AMINO-PYRIMIDONYL DERIVATIVES, A PROCESS FOR THEIR

PREPARATION AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM

The present invention relates to new amino -pyrimidonyl derivatives, to a process for their preparation and to pharmaceutical compositions containing them.

The compounds of the present invention are new and have very valuable pharmacological characteristics in the field of apoptosis and oncology.

Ubiquitination is a process controlling essential cellular functions such as protein turnover and homeostasis, protein activation and localisation. Ubiquitin is a 76 amino acids polypeptide which is covalently attached to postranslationnaly modified protein substrates via an isopeptide bond. Deubiquinating enzymes (DUBs) are in majority cysteine proteases that cleave the ubiquitin-ubiquitin bond or ubiquitin-protein bond at the Cter glycine of Ubiquitin. Approximately 100 DUBs regulate the thousands ubiquitinated proteins and then some redundancy of deubiquitinase substrates regulation are observed.

Dysregulation of DUBs have been associated with several diseases such as neurodegenerative and infectious diseases (Edelman et al, Expert Rev. Mol. Med. 2011, 13, 1-17) and human malignancies (Pal et al, Cancer Res. 2014, 74, 4955-4966). Accordingly, overexpression of DUBs or increase of their activity have been associated to numerous types of cancers (Luise et al, Plos One 2011, 6, el589l; Rolen et al, Mol. Carcinog. 2006, 45, 260-269) and poor prognosis.

Ubiquitin Specific Protease 7 (USP7), also known as Herpes-virus-Associated Ubiquitin- Specific Protease (HAUSP), belongs to the deubiquitinating family. USP7 has been reported to stabilize numerous oncogenes involved in survival and proliferations via cell cycle progression, apoptosis, DNA repair, DNA replication and epigenetic factors regulation (Nicholson et al, Cell Biochem. Biophys. 2011, 60, 61-68). In addition, USP7 has been shown to regulate immune response via inflammation and Treg modulation (Van Loosdregt et al, Immunity 2013, 39, 259-27; Colleran et al, Proc. Natl. Acad. Sci. USA 2013, 110, 618-623; Wang et al, EBio Medicine 2016, 99-112; Wang et al, PLoS One 2017, 12, e0l8977). USP7 has also been implicated in other pathologic states such as neurodevelopmental disorder (Hao et al, Mol. Cell 2015, 59, 956-969) and viral infection (Holowaty et al, Biochem. Soc. Trans. 2004, 32, 731-732).

USP7 overexpression has been associated with late stages of cancers and poor prognosis in lung, neuroblastoma, myeloma, prostate, colon and breast cancers. Numerous USP7 inhibitors have been recently published in the literature (Turnbull et al, Nature 2017, 550, 481-486; Kategaya et al., Nature 2017, 550, 534-538; Gavory et al., Nat. Chem. Biol. 2018, 14, 118-125; O’Dowd et al, ACS Med. Chem. Lett. 2018, 9, 238-243; Pozhidaeva et al, Cell Chem. Biol. 2017, 24, 1501-1512; Lamberto et al, Cell Chem. Biol. 2017, 24, 1490- 1500) and, particularly, pyrimidonyl derivatives claimed as USP7 inhibitors have been disclosed in PCT/GB2017/053175. However, PCT/GB2017/053175 shows that 5,6- disubstituted pyrimidonyl derivatives provide compounds with weakest affinity on USP7. Despite an intense research in the field, no USP7 inhibitors have entered the clinic (Kemp et al, Progress in Medicinal Chemistry 2016, 55, 149-192; Wu et al, J. Med. Chem. 2018, 61, 422-443). There is, therefore, a therapeutic need for compounds that inhibit the activity of the protein USP7.

In addition to being new and very potent on their target, the compounds of the present invention have pro-apoptotic and/or anti-proliferative properties making it possible to use them in pathologies involving a defect in apoptosis, such as, for example, in the treatment of cancer and of immune and auto-immune diseases. The present invention relates more especially to compounds of formula (I):

wherein:

¨ J represents an oxygen atom or a sulphur atom,

¨ Ri represents a cycloalkyl group, a heterocycloalkyl group, an aryl group, or a heteroaryl group, ¨ R ₂ represents a hydrogen atom, a halogen atom, a hydroxy group, or a linear or branched (Ci-C ₆ )alkoxy group,

¨ R ₃ represents a hydrogen atom, a halogen atom, a linear or branched (Ci-C ₆ )alkyl group, a linear or branched (C2-C ₆ )alkenyl group, a linear or branched (C2-C ₆ )alkynyl group, a linear or branched (C2-C ₆ )alkynyl-R7 group, a cycloalkyl group, an aryl group, a heteroaryl group, an aryl(Ci-C ₆ )alkyl group, or a heteroaryl(Ci-C6)alkyl group,

¨ R4 represents a hydrogen atom or a halogen atom,

¨ R5 represents a hydrogen atom, a linear or branched (Ci-C ₆ )alkyl group, a linear or branched halo(Ci-C6)alkyl group, or an aryl(Ci-C ₆ )alkyl group,

¨ R6 represents an aryl group or a heteroaryl group,

¨ R ₇ represents a cycloalkyl group, an aryl group, a heteroaryl group, or a -Yi-OR’ group,

¨ n is an integer equal to 0, 1 or 2,

¨ means a single bond or a double bond, it being understood that:

-“aryl” means a phenyl, naphthyl, or indanyl group,

-“heteroaryl” means any mono- or fused bi-cyclic group composed of from 5 to 10 ring members, having at least one aromatic moiety and containing from 1 to 3 heteroatoms selected from oxygen, sulphur and nitrogen,

-“cycloalkyl” means any mono- or fused bi-cyclic non-aromatic carbocyclic group containing from 3 to 7 ring members,

-“heterocycloalkyl” means any non-aromatic mono- or fused bi-cyclic group containing from 3 to 10 ring members, and containing from 1 to 3 heteroatoms selected from oxygen, sulphur and nitrogen, it being possible for the aryl, heteroaryl, cycloalkyl and heterocycloalkyl groups so defined to be substituted by from 1 to 4 groups selected from linear or branched (Ci-C ₆ )alkyl, linear or branched (C2-C ₆ )alkenyl, linear or branched (C2-C ₆ )alkynyl, linear or branched halo(Ci-C ₆ )alkyl, -Y ₂ -OR’, -Y ₂ -NR’R”, -Y ₂ -S(0) _m -R’, oxo (or N- oxide where appropriate), pentafluorosulfide, nitro, -Y ₂ -CN, -C(0)-R’, -C(0)-OR’, -0-C(0)-R’, -Y ₂ -C(0)-NR’R”, -Y ₂ -NR’-C(0)-R”, -Y ₂ -NR’-C(0)-0R”, halogen, cyclopropyl and - Y ₂ -heterocycloalkyl, it being understood that:

- Yi and Y ₂ independently of one another represent a bond, a linear or branched (Ci-C ₄ )alkylene group, or a linear or branched halo(Ci-C ₄ )alkylene group,

- R’ and R” independently of one another represent a hydrogen atom, a linear or branched (Ci-C ₆ )alkyl group, a linear or branched (C ₂ -C ₆ )alkenyl group, a linear or branched (C ₂ -C ₆ )alkynyl group, a linear or branched (Ci-C ₆ )alkoxy group, a linear or branched halo(Ci-C ₆ )alkyl, a linear or branched hydroxy(Ci-C ₆ )alkyl group, a linear or branched (Ci-C ₆ )alkoxy(Ci-C ₆ )alkyl group, a formyl group, a phenyl group, a benzyl group, a cyclopropyl group, a cyclopropylmethyl group,

or the pair (R’, R”) form together with the nitrogen atom carrying them a non aromatic ring composed of from 5 to 7 ring members, which may contain in addition to the nitrogen a second heteroatom selected from oxygen and nitrogen, it being understood that the nitrogen in question may be substituted by from 1 to 2 groups representing a hydrogen atom, or a linear or branched (Ci-C ₆ )alkyl group,

- m is an integer equal to 0, 1 and 2, their enantiomers, diastereoisomers, and addition salts thereof with a pharmaceutically acceptable acid or base.

In a preferred embodiment of the invention, the present invention relates to compounds of formula (I) wherein:

¨ Ri represents an aryl group or a heteroaryl group,

¨ R ₂ represents a halogen atom, a hydroxy group or a linear or branched (Ci-C ₆ )alkoxy group,

¨ R ₃ represents a halogen atom, a linear or branched (Ci-C ₆ )alkyl group, a linear or branched (C ₂ -C ₆ )alkynyl group, a linear or branched (C ₂ -C ₆ )alkynyl-R ₇ group, an aryl group, an aryl(Ci-C ₆ )alkyl group, or a heteroaryl(Ci-C ₆ )alkyl group,

¨ R ₄ represents a hydrogen atom or a halogen atom,

¨ R ₅ represents a hydrogen atom, a linear or branched (Ci-C ₆ )alkyl group, a linear or branched halo(Ci-C ₆ )alkyl group, or an aryl(Ci-C ₆ )alkyl group,

¨ R ₆ represents an aryl group,

¨ R ₇ represents a cycloalkyl group, an aryl group, or a heteroaryl group, it being possible for the aryl and heteroaryl groups so defined to be substituted by from 1 to 4 groups selected from linear or branched (Ci-C ₆ )alkyl, linear or branched halo(Ci-C ₆ )alkyl, -Y ₂ -OR’, -Y ₂ -NR’R”, pentafluorosulfide, -Y ₂ -CN, -C(0)-R’,

-C(0)-OR’, -Y ₂ -C(0)-NR’R”, halogen and -Y ₂ -heterocycloalkyl, it being understood that Y ₂ is as defined for formula (I) and R’ and R” independently of one another represent a hydrogen atom, a linear or branched (Ci-C ₆ )alkyl group, a linear or branched halo(Ci-C ₆ )alkyl, a linear or branched hydroxy(Ci-C ₆ )alkyl group, a formyl group, a phenyl group, a benzyl group, or a cyclopropyl group,

or the pair (R’, R”) form together with the nitrogen atom carrying them a non-aromatic ring composed of from 5 to 7 ring members, which may contain in addition to the nitrogen a second heteroatom selected from oxygen and nitrogen, it being understood that the nitrogen in question may be substituted by from 1 to 2 groups representing a hydrogen atom or a linear or branched (Ci-C ₆ )alkyl group.

Among the pharmaceutically acceptable acids there may be mentioned, without implying any limitation, hydrochloric acid, hydrobromic acid, sulphuric acid, phosphonic acid, acetic acid, trifluoroacetic acid, lactic acid, pyruvic acid, malonic acid, succinic acid, glutaric acid, fumaric acid, tartaric acid, maleic acid, citric acid, ascorbic acid, oxalic acid, methanesulphonic acid, camphoric acid etc.

Among the pharmaceutically acceptable bases there may be mentioned, without implying any limitation, sodium hydroxide, potassium hydroxide, triethylamine, fc/ -butylaminc etc.

Among the heteroaryl groups there may be mentioned, without implying any limitation, pyrrolyl, furyl, thienyl, thiazolyl, isothiazolyl, oxazolyl, isoxazolyl, pyrazolyl, imidazolyl, pyridinyl, pyrazinyl, pyridazinyl, pyrimidinyl, pyridinonyl, indolyl, dihydro indolyl, dihydroisoindolyl, indazolyl, dihydrocyclopentathienyl, benzothienyl, tetrahydrobenzo thienyl, benzofuranyl, imidazopyridinyl, imidazopyrazinyl, benzotriazolyl, benzodioxolyl, dihydrobenzodioxinyl, quinolinyl, isoquinolinyl, tetrahydroquinolinyl, tetrahydroisoquinolinyl, quinoxalinyl, dihydroquinoxalinyl, dihydrothienodioxinyl, quinazolinonyl, pyrrolopyridazinyl, pyrazolopyrazinyl, pyrrolopyridinyl, dihydropyrrolizinyl, tetrahydroindolizinyl, etc.

Among the cycloalkyl groups there may be mentioned, without implying any limitation, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, etc.

Among the heterocycloalkyl groups there may be mentioned, without implying any limitation, pyrrolidinyl, tetrahydropyranyl, piperidinyl, piperazinyl, morpholinyl, etc. Advantageously, the compounds of formula (I) display a trans configuration as follows:

or

Preferably, the compounds of formula (I) display a trans configuration as follows:

In another embodiment, when R ₄ represents a halogen atom and n is an integer equal to 1 or 2, a new asymmetric carbon can be created providing two possible isomers as follows:

Preferably, when R ₄ represents a halogen atom and n is an integer equal to 2, having the following formula: the preferred isomer has the ^-configuration as follows:

Preferably, is a single bond. J advantageously represents an oxygen atom.

Ri preferably represents an aryl group or a heteroaryl group. More preferably, Ri represents a phenyl group, an indanyl group, a benzodioxolyl group, a tetrahydroisoquinolyl group, an isoindolinyl group, an indazolyl group, a thiazolyl group, a pyridinyl group, a pyrrolopyridinyl group or a pyrimidinyl group. Even more preferably, Ri represents a phenyl group. In a preferred embodiment of the invention, Ri represents a phenyl group which is substituted by from 1 to 2 groups selected from linear or branched (Ci-C ₆ )alkyl; linear or branched halo(Ci-C ₆ )alkyl; -Y ₂ -OR’; -Y ₂ -NR’R”; pentafluorosulfide; -Y ₂ -CN; -C(0)-R’; -C(0)-OR’ wherein R’ represents a linear or branched (Ci-C ₆ )alkyl; -Y ₂ -C(0)-NR’R”; halogen; and -Y ₂ -heterocyclo alkyl. In another preferred embodiment of the invention, Ri represents a phenyl group which is substituted by from 1 to 2 groups selected from linear or branched (Ci-C ₆ )alkyl, linear or branched halo(Ci-C ₆ )alkyl, -Y ₂ -OR’, -Y ₂ -NR’R”, -Y ₂ -CN, -C(0)-R’, halogen and

-Y ₂ -heterocycloalkyl. More advantageously, Ri represents a phenyl group which is substituted by from 1 to 2 groups selected from -Y ₂ -OR’, -Y ₂ -NR’R”, halogen, pyrrolidinyl, -Y2-piperidinyl and -Y2-morpholinyl. Even more advantageously, Ri represents a phenyl group which is substituted by from 1 to 2 groups selected from hydroxy, methoxy, -Y ₂ -NR’R”, fluorine, chlorine, pyrrolidinyl and piperidinyl.

R ₂ preferably represents a halogen atom, a hydroxy group, or a linear or branched (Ci-C ₆ )alkoxy group. More preferably, R ₂ represents a fluorine atom, a hydroxy group, or a methoxy group. Even more preferably, R ₂ represents a fluorine atom.

R ₃ preferably represents a halogen atom, a linear or branched (Ci-C ₆ )alkyl, a linear or branched (C2-C ₆ )alkynyl group, a linear or branched (C2-C ₆ )alkynyl-R7 group, an aryl group, an aryl(Ci-C ₆ )alkyl group, or a heteroaryl(Ci-C ₆ )alkyl group. More preferably, R ₃ represents a fluorine atom; a phenyl group; a benzyl group; a -CºCH group; a -CºC-R ₇ group wherein R ₇ represents a cycloalkyl group, an aryl group or a heteroaryl group; or a heteroaryl(Ci-C ₆ )alkyl group wherein the heteroaryl ring is selected from pyridinyl, pyrimidinyl, pyrazinyl, pyridazinyl, thiazolyl or imidazolyl. Even more preferably, R ₃ represents a fluorine atom; a phenyl group; a benzyl group; a -CºC-R ₇ group wherein R ₇ represents a cycloalkyl group, an aryl group or a heteroaryl group; or a heteroaryl(Ci-C ₆ )alkyl group wherein the heteroaryl ring is selected from pyridinyl, pyrimidinyl, pyrazinyl, pyridazinyl, thiazolyl or imidazolyl. In another preferred embodiment, R ₃ represents a fluorine atom. In another preferred embodiment, R ₃ represents a -CºC-R ₇ group wherein R ₇ represents a cyclopropyl group, a phenyl group, a imidazolyl group, a pyridinyl group, a pyrimidinyl group, a pyrazinyl group, or a pyridazinyl group. In another preferred embodiment, R ₃ represents a -CºC-R ₇ group wherein R ₇ represents a heteroaryl group selected from imidazolyl, pyridinyl, pyrimidinyl, pyrazinyl or pyridazinyl. In another preferred embodiment, R ₃ represents a -CºC-R ₇ group wherein R ₇ represents a pyridinyl group, a pyrimidinyl group, a pyrazinyl group, or a pyridazinyl group.

Advantageously, R ₂ and R ₃ are geminal groups. More advantageously, R ₂ and R ₃ are geminal groups and R ₂ and R ₃ represent a fluorine atom (also called a gem-difluoro group). In another preferred embodiment, R ₂ and R ₃ are geminal groups wherein R ₂ represents a halogen atom or a linear or branched (Ci-C ₆ )alkoxy group and R ₃ represents a -CºC-R ₇ group wherein R ₇ represents a heteroaryl group selected from imidazolyl, pyridinyl, pyrimidinyl, pyrazinyl or pyridazinyl.

More preferably, R ₂ and R ₃ are geminal groups wherein R ₂ represents a halogen atom, more preferably a fluorine atom, and R ₃ represents a -CºC-R ₇ group wherein R ₇ represents a pyridinyl group, a pyrazinyl group or a pyridazinyl group.

In another preferred embodiment, R ₂ and R ₃ are geminal groups wherein R ₂ represents a linear or branched (Ci-C ₆ )alkoxy group, more preferably a methoxy group, and R ₃ represents a -CºC-R ₇ group wherein R ₇ represents a pyridinyl group, a pyrimidinyl group, a pyrazinyl group or a pyridazinyl group.

Advantageously, R ₄ represents a hydrogen atom or a fluorine atom. More preferably, R ₄ represents a hydrogen atom. In another embodiment, when R ₄ represents a fluorine atom and n is equal to 2, both fluorine atoms preferably represent a gem-difluoro group.

Preferably, R ₅ represents a hydrogen atom.

R ₆ preferably represents an aryl group or a heteroaryl group selected from pyridinyl, thienyl, oxazolyl, pyrazolyl, thiazolyl, or furyl. More preferably, R ₆ represents an aryl group, even more preferably, a phenyl group.

R ₇ preferably represents a cycloalkyl group, an aryl group, or a heteroaryl group. More preferably, R ₇ represents a cyclopropyl group, a phenyl group, a imidazolyl group, a pyridinyl group, a pyrimidinyl group, a pyrazinyl group, or a pyridazinyl group. Even more preferably, R ₇ represents an imidazolyl group, a pyridinyl group, a pyrimidinyl group, a pyrazinyl group, or a pyridazinyl group. More advantageously, R ₇ represents a pyridinyl group, a pyrimidinyl group, a pyrazinyl group, or a pyridazinyl group. In another preferred embodiment, R ₇ represents a cycloalkyl group, an aryl group, or a heteroaryl group which is substituted by from 1 to 2 groups selected from halogen atom, linear or branched (Ci-C ₆ )alkyl group, linear or branched (Ci-C ₆ )alkoxy group, or amino group. More preferably, R ₇ represents a cycloalkyl group, an aryl group, or a heteroaryl group which is substituted by from 1 to 2 groups selected from a fluorine atom, a methyl group, a methoxy group, or an ammo group.

In a preferred embodiment of the invention, the present invention relates to compounds of formula (I-a):

wherein Ri, R ₂ , R3, R4 and n are as defined for formula (I).

In a preferred embodiment of the invention, the present invention relates to compounds of formula (I-a):

wherein Ri represents a phenyl group which may be substituted by from 1 to 2 groups selected from linear or branched (Ci-C ₆ )alkyl, linear or branched halo(Ci-C ₆ )alkyl, -Y ₂ -OR’, -Y ₂ -NR’R”, pentafluorosulfide, -Y ₂ -CN, -C(0)-R’, -C(0)-OR’ wherein R’ represents a linear or branched (Ci-C ₆ )alkyl, -Y ₂ -C(0)-NR’R”, halogen and -Y ₂ -heterocycloalkyl, and R ₂ , R3, R ₄ and n are as defined for formula (I). In a more preferred embodiment of the invention, the present invention relates to compounds of formula (I-a):

wherein Ri represents a phenyl group which may be substituted by from 1 to 2 groups selected from -Y ₂ -OR’, -Y ₂ -NR’R”, halogen, pyrrolidinyl, -Y ₂ -piperidinyl and -Y ₂ -morpholinyl, and R ₂ , R ₃ , R ₄ and n are as defined for formula (I).

Among the preferred compounds of the invention there may be mentioned:

5-amino-3-[[l-[(lR,2R)-4,4-difluoro-2-phenyl-cyclohexanecarb onyl]-4-hydroxy-4- piperidyljmethyl] -6-(3 -hydroxy-5 -methoxy-phenoxy)pyrimidin-4-one;

- 5-amino-3-( { 1 -[(li?,2i?)-4,4-difluoro-2-phenylcyclohexane- 1 -carbonyl]-4- hydroxypipcridin-4-yl [methyl )-6-[4-(pyrrolidin-2-yl)phcnoxy]pyri midi n-4(3//)- one;

5-amino-3-( { 1 -[(li?,2i?)-4,4-difluoro-2-phenylcyclohexane- 1 -carbonyl]-4- hydroxypipcridin-4-yl [methyl )-6-(4-fluoro-3-hydroxyphcnoxy )pyri midi n-4(3//)- one;

5-amino-3-[[ 1 -[( 1 ?,2 ?)-4,4-difluoro-2-phcnyl-cyclohcxanccarbonyl]-4-hydroxy-4- piperidyl]methyl]-6-[3-(2-piperidyl)phenoxy]pyrimidin-4-one;

5-amino-6-[4-( 1 -aminocthyl)phcnoxy]-3-( [ 1 -[( 1 /?,2/?)-4,4-difluoro-2- phenylcyclo hexane- l-carbonyl]-4-hydroxypiperidin-4-yl}methyl)pyrimidin-4(3 )- one;

5-amino-6-[4-(aminomethyl)phenoxy]-3-({l-[(li?,2i?)-4,4-difl uoro-2- phenylcyclo hexane- l-carbonyl]-4-hydroxypiperidin-4-yl}methyl)pyrimidin-4(3 )- one; 5-amino-3-( { 1 -[( 1 /?,2/?)-4,4-difluoro-2-phcnylcyclohcxanc- 1 -carbonyl]-4- hydroxypiperidin-4-yl}methyl)-6-{4-[(methylamino)methyl]phen oxy}pyrimidin-

4(3 )-one;

5 -amino-6- [3 -(aminomethyl)phenoxy] -3 -( { 1 - [( li?,2i?)-4,4-difluoro-2- phenylcyclo hexane- l-carbonyl]-4-hydroxypiperidin-4-yl}methyl)pyrimidin-4(3 )- one;

5-amino-3-[[l-[(lR,2R)-4,4-difluoro-2-phenyl-cyclohexanecarb onyl]-4-hydroxy-4- piperidyljmethyl] -6-(3 -hydroxyphenoxy)pyrimidin-4-one;

5-amino-6-[4-(aminomethyl)-3-fluorophenoxy]-3-({l-[(li?,2 i?)-4,4-difluoro-2- phenylcyclo hexane- l-carbonyl]-4-hydroxypiperidin-4-yl}methyl)pyrimidin-4(3 )- one;

5-amino-6-[4-(aminomethyl)-3-chlorophenoxy]-3-({l-[(li?,2i?) -4,4-difluoro-2- phenylcyclo hexane- l-carbonyl]-4-hydroxypiperidin-4-yl}methyl)pyrimidin-4(3 )- one;

5-amino-6- {4-[(/er/-butylamino)methyl]phenoxy} -3-( { 1 -[( 1 /?,2/?)-4,4-difluoro-2- phenylcyclo hexane- l-carbonyl]-4-hydroxypiperidin-4-yl}methyl)pyrimidin-4(3 )- one;

5-amino-6-[4-(aminomethyl)phenoxy]-3-( {(45)- 1 -[(li?,2i?)-4,4-difluoro-2- phenylcyclo hexane- 1 -carbonyl] -3, 3-difluoro-4-hydroxypiperidin-4- yl}methyl)pyrimidin-4(3 )-one;

5-amino-3-( {(45)- 1 -[(li?,2i?)-4,4-difluoro-2-phenylcyclohexane- 1 -carbonyl]-3,3- difluoro-4-hydroxypipcridin-4-yl [methyl )-6-(3-hydroxyphcnoxy)pyri midi n-4(3 /)- one;

5-amino-3-( {(4S)- 1 -[(lR,2R)-4, 4-difluoro-2-phenylcyclo hexane- 1 -carbonyl]-3, 3- difluoro-4-hydroxypiperidin-4-yl}methyl)-6-(4-fluoro-3- hydroxyphenoxy)pyrimidin-4(3H)-one;

5-amino-3-( { 1 -[(lR,2R)-4,4-difluoro-2-phenylcyclohexane- 1 -carbonyl]-4- hydroxypiperidin-4-yl}methyl)-6-[4-(piperidin-2-yl)phenoxy]p yrimidin-4(3H)-one;

5-amino-3-[(l-{[(lR,2R,4R)-4-fluoro-2-phenyl-4-[2-(pyridi n-3- yl)ethynyl]cyclohexyl]carbonyl}-4-hydroxypiperidin-4-yl)meth yl]-6-(4- fluorophenoxy)pyrimidin-4-one; 5-amino-3-[(l-{[(li?,2i?,4i?)-4-fluoro-2-phenyl-4-[2-(pyridi n-2- yl)ethynyl]cyclohexyl]carbonyl}-4-hydroxypiperidin-4-yl)meth yl]-6-(4- fluorophenoxy)pyrimidin-4-one;

5-amino-3-[(l-{[(lR,2R,4R)-4-fluoro-4-[2-(5-fluoropyridin-2- yl)ethynyl]-2- phenylcyclohexyl]carbonyl}-4-hydroxypiperidin-4-yl)methyl]-6 -(4- fluorophenoxy)pyrimidin-4-one;

5-amino-3-({l-[(lR,2R,4S)-4-fluoro-2-phenyl-4-[2-(pyrazin-2- yl)ethynyl]cyclohexanecarbonyl]-4-hydroxypiperidin-4-yl}meth yl)-6-(4- fluorophenoxy ) -3,4- dihy dropyrimidin- 4 - one ;

5-amino-3-({l-[(lR,2R,4R)-4-fluoro-2-phenyl-4-[2-(pyrazin -2- yl)ethynyl]cyclohexanecarbonyl]-4-hydroxypiperidin-4-yl}meth yl)-6-(4- fluorophenoxy ) -3,4- dihy dropyrimidin- 4 - one ;

5-amino-6-(4-fluorophenoxy)-3-[(4-hydroxy-l-{[(lR,2R,4R)-4-m ethoxy-2-phenyl-

4- [2-(pyrimidin-5 -yl)ethynyl]cyclo hexyl] carbonyl } piperidin-4- yl)methyl]pyrimidin-4-one;

5-amino-3-[(l-{[(lR,2R,4R)-4-fluoro-2-phenyl-4-[2-(pyridazin -3- yl)ethynyl]cyclohexyl]carbonyl}-4-hydroxypiperidin-4-yl)meth yl]-6-(4- fluorophenoxy)pyrimidin-4-one;

5-amino-6-(4-fluorophenoxy)-3-[(4-hydroxy-l-{[(lR,2R,4R)-4-m ethoxy-2-phenyl-

4-[2-(pyridazin-3-yl)ethynyl]cyclohexyl]carbonyl}piperidi n-4- yl)methyl]pyrimidin-4-one;

5-amino-6-(4-fluorophenoxy)-3-( {4-hydroxy- l-[(lR,2R, 4R)-4-methoxy-2-phenyl-

4-[2-(pyrazin-2-yl)ethynyl]cyclohexanecarbonyl]piperidin- 4-yl}methyl)-3,4- dihydropyrimidin-4-one;

5-amino-3-({l-[(lR,2R,4R)-4-fluoro-4-[2-(4-fluoropyridin-2-y l)ethynyl]-2- pheny lcyclo hexanecarbony 1] 4 hy droxypiperidin- 4-yl} methyl) - 6 - (4 - fluorophenoxy ) -3,4- dihy dropyrimidin- 4 - one ;

5-amino-3-{[(4S)-3,3-difluoro-l-[(lR,2R,4R)-4-fluoro-4-[2-(6 -methylpyridazin-3- yl)ethynyl] -2-phenylcyclohexanecarbonyl] -4-hydroxypiperidin-4-yl]methyl} -6-(4- fluorophenoxy ) -3,4- dihy dropyrimidin- 4 - one ; 5-amino-3-{[(4S)-3,3-difluoro-4-hydroxy-l-{[(lR,2R,4R)-4-met hoxy-2-phenyl-4-

[2-(pyridazin-3-yl)ethynyl]cyclohexyl]carbonyl}piperidin- 4-yl]methyl}-6-(4- fluorophenoxy)pyrimidin-4-one;

5-amino-3-{[(4S)-3,3-difluoro-4-hydroxy-l-[(lR,2R,4R)-4-meth oxy-2-phenyl-4- [2-(pyridin-2-yl)ethynyl]cyclohexanecarbonyl]piperidin-4-yl] methyl}-6-(4- fluorophenoxy ) -3,4- dihy dropyrimidin- 4 - one ;

5-amino-3-{[(4S)-3,3-difluoro-l-{[(lR,2R,4R)-4-fluoro-2-phen yl-4-[2-(pyridazin-

3-yl)ethynyl]cyclohexyl]carbonyl}-4-hydroxypiperidin-4-yl ]methyl}-6-(4- fluorophenoxy)pyrimidin-4-one;

- 5-amino-3-{[(4S)-3,3-difluoro-4-hydroxy-l-[(lR,2R,4R)-4-meth oxy-4-[2-(5- methylpyridazin-3-yl)ethynyl]-2-phenylcyclohexanecarbonyl]pi peridin-4- y ljmethy 1 } - 6 - (4 - fluorophenoxy ) -3,4- dihy dropyrimidin- 4 - one ;

5-amino-3-{[(4S)-3,3-difluoro-l-[(lR,2R,4R)-4-fluoro-4-[2-(5 -methylpyridazin-3- yl)ethynyl] -2-phenylcyclohexanecarbonyl] -4-hydroxypiperidin-4-yl]methyl} -6-(4- fluorophenoxy) -3 ,4-dihydropyrimidin-4-one;

5-amino-3-{[(4S)-3,3-difluoro-4-hydroxy-l-[(lR,2R,4R)-4-meth oxy-4-[2-(5- methoxypyridazin-3-yl)ethynyl]-2-phenylcyclohexanecarbonyl]p iperidin-4- y ljmethy 1 } - 6 - (4 - fluorophenoxy) -3,4- dihy dropyrimidin- 4 - one ;

5-amino-3-{[(4S)-3,3-difluoro-4-hydroxy-l-[(lR,2R,4R)-4-meth oxy-2-phenyl-4- [2-(pyrimidin-5-yl)ethynyl]cyclohexanecarbonyl]piperidin-4-y l]methyl}-6-(4- fluorophenoxy ) -3,4- dihy dropyrimidin- 4 - one .

The invention relates also to a process for the preparation of compounds of formula (I), which process is characterized in that there is used as starting material the compound of formula (II):

wherein R ₄ and n are as defined for formula (I), which is subjected to coupling with a compound of formula (III):

wherein R ₂ , R3 and R ₆ are as defined for formula (I), to yield the compound of formula (IV):

wherein R ₂ , R ₃ , R ₄ , Re and n are as defined hereinbefore, compound of formula (IV) which is further converted to compound of formula (V):

wherein R ₂ , R ₃ , R ₄ , R ₆ and n are as defined hereinbefore, compound of formula (V) which is further subjected to coupling with compound of formula (VI): wherein Ri, R ₅ and J are as defined for formula (I), to yield the compound of formula (I), which may then be purified according to a conventional separation technique, which is converted, if desired, into its addition salts with a pharmaceutically acceptable acid or base and which is optionally separated into its isomers according to a conventional separation technique,

it being understood that at any moment considered appropriate during the course of the process described above, some groups (hydroxy, amino...) of the starting reagents or of the synthesis intermediates can be protected, subsequently deprotected and functionalized, as required by the synthesis.

In another embodiment of the invention, compounds of formula (I) may be obtained using an alternative process, which process is characterized in that there is used as starting material the compound of formula (VII):

wherein R ₄ and n are as defined for formula (I) and PG represents a protecting group of the amine function, which is further converted to compound of formula (VIII):

wherein R ₄ , PG and n are as defined hereinbefore, compound of formula (VIII) which is subjected to coupling with compound of formula (VI):

wherein Ri, R ₅ and J are as defined for formula (I), to yield the compound of formula (IX):

wherein Ri, R4, R ₅ , J, PG and n are as defined for formula (I), which is further subjected, after removing the protecting group of the amine function, to coupling with a compound of formula (III):

wherein R ₂ , R3 and R ₆ are as defined for formula (I), to yield the compound of formula (I), which may then be purified according to a conventional separation technique, which is converted, if desired, into its addition salts with a pharmaceutically acceptable acid or base and which is optionally separated into its isomers according to a conventional separation technique,

it being understood that at any moment considered appropriate during the course of the process described above, some groups (hydroxy, amino...) of the starting reagents or of the synthesis intermediates can be protected, subsequently deprotected and functionalized, as required by the synthesis.

The compounds of formulae (II), (III), (VI) and (VII) are either commercially available or can be obtained by the person skilled in the art using conventional chemical reactions described in the literature. Pharmacological studies of the compounds of the invention have shown pro-apoptotic and/or anti-proliferative properties. The ability to reactivate the apoptotic process in cancerous cells is of major therapeutic interest in the treatment of cancers and of immune and auto-immune diseases.

Among the cancer treatments envisaged there may be mentioned, without implying any limitation, treatment of cancers of the bladder, brain, breast and uterus, chronic lymphoid leukemia, cancer of the colon, esophagus and liver, lymphoblastic leukemia, acute myeloid leukemia, lymphomas, melanomas, malignant haemopathies, myelomas, ovarian cancer, non-small-cell lung cancer, prostate cancer, pancreatic cancer and small-cell lung cancer. More especially, the compounds according to the invention will be useful in the treatment of chemo-, targeted therapy- or radio -resistant cancers.

The present invention relates also to pharmaceutical compositions comprising at least one compound of formula (I) in combination with one or more pharmaceutically acceptable excipients. In particular, these pharmaceutical compositions are interesting for use as pro- apoptotic and/or anti-proliferative agents, particularly, in the treatment of cancers and of auto-immune and immune system diseases. Preferably, these pharmaceutical compositions can be used in the treatment of cancers of the bladder, brain, breast and uterus, chronic lymphoid leukemia, cancer of the colon, esophagus and liver, lymphoblastic leukemia, acute myeloid leukemia, lymphomas, melanomas, malignant haemopathies, myelomas, ovarian cancer, non-small-cell lung cancer, prostate cancer, pancreatic cancer and small cell lung cancer.

Among the pharmaceutical compositions according to the invention there may be mentioned more especially those that are suitable for oral, parenteral, nasal, per- or trans-cutaneous, rectal, perlingual, ocular or respiratory administration, especially tablets or dragees, sublingual tablets, sachets, paquets, capsules, glossettes, lozenges, suppositories, creams, ointments, dermal gels, and drinkable or injectable ampoules.

The pharmaceutical compositions according to the invention comprise one or more excipients or carriers selected from diluents, lubricants, binders, disintegration agents, stabilisers, preservatives, absorbents, colorants, sweeteners, flavourings etc.

By way of non-limiting example there may be mentioned:

¨ as diluents : lactose, dextrose, sucrose, mannitol, sorbitol, cellulose, glycerol,

¨ as lubricants : silica, talc, stearic acid and its magnesium and calcium salts, polyethylene glycol,

¨ as binders magnesium aluminium silicate, starch, gelatin, tragacanth, methylcellulose, sodium carboxymethylcellulose and polyvinylpyrrolidone,

¨ as disintegrants: agar, alginic acid and its sodium salt, effervescent mixtures.

The dosage varies according to the sex, age and weight of the patient, the administration route, the nature of the therapeutic indication, or of any associated treatments, and ranges from 0.01 mg to 1 g per 24 hours in one or more administrations.

Furthermore, the present invention relates also to the combination of a compound of formula (I) with anti-cancer agents selected from genotoxic agents, mitotic poisons, anti metabolites, proteasome inhibitors, kinase inhibitors, protein-protein interaction inhibitors, immunomodulators, E3 ligase inhibitors, chimeric antigen receptor T-cell therapy and antibodies, and also to pharmaceutical compositions comprising that type of combination and their use in the manufacture of medicaments for use in the treatment of cancers, particularly, cancers of the bladder, brain, breast and uterus, chronic lymphoid leukemia, cancer of the colon, esophagus and liver, lymphoblastic leukemia, acute myeloid leukemia, lymphomas, melanomas, malignant haemopathies, myelomas, ovarian cancer, non-small- cell lung cancer, prostate cancer, pancreatic cancer and small-cell lung cancer.

The combination of a compound of formula (I) with an anticancer agent may be administered simultaneously or sequentially. The administration route is preferably the oral route, and the corresponding pharmaceutical compositions may allow the instantaneous or delayed release of the active ingredients. The compounds of the combination may moreover be administered in the form of two separate pharmaceutical compositions, each containing one of the active ingredients, or in the form of a single pharmaceutical composition, in which the active ingredients are in admixture.

The compounds of formula (I) may also be used in combination with radiotherapy in the treatment of cancer.

The following Preparations and Examples illustrate the invention but do not limit it in any way.

General Procedures for Preparations R2a-R2ce, R3a-R3ce, R4a-R4ce, R5a-R51 and EXAMPLES 1 to 90 and 104 to 121 All reagents obtained from commercial sources were used without further purification. Anhydrous solvents were obtained from commercial sources and used without further drying.

Flash chromatography was performed on ISCO CombiFlash Rf 200i with pre-packed silica-gel cartridges (RediSb/?®i?f Gold High Performance). Thin layer chromatography was conducted with 5 x 10 cm plates coated with Merck Type 60 F254 silica-gel. Microwave heating was performed in an Anton Parr MonoWave or CEM Discover® instrument.

Preparative HPLC purifications were performed on an HANBON NP7000 Liquid Chromatography system with a Gemini-NX® 5 pm Cl 8, 250 mm x 50 mm i.d. column running at a flow rate of 99.9 mL x min ¹ with UV diode array detection (210-400 nm) using 5 mM aqueous NH4HCO3 solution and MeCN as eluents unless specified otherwise.

Chiral Chromatography was performed on Daicel columns in the mixture of heptane and alcohols.

Analytical LC-MS: The compounds of the present invention were characterized by high performance liquid chromatography-mass spectroscopy (HPLC-MS) on Agilent HP 1200 with Agilent 6140 quadrupole LC/MS, operating in positive or negative ion electrospray ionisation mode. Molecular weight scan range is 100 to 1350. Parallel UV detection was done at 210 nm and 254 nm. Samples were supplied as a 1 mM solution in acetonitrile, or in THF/H2O (1 :1) with 5 pL loop injection. LCMS analyses were performed on two instruments, one of which was operated with basic, and the other with acidic eluents.

Basic LCMS: Gemini-NX, 3 pm, Cl 8, 50 mm x 3.00 mm i.d. column at 23 °C, at a flow rate of 1 mL x min ¹ using 5 mM ammonium bicarbonate (Solvent A) and acetonitrile (Solvent B) with a gradient starting from 100 % Solvent A and finishing at 100 % Solvent B over various/certain duration of time. Acidic LCMS: ZORBAX Eclipse XDB-C18, 1.8 pm, 50 mm x 4.6 mm i.d. column at 40 °C, at a flow rate of 1 mL x min ¹ using 0.02 % v/v aqueous formic acid (Solvent A) and 0.02 % v/v formic acid in acetonitrile (Solvent B) with a gradient starting from 100 % Solvent A and finishing at 100 % Solvent B over various/certain duration of time.

1H-NMR measurements were performed on Bruker Avance III 500 MHz spectrometer and Bruker Avance III 400 MHz spectrometer, using DMSO-d6 or CDCI ₃ as solvent. 1H NMR data is in the form of delta values, given in part per million (ppm), using the residual peak of the solvent (2.50 ppm for DMSO-d6 and 7.26 ppm for CDCf) as internal standard. Splitting patterns are designated as: s (singlet), d (doublet), t (triplet), q (quartet), qn (quintet), sept (septet), m (multiplet), brs (broad singlet), brd (broad doublet), brt (broad triplet), brq (broad quartet), brm (broad multiplet), vbrs (very broad singlet), br. (broad singlet or doublet), dd (doublet of doublets), td (triplet of doublets), dt (doublet of triplets), dq (doublet of quartet), ddd (doublet of doublet of doublets), dm (doublet of multiplets), tm (triplet of multiplets), qm (quartet of multiplets).

Combination gas chromatography and low resolution mass spectrometry were performed on Agilent 6850 gas chromatograph and Agilent 5975C mass spectrometer using 15 m x 0.25 mm column with 0.25 pm HP-5MS coating and helium as carrier gas. Ion source:

EI+, 70 eV, 230 °C, quadrupole: 150 °C, interface: 300 °C.

High resolution mass spectrometry was performed on JEOL AccuTOF MS instrument connected to Agilent 7693A gas chromatograph on Rxi-5Sil MS coloumn 15 m x 0.25 mm column and helium was used as carrier gas. Ion source: EI+, 70 eV, 200 °C, interface: 250 °C. HRMS were determined on a Shimadzu IT-TOF, ion source temperature 200 °C,

ESI +/-, ionization voltage: (+-)4.5 kV. Mass resolution min. 10000.

Elementary analyses were performed on a Thermo Flash EA 1112 Elemental Analyzer.

IUPAC chemical names were generated using ACD/Name 2015 Pack 2 (File Version N20E41, Build 75170, 19 Dec 2014) or using‘Structure to Name’ functionality within Accelrys Draw 4.2.

List of abbreviations

Abbreviation Name

abs. absolute

aq. aqueous

Boc fc/ -butoxycarbonyl

cc. concentrated DAST diethylaminosulfur trifluoride

DBU l,8-diazabicyclo[5.4.0]undec-7-ene

DCM methylene chloride

DEE diethylether

DIPO diisopropyl oxide

DMAP 4-dimethylaminopyridine

DMF dimethylformamide

DMSO dimethy lsulfo xide

EEO ethyl ethanoate

eq. equivalent

Et ₃ N.3HF triethylamine trihydro fluoride

EtOAc ethyl acetate

HATU 1 -[bis(dimethylamino)methylene]- \H- 1 ,2,3-triazolo[4,5-h] pyridinium 3-oxid hexafluorophosphate

HBTU 3-[bis(dimcthylamino)mcthyliumyl]-3//-bcnzotriazol- 1 -oxide hexafluorophosphate

LC liquid chromatography

MeCN acetonitrile

MeOH methanol

MSM methylsulfmylmethane

MTBE /e/t-butyl methylether

r.t. room temperature

sat. saturated

TBAF tetra-n-butylammonium fluoride

TFA trifluoroacetic acid

TCEP tris(2-carboxyethyl)phosphine

THF tetrahydrofurane

TMSC1 trimethylsilyl chloride

TMSOTf trimethylsilyl triflate

XtalFluor-E® (diethylamino)difluorosulfonium tetrafluoroborate

XtalFluor-M® difluoro(morpholino)sulfonium tetrafluoroborate General Procedure 1

4-chloro-6-methoxy-5-nitro-pyrimidine (Preparation Rla; 1.0 eq.), the appropriate phenol (1.2 eq.), and potassium carbonate (1.2 eq.) were dissolved in acetonitrile. It was stirred at 80 °C till completion, then water was added to the reaction mixture. MeCN was evaporated. The residue extracted with DCM. The combined organic phase was dried over MgS0 ₄ and evaporated under reduced pressure to give R2a-R2ce.

General Procedure 2

Autoclave was charged with R2a-R2ce (1.0 eq.), Raney-nickel catalyst (10 w/w%) and l,4-dioxane and then placed under a nitrogen atmosphere. After that it was filled with lO bar ¾ gas. The reaction mixture was stirred in autoclave at r.t. for 20 hours. The reaction mixture was removed from the autoclave and filtered. The filtrate was purified by preparative LC (on C-18 Gemini-NX 5 pm column, 5 mM aqueous NH ₄ HC0 ₃ -MeCN, gradient). Solvent was evaporated under reduced pressure to give R3a-R3ce.

General Procedure 3

R2a-R2ce (1.0 eq.), and tin(II) chloride dihydrate (3.5 eq.) were dissolved in l,4-dioxane. The reaction mixture was stirred till completion at r.t. Then sat. NaHCCh solution and EtOAc were added, the suspension was filtered through Celite, washed with EtOAc, the layers were separated. The aqueous phase extracted with EtOAc. The Celite washed with DCM-MeOH. The organic phase evaporated to give R3a-R3ce. General Procedure 4

R3a-R3ce (1.0 eq.) was dissolved in l,4-dioxane, then 1N hydrochloric acid (3.0-5.0 eq.) was added. It was stirred at 95 °C till completion, then the reaction mixture concentrated under reduced pressure to give R4a-R4ce.

General Procedure 5

R4a-R4ce (1.0 eq.), R5a-R51 (1.0 eq.) and potassium carbonate (3.0 eq.) were dissolved in N,N-dimethylformamide. It was stirred at 70 °C till completion. The reaction mixture was directly injected through syringe filter to preparative HPLC (on C-18 Gemini-NX 5 pm column, 5 mM NH4HCO3 aqueous solution - MeCN, gradient 5-90 %). Fractions were collected and concentrated under reduced pressure, then dried in vacuum at 50 °C for overnight.

General Procedure 6: Boc Protection

The appropriate amine (1.0 eq.), tert-butoxycarbonyl tert-butyl carbonate (1.5 eq.), and sodium hydrogen carbonate (2.0 eq.) were dissolved in THF and water (1 :1). It was stirred at r.t. till completion. The reaction mixture was extracted with EtOAc. The combined organic phase dried on MgS0 ₄ and the solvent was evaporated under reduced pressure to give the appropriate Boc protected amine. General Procedure 7: Boc deprotection

The appropriate Boc protected amine (1.0 eq.) was dissolved in l,4-dioxane and 1N hydrochloric acid solution (5.0 eq.) was added. It was stirred at 70 °C till completion, then the solvents were evaporated under reduced pressure to give the appropriate amine derivative. General procedure 8

Step 1:

Corresponding aryl-carbaldehyde (1.0 eq.) and l-(triphenyl-phosphanylidene)propan-2-one (1.2 eq.) were dissolved in DCM. The mixture was stirred at r.t. for 1-168 hours. The solvent was evaporated. The residue was purified by flash chromatography (hexane:EEO) to give the appropriate (£)-4-(aryl)but-3-en-2-one.

Step 2:

A solution of corresponding (£)-4-(aryl)but-3-cn-2-onc obtained in Step 1 above (2.1 eq.), triethylamine (1.5 eq.) and abs. DCM were cooled to -20 °C and TMSOTf (2.0 eq.) was added dropwise. The solution was stirred for 1 hour at this temperature. The mixture was washed with aq. NaHCCF solution (15 ml) 3 times. The organic layer was dried over MgS0 ₄ , then the solvent was evaporated in reduced pressure. The residue was used without further purification. Step 3:

Corresponding (£')-((4-(aryl)buta-l,3-dien-2-yl)oxy)trimethylsilane obtained in Step 2 above (1.0 eq.) and ethyl acrylate (2.0 eq.) were dissolved in abs. toluene. The mixture was stirred at 120 °C for 1-2 days. The solvent was evaporated. The residue was dissolved in THF/1M aq. HC1 1 :1 v/v mixture and stirred for 1 hour at 25 °C. Then the emulsion was diluted with DEE and washed 3 times with NaHCCf solution and with brine. The organic layer was dried over MgS0 ₄ and then the solvent was evaporated under reduced pressure. The crude product was purified by flash chromatography (hexane:EEO) to give the corresponding ethyl 2-(aryl)-4-oxocyclohexane-l-carboxylate. Step 4:

Oven-dried flask was inertized then filled with ethyl 2-(aryl)-4-oxocyclo hexane- 1- carboxylate obtained in Step 3 above (1.0 eq.) and abs. DCM (c = 0.05M). The solution was cooled to 10 °C and DAST (5.0 eq.) was added dropwise. After that the reaction mixture was stirred for 3 hours at 25 °C. The reaction mixture was quenched with aq. NaHC0 ₃ solution (25 ml), and the mixture was washed with aq. NaHC0 ₃ solution twice. The organic layer was dried over MgS0 ₄ , and then the solvent was evaporated under reduced pressure. The crude product was purified by column chromatography (hexane:EEO) to give the corresponding ethyl 4, 4-difluoro-2-(aryl)cyclo hexane- 1- carboxylate. Step 5:

The corresponding ester obtained in Step 4 above was dissolved in the mixture of ethanol and water (5:1, v/v) and lithium hydroxide hydrate (2.0-3.0 eq.) was added. It was stirred at r.t. for 44-435 hours.

Work-up 1 :

The reaction mixture was partially evaporated to water and isolated as lithium salt.

Work-up 2:

The reaction mixture was evaporated to water, then 1N HC1 was added. The obtained solid was filtered off.

Work-up 3 :

The reaction mixture was evaporated to water, 1N HC1 was added, and then it was evaporated again. The residue was purified by preparative HPLC (on C-18 Gemini-NX 5 pm column, 5 mM aqueous NH ₄ HC0 ₃ -MeCN, gradient).

Step 6:

The appropriate 4-piperidone hydrochloride hydrate, HBTU (1.6 eq.), 2-aryl-4,4- difluoroyclohexanecarboxylic acid (1.0 eq.) and N, /V- d i i so p ro p y 1 c th y 1 am i n c (5.0 eq.) were dissolved in MeCN (50 mL) and stirred till completion. After evaporation, the residue was dissolved in DCM and it was washed with 1N NaOH and then with 1N HC1 and then with water. Organic layer was dried (MgS0 ₄ ) and evaporated. DIPO was added, solid compound was formed, which was filtered off to give the appropriate l-(2-aryl-4,4- difluorocyclohexanecarbonyl)piperidin-4-one.

Step 7:

l-(2 -Aryl-4, 4-difluorocyclohexanecarbonyl)piperidin-4-one (1.0 eq.) and trimethylsulfoxonium- iodide (5.0 eq.) was charged into a round bottom flask and dissolved/suspended in MeCN and MTBE (1 :1). NaOH (2.5 eq.) was dissolved in water and the obtained solution was added to the mixture and stirred at 60 °C for 6 hours. After the reaction completed, the reaction mixture was filtered through Celite, and washed with MTBE. Water was added to the solution, layers were separated, and the aqueous layer was extracted with MTBE. Combined organic layers were dried over MgS0 ₄ and after filtration evaporated to give the appropriate (2-aryl-4,4-difluorocyclohexyl)-(l-oxa-6- azaspiro [2.5 ]octan-6-yl)methanone.

Preparation R2a: 6-methoxy-5-nitro-4-phenoxy- 1 ,6-dihydropyrimidine

Using General Procedure 1 starting from Preparation Rla and phenol as reagents, Preparation R2a was obtained. 1H-NMR (500 MHz, dmso-d6) d ppm 8.59 (s, 1H), 7.48 (m, 2H), 7.33 (tm, 1H), 7.27 (dm, 2H), 4.1 (s, 3H) ¹³ C-NMR (125 MHz, dmso-d6) d ppm 162.4, 161.1, 158.7, 152, 130.4, 126.8, 122.1, 56.6

Preparation R2b: 4-(2-fluorophenoxy)-6-methoxy-5-nitro-pyrimidine

Using General Procedure 1 starting from Preparation Rla and 2-fluorophenol as reagents, Preparation R2b was obtained. HRMS calculated for C ₁₁ H ₈ FN ₃ O ₄ : 265.0499; found 265.04976 (M ⁺ form).

1H-NMR (400 MHz, dmso-d6) d ppm 8.62 (s, 1H), 7.48 (dd, 1H), 7.45 (dd, 1H), 7.41 (m, 1H), 7.31 (m, 1H), 4.12 (s, 3H)

¹³ C-NMR (125 MHz, dmso-d6) d ppm 162.6, 160.3, 158.8, 153.9, 138.8, 128.8, 126, 124.5, 117.4, 56.8 Preparation R2c: 4-methoxy-6-(4-methoxyphenoxy)pyrimidin-5-amine

Using General Procedure 1 starting from Preparation Rla and 4-methoxyphenol as reagents, Preparation R2c was obtained. HRMS calculated for C ₁₂ H ₁₃ N ₃ O ₃ : 247.0957; found 248.10318 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 7.72 (s, 1H), 7.06 (m, 2H), 6.94 (m, 2H), 4.79 (s, 2H), 3.94 (s, 3H), 3.75 (s, 3H)

¹³ C-NMR (125 MHz, dmso-d6) d ppm 157.7, 156.5, 155.4, 147.3, 142.9, 122.8, 116.7, 114.9

Preparation R2d: 4-methoxy-6-(3-methoxyphenoxy)-5-nitro-pyrimidine

Using General Procedure 1 starting from Preparation Rla and 3-methoxyphenol as reagents, Preparation R2d was obtained. HRMS calculated for C ₁₂ H ₁₁ N ₃ O ₅ : 277.0699; found 278.0773 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 8.6 (s, 1H), 7.36 (t, 1H), 6.9 (dm, 1H), 6.89 (m, 1H), 6.83 (dm, 1H), 4.1 (s, 3H), 3.76 (s, 3H)

¹³ C-NMR (125 MHz, dmso-d6) d ppm 162.4, 161.1, 160.9, 158.7, 152.2, 130.7, 114, 112.7, 108

Preparation R2e: 4-(4-fluorophenoxy)-6-methoxy-5-nitro-pyrimidine

Using General Procedure 1 starting from Preparation Rla and 4-fluorophenol as reagents, Preparation R2e was obtained. HRMS calculated for C ₁₁ H ₈ FN ₃ O ₄ : 265.0499; found 265.04956 (M ⁺ form).

1H-NMR (400 MHz, dmso-d6) d ppm 8.59 (s, 1H), 7.33 (m, 2H), 7.33 (m, 2H), 4.1 (s, 3H) ¹³ C-NMR (125 MHz, dmso-d6) d ppm 162.4, 161.6, 158.6, 124.1, 117, 56.7

Preparation R2f: 4-(3-fluorophenoxy)-6-methoxy-5-nitro-pyrimidine

Using General Procedure 1 starting from Preparation Rla and 3-fluorophenol as reagents, Preparation R2f was obtained. HRMS calculated for C ₁₁ H ₈ FN ₃ O ₄ : 265.0499; found 266.05704 ((M+H) ⁺ form).

1H-NMR (400 MHz, dmso-d6) d ppm 8.62 (s, 1H), 7.52 (m, 1H), 7.31 (m, 1H), 7.2 (m, 1H), 7.16 (dd, 1H), 4.11 (s, 3H).

1 ³ C-NMR (125 MHz, dmso-d6) d ppm 163, 162.5, 158.7, 152.8, 131.6, 118.4, 113.9, 110.3, 56.7.

Preparation R2g: 4-(3,5-dimethoxyphenoxy)-6-methoxy-5-nitro-pyrimidine

Using General Procedure 1 starting from Preparation Rla and 3,5-dimethoxyphenol as reagents, Preparation R2g was obtained. HRMS calculated for C ₁₃ H ₁₃ N ₃ O ₆ : 307.0804; found 308.0882 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 8.61 (s, 1H), 6.47 (m, 2H), 6.45 (m, 1H), 4.1 (s, 3H), 3.74 (s, 6H).

¹³ C-NMR (125 MHz, dmso-d6) d ppm 162.4, 161.5, 161.1, 158.7, 153.6, 121, 100.6, 98.9, 56.6, 56.1. Preparation R2h: 4-(3,5-difluorophenoxy)-6-methoxy-5-nitro-pyrimidine

Using General Procedure 1 starting from Preparation Rla and 3,5-difluorophenol as reagents, Preparation R2h was obtained. HRMS calculated for C _{1 1} H ₇ F ₂ N ₃ O ₄ : 283.0405; found 284.0477 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 8.65 (s, 1H), 7.28 (t, 1H), 7.24 (d, 2H), 4.12 (s, 3H) ¹³ C-NMR (125 MHz, dmso-d6) d ppm 163, 162.6, 160.5, 158.7, 153.3, 121, 107, 102.8, 56.8

Preparation R2i: 4-(4-chlorophenoxy)-6-methoxy-5-nitro-pyrimidine

Using General Procedure 1 starting from Preparation Rla and 4-chlorophenol as reagents, Preparation R2j was obtained. HRMS calculated for C ₁₁ H ₈ CIN ₃ O ₄ : 281.0203; found 281.01978 (M ⁺ form).

1H-NMR (400 MHz, dmso-d6) d ppm 8.6 (s, 1H), 7.54 (m, 2H), 7.34 (m, 2H), 4.1 (s, 3H). ¹³ C-NMR (125 MHz, dmso-d6) d ppm 162.5, 161, 158.7, 150.7, 131, 130.3, 124.1, 56.7.

Preparation R2k: 4-(4-chloro-3-methoxy-phenoxy)-6-methoxy-5-nitro-pyrimidine Using General Procedure 1 starting from Preparation Rla and 4-chloro-3-methoxy- phenol as reagents, Preparation R2k was obtained. HRMS calculated for C ₁₂ H ₁₀ CIN ₃ O ₅ : 311.0309; found 312.038 ((M+H) ⁺ form).

1H-NMR (400 MHz, dmso-d6) d ppm 8.61 (s, 1H), 7.51 (d, 1H), 7.17 (d, 1H), 6.9 (dd, 1H), 4.11 (s, 3H), 3.83 (s, 3H).

¹³ C-NMR (125 MHz, dmso-d6) d ppm 162.4, 161, 158.7, 155.8, 151.6, 130.7, 119, 114.9, 107.7, 57, 56.7.

Preparation R21: 4-(3-chlorophenoxy)-6-methoxy-5-nitro-pyrimidine

Using General Procedure 1 starting from Preparation Rla and 3-chlorophenol as reagents, Preparation R21 was obtained. HRMS calculated for C ₁₁ H ₈ CIN ₃ O ₄ : 281.0203; found 282.0276 ((M+H) ⁺ form).

1H-NMR (400 MHz, dmso-d6) d ppm 8.62 (s, 1H), 7.51 (t, 1H), 7.51 (brs, 1H), 7.42 (dm, 1H), 7.29 (dm, lH), 4.l l (s, 3H)

¹³ C-NMR (125 MHz, dmso-d6) d ppm 162.5, 160.9, 158.7, 152.6, 134.1, 131.7, 127, 122.6, 121.1, 56.7

Preparation R2n: 4-(l,3-benzodioxol-5-yloxy)-6-methoxy-5-nitro-pyrimidine

Using General Procedure 1 starting from Preparation Rla and l,3-benzodioxol-5-ol as reagents, Preparation R2n was obtained. HRMS calculated for C ₁₂ H ₉ N ₃ O ₆ : 291.0491; found 292.057 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 8.59 (s, 1H), 6.97 (d, 1H), 6.95 (d, 1H), 6.7 (dd, 1H), 6.09 (s, 2H), 4.09 (s, 3H).

¹³ C-NMR (125 MHz, dmso-d6) d ppm 162.3, 161.4, 158.6, 148.9, 148.3, 146.1, 120.8, 114.5, 108.6, 104.4, 102.4, 56.6. Preparation R2o: 3-methoxy-5-(6-methoxy-5-nitro-pyrimidin-4-yl)oxy-phenol

Using General Procedure 1 starting from Preparation Rla and 5-methoxybenzene-l,3- diol as reagents, Preparation R2o was obtained. HRMS calculated for C ₁₂ H ₁₁ N ₃ O ₆ : 293.0648; found 294.0718 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 9.86 (s, 1H), 8.6 (s, 1H), 6.29/6.28/6.21 (t+t+t, 3H), 4.09 (s, 3H), 3.69 (s, 3H).

¹³ C-NMR (125 MHz, dmso-d6) d ppm 162.3, 161.5, 161, 159.6/153.4, 158.7, 101.8/99.8/99, 56.6, 55.8.

Preparation R2p: 4-(4-fluoro-3-methoxy-phenoxy)-6-methoxy-5-nitro-pyrimidine Using General Procedure 1 starting from Preparation Rla and 4-fluoro-3-methoxy- phenol as reagents, Preparation R2p was obtained. HRMS calculated for C ₁₂ H ₁₀ FN ₃ O ₅ : 295.0605; found 296.0675 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 8.84 (s, 1H), 7.33 (dd, 1H), 7.26 (dd, 1H), 6.91 (ddd, 1H), 3.81 (s, 3H), 3.81 (s, 3H)

1 ³ C-NMR (125 MHz, dmso-d6) d ppm 159.1, 116.8, 113.8, 108.5, 56.9, 56.9

Preparation R2r: 4-methoxy-5-nitro-6- [3-(trifluoromethoxy)phenoxy] pyrimidine

Using General Procedure 1 starting from Preparation Rla and 3-(trifluoromethoxy)phenol as reagents, Preparation R2r was obtained. HRMS calculated for C ₁₂ H ₈ F ₃ N ₃ O ₅ : 331.0416; found 332.0488 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 8.62 (s, 1H), 7.62 (t, 1H), 7.47 (s, 1H), 7.37 (m, 1H), 7.36 (m, 1H), 4.11 (s, 3H).

¹³ C-NMR (125 MHz, dmso-d6) d ppm 162.5, 160.8, 158.7, 152.6, 149.2, 131.8, 121.5, 121.4, 120.1, 119.4, 115.8, 56.7.

Preparation R2s: 4-methoxy-6-(3-methylphenoxy)-5-nitro-pyrimidine

Using General Procedure 1 starting from Preparation Rla and m-cresol as reagents, Preparation R2s was obtained. HRMS calculated for C ₁₂ H ₁₁ N ₃ O ₄ : 261.075; found 262.0825 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 8.59 (s, 1H), 7.35 (t, 1H), 7.14 (dm, 1H), 7.09 (m, 1H), 7.05 (dm, 1H), 4.1 (s, 3H), 2.33 (s, 3H). ¹³ C-NMR (125 MHz, dmso-d6) d ppm 162.3, 161.1, 158.7, 140.2, 130, 127.5, 122.4, 121, 119, 56.6, 21.2.

Preparation R2t: 4-(3-bromophenoxy)-6-methoxy-5-nitro-pyrimidine

Using General Procedure 1 starting from Preparation Rla and 3-bromophenol as reagents, Preparation R2t was obtained. HRMS calculated for CnHsBrNsCU 324.9698; found 325.9771 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 8.62 (s, 1H), 7.63 (m, 1H), 7.55 (dm, 1H), 7.44 (t, 1H), 7.33 (dm, lH), 4.l l (s, 3H).

13C-NMR (125 MHz, dmso-d6) d ppm 1600.9, 162.5, 158.7, 132, 129.9, 125.4, 121.4, 120.9, 56.7.

Preparation R2u: 4-methoxy-5-nitro-6- [3-(pentafluoro^ ⁶ -sulfanyl)phenoxy] pyrimidine

Using General Procedure 1 starting from Preparation Rla and 3-(pentafluoro^ ⁶ - sulfanyl)phenol as reagents, Preparation R2u was obtained. HRMS calculated for CiiHsFsNsCUS: 373.0156; found 374.022 ((M+H) ⁺ form).

1H-NMR (400 MHz, dmso-d6) d ppm 8.62 (s, 1H), 8.02 (t, 1H), 7.74 (t, 1H), 7.66 (dd, 1H), 4.12 (s, 3H).

¹³ C-NMR (125 MHz, dmso-d6) d ppm 162.6, 160.9, 158.6, 151.7, 131.3, 126.8, 120.6, 56.7

¹⁹ F -NMR (376 MHz, dmso-d6) d ppm 86, 64.2.

Preparation R2v: 4-methoxy-5-nitro-6- [3-(trifluoromethyl)phenoxy] pyrimidine

Using General Procedure 1 starting from Preparation Rla and 3-(trifluoromethyl)phenol as reagents, Preparation R2v was obtained. HRMS calculated for CizHsFsNsCU 315.0467; found 316.0545 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 8.62 (s, 1H), 7.79 (m, 1H), 7.72 (m, 1H), 7.72 (m, 1H), 7.65 (m, lH), 4.l2 (s, 3H).

¹³ C-NMR (125 MHz, dmso-d6) d ppm 162.5, 160.9, 158.7, 152.2, 131.7, 131, 126.6, 124, 123.7, 119.5, 56.7. Preparation R2w: [4-(6-methoxy-5-nitro-pyrimidin-4-yl)oxyphenyl] methanol

Using General Procedure 1 starting from Preparation Rla and 4-(hydroxymethyl)phenol as reagents, Preparation R2w was obtained. HRMS calculated for C ₁₂ H ₁₁ N ₃ O ₅ : 277.0699; found 278.0764 ((M+H) ⁺ form).

1H-NMR (400 MHz, dmso-d6) d ppm 8.58 (s, 1H), 7.4 (d, 2H), 7.22 (d, 2H), 5.27 (t, 1H), 4.53 (d, 2H), 4.11 (s, 3H).

¹³ C-NMR (125 MHz, dmso-d6) d ppm 162.4, 161.3, 158.6, 150.5, 141.2, 128.4, 121.7, 120.9, 62.7, 56.6.

Preparation R2z: 4-(6-methoxy-5-nitro-pyrimidin-4-yl)oxybenzonitrile

Using General Procedure 1 starting from Preparation Rla and 4-hydroxybenzonitrile as reagents, Preparation R2z was obtained. HRMS calculated for C ₁₂ H ₈ N ₄ O ₄ : 272.0546; found 273.0621 ((M+H) ⁺ form).

1H-NMR (400 MHz, dmso-d6) d ppm 8.63 (s, 1H), 7.99 (d, 2H), 7.55 (d, 2H), 4.12 (s, 3H) ¹³ C-NMR (125 MHz, dmso-d6) d ppm 162.6, 160.6, 158.7, 155.4, 134.9, 123.5, 118.8, 109.9, 56.8

Preparation R2aa: 3-(6-methoxy-5-nitro-pyrimidin-4-yl)oxybenzonitrile

Using General Procedure 1 starting from Preparation Rla and 3-hydroxybenzonitrile as reagents, Preparation R2aa was obtained. HRMS calculated for C ₁₂ H ₈ N ₄ O ₄ : 272.0546; found 272.05401 (M ⁺ form).

1H-NMR (400 MHz, dmso-d6) d ppm 8.62 (s, 1H), 7.92 (m, 1H), 7.83 (m, 1H), 7.69 (m, 1H), 7.69 (m, lH), 4.l2 (s, 3H).

¹³ C-NMR (125 MHz, dmso-d6) d ppm 162.6, 160.7, 158.7, 152, 131.8, 130.9, 127.7, 126.1, 118.2, 113, 56.8.

Preparation R2ab: tert-butyl 7-(6-methoxy-5-nitro-pyrimidin-4-yl)oxy-3,4-dihydro- lH-isoquinoline-2-carboxylate

Using General Procedure 1 starting from Preparation Rla and tert-butyl 7-hydroxy- 3,4-dihydro-lH-isoquinoline-2-carboxylate as reagents, Preparation R2ab was obtained. HRMS calculated for C ₁₉ H ₂₂ N ₄ O ₆ : 402.1539; found 425.1421 ((M+Na) ⁺ form). 1H-NMR (400 MHz, dmso-d6) d ppm 8.6 (s, 1H), 7.25 (d, 1H), 7.12 (d, 1H), 7.08 (dd, 1H), 4.51 (brs, 2H), 4.11 (s, 3H), 3.57 (t, 2H), 2.8 (t, 2H), 1.43 (s, 9H).

¹³ C-NMR (125 MHz, dmso-d6) d ppm 162.4, 161.1, 158.7, 154.1, 150.2, 135.7, 133.3,

130.6, 120.2, 119.6, 79.5, 56.6, 45.4, 41.5, 28.6, 28.2.

Preparation R2ac: methyl 3-(6-methoxy-5-nitro-pyrimidin-4-yl)oxybenzoate

Using General Procedure 1 starting from Preparation Rla and methyl 3-hydroxybenzoate as reagents, Preparation R2ac was obtained. HRMS calculated for C _I3 H _{I I} N ₃ 0 ₆ : 305.0648; found 306.0714 ((M+H) ⁺ form).

1H-NMR (400 MHz, dmso-d6) d ppm 8.6 (s, 1H), 7.93 (dd, 1H), 7.83 (t, 1H), 7.65 (t, 1H), 7.61 (dd, 1H), 4.11 (s, 3H), 3.88 (s, 3H).

¹³ C-NMR (125 MHz, dmso-d6) d ppm 165.7, 162.5, 161, 158.6, 152, 131.9, 131, 127.6,

127.2, 122.8, 121, 56.7, 52.9.

Preparation R2ad: [3-(6-methoxy-5-nitro-pyrimidin-4-yl)oxyphenyl] methanol

Using General Procedure 1 starting from Preparation Rla and

3-(hydroxymethyl)phenol as reagents, Preparation R2ad was obtained. HRMS calculated for C _I2 H _{I I} N ₃ 0 ₅ : 277.0699; found 278.077 ((M+H) ⁺ form).

1H-NMR (400 MHz, dmso-d6) d ppm 8.6 (s, 1H), 7.43 (t, 1H), 7.27 (dd, 1H), 7.19 (t, 1H), 7.13 (dd, 1H), 5.33 (t, 1H), 4.54 (d, 2H), 4.11 (s, 3H).

¹³ C-NMR (125 MHz, dmso-d6) d ppm 162.4, 161.2, 158.7, 152, 145.5, 130, 124.6, 121,

120.3, 119.7, 62.7, 56.6.

Preparation R2ae: 3-[4-(6-methoxy-5-nitro-pyrimidin-4-yl)oxyphenyl]propan-l-ol Using General Procedure 1 starting from Preparation Rla and

4-(3-hydroxypropyl)phenol as reagents, Preparation R2ae was obtained. HRMS calculated for C _I4 H _{I 5} N ₃ 0 ₅ : 305.1012; found 306.1082 ((M+H) ⁺ form).

1H-NMR (400 MHz, dmso-d6) d ppm 8.59 (s, 1H), 7.29 (dm, 2H), 7.17 (dm, 2H), 4.51 (t, 1H), 4.11 (s, 3H), 3.43 (m, 2H), 2.65 (t, 2H), 1.74 (quin, 2H).

¹³ C-NMR (125 MHz, dmso-d6) d ppm 162.3, 161.2, 158.6, 149.9, 140.8, 130.1, 121.8,

60.4. 56.6, 34.7, 31.5.

Preparation R2af: 4-methoxy-5-nitro-6-phenylsulfanyl-pyrimidine Using General Procedure 1 starting from Preparation Rla and benzenethiol as reagents, Preparation R2af was obtained. HRMS calculated for C _{1 1} H ₉ N ₃ O ₃ S: 263.0365; found 264.0434 ((M+H) ⁺ form).

1H-NMR (400 MHz, dmso-d6) d ppm 8.61 (s, 1H), 7.63-7.44 (m, 5H), 4.07 (s, 3H).

1 ³ C-NMR (125 MHz, dmso-d6) 5 ppm 165.4, 161.9, 158.3, 127.5, 56.4.

Preparation R2ag: tert-butyl 6-(6-methoxy-5-nitro-pyrimidin-4-yl)oxy-3,4-dihydro- lH-isoquinoline-2-carboxylate

Using General Procedure 1 starting from Preparation Rla and tert-butyl 6-hydroxy- 3,4-dihydro-lH-isoquinoline-2-carboxylate as reagents, Preparation R2ag was obtained. HRMS calculated for C ₁₉ H ₂₂ N ₄ O ₆ : 402.1539; found 347.0988 ((M+H-tBu) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 8.58 (s, 1H), 7.26 (m, 1H), 7.08 (m, 1H), 7.08 (m, 1H), 4.52 (brs, 2H), 4.1 (s, 3H), 3.55 (t, 2H), 2.78 (t, 2H), 1.43 (s, 9H).

¹³ C-NMR (125 MHz, dmso-d6) d ppm 158.6, 128.2, 121.8, 119.9, 56.6, 45.3, 41, 28.6, 28.6.

Preparation R2ah: tert-butyl 5-(6-methoxy-5-nitro-pyrimidin-4-yl)oxyisoindoline-2- carboxylate

Using General Procedure 1 starting from Preparation Rla and tert-butyl 5-hydroxyisoindoline-2-carboxylate as reagents, Preparation R2ah was obtained. HRMS calculated for C ₁₈ H ₂₀ N ₄ O ₆ : 388.1383; found 333.0826 ((M+H-tBu) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 8.58 (s, 1H), 7.41/7.4 (d, 1H), 7.26/7.24 (d, 1H), 7.18 (dd, 1H), 4.63-4.55 (brs, 4H), 4.1 (s, 3H), 1.46 (s, 9H).

¹³ C-NMR (125 MHz, dmso-d6) d ppm 158.7, 124.6, 121.3, 116.7, 56.6, 28.6.

Preparation R2ai: 2-[4-(6-methoxy-5-nitro-pyrimidin-4-yl)oxyphenoxy] ethanol

Using General Procedure 1 starting from Preparation Rla and 4-(2-hydroxyethoxy)phenol as reagents, Preparation R2ai was obtained. HRMS calculated for C ₁₃ H ₁₃ N ₃ O ₆ : 307.0804; found 308.088 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 8.57 (s, 1H), 7.17 (dm, 2H), 7 (dm, 2H), 4.89 (t, 1H), 4.09 (s, 3H), 4 (t, 2H), 3.72 (q, 2H). ¹³ C-NMR (125 MHz, dmso-d6) d ppm 162.3, 161.4, 158.6, 145.2, 145.2, 123, 115.7, 70.4, 60, 56.6.

Preparation R2ai: tert-butyl 2-[4-(6-methoxy-5-nitro-pyrimidin-4- yl)oxyphenyl]pyrrolidine-l-carboxylate

4-Pyrrolidin-2-ylphenol, hydrogen bromide (1 :1) (1 g, 4.0962 mmol), tert-butoxycarbonyl tert-butyl carbonate (1.5 eq., 6.1443 mmol) and sodium hydrogencarbonate (4.0 eq., 16.385 mmol) were dissolved in THF (10 mL) and water (10 mL). The reaction mixture was stirred at r.t. for 20 hours. The reaction mixture was extracted with EtOAc (3 x 10 ml). The organic layer was evaporated after drying with brine and MgS0 ₄ .The residue was washed with diisopropyl ether and the solid compound was filtered off to give tert-butyl 2-(4-hydroxyphenyl)pyrrolidine-l-carboxylate as a crude product.

Using General Procedure 1 starting from Preparation Rla and tert-butyl 2-(4-hydroxyphenyl)pyrrolidine-l-carboxylate as reagents, Preparation R2aj was obtained. HRMS calculated for C ₂₀ H ₂₄ N ₄ O ₆ : 416.1696; found 439.1581 ((M+Na) ⁺ form). 1H-NMR (500 MHz, dmso-d6) d ppm 8.56 (s, 1H), 7.226 (m, 2H), 7.19 (m, 2H), 4.8 (brm, 1H), 4.12 (s, 3H), 3.58-3.45 (m, 2H), 2.32/1.75 (m+m, 2H), 1.9-1.8 (m, 2H), 1.26 (brs, 9H).

¹³ C-NMR (125 MHz, dmso-d6) d ppm 158.5, 127.3, 121.5, 60.6, 56.5, 47.4, 35.7, 28.5, 23.4. Preparation R2al: 6-(6-methoxy-5-nitro-pyrimidin-4-yl)oxy-lH-indazole

Using General Procedure 1 starting from Preparation Rla and lH-indazol-6-ol as reagents, Preparation R2al was obtained. HRMS calculated for C ₁₂ H ₉ N ₅ O ₄ : 287.0655; found 288.0729 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 13.21 (s, 1H), 8.58 (s, 1H), 8.12 (m, 1H), 7.83 (d, 1H), 7.45 (m, 1H), 7 (dd, 1H), 4.11 (s, 3H)

¹³ C-NMR (125 MHz, dmso-d6) d ppm 162.4, 161.4, 158.7, 150.4, 140.3, 134.2, 122.2, 121.6, 115.7, 103.1, 56.6

Preparation R2am: 2- [4-(6-methoxy-5-nitro-pyrimidin-4-yl)oxyphenyl] ethanol

Using General Procedure 1 starting from Preparation Rla and 4-(2-hydroxyethyl)phenol as reagents, Preparation R2am was obtained. HRMS calculated for C ₁₃ H ₁₃ N ₃ O ₅ : 291.0855; found 292.093 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 8.58 (s, 1H), 7.3 (dm, 2H), 7.15 (dm, 2H), 4.68 (t, 1H), 4.1 (s, 3H), 3.62 (m, 2H), 2.74 (t, 2H)

1 ³ C-NMR (125 MHz, dmso-d6) d ppm 162.3, 161.2, 158.6, 150.2, 138.3, 130.7, 121.6, 62.4, 56.6, 38.7

Preparation R2an: 4-methoxy-5-nitro-6- [4-(2,2,2-trifluoroethyl)phenoxy] pyrimidine Using General Procedure 1 starting from Preparation Rla and 4-(2,2,2-trifluoroethyl) phenol as reagents, Preparation R2an was obtained. HRMS calculated for C ₁₃ H ₁₀ F ₃ N ₃ O ₄ : 329.0623; found 330.0707 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 8.6 (s, 1H), 7.46 (m, 2H), 7.3 (m, 2H), 4.1 (s, 3H), 3.71 (q, 2H)

¹³ C-NMR (125 MHz, dmso-d6) d ppm 158.7, 132.3, 126.8, 122.2, 38.2

Preparation R2ao: 4- [4-(2,2-difluoroethyl)phenoxy] -6-methoxy-5-nitro-pyrimidine Using General Procedure 1 starting from Preparation Rla and 4-(2,2-difluoroethyl) phenol as reagents, Preparation R2ao was obtained. HRMS calculated for C ₁₃ H ₁₁ F ₂ N ₃ O ₄ : 311.0717; found 312.0786 ((M+H) ⁺ form).

1H-NMR (400 MHz, dmso-d6) d ppm 8.59 (s, 1H), 7.4 (dm, 2H), 7.25 (dm, 2H), 6.28 (tt, 1H), 4.1 (s, 3H), 3.22 (td, 2H)

1 ³ C-NMR (125 MHz, dmso-d6) d ppm 162.4, 161.1, 158.6, 151.1, 131.8, 131.4, 122.1, 117.4, 58.6, 39.4

Preparation R2ap: 4- [4-(2-fluoroethyl)phenoxy] -6-methoxy-5-nitro-pyrimidine

Using General Procedure 1 starting from Preparation Rla and 4-(2-fluoroethyl)phenol as reagents, Preparation R2ap was obtained. HRMS calculated for C ₁₃ H ₁₂ FN ₃ O ₄ : 293.0812; found 294.0883 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 8.58 (s, 1H), 7.37 (dm, 2H), 7.21 (dm, 2H), 4.66 (dt, 2H), 4.1 (s, 3H), 3.01 (dt, 2H).

¹³ C-NMR (125 MHz, dmso-d6) d ppm 162.4, 161.2, 158.6, 150.6, 136.1, 130.8, 121.9, 120.9, 84.3, 56.6, 35.9 Preparation R2aq: 4- [4-fluoro-3-(trifluoromethoxy)phenoxy] -6-methoxy-5-nitro- pyrimidine

Using General Procedure 1 starting from Preparation Rla and 4-fluoro-3- (trifluoromethoxy)phenol as reagents, Preparation R2aq was obtained. HRMS calculated for C ₁₂ H ₇ F ₄ N ₃ O ₅ : 349.0322; found 350.0392 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 8.63 (s, 1H), 7.75 (dm, 1H), 7.65 (t, 1H), 7.46 (dm, 1H), 4.11 (s, 3H).

¹³ C-NMR (125 MHz, dmso-d6) d ppm 162.5, 160.9, 158.7, 152.2, 147.7, 135.7, 123.5, 118.9, 118.7, 56.7. Preparation R2as: 4-(4-chloro-3-ethyl-phenoxy)-6-methoxy-5-nitro-pyrimidine

Using General Procedure 1 starting from Preparation Rla and 4-chloro-3-ethyl-phenol as reagents, Preparation R2as was obtained. HRMS calculated for C ₁₃ H ₁₂ CIN ₃ O ₄ : 309.0516; found 310.0589 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 8.6 (s, 1H), 7.53 (d, 1H), 7.33 (d, 1H), 7.2 (dd, 1H), 4.1 (s, 3H), 2.72 (q, 2H), 1.17 (t, 3H)

¹³ C-NMR (125 MHz, dmso-d6) d ppm 162.5, 161.7, 161, 158.7, 150.8, 143.4, 130.8, 130.6, 123.3, 121.5, 56.7, 26.6, 14.1

Preparation R2at: 4-(3-benzyloxyphenoxy)-6-methoxy-5-nitro-pyrimidine

Using General Procedure 1 starting from Preparation Rla and 3-benzyloxyphenol as reagents, Preparation R2at was obtained. HRMS calculated for C ₁₈ H ₁₅ N ₃ O ₅ : 353.1012; found 354.1084 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 8.6 (s, 1H), 7.48-7.3 (m, 5H), 7.37 (t, 1H), 6.99 (m, 1H), 6.98 (dm, 1H), 6.85 (dm, 1H), 5.1 (s, 2H), 4.1 (s, 3H).

¹³ C-NMR (125 MHz, dmso-d6) d ppm 158.7, 130.8, 114.2, 113.5, 108.8, 70, 56.6. Preparation R2au: 4-(6-methoxy-5-nitro-pyrimidin-4-yl)oxybenzaldehyde

Using General Procedure 1 starting from Preparation Rla and 4-hydroxybenzaldehyde as reagents, Preparation R2au was obtained. HRMS calculated for C ₁₂ H ₉ N ₃ O ₅ : 275.0542; found 276.0612 ((M+H) ⁺ form). 1H-NMR (500 MHz, dmso-d6) d ppm 10.03 (s, 1H), 8.63 (s, 1H), 8.03 (dm, 2H), 7.53 (dm, 2H), 4.12 (s, 3H).

¹³ C-NMR (125 MHz, dmso-d6) d ppm 192.4, 162.6, 160.7, 158.7, 156.4, 134.7, 131.9, 122.9, 121.2, 56.7.

Preparation R2av: tert-butyl N-[(lR)-2,2,2-trifluoro-l-[4-(6-methoxy-5-nitro- pyrimidin-4-yl)oxyphenyl] ethyl] carbamate

4-[(lR)-l-amino-2,2,2-trifluoro-ethyl]phenol, hydrochloride (850 mg, 3.7345 mmol), tert-butoxycarbonyl tert-butyl carbonate (1.5 eq., 5.6017 mmol), and sodium hydrogencarbonate (2.0 eq., 7.4689 mmol) were dissolved in THF (10 mL) and water (10 mL). The reaction mixture was stirred at r.t. for 20 hours. The reaction mixture was extracted with EtOAc (3 x 10 ml). The organic layer was evaporated after drying with brine and MgS0 ₄ to give tert-butyl N-[(lR)-2,2,2-trifluoro-l-(4-hydroxyphenyl)ethyl] carbamate as a crude product.

Using General Procedure 1 starting from Preparation Rla and tert-butyl N-[(lR)-2,2,2- trifluoro-l-(4-hydroxyphenyl)ethyl] carbamate as reagents, Preparation R2av was obtained. HRMS calculated for C ₁₈ H ₁₉ F ₃ N ₄ O ₆ : 444.1257; found 462.1587 ((M+NH ₄ ) ⁺ form).

1H-NMR (400 MHz, dmso-d6) d ppm 8.91/8.6 (s, 1H), 8.42/8.4 (d, 1H), 7.7/7.62 (dm, 2H), 7.35/7.24 (dm, 2H), 5.51 (m, 1H), 4.12/4.11 (s, 3H), 1.41/1.4 (s, 9H)

¹³ C-NMR (125 MHz, dmso-d6) d ppm 162.5, 161, 159.1/158.6, 152.2, 132.1, 130.6/130.3, 122.2/122.1, 79.9, 57.1/56.7, 55, 28.5

Preparation R2aw: tert-butyl N-[(lS)-2,2,2-trifluoro-l-[4-(6-methoxy-5-nitro- pyrimidin-4-yl)oxyphenyl] ethyl] carbamate

4-[(lS)-l -amino-2, 2, 2-trifluoro-ethyl]phenol, hydrochloride (960 mg, 4.2177 mmol), tert-butoxycarbonyl tert-butyl carbonate (1.5 eq., 6.3266 mmol) and sodium hydrogencarbonate (2.0 eq., 8.4355 mmol) were dissolved in THF (10 mF), and water (10 mF). The reaction mixture was stirred at r.t. for 20 hours. The reaction mixture was extracted with EtOAc (3 x 10 ml). The organic layer was evaporated after drying with brine and MgS0 ₄ to give tert-butyl N-[(lS)-2,2,2-trifluoro-l-(4-hydroxyphenyl) ethyl] carbamate . Using General Procedure 1 starting from Preparation Rla and tert-butyl N-[(lS)-2,2,2- trifluoro-l-(4-hydroxyphenyl)ethyl] carbamate as reagents, Preparation R2aw was obtained. HRMS calculated for C ₁₈ H ₁₉ F ₃ N ₄ O ₆ : 444.1257; found 389.0703 ((M+H- C ₄ H ₈ ) ⁺ form). Preparation R2az: tert-butyl 2-[3-(6-methoxy-5-nitro-pyrimidin-4-yl)oxyphenyl] piperidine-l-carboxylate

3-(2-piperidyl)phenol, tert-butoxycarbonyl tert-butyl carbonate (1.5 eq.) and sodium hydrogencarbonate (4.0 eq.) were dissolved in THF (10 mL), and water (10 mL). The reaction mixture was stirred at r.t. for 20 hours. The reaction mixture was extracted with EtOAc (3 x 10 ml). The organic layer was evaporated after drying with brine and MgS0 ₄ to give tert-butyl 2-(3-hydroxyphenyl)piperidine-l-carboxylate.

Using General Procedure 1 starting from Preparation Rla and tert-butyl 2-(3-hydroxyphenyl)piperidine-l-carboxylate as reagents, Preparation R2az was obtained. HRMS calculated for C _2i H ₂₆ N ₄ 0 ₆ : 430.1852; found 453.1741 ((M+Na) ⁺ form). 1H-NMR (500 MHz, dmso-d6) d ppm 8.58 (s, 1H), 7.47 (t, 1H), 7.16 (dm, 1H), 7.13 (dm, 1H), 7.05 (brs, 1H), 5.28 (br„ 1H), 4.1 (s, 3H), 3.92/2.7 (d+td, 2H), 2.28/1.76 (d+tm, 2H), 1.54/1.38 (d+m, 2H), 1.54/1.24 (d+m, 2H), 1.37 (s, 9H).

¹³ C-NMR (125 MHz, dmso-d6) d ppm 162.4, 161.1, 158.6, 155.1, 152.4, 143.3, 130.5, 124.6, 120.1, 119.9, 79.5, 56.6, 53.2, 40.3, 28.5, 28.3, 25.2, 19.4 Preparation R2bc: 5-(6-methoxy-5-nitro-pyrimidin-4-yl)oxyindan-2-ol

Using General Procedure 1 starting from Preparation Rla and indane-2,5-diol as reagents, Preparation R2bc was obtained. HRMS calculated for C _I4 H _I3 N ₃ 0 ₅ : 303.0855; found 304.0927 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 8.57 (s, 1H), 7.26 (d, 1H), 7.09 (d, 1H), 6.98 (dd, 1H), 4.91 (d, 1H), 4.53 (m, 1H), 4.09 (s, 3H), 3.06/2.74 (dt+dt, 2H), 3.06/2.74 (dt+dt, 2H).

¹³ C-NMR (125 MHz, dmso-d6) d ppm 162.3, 161.4, 158.6, 150.7, 144.1, 140.3, 126, 120.9, 119.7, 118.4, 72, 56.6, 42.7, 42

Preparation R2bf: 2- [3-(6-methoxy-5-nitro-pyrimidin-4-yl)oxyphenyl] propan-2-ol Using General Procedure 1 starting from Preparation Rla and 3-(l-hydroxy-l-methyl- ethyl)phenol as reagents, Preparation R2bf was obtained. HRMS calculated for C14H15N3O5: 305.1012; found 306.1083 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 8.59 (s, 1H), 7.42-7.07 (m, 4H), 5.13 (br., 1H), 4.1 (s, 3H), 1.42 (s, 6H).

¹³ C-NMR (125 MHz, dmso-d6) d ppm 162.4, 161.2, 158.7, 153.6, 151.7,

129.6/123.1/119.6/118, 71, 56.6, 32.3.

Preparation R2bg: 2-fluoro-4-(6-methoxy-5-nitro-pyrimidin-4-yl)oxy-benzonitril e Using General Procedure 1 starting from Preparation Rla and 2-fluoro-4-hydroxy- benzonitrile as reagents, Preparation R2bg was obtained. HRMS calculated for C12H7FN4O4: 290.0451; found 291.0522 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 8.66 (s, 1H), 8.09 (dd, 1H), 7.74 (dd, 1H), 7.44 (dm, 1H), 4.13 (s, 3H).

¹³ C-NMR (125 MHz, dmso-d6) d ppm 163.5, 162.7, 160.2, 158.8, 156.8, 135.6, 119.8, 114, 111.6, 98.7, 56.9.

Preparation R2bh: 2-chloro-4-(6-methoxy-5-nitro-pyrimidin-4-yl)oxy-benzonitril e Using General Procedure 1 starting from Preparation Rla and 2-chloro-4-hydroxy- benzonitrile as reagents, Preparation R2bh was obtained. HRMS calculated for C12H7CIN4O4: 306.0156; found 307.0226 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 8.66 (s, 1H), 8.13 (d, 1H), 7.92 (d, 1H), 7.56 (dd, 1H), 4.12 (s, 3H).

¹³ C-NMR (125 MHz, dmso-d6) d ppm 162.7, 160.3, 158.8, 155.8, 137.1, 136.6, 124.3, 122.3, 116, 110.5, 56.8.

Preparation R2bi: 2- [4-(6-methoxy-5-nitro-pyrimidin-4-yl)oxyphenyl] acetonitrile Using General Procedure 1 starting from Preparation Rla and 2-(4-hydroxyphenyl)acetonitrile as reagents, Preparation R2bi was obtained. HRMS calculated for C13H10N4O4: 286.0702; found 287.077 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 8.58 (s, 1H), 7.45 (m, 2H), 7.31 (m, 2H), 4.1 (s, 2H), 4.09 (s, 3H) ¹³ C-NMR (125 MHz, dmso-d6) d ppm 162.4, 161.1, 158.6, 151.3, 130.2, 130.1, 122.7, 119.6, 56.6, 22.3

Preparation R2bi: 3- [4-(6-methoxy-5-nitro-pyrimidin-4-yl)oxyphenyl] propanenitrile Using General Procedure 1 starting from Preparation Rla and 3-(4-hydroxyphenyl)propanenitrile as reagents, Preparation R2bj was obtained. HRMS calculated for C14H12N4O4: 300.0858; found 300.08627 (M ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 8.59 (s, 1H), 7.39 (m, 2H), 7.23 (m, 2H), 4.1 (s, 3H), 2.92 (m, 2H), 2.84 (m, 2H).

¹³ C-NMR (125 MHz, dmso-d6) d ppm 158.6, 130.3, 122, 120.7, 56.6, 30.3, 18.6.

Preparation R2bk: 3-chloro-4-(6-methoxy-5-nitro-pyrimidin-4-yl)oxy-benzonitril e Using General Procedure 1 starting from Preparation Rla and 3-chloro-4-hydroxy- benzonitrile as reagents, Preparation R2bk was obtained. HRMS calculated for C12H7CIN4O4: 306.0156; found 307.0227 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 8.63 (s, 1H), 8.33 (d, 1H), 8 (dd, 1H), 7.76 (d, 1H), 4.13 (s, 3H).

¹³ C-NMR (125 MHz, dmso-d6) d ppm 162.7, 159.8, 158.8, 151.3, 135, 133.7, 127.6, 126, 117.5, 111.6, 57.

Preparation R2bm: tert-butyl N- [ 1- [4-(6-methoxy-5-nitro-pyrimidin-4-yl)oxyphenyl] ethyl] carbamate

Using General Procedure 1 starting from Preparation Rla and tert-butyl N-[l-(4- hydroxyphenyl)ethyl] carbamate as reagents, Preparation R2bm was obtained. HRMS calculated for C18H22N4O6: 390.1539; found 408.1877 ((M+NH ₄ ) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 8.58 (s, 1H), 7.44 (d, 1H), 7.37 (m, 2H), 7.2 (m, 2H), 4.65 (m, 1H), 4.1 (s, 3H), 1.37 (s, 9H), 1.31 (d, 3H).

¹³ C-NMR (125 MHz, dmso-d6) d ppm 158.6, 127.6, 121.7, 56.6, 49.5, 28.7, 23.3.

Preparation R2bn: tert-butyl N-[l-[4-(6-methoxy-5-nitro-pyrimidin-4-yl)oxyphenyl] propyl] carbamate

4-(l-Aminopropyl)phenol, hydrochloride (1 :1) (1 g, 5.3286 mmol) tert-butoxycarbonyl tert-butyl carbonate (1.5 eq., 7.9929 mmol) and sodium hydrogen carbonate (3.0 eq., 15.9858 mmol) were dissolved in THF (10 mL), and water (10 mL). The reaction mixture was stirred at r.t. for 20 hours. The reaction mixture was extracted with EtOAc (3 x 10 ml). The organic layer was evaporated after drying with brine and MgS0 ₄ to give tert-butyl N-[ 1 -[4-(6-mcthoxy-5-nitro-pyrimidin-4-yl)oxyphcnyl]propyl]carba matc.

Using General Procedure 1 starting from Preparation Rla and tert-butyl N-[l-[4-(6- methoxy-5-nitro-pyrimidin-4-yl)oxyphenyl] propyl] carbamate as reagents,

Preparation R2bn was obtained. HRMS calculated for C ₁₉ H ₂₄ N ₄ O ₆ : 404.1696; found 422.2022 ((M+NH ₄ ) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 8.59 (s, 1H), 7.4 (d, 1H), 7.35 (m, 2H), 7.2 (m, 2H), 4.39 (m, 1H), 4.1 (s, 3H), 1.66/1.61 (m+m, 2H), 1.37 (s, 3H), 0.83 (t, 3H).

¹³ C-NMR (125 MHz, dmso-d6) d ppm 158.7, 128.2, 121.7, 56.6, 55.8, 29.9, 28.7, 11.6.

Preparation R2bq: 4-methoxy-5-nitro-6-(3-pyridyloxy)pyrimidine

Using General Procedure 1 starting from Preparation Rla and pyridin-3-ol as reagents, Preparation R2bq was obtained. HRMS calculated for C ₁₀ H ₈ N ₄ O ₄ : 248.0546; found 249.0615 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 8.61 (s, 1H), 8.58 (d, 1H), 8.54 (dd, 1H), 7.82 (ddd, 1H), 7.55 (dd, lH), 4T2 (s, 3H)

¹³ C-NMR (125 MHz, dmso-d6) d ppm 162.5, 160.9, 158.7, 148.8, 147.9, 143.8, 130.2, 125.1, 120.9, 56.7

Preparation R2bs: 6-(6-methoxy-5-nitro-pyrimidin-4-yl)oxy-lH-pyrrolo[3,2-b] pyridine

Using General Procedure 1 starting from Preparation Rla and lH-pyrrolo[3,2-b] pyridin-6-ol as reagents, Preparation R2bs was obtained. HRMS calculated for C ₁₂ H ₉ N ₅ O ₄ : 287.0655; found 288.0733 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 11.49 (br., 1H), 8.57 (s, 1H), 8.25 (d, 1H), 7.77 (dd, 1H), 7.71 (dd, 1H), 6.61 (m, 1H), 4.11 (s, 3H)

¹³ C-NMR (125 MHz, dmso-d6) d ppm 162.4, 161.7, 158.6, 145/143.6/128.3, 136.9, 131.2, 120.9, 112.4, 102.2, 56.6 Preparation R2bt: 4-(3-benzyloxy-4-chloro-phenoxy)-6-methoxy-5-nitro-pyrimidin e Using General Procedure 1 starting from Preparation Rla and 3-benzyloxy-4-chloro- phenol as reagents, Preparation R2bt was obtained. HRMS calculated for C ₁₈ H ₁₄ CIN ₃ O ₅ : 387.0622; found 388.0696 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 8.6 (s, 1H), 7.49-7.31 (m, 5H), 7.53 (d, 1H), 7.3 (d, 1H), 6.92 (dd, 1H), 5.18 (s, 2H), 4.11 (s, 3H)

¹³ C-NMR (125 MHz, dmso-d6) d ppm 158.7, 130.8, 115.2, 108.9, 70.8, 56.7

Preparation R2bu: 4-(3-benzyloxy-4-methyl-phenoxy)-6-methoxy-5-nitro-pyrimidin e Using General Procedure 1 starting from Preparation Rla and 3-benzyloxy-4-methyl- phenol as reagents, Preparation R2bu was obtained. HRMS calculated for C ₁₉ H ₁₇ N ₃ O ₅ : 367.1168; found 368.1237 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 8.57 (s, 1H), 7.48-7.30 (m, 5H), 7.22 (dm, 1H), 7.01 (d, 1H), 6.75 (dd, 1H), 5.08 (s, 2H), 4.1 (s, 3H), 2.2 (brs, 3H)

¹³ C-NMR (125 MHz, dmso-d6) d ppm 158.6, 131.1, 113.5, 106.3, 69.9, 56.6, 16.2

Preparation R2bv: tert-butyl 4- [2- [4-(6-methoxy-5-nitro-pyrimidin-4-yl)oxyphenyl] ethyl] piperidine- 1-carboxylate

4-[2-(4-piperidyl)ethyl]phenol (1 g, 4.871 mmol), tert-butoxycarbonyl tert-butyl carbonate (1.5 eq., 7.306 mmol) and sodium hydrogencarbonate (4.0 eq., 19.48 mmol) were dissolved in THF (10 mL) and water (10 mL). The reaction mixture was stirred at r.t. for 20 hours. Then water was added (30 ml) and it was extracted with EtOAc (3 x 30 ml). The organic layer was evaporated after drying with MgS0 ₄ .The residue was washed with diisopropyl ether and the solid compound was filtered off to give tert-butyl 4-[2-(4- hydroxyphenyl)ethyl]piperidine-l-carboxylate as a crude product.

Using General Procedure 1 starting from Preparation Rla and tert-butyl 4-[2-(4- hydroxyphenyl)ethyl]piperidine-l-carboxylate as reagents, Preparation R2bv was obtained. HRMS calculated for C ₂₃ H ₃₀ N ₄ O ₆ : 458.2165; found 403.1608 ((M+H-C ₄ H _¾ ) form).

1H-NMR (500 MHz, dmso-d6) d ppm 8.58 (s, 1H), 7.28 (m, 2H), 7.15 (m, 2H), 4.1 (s, 3H), 3.92/2.67 (m+m, 4H), 2.62 (m, 2H), 1.69/1.01 (m+m, 4H), 1.51 (m, 2H), 1.4 (m, 1H), 1.38 (s, 3H) ¹³ C-NMR (125 MHz, dmso-d6) d ppm 158.7, 130, 121.8, 56.6, 44, 38.6, 38.3, 35.3, 32.1, 32

Preparation R2bw: 4- [ [4- [(6-methoxy-5-nitro- 1 ,4-dihydropyrimidin-4-yl)oxy] phenyl] methyl] morpholine

Using General Procedure 1 starting from Preparation Rla and 4-(morpholinomethyl)phenol as reagents, Preparation R2bw was obtained. HRMS calculated for C ₁₆ H ₁₈ N ₄ O ₅ : 346.1277; found 347.1351 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 8.59 (s, 1H), 7.39 (dm, 2H), 7.21 (dm, 2H), 4.1 (s, 3H), 3.58 (t, 4H), 3.48 (s, 2H), 2.36 (br„ 4H)

1 ³ C-NMR (125 MHz, dmso-d6) d ppm 162.4, 161.1, 158.7, 150.9, 136.5, 130.6, 121.7, 66.7, 61.2, 56.6, 53.6

Preparation R2bx: tert-butyl 2- [2- [4-(6-methoxy-5-nitro-pyrimidin-4-yl)oxyphenyl] ethyl] piperidine- 1-carboxylate

4-[2-(2-piperidyl)ethyl]phenol (1 g, 4.871 mmol), tert-butoxycarbonyl tert-butyl carbonate (1.5 eq., 7.306 mmol) and sodium hydrogencarbonate (4.0 eq., 19.48 mmol) were dissolved in THF (10 mL) and water (10 mL). The reaction mixture was stirred at r.t. for 20 hours. Then water was added (30 ml) and it was extracted with EtOAc (3 x 30 ml). The organic layer was evaporated after drying with MgS0 ₄ .The residue was crystalized from the mixture of diisopropyl ether pentane, and the solid compound was filtered off to give tert-butyl 2-[2-(4-hydroxyphenyl)ethyl]piperidine-l-carboxylate as a crude product.

Using General Procedure 1 starting from Preparation Rla and tert-butyl 2-[2-(4- hydroxyphenyl)ethyl]piperidine-l-carboxylate as reagents, Preparation R2bx was obtained. HRMS calculated for C ₂₃ H ₃₀ N ₄ O ₆ : 458.2165; found 481.20517 ((M+Na) ⁺ form). 1H-NMR (500 MHz, dmso-d6) d ppm 8.57 (s, 1H), 7.3 (dm, 2H), 7.16 (dm, 2H), 4.16 (br., 1H), 4.1 (s, 3H), 3.85/2.81 (br.+br., 2H), 2.57/2.46 (m+m, 2H), 1.95/1.73 (m+m, 2H),

1.58/1.48 (m+m, 2H), 1.57/1.26 (m+m, 2H), 1.56/1.51 (m+m, 2H), 1.37 (s, 9H).

¹³ C-NMR (125 MHz, dmso-d6) d ppm 162.4, 161.2, 158.6, 156, 140.5, 130, 121.8, 78.8, 56.6, 50.2, 38.9, 31.9, 31.4, 28.6, 28.4, 25.6, 19 Preparation R2bv: tert-butyl 2-[3-(6-methoxy-5-nitro-pyrimidin-4-yl)oxyphenyl] morpholine-4-carboxylate

3-morpholin-2-ylphenol (1 g, 5.579 mmol), tert-butoxycarbonyl tert-butyl carbonate (1.5 eq., 8.369 mmol) and sodium hydrogencarbonate (4.0 eq., 22.319 mmol) were dissolved in THF (10 mL) and water (10 mL). The reaction mixture was stirred at r.t. for 20 hours. Then water was added (30 ml) and it was extracted with EtOAc (3 x 30 ml). The organic layer was evaporated after drying with MgS0 ₄ to give tert-butyl 2-(3-hydroxyphenyl)morpholine-4-carboxylate as a crude product.

Using General Procedure 1 starting from Preparation Rla and tert-butyl 2-(3- hydroxyphenyl)morpholine-4-carboxylate as reagents, Preparation R2by was obtained. HRMS calculated for C ₂₀ H ₂₄ N ₄ O ₇ : 432.1645; found 455.153 ((M+Na) ⁺ form).

1H-NMR (400 MHz, dmso-d6) d ppm 8.6 (s, 1H), 7.47 (t, 1H), 7.34 (dm, 1H), 7.28 (t, 1H), 7.23 (dm, 1H), 4.45 (dd, 1H), 4.1 (s, 3H), 3.94/3.55 (m+m, 2H), 3.91/2.78 (brm, 2H), 3.78/2.97 (brm, 2H), 1.41 (s, 3H).

¹³ C-NMR (100 MHz, dmso-d6) d ppm 158.7, 130.3, 124.7, 121.6, 119.8, 76.5, 66.4, 56.6, 49.7, 43.2, 28.5

Preparation R2bz: tert-butyl N-[(lR)-2,2,2-trifluoro-l-[4-(6-methoxy-5-nitro- pyrimidin-4-yl)oxyphenyl] ethyl] carbamate

4-[(lR)-l-amino-2,2,2-trifluoro-ethyl]phenol (850 mg, 3.734 mmol), tert-butoxycarbonyl tert-butyl carbonate (1.5 eq., 5.601 mmol) and sodium hydrogencarbonate (2.0 eq., 7.468 mmol) were dissolved in THF (10 mL) and water (10 mL). The reaction mixture was stirred at r.t. for 18 hours. It was extracted with EtOAc (3 x 10 ml). The organic layer was evaporated after drying with MgS0 ₄ to give tert-butyl N-[(lR)-2,2,2-trifluoro-l-(4- hydroxyphenyl)ethyl] carbamate as a crude product.

Using General Procedure 1 starting from Preparation Rla and tert-butyl N-[(lR)-2,2,2- trifluoro-l-(4-hydroxyphenyl)ethyl] carbamate as reagents, Preparation R2bz was obtained. HRMS calculated for C ₁₈ H ₁₉ F ₃ N ₄ O ₆ : 444.1257; found 462.1587 ((M+NH ₄ ) ⁺ form).

1H-NMR (400 MHz, dmso-d6) d ppm 8.91/8.6 (s, 1H), 8.42/8.4 (d, 1H), 7.7/7.62 (dm, 2H), 7.35/7.24 (dm, 2H), 5.51 (m, 1H), 4.12/4.11 (s, 3H), 1.41/1.4 (s, 9H) ¹³ C-NMR (100 MHz, dmso-d6) d ppm 162.5, 161, 159.1/158.6, 152.2, 132.1, 130.6/130.3, 122.2/122.1, 79.9, 57.1/56.7, 55, 28.5

Preparation R2ca: 2- [4-(6-methoxy-5-nitro-pyrimidin-4-yl)oxyphenyl] acetonitrile Using General Procedure 1 starting from Preparation Rla and 2-(4- hydroxyphenyl)acetonitrile as reagents, Preparation R2ca was obtained. HRMS calculated for C ₁₃ H ₁₀ N ₄ O ₄ : 286.0702; found 287.0770 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 8.58 (s, 1H), 7.45 (m, 2H), 7.31 (m, 2H), 4.1 (s, 2H), 4.09 (s, 3H)

¹³ C-NMR (125 MHz, dmso-d6) d ppm 162.4, 161.1, 158.6, 151.3, 130.2, 130.1, 122.7, 119.6, 56.6, 22.3

Preparation R2cb: [2-fluoro-5-(6-methoxy-5-nitro-pyrimidin-4-yl)oxy- phenyl] methanol

Using General Procedure 1 starting from Preparation Rla and 4-fluoro-3- (hydroxymethyl)phenol as reagents, Preparation R2cb was obtained. HRMS calculated for C ₁₂ H ₁₀ FN ₃ O ₅ : 295.0605; found 296.06726 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 8.59 (s, 1H), 7.32 (dd, 1H), 7.26 (t, 1H), 7.21 (ddd, 1H), 5.4 (t, 1H), 4.56 (d, 2H), 4.1 (s, 3H)

¹³ C-NMR (125 MHz, dmso-d6) d ppm 162.4, 161.2, 158.6, 157.5, 147.9, 131.5, 122.1, 122, 120.9, 116.5, 56.9, 56.6 Preparation R2cc: 4-(4-fluoro-3-nitro-phenoxy)-6-methoxy-5-nitro-pyrimidine

Using General Procedure 1 starting from Preparation Rla and 4-fluoro-3-nitro-phenol as reagents, Preparation R2cc was obtained. HRMS calculated for CnH ₇ FN ₄ 0 ₆ : 310.035; found 311.0429 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 8.63 (s, 1H), 8.25 (dd, 1H), 7.83 (ddd, 1H), 7.74 (dd, 1H), 4.12 (s, 3H)

¹³ C-NMR (125 MHz, dmso-d6) d ppm 162.6, 160.8, 158.6, 153.1, 147.3, 137.5, 130.6, 120.9, 120.4, 120.2, 56.8 Preparation R2cd: 4-(4-isopropenyl-3-methoxy-phenoxy)-6-methoxy-5-nitro- pyrimidine

Using General Procedure 1 starting from Preparation Rla and 4-bromo-3-methoxy- phenol as reagents, 4-(4-bromo-3-methoxy-phenoxy)-6-methoxy-5-nitro-pyrimidine was obtained.

4-(4-bromo-3-methoxy-phenoxy)-6-methoxy-5-nitro-pyrimidine (500 mg, 1.4 mmol), 2-isopropenyl-4,4,5,5-tetramethyl-l,3,2-dioxaborolane (2.8 mmol, 2.0 eq.), potassium carbonate (4.3 mmol, 3.07 eq.), tetrakis(triphenylphosphine)palladium(0) (0.14 mmol, 0.1 eq.) were dissolved in dry toluene. The resulted mixture was heated and stirred at 100 °C till completion. Then ethyl acetate and brine were added. The layers were separated. The organic layer was dried over magnesium sulfate and evaporated. It was purified by Flash chromatography (eluent: heptane:ethyl acetate= 3:2) to give Preparation R2cd.

1H-NMR (500 MHz, dmso-d6) d ppm 8.61 (s, 1H), 7.21 (d, 1H), 6.96 (d, 1H), 6.81 (dd, 1H), 5.13/5.05 (m+m, 2H), 4.11 (s, 3H), 3.75 (s, 3H), 2.05 (dd, 3H)

¹³ C-NMR (125 MHz, dmso-d6) d ppm 158.7, 129.9, 116.2, 113.6, 105.9, 56.6, 56.3, 23.5

Preparation R2ce: tert-butyl 2-[4-(6-methoxy-5-nitro-pyrimidin-4- yl)oxyphenyl] piperidine- 1-carboxylate

4-(2-piperidyl)phenol hydrochloride(l.2 g, 5.615 mmol), tert-butoxycarbonyl tert-butyl carbonate (1.5 eq., 8.423 mmol) and sodium hydrogencarbonate (4.0 eq., 22.461 mmol) were dissolved in THF (15 mL) and water (15 mL). The reaction mixture was stirred at r.t. for 20 hours. Then water was added (30 ml) and it was extracted with EtOAc (3 x 30 ml). The organic layer was evaporated after drying with MgS0 ₄ .The residue was washed with mixture of diisopropyl ether and ethanol and the solid compound was filtered off to give tert-butyl 2-(4-hydroxyphenyl)piperidine-l-carboxylate as a crude product.

Using General Procedure 1 starting from Preparation Rla and tert-butyl 2-(4- hydroxyphenyl)piperidine-l-carboxylate as reagents, Preparation R2ce was obtained. HRMS calculated for C21H26N4O6: 430.1852; found 375.1292 ((M+H-C ₄ H ₈ ) ⁺ form).

1H-NMR (400 MHz, dmso-d6) d ppm 8.6 (s, 1H), 7.27 (s, 2H), 7.27 (s, 2H), 5.29 (d, 1H), 4.1 (s, 3H), 3.94/2.72 (m+m, 2H), 2.38-1.18 (m, 6H), 1.4 (s, 9H)

¹³ C-NMR (100 MHz, dmso-d6) d ppm 158.8, 128.1, 122.2, 56.6, 53, 40.3, 28.6 Preparation R3a: 6-methoxy-4-phenoxy- 1 ,6-dihydropyrimidin-5-amine

Using General Procedure 2 starting from Preparation R2a as reagent, Preparation R3a was obtained. HRMS calculated for C ₁₁ H ₁₁ N ₃ O ₂ : 217.0851; found 218.092 ((M+H) ⁺ form). 1H-NMR (500 MHz, dmso-d6) d ppm 7.75 (s, 1H), 7.4 (m, 2H), 7.19 (m, 1H), 7.12 (m, 2H), 4.85 (brs, 2H), 3.95 (s, 3H).

¹³ C-NMR (125 MHz, dmso-d6) d ppm 158, 154.7, 154.1, 142.9, 129.9, 124.9, 121.4,

117.3. 54.4.

Preparation R3b: 4-(2-fluorophenoxy)-6-methoxy-pyrimidin-5-amine

Using General Procedure 2 starting from Preparation R2b as reagent, Preparation R3b was obtained. HRMS calculated for C ₁₁ H ₁₀ FN ₃ O ₂ : 235.0757; found 235.07507 (M ⁺ form). 1H-NMR (500 MHz, dmso-d6) d ppm 7.71 (s, 1H), 7.35 (m, 1H), 7.31 (m, 1H), 7.28 (m, 1H), 7.24 (m, 1H), 4.92 (s, 2H), 3.95 (s, 3H).

¹³ C-NMR (125 MHz, dmso-d6) d ppm 157.9, 154.5, 142.7, 140.9, 127, 125.5, 124.7,

117.1. 54.5. Preparation R3c: 4-methoxy-6-(4-methoxyphenoxy)pyrimidin-5-amine

Using General Procedure 2 starting from Preparation R2c as reagent, Preparation R3c was obtained. HRMS calculated for C ₁₂ H ₁₃ N ₃ O ₃ : 247.0957; found 248.10318 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 7.72 (s, 1H), 7.06 (m, 2H), 6.94 (m, 2H), 4.79 (s, 2H), 3.94 (s, 3H), 3.75 (s, 3H).

¹³ C-NMR (125 MHz, dmso-d6) d ppm 157.7, 156.5, 155.4, 147.3, 142.9, 122.8, 116.7, 114.9.

Preparation R3d: 4-methoxy-6-(3-methoxyphenoxy)pyrimidin-5-amine

Using General Procedure 2 starting from Preparation R2d as reagent, Preparation R3d was obtained. HRMS calculated for C ₁₂ H ₁₃ N ₃ O ₃ : 247.0957; found 248.10317 ((M+H) ⁺ form).

1H-NMR (400 MHz, dmso-d6) d ppm 7.76 (s, 1H), 7.29 (t, 1H), 6.77 (dd, 1H), 6.71 (t, 1H), 6.69 (dd, 1H), 4.83 (s, 2H), 3.95 (s, 3H), 3.74 (s, 3H).

¹³ C-NMR (125 MHz, dmso-d6) d ppm 160.7, 158.1, 155.2, 142.9, 130.3, 113.5, 110.6, 107.4, 55.8, 54.4.

Preparation R3e: 4-(4-fluorophenoxy)-6-methoxy-pyrimidin-5-amine

Using General Procedure 2 starting from Preparation R2e as reagent, Preparation R3e was obtained. HRMS calculated for C ₁₁ H ₁₀ FN ₃ O ₂ : 235.0757; found 235.07503 (M ⁺ form). 1H-NMR (500 MHz, dmso-d6) d ppm 7.74 (s, 1H), 7.23 (m, 2H), 7.18 (m, 2H), 4.86 (s, 2H), 3.95 (s, 3H).

¹³ C-NMR (125 MHz, dmso-d6) d ppm 159.2, 157.9, 154.9, 150.1, 142.9, 123.4, 116.4, 54.4.

Preparation R3f: 4-(3-fluorophenoxy)-6-methoxy-pyrimidin-5-amine

Using General Procedure 2 starting from Preparation R2f as reagent, Preparation R3f was obtained. HRMS calculated for C ₁₁ H ₁₀ FN ₃ O ₂ : 235.0757; found 236.0824 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 7.78 (s, 1H), 7.43 (m, 1H), 7.08-7.01 (m, 1H), 7.08- 7.01 (m, 1H), 6.99 (m, 1H), 4.92 (br„ 2H), 3.96 (s, 3H).

¹³ C-NMR (125 MHz, dmso-d6) d ppm 162.8, 158.2, 155.3, 154, 142.8, 131.2, 117.7, 116.8, 111.7, 108.5, 54.5.

Preparation R3g: 4-(3,5-dimethoxyphenoxy)-6-methoxy-pyrimidin-5-amine

Using General Procedure 2 starting from Preparation R2g as reagent, Preparation R3g was obtained. HRMS calculated for C ₁₃ H ₁₅ N ₃ O ₄ : 277.1063; found 278.1141 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 7.77 (s, 1H), 6.35 (t, 1H), 6.3 (d, 2H), 4.83 (br., 2H), 3.95 (s, 3H), 3.72 (s, 6H).

¹³ C-NMR (125 MHz, dmso-d6) d ppm 161.3, 158.1, 155.9, 154.4, 142.9, 117.5, 99.9, 97, 55.9, 54.4.

Preparation R3h: 4-(3,5-difluorophenoxy)-6-methoxy-pyrimidin-5-amine

Using General Procedure 2 starting from Preparation R2h as reagent, Preparation R3h was obtained. HRMS calculated for C ₁₁ H ₉ F ₂ N ₃ O ₂ : 253.0663; found 254.0738 ((M+H) ⁺ form).

1H-NMR (400 MHz, dmso-d6) d ppm 7.81 (s, 1H), 7.09 (m, 1H), 6.98 (m, 2H), 4.98 (OT., 2H), 3.96 (s, 3H).

¹³ C-NMR (125 MHz, dmso-d6) d ppm 163, 158.5, 156.2, 153.2, 142.8, 118.1, 105.2,

100.4, 54.5.

Preparation R3i: 4-methoxy-N-methyl-6-phenoxy-pyrimidin-5-amine

To the solution (in THF) of 4,6-dichloro-N-methyl-pyrimidin-5-amine freshly prepared sodium phenoxide (1.1 eq.) in THF was added and it was stirred at r.t. for 40 hours. The reaction mixture was purified by Hanbon preparative HPLC (C 18 Silica, Gemini NX 5 pm, 5 mM NH ₄ HC0 ₃ -MeCN) using gradient method 5-90 %. Solvent was evaporated under reduced pressure to give 4-chloro-N-methyl-6-phenoxy-pyrimidin-5-amine as a crude product. It was dissolved in methanol and sodium methoxide (2.2 eq.) was added. The reaction mixture was heated and stirred at 50 °C for 3 hours. The reaction mixture was filtered and the filtrate was purified by Hanbon preparative HPLC (Cl 8 Silica, Gemini NX 5 pm, 5 mM NH ₄ HC0 ₃ -MeCN) using gradient method 5-90 %. Solvent was evaporated under reduced pressure to give Preparation R3i. HRMS calculated for C ₁₂ H ₁₃ N ₃ O ₂ : 231.1008; found 232.108 ((M+H ⁾⁺ form).

1H-NMR (400 MHz, dmso-d6) d ppm 7.81 (s, 1H), 7.39 (m, 2H), 7.18 (tm, 1H), 7.1 (dm, 2H), 4.8 (q, 1H), 3.95 (s, 3H), 2.89 (d, 3H).

¹³ C-NMR (125 MHz, dmso-d6) d ppm 159.8, 155.7, 154.5, 144.3, 130, 124.7, 121, 120, 54.6, 33.1.

Preparation R3i: 4-(4-chlorophenoxy)-6-methoxy-pyrimidin-5-amine

Using General Procedure 2 starting from Preparation R2j as reagent, Preparation R3j was obtained. HRMS calculated for C ₁₁ H ₁₀ CIN ₃ O ₂ : 251.0462; found 252.0523 ((M+H) ⁺ form).

1H-NMR (400 MHz, dmso-d6) d ppm 7.76 (s, 1H), 7.45 (m, 2H), 7.18 (m, 2H), 4.9 (s, 2H), 3.95 (s, 3H).

¹³ C-NMR (125 MHz, dmso-d6) d ppm 158.1, 154.3, 153, 142.8, 129.8, 128.8, 123.3,

117.4, 54.4. Preparation R3k: 4-(4-chloro-3-methoxy-phenoxy)-6-methoxy-pyrimidin-5-amine Using General Procedure 3 starting from Preparation R2k as reagent, Preparation R3k was obtained. HRMS calculated for C12H12CIN3O3: 281.0567; found 282.0637 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 7.77 (s, 1H), 7.42 (d, 1H), 6.99 (d, 1H), 6.73 (dd, 1H), 4.89 (s, 2H), 3.95 (s, 3H), 3.82 (s, 3H).

¹³ C-NMR (125 MHz, dmso-d6) d ppm 158.1, 155.6, 154.3, 154, 142.8, 130.3, 117.4, 117,

114.1, 106.9.

Preparation R31: 4-(3-chlorophenoxy)-6-methoxy-pyrimidin-5-amine

Using General Procedure 3 starting from Preparation R21 as reagent, Preparation R31 was obtained. HRMS calculated for C1 1H10CIN3O2: 251.0462; found 252.0533 ((M+H) ⁺ form).

1H-NMR (400 MHz, dmso-d6) d ppm 7.78 (s, 1H), 7.43 (t, 1H), 7.27 (dm, 1H), 7.26 (m, 1H), 7.13 (dm, 1H), 4.93 (brs, 2H), 3.96 (s, 3H)

1 ³ C-NMR (125 MHz, dmso-d6) d ppm 158.3, 155.1, 153.9, 142.8, 131.4, 124.9, 121.5,

120.2, 54.6, 7.26

Preparation R3n: 4-(l,3-benzodioxol-5-yloxy)-6-methoxy-pyrimidin-5-amine

Using General Procedure 2 starting from Preparation R2n as reagent, Preparation R3n was obtained. HRMS calculated for C12H1 1N3O4: 261.075; found 262.0819 ((M+H) ⁺ form). 1H-NMR (500 MHz, dmso-d6) d ppm 7.74 (s, 1H), 6.9 (d, 1H), 6.8 (d, 1H), 6.59 (dd, 1H), 6.05 (s, 2H), 4.79 (br„ 2H), 3.94 (s, 3H)

¹³ C-NMR (125 MHz, dmso-d6) d ppm 157.8, 155.3, 148.3, 148.1, 144.5, 142.9, 116.8, 114.1, 108.4, 104.3, 102, 54.4

Preparation R3o: 3-(5-amino-6-methoxy-pyrimidin-4-yl)oxy-5-methoxy-phenol

Using General Procedure 2 starting from Preparation R2o as reagent, Preparation R3o was obtained. HRMS calculated for C12H13N3O4: 263.0906; found 263.09017 (M ⁺ form). 1H-NMR (500 MHz, dmso-d6) d ppm 7.78 (s, 1H), 6.16 (t, 1H), 6.14 (t, 1H), 6.08 (t, 1H), 4.81 (s, 2H), 3.95 (s, 3H), 3.67 (s, 3H). ¹³ C-NMR (125 MHz, dmso-d6) d ppm 161.3, 159.4, 158.1, 155.9, 154.4, 143, 117.6, 100.9, 98.2, 97.9, 55.6, 54.4.

Preparation R3p: 4-(4-fluoro-3-methoxy-phenoxy)-6-methoxy-pyrimidin-5-amine Using General Procedure 2 starting from Preparation R2p as reagent, Preparation R3p was obtained. HRMS calculated for C12H12FN3O3: 265.0863; found 266.0931 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 7.76 (s, 1H), 7.21 (dd, 1H), 7 (dd, 1H), 6.69 (dm, 1H), 4.85 (s, 2H), 3.95 (s, 3H), 3.8 (s, 3H).

¹³ C-NMR (125 MHz, dmso-d6) d ppm 142.9, 116.2, 113.3, 108.1. Preparation R3q: 4-methoxy-6-phenoxy-N-(2,2,2-trifluoroethyl)pyrimidin-5-amin e

Preparation R3a and triethylamine (1.5 eq.) were dissolved in abs. THF and 2,2,2-trifluoroethyl-trifluoromethanesulfonate (1.2 eq.) was added. The reaction mixture was heated and stirred at 70 °C for 214 hours. The reaction mixture was purified by Hanbon preparative HPLC (Cl 8 Silica, Gemini NX 5 pm, 5 mM NH ₄ HC03-MeCN) using gradient method 5-90 %. Solvent was evaporated under reduced pressure to give Preparation R3q. HRMS calculated for C13H12F3N3O2: 299.0882; found 300.0946 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 7.91 (s, 1H), 7.42 (tm, 2H), 7.23 (tm, 1H), 7.11 (dm, 2H), 5.5 (t, 1H), 4.06 (m, 2H), 3.99 (s, 3H)

1 ³ C-NMR (125 MHz, dmso-d6) d ppm 160, 157.1, 153.6, 146.1, 130.1, 126.2, 125.3, 121.6, 115.6, 54.8, 45.6

Preparation R3r: 4-methoxy-6- [3-(trifluor omethoxy)phenoxy] pyrimidin-5-amine Using General Procedure 2 starting from Preparation R2r as reagent, Preparation R3r was obtained. HRMS calculated for C12H10F3N3O3: 301.0674; found 302.0742 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 7.79 (s, 1H), 7.53 (m, 1H), 7.23-7.18 (m, 3H), 4.96 (br„ 2H), 3.96 (s, 3H).

¹³ C-NMR (125 MHz, dmso-d6) d ppm 158.3, 153.8, 152.2, 149.2, 142.8, 131.3, 120.5, 120.4/117.2/114.4, 117.8, 54.5. Preparation R3s: 4-methoxy-6-(3-methylphenoxy)pyrimidin-5-amine

Using General Procedure 2 starting from Preparation R2s as reagent, Preparation R3s was obtained. HRMS calculated for C ₁₂ H ₁₃ N ₃ O ₂ : 231.1008; found 232.1083 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 7.75 (s, 1H), 7.27 (t, 1H), 7.01 (brd, 1H), 6.93 (br., 1H), 6.91 (dm, 1H), 4.82 (br., 2H), 3.95 (s, 3H), 2.31 (s, 3H).

¹³ C-NMR (125 MHz, dmso-d6) d ppm 158, 154.8, 154.2, 143, 139.6, 129.6, 125.5, 121.8, 118.4, 117.3, 54.4, 21.3.

Preparation R3t: 4-(3-bromophenoxy)-6-methoxy-pyrimidin-5-amine

Using General Procedure 2 starting from Preparation R2t as reagent, Preparation R3t was obtained. HRMS calculated for CnHioBr^CU 294.9956; found 296.00304 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 7.78 (s, 1H), 7.4 (m, 1H), 7.39 (m, 1H), 7.36 (m, 1H), 7.17 (m, 1H), 4.93 (s, 2H), 3.96 (s, 3H).

¹³ C-NMR (125 MHz, dmso-d6) d ppm 158.2, 154, 142.8, 131.7, 127.7, 124.2, 120.5, 117.7.

Preparation R3u: 4-methoxy-6- [3-(pentafluoro^ ⁶ -sulfanyl)phenoxy] pyrimidin-5- amine

Using General Procedure 2 starting from Preparation R2u as reagent, Preparation R3u was obtained. HRMS calculated for C _{1 1} H ₁₀ F ₅ N ₃ O ₂ S: 343.0414; found 344.0484 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 7.79 (s, 1H), 7.75 (dm, 1H), 7.72 (t, 1H), 7.65 (t, 1H), 7.5 (dm, 1H), 5.01 (s, 2H), 3.97 (s, 3H).

¹³ C-NMR (125 MHz, dmso-d6) d ppm 158.3, 154, 153.7, 153.6, 142.7, 130.8, 125.6, 122.2, 119, 117.8, 54.5.

Preparation R3v: 4-methoxy-6- [3-(trifluor omethyl)phenoxy] pyrimidin-5-amine

Using General Procedure 2 starting from Preparation R2v as reagent, Preparation R3v was obtained. HRMS calculated for C ₁₂ H ₁₀ F ₃ N ₃ O ₂ : 285.0725; found 286.0796 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 7.79 (s, 1H), 7.64 (brt, 1H), 7.57 (dm, 1H), 7.52 (m, 1H), 7.48 (dm, 1H), 4.97 (br„ 2H), 3.97 (s, 3H).

¹³ C-NMR (125 MHz, dmso-d6) d ppm 158.3, 154.5, 153.9, 142.8, 131.3, 130.7, 125.5, 124.3, 121.5, 118.1, 54.5.

Preparation R3w: [4-(5-amino-6-methoxy-pyrimidin-4-yl)oxyphenyl] methanol

Using General Procedure 2 starting from Preparation R2w as reagent, Preparation R3w was obtained. HRMS calculated for C ₁₂ H ₁₃ N ₃ O ₃ : 247.0957; found 247.09514 (M ⁺ (GCTOF) form).

1H-NMR (500 MHz, dmso-d6) d ppm 7.73 (s, 1H), 7.33 (dm, 2H), 7.07 (dm, 2H), 5.19 (t, 1H), 4.83 (brs, 2H), 4.49 (d, 2H), 3.95 (s, 3H).

¹³ C-NMR (125 MHz, dmso-d6) d ppm 157.9, 155, 152.8, 142.9, 142.9, 128, 121.2, 117.1, 62.9, 54.4.

Preparation R3z: 4-(5-amino-6-methoxy-pyrimidin-4-yl)oxybenzonitrile

Using General Procedure 3 starting from Preparation R2z as reagent, Preparation R3z was obtained. HRMS calculated for C ₁₂ H ₁₀ N ₄ O ₂ : 242.0804; found 243.088 ((M+H) ⁺ form). 1H-NMR (500 MHz, dmso-d6) d ppm 7.88 (dm, 2H), 7.81 (s, 1H), 7.32 (dm, 2H), 5.04 (br., 2H), 3.97 (s, 3H).

¹³ C-NMR (125 MHz, dmso-d6) d ppm 158.6, 158.1, 152.9, 142.8, 134.5, 121.6, 119.1, 118.5, 107, 54.6.

Preparation R3aa: 3-(5-amino-6-methoxy-pyrimidin-4-yl)oxybenzonitrile

Using General Procedure 3 starting from Preparation R2aa as reagent, Preparation R3aa was obtained. HRMS calculated for C ₁₂ H ₁₀ N ₄ O ₂ : 242.0804; found 243.0874 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 7.78 (s, 1H), 7.71 (m, 1H), 7.68 (dm, 1H), 7.61 (t, 1H), 7.51 (dm, 1H), 4.98 (s, 2H), 3.96 (s, 3H).

¹³ C-NMR (125 MHz, dmso-d6) d ppm 142.7, 131.4, 128.8, 126.7, 124.9, 118.6, 54.5.

Preparation R3ab: tert-butyl 7-(5-amino-6-methoxy-pyrimidin-4-yl)oxy-3, 4-dihydro- lH-isoquinoline-2-carboxylate

Using General Procedure 2 starting from Preparation R2ab as reagent,

Preparation R3ab was obtained. HRMS calculated for C ₁₉ H ₂₄ N ₄ O ₄ : 372.1797; found 373.1876 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 7.74 (s, 1H), 7.17 (d, 1H), 6.96 (d, 1H), 6.93 (dd,

1H), 4.81 (s, 2H), 4.48 (s, 2H), 3.95 (s, 3H), 3.56 (t, 2H), 2.76 (t, 2H), 1.42 (s, 9H).

¹³ C-NMR (125 MHz, dmso-d6) d ppm 142.9, 130, 119.8, 119.1, 54.4, 45.5, 41.7, 28.6, 28.1.

Preparation R3ac: methyl 3-(5-amino-6-methoxy-pyrimidin-4-yl)oxybenzoate

Using General Procedure 2 starting from Preparation R2ac as reagent,

Preparation R3ac was obtained. HRMS calculated for C ₁₃ H ₁₃ N ₃ O ₄ : 275.0906; found 276.0977 ((M+H) ⁺ form).

1H-NMR (400 MHz, dmso-d6) d ppm 7.79 (dm, 1H), 7.78 (s, 1H), 7.64 (m, 1H), 7.56 (t, 1H), 7.47 (dm, 1H), 4.95 (s, 2H), 3.97 (s, 3H), 3.85 (s, 3H).

1 ³ C-NMR (125 MHz, dmso-d6) d ppm 142.8, 130.5, 126.3, 125.5, 121.6, 54.5, 52.8.

Preparation R3ad: [3-(5-amino-6-methoxy-pyrimidin-4-yl)oxyphenyl] methanol

Using General Procedure 2 starting from Preparation R2ad as reagent,

Preparation R3ad was obtained. HRMS calculated for C ₁₂ H ₁₃ N ₃ O ₃ : 247.0957; found 248.1034 ((M+H) ⁺ form).

1H-NMR (400 MHz, dmso-d6) d ppm 7.75 (s, 1H), 7.34 (t, 1H), 7.13 (dm, 1H), 7.05 (m, 1H), 6.98 (dm, 1H), 5.26 (brt, 1H), 4.84 (brs, 2H), 4.5 (d, 2H), 3.95 (s, 3H).

¹³ C-NMR (125 MHz, dmso-d6) d ppm 143, 129.5, 122.7, 119.6, 119, 62.9, 54.4.

Preparation R3ae: 3-[4-(5-amino-6-methoxy-pyrimidin-4-yl)oxyphenyl]propan-l-ol Using General Procedure 2 starting from Preparation R2ae as reagent, Preparation R3ae was obtained. HRMS calculated for C ₁₄ H ₁₇ N ₃ O ₃ : 275.127; found 276.1348 ((M+H) ⁺ form).

1H-NMR (400 MHz, dmso-d6) d ppm 7.75 (s, 1H), 7.21 (dm, 2H), 7.03 (tm, 2H), 4.83 (brs, 2H), 4.49 (t, 1H), 3.95 (s, 3H), 3.43 (q, 2H), 2.62 (t, 2H), 1.73 (quin, 2H).

¹³ C-NMR (125 MHz, dmso-d6) d ppm 157.9, 155, 152, 142.9, 138.7, 129.7, 121.3, 117.1, 60.5. 54.4, 34.8, 31.5.

Preparation R3af: 4-methoxy-6-phenylsulfanyl-pyrimidin-5-amine

Using General Procedure 2 starting from Preparation R2af as reagent, Preparation R3af was obtained. HRMS calculated for C ₁₁ H ₁₁ N ₃ OS: 233.0623; found 234.0703 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 7.94 (s, 1H), 7.38 (m, 4H), 7.34 (m, 1H), 5.13 (brs, 2H), 3.94 (s, 3H).

¹³ C-NMR (125 MHz, dmso-d6) d ppm 156.8, 145.1, 142.9, 132.6/129.7, 131.5, 129.5,

128.3. 54.4. Preparation R3ag: tert-butyl 6-(5-amino-6-methoxy-pyrimidin-4-yl)oxy-3,4-dihydro- lH-isoquinoline-2-carboxylate

Using General Procedure 2 starting from Preparation R2ag as reagent,

Preparation R3ag was obtained. HRMS calculated for C ₁₉ H ₂₄ N ₄ O ₄ : 372.1797; found 373.1868 ((M+H) ⁺ form).

1H-NMR (400 MHz, dmso-d6) d ppm 7.73 (s, 1H), 7.18 (d, 1H), 6.94 (dd, 1H), 6.93 (d, 1H), 4.82 (s, 2H), 4.49 (brs, 2H), 3.95 (s, 3H), 3.54 (t, 2H), 2.76 (t, 2H), 1.43 (s, 9H).

1 ³ C-NMR (125 MHz, dmso-d6) d ppm 142.9, 127.7, 121.3, 119.6, 54.4, 45.2, 41.2, 28.7, 28.6.

Preparation R3ah: tert-butyl 5-(5-amino-6-methoxy-pyrimidin-4-yl)oxyisoindoline-2- carboxylate

Using General Procedure 2 starting from Preparation R2ah as reagent,

Preparation R3ah was obtained. HRMS calculated for C ₁₈ H ₂₂ N ₄ O ₄ : 358.1641; found 359.1713 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 7.74/7.73 (s/s, 1H), 7.33/7.32 (d/d, 1H), 7.11 (d, 1H), 7.04/7.02 (dd/dd, 1H), 4.85 (s, 2H), 4.59/4.56 (brs+brs, 4H), 3.95 (s, 3H), 1.46/1.45

(s/s, 9H).

¹³ C-NMR (125 MHz, dmso-d6) d ppm 158, 154.9, 142.9, 139/138.1, 133.6/133.1, 124.1, 120.9, 116.2/116.1, 54.4, 52.3/52.2/51.9/51.8, 28.6. Preparation R3ai: 2- [4-(5-amino-6-methoxy-pyrimidin-4-yl)oxyphenoxy] ethanol

Using General Procedure 2 starting from Preparation R2ai as reagent, Preparation R3ai was obtained. HRMS calculated for C ₁₃ H ₁₅ N ₃ O ₄ : 277.1063; found 278.1134 ((M+H) ⁺ form).

1H-NMR (400 MHz, dmso-d6) d ppm 7.73 (s, 1H), 7.06 (d, 2H), 6.96 (d, 2H), 4.88 (t, 1H), 4.8 (brs, 2H), 3.99 (t, 2H), 3.95 (s, 3H), 3.72 (m, 2H).

¹³ C-NMR (125 MHz, dmso-d6) d ppm 157.7, 156, 155.4, 147.2, 142.9, 122.7, 115.5, 70.4,

60.1. 54.4.

Preparation R3ai: tert-butyl 2-[4-(5-amino-6-methoxy-pyrimidin-4-yl)oxyphenyl] pyrrolidine-l-carboxylate

Using General Procedure 2 starting from Preparation R2aj as reagent,

Preparation R3aj was obtained. HRMS calculated for C ₂₀ H ₂₆ N ₄ O ₄ : 386.1954; found 387.2031 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 7.76 (s, 1H), 7.19 (m, 2H), 7.07 (m, 2H), 4.79 (m, 1H), 4.6 (s, 2H), 3.98 (s, 3H), 3.52/3.48 (m+m, 2H), 2.3/1.76 (m+m, 2H), 1.9-1.8 (m, 2H),

1.27 (brs, 9H).

¹³ C-NMR (125 MHz, dmso-d6) d ppm 143.2, 126.9, 120.9, 60.7, 54.3, 47.4, 35.6, 28.6,

23.4.

Preparation R3al: 4-(lH-indazol-6-yloxy)-6-methoxy-pyrimidin-5-amine

Using General Procedure 2 starting from Preparation R2al as reagent,

Preparation R3al was obtained. HRMS calculated for C ₁₂ H ₁₁ N ₅ O ₂ : 257.0913; found 258.0985 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 12.99 (s, 1H), 8.06 (s, 1H), 7.76 (s, 1H), 7.75 (d, 1H), 7.24 (d, 1H), 6.91 (d, 1H), 4.9 (brs, 2H), 3.96 (s, 3H).

¹³ C-NMR (125 MHz, dmso-d6) d ppm 158.1, 154.8, 152.9, 142.9, 140.7, 134, 121.6, 120.5, 117.5, 116, 101.5, 54.4.

Preparation R3am: 2- [4-(5-amino-6-methoxy-pyrimidin-4-yl)oxyphenyl] ethanol

Using General Procedure 2 starting from Preparation R2am as reagent, Preparation R3am was obtained. HRMS calculated for C ₁₃ H ₁₅ N ₃ O ₃ : 261.1113; found 262.1186 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 7.73 (s, 1H), 7.23 (m, 2H), 7.02 (m, 2H), 4.81 (s, 2H), 4.66 (t, 1H), 3.95 (s, 3H), 3.61 (m, 2H), 2.72 (t, 2H).

¹³ C-NMR (125 MHz, dmso-d6) d ppm 142.9, 130.2, 121.2, 62.7, 54.4, 38.8. Preparation R3an: 4-methoxy-6- [4-(2,2,2-trifluoroethyl)phenoxy] pyrimidin-5-amine Using General Procedure 2 starting from Preparation R2an as reagent, Preparation R3an was obtained. HRMS calculated for C ₁₃ H ₁₂ F ₃ N ₃ O ₂ : 299.0882; found 299.08761 ((M ⁺ ) form).

1H-NMR (500 MHz, dmso-d6) d ppm 7.76 (s, 1H), 7.37 (m, 2H), 7.13 (m, 2H), 4.87 (s, 2H), 3.96 (s, 3H), 3.65 (q, 2H)

¹³ C-NMR (125 MHz, dmso-d6) d ppm 158.1, 154.5, 153.9, 142.9, 131.9, 126.8, 126.8,

121.4, 117.5, 54.4, 38.2

Preparation R3ao: 4- [4-(2,2-difluoroethyl)phenoxy] -6-methoxy-pyrimidin-5-amine Using General Procedure 2 starting from Preparation R2ao as reagent, Preparation R3ao was obtained. HRMS calculated for C ₁₃ H ₁₃ F ₂ N ₃ O ₂ : 281.0976; found 282.1045 ((M+H) ⁺ form).

1H-NMR (400 MHz, dmso-d6) d ppm 7.75 (s, 1H), 7.32 (dm, 2H), 7.1 (dm, 2H), 6.25 (tt, 1H), 4.85 (br., 2H), 3.95 (s, 3H), 3.18 (td, 2H)

¹³ C-NMR (125 MHz, dmso-d6) d ppm 142.9, 131.4, 121.4, 117.5, 66.8, 54.4 Preparation R3ap: 4-[4-(2-fluoroethyl)phenoxy]-6-methoxy-pyrimidin-5-amine

Using General Procedure 2 starting from Preparation R2ap as reagent,

Preparation R3ap was obtained. HRMS calculated for C ₁₃ H ₁₄ FN ₃ O ₂ : 263.107; found 264.1140 ((M+H) ⁺ form).

1H NMR (400 MHz, dmso-d6) d ppm 7.75 (s, 1H), 7.3 (d, 2H), 7.08 (d, 2H), 4.84 (s, 2H), 4.66 (dt, 2H), 3.96 (s, 3H), 2.99 (dt, 2H).

¹³ C-NMR (125 MHz, dmso-d6) d ppm 158, 154.9, 152.7, 142.9, 134, 130.4, 121.4, 117.2,

84.4, 54.4, 35.9

Preparation R3aq: 4- [4-fluoro-3-(trifluoromethoxy)phenoxy] -6-methoxy-pyrimidin-5- amine

Using General Procedure 2 starting from Preparation R2aq as reagent,

Preparation R3aq was obtained. HRMS calculated for C12H9F4N3O3: 319.058; found 319.05479 (M ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 7.77 (s, 1H), 7.55 (dd, 1H), 7.49 (dm, 1H), 7.29 (dm, 1H), 4.95 (s, 2H), 3.96 (s, 3H).

¹³ C-NMR (125 MHz, dmso-d6) d ppm 158.2, 154, 151, 150.2, 142.7, 135.5, 122.5, 120.4, 118.2, 117.7, 117.5, 54.5.

Preparation R3as: 4-(4-chloro-3-ethyl-phenoxy)-6-methoxy-pyrimidin-5-amine

Using General Procedure 2 starting from Preparation R2as as reagent,

Preparation R3as was obtained. HRMS calculated for C13H14CIN3O2: 279.0775; found 280.0842 ((M+H) ⁺ form).

1H-NMR (400 MHz, dmso-d6) d ppm 7.77 (s, 1H), 7.42 (d, 1H), 7.15 (d, 1H), 7.01 (dd, 1H), 4.89 (s, 2H), 3.96 (s, 3H), 2.7 (q, 2H), 1.17 (t, 3H).

1 ³ C-NMR (125 MHz, dmso-d6) d ppm 158.1, 154.4, 153.1, 142.8, 142.7, 130.3, 128.4, 122.6, 120.7, 117.4, 54.4, 26.6, 14.4.

Preparation R3at: 4-(3-benzyloxyphenoxy)-6-methoxy-pyrimidin-5-amine

Using General Procedure 2 starting from Preparation R2at as reagent,

Preparation R3at was obtained. HRMS calculated for C18H17N3O3: 323.127; found 324.1347 ((M+H) ⁺ form).

1H-NMR (400 MHz, dmso-d6) d ppm 7.76 (s, 1H), 7.48-7.3 (m, 5H), 7.29 (t, 1H), 6.85 (dm, 1H), 6.8 (t, 1H), 6.7 (dm, 1H), 5.09 (s, 2H), 4.84 (s, 2H), 3.95 (s, 3H).

¹³ C-NMR (125 MHz, dmso-d6) d ppm 142.9, 130.4, 113.7, 111.4, 108.2, 69.9, 54.4.

Preparation R3au: 4-(5-amino-6-methoxy-pyrimidin-4-yl)oxybenzaldehyde

Using General Procedure 2 starting from Preparation R2au as reagent,

Preparation R3au was obtained. HRMS calculated for C12H1 1N3O3: 245.08; found 246.0873 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 9.97 (s, 1H), 7.95 (m, 2H), 7.81 (s, 1H), 7.32 (m, 2H), 5.02 (s, 2H), 3.97 (s, 3H). ¹³ C-NMR (125 MHz, dmso-d6) d ppm 192.3, 159.4, 158.6, 153.1, 142.8, 132.8, 131.8, 121, 118.5, 54.6.

Preparation R3av: tert-butyl N-[(lR)-l-[4-(5-amino-6-methoxy-pyrimidin-4-yl) oxyphenyl] -2,2,2-trifluoro-ethyl] carbamate

Using General Procedure 2 starting from Preparation R2av as reagent,

Preparation R3av was obtained. HRMS calculated for C ₁₈ H ₂₁ F ₃ N ₄ O ₄ : 414.1515; found 415.1578 ((M+H) ⁺ form).

Preparation R3aw: tert-butyl N-[(lS)-l-[4-(5-amino-6-methoxy-pyrimidin-4- yl)oxyphenyl] -2,2,2-trifluoro-ethyl] carbamate

Using General Procedure 2 starting from Preparation R2aw as reagent,

Preparation R3aw was obtained. HRMS calculated for C ₁₈ H ₂₁ F ₃ N ₄ O ₄ : 414.1515; found 415.1586 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 8.39 (d, 1H), 7.76 (s, 1H), 7.59 (m, 2H), 7.16 (m, 2H), 5.44 (m, 1H), 4.88 (brs, 2H), 3.96 (s, 3H), 1.41 (s, 9H)

1 ³ C-NMR (125 MHz, dmso-d6) d ppm 142.9, 130.2, 121.3, 55.3, 54.5, 28.5

Preparation R3az: tert-butyl 2-[3-(5-amino-6-methoxy-pyrimidin-4- yl)oxyphenyl] piperidine- 1-carboxylate

Using General Procedure 2 starting from Preparation R2az as reagent,

Preparation R3az was obtained. HRMS calculated for C ₂₁ H ₂₈ N ₄ O ₄ : 400.2111; found 401.2183 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 7.74 (s, 1H), 7.39 (t, 1H), 7.03 (d, 1H), 7 (d, 1H), 6.88 (brs, 1H), 5.28 (br„ 1H), 3.95 (s, 3H), 3.91/2.68 (d+t, 2H), 2.28/1.75 (d+tm, 2H), 1.54/1.4 (d+m, 2H), 1.54/1.25 (d+q, 2H), 1.36 (s, 9H).

¹³ C-NMR (125 MHz, dmso-d6) d ppm 158.1, 155, 154.7, 154.5, 142.9, 142.5, 130.1, 122.6, 119.3, 119.1, 79.4, 54.4, 53, 40.3, 28.5, 28.3, 25.3, 19.4

Preparation R3bc: 5-(5-amino-6-methoxy-pyrimidin-4-yl)oxyindan-2-ol Using General Procedure 2 starting from Preparation R2bc as reagent,

Preparation R3bc was obtained. HRMS calculated for C14H15N3O3: 273.1113; found 274.1188 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 7.73 (s, 1H), 7.19 (d, 1H), 6.95 (d, 1H), 6.86 (dd, 1H), 4.89 (d, 1H), 4.78 (br„ 2H), 4.52 (m, 1H), 3.94 (s, 3H), 3.09-3.00+2.77-2.68 (m, 2H),

3.09-3.00+2.77-2.68 (m, 2H).

¹³ C-NMR (125 MHz, dmso-d6) d ppm 157.8, 155.3, 152.7, 143.5, 143, 138.2, 125.5,

119.5, 118, 117, 72.1, 54.4, 42.7, 41.9

Preparation R3bf: 2- [3-(5-amino-6-methoxy-pyrimidin-4-yl)oxyphenyl] propan-2-ol Using General Procedure 2 starting from Preparation R2bf as reagent,

Preparation R3bf was obtained. HRMS calculated for C14H17N3O3: 275.127; found 276.1342 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 7.75 (s, 1H), 7.31 (t, 1H), 7.26 (dm, 1H), 7.2 (t, 1H), 6.93 (dm, 1H), 5.07 (s, 1H), 4.83 (s, 2H), 3.95 (s, 3H), 1.41 (s, 6H)

1 ³ C-NMR (125 MHz, dmso-d6) d ppm 158, 154.9, 153.9, 153, 143, 129.1, 121.1, 118.9, 117.6, 71, 54.4, 32.3

Preparation R3bg: 4-(5-amino-6-methoxy-pyrimidin-4-yl)oxy-2-fluoro-benzonitril e Using General Procedure 3 starting from Preparation R2bg as reagent,

Preparation R3bg was obtained. HRMS calculated for C12H9FN4O2: 260.071; found 261.0779 ((M+H) ⁺ form).

1H-NMR (400 MHz, dmso-d6) d ppm 7.95 (dd, 1H), 7.84 (s, 1H), 7.42 (dd, 1H), 7.18 (dm, 1H), 5.1 (s, 2H), 3.98 (s, 3H).

¹³ C-NMR (125 MHz, dmso-d6) d ppm 163.8, 160, 158.9, 152.1, 142.7, 135.3, 117.6,

114.5, 109, 95.8, 54.7. Preparation R3bh: 4-(5-amino-6-methoxy-pyrimidin-4-yl)oxy-2-chloro-benzonitril e Using General Procedure 3 starting from Preparation R2bh as reagent,

Preparation R3bh was obtained. HRMS calculated for C12H9CIN4O2: 276.0414; found 277.0486 ((M+H) ⁺ form).

1H-NMR (400 MHz, dmso-d6) d ppm 8.00 (d, 1H), 7.84 (s, 1H), 7.61 (d, 1H), 7.32 (dd, 1H), 5.1 (s, 2H), 3.98 (s, 3H).

¹³ C-NMR (125 MHz, dmso-d6) d ppm 158.9, 158.8, 152.2, 142.7, 137, 136.2, 122, 120.1,

116.4, 107.5, 54.7.

Preparation R3bi: 2- [4-(5-amino-6-methoxy-pyrimidin-4-yl)oxyphenyl] acetonitrile Using General Procedure 3 starting from Preparation R2bi as reagent, Preparation R3bi was obtained. HRMS calculated for C ₁₃ H ₁₂ N ₄ O ₂ : 256.096; found 257.1034 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 7.74 (s, 1H), 7.37 (m, 2H), 7.15 (m, 2H), 4.87 (s, 2H), 4.04 (s, 2H), 3.95 (s, 3H).

1 ³ C-NMR (125 MHz, dmso-d6) d ppm 158.1, 154.6, 153.5, 142.8, 129.7, 127.8, 122,

119.8. 54.4, 22.2.

Preparation R3bi: 3- [4-(5-amino-6-methoxy-pyrimidin-4-yl)oxyphenyl] propanenitrile Using General Procedure 3 starting from Preparation R2bj as reagent,

Preparation R3bj was obtained. HRMS calculated for C ₁₄ H ₁₄ N ₄ O ₂ : 270.1117; found 271.1192 ((M+H) ⁺ form).

1H-NMR (400 MHz, dmso-d6) d ppm 7.75 (s, 1H), 7.31 (dm, 2H), 7.08 (dm, 2H), 4.83 (br„ 2H), 3.95 (s, 3H), 2.89 (m, 2H), 2.82 (m, 2H).

¹³ C-NMR (125 MHz, dmso-d6) d ppm 158, 154.8, 152.9, 142.9, 135.4, 129.9, 121.5,

120.8. 54.4. 30.4, 18.8. Preparation R3bk: 4-(5-amino-6-methoxy-pyrimidin-4-yl)oxy-3-chloro-benzonitril e Using General Procedure 3 starting from Preparation R2bk as reagent,

Preparation R3bk was obtained. HRMS calculated for C ₁₂ H ₉ CIN ₄ O ₂ : 276.0414; found 277.0484 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 8.23 (d, 1H), 7.89 (dd, 1H), 7.73 (s, 1H), 7.48 (d, 1H), 5.05 (s, 2H), 3.97 (s, 3H).

¹³ C-NMR (125 MHz, dmso-d6) d ppm 158.4, 154, 153.2, 142.6, 134.7, 133.3, 127.3, 124.9, 117.9, 117.5, 109.3, 54.6.

Preparation R3bm: tert-butyl N-[l-[4-(5-amino-6-methoxy-pyrimidin-4- yl)oxyphenyl] ethyl] carbamate

Using General Procedure 2 starting from Preparation R2bm as reagent,

Preparation R3bm was obtained. HRMS calculated for C ₁₈ H ₂₄ N ₄ O ₄ : 360.1797; found 361.1862 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 7.77 (s, 1H), 7.32 (m, 2H), 7.07 (m, 2H), 7.06 (brs, 1H), 4.64 (m, 1H), 4.59 (brs, 2H), 3.98 (s, 3H), 1.37 (s, 9H), 1.35 (d, 3H).

¹³ C-NMR (125 MHz, dmso-d6) d ppm 143.2, 127.3, 120.9, 54.3, 49.9, 28.8, 23.1.

Preparation R3bn: tert-butyl N-[l-[4-(5-amino-6-methoxy-pyrimidin-4- yl)oxyphenyl] propyl] carbamate

Using General Procedure 2 starting from Preparation R2bn as reagent,

Preparation R3bn was obtained. HRMS calculated for C ₁₉ H ₂₆ N ₄ O ₄ : 374.1954; found 375.2024 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 7.77 (s, 1H), 7.3 (m, 2H), 7.06 (m, 2H), 7.01 (brs, 1H), 4.6 (s, 2H), 4.38 (m, 1H), 3.98 (s, 3H), 1.7/1.65 (m+m, 2H), 1.37 (s, 3H), 0.85 (t, 3H). ¹³ C-NMR (125 MHz, dmso-d6) d ppm 142.9, 127.8, 121.1, 56.2, 54.4, 30, 28.8, 11.

Preparation R3bq: 4-methoxy-6-(3-pyridyloxy)pyrimidin-5-amine

Using General Procedure 2 starting from Preparation R2bq as reagent,

Preparation R3bq was obtained. HRMS calculated for C ₁₀ H ₁₀ N ₄ O ₂ : 218.0804; found 219.0878 ((M+H) ⁺ form).

1H-NMR (400 MHz, dmso-d6) d ppm 8.46 (d, 1H), 8.42 (dd, 1H), 7.76 (s, 1H), 7.63 (dm, 1H), 7.46 (dd, 1H), 4.97 (br„ 2H), 3.96 (s, 3H)

¹³ C-NMR (125 MHz, dmso-d6) d ppm 158.2, 154.1, 150.7, 146, 143.4, 142.7, 129.1, 124.8, 117.4, 54.5

Preparation R3bs: 4-methoxy-6-(lH-pyrrolo[3,2-b]pyridin-6-yloxy)pyrimidin-5- amine

Using General Procedure 2 starting from Preparation R2bs as reagent,

Preparation R3bs was obtained. HRMS calculated for C ₁₂ H ₁₁ N ₅ O ₂ : 257.0913; found 258.0990 ((M+H) ⁺ form). 1H-NMR (500 MHz, dmso-d6) d ppm 11.3 (brs, 1H), 8.19 (d, 1H), 7.72 (s, 1H), 7.63 (dd, 1H), 7.6 (dd, 1H), 6.56 (d, 1H), 4.91 (s, 2H), 3.96 (s, 3H)

¹³ C-NMR (125 MHz, dmso-d6) d ppm 142.8, 137.5, 130.1, 111.8, 102.1

Preparation R3bt: 4-(3-benzyloxy-4-chloro-phenoxy)-6-methoxy-pyrimidin-5-amine Using General Procedure 2 starting from Preparation R2bt as reagent, Preparation R3bt was obtained. HRMS calculated for C ₁₈ H ₁₆ CIN ₃ O ₃ : 357.088; found 358.0962 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 7.76 (s, 1H), 7.51-7.29 (m, 5H), 7.44 (d, 1H), 7.11 (d, 1H), 6.75 (dd, 1H), 5.18 (s, 2H), 4.89 (s, 2H), 3.96 (s, 3H)

1 ³ C-NMR (125 MHz, dmso-d6) d ppm 142.8, 130.4, 114.5, 108.3, 70.6, 54.5

Preparation R3bu: 4-(3-benzyloxy-4-methyl-phenoxy)-6-methoxy-pyrimidin-5-amine Using General Procedure 2 starting from Preparation R2bu as reagent, Preparation

R3bu was obtained. HRMS calculated for C ₁₉ H ₁₉ N ₃ O ₃ : 337.1426; found 338.1509 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 7.74 (s, 1H), 7.49-7.28 (m, 5H), 7.15 (d, 1H), 6.85 (d, 1H), 6.62 (dd, 1H), 5.08 (s, 2H), 4.8 (s, 2H), 3.95 (s, 3H), 2.19 (s, 3H)

¹³ C-NMR (125 MHz, dmso-d6) d ppm 142.9, 130.9, 113.2, 106.1, 69.7, 54.4, 16.1

Preparation R3bv: tert-butyl 4- [2- [4-(5-amino-6-methoxy-pyrimidin-4-yl)oxyphenyl] ethyl] piperidine- 1-carboxylate

Using General Procedure 2 starting from Preparation R2bv as reagent, Preparation R3bv was obtained. HRMS calculated for C ₁₆ H ₂₀ N ₄ O ₃ : 316.1535; found 317.1615 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 7.75 (s, 1H), 7.31 (dm, 2H), 7.07 (dm, 2H), 4.83 (br., 2H), 3.95 (s, 3H), 3.57 (t, 4H), 3.45 (s, 2H), 2.35 (br., 4H)

¹³ C-NMR (125 MHz, dmso-d6) d ppm 158, 154.7, 153.1, 142.9, 134.3, 130.4, 121.1, 117.3, 66.7, 62.3, 54.4, 53.6

Preparation R3bw: 4-methoxy-6- [4-(morpholinomethyl)phenoxy] pyrimidin-5-amine Using General Procedure 2 starting from Preparation R2bw as reagent, Preparation R3bw was obtained. HRMS calculated for C ₁₆ H ₂₀ N ₄ O ₃ : 316.1535; found 317.1615 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 7.75 (s, 1H), 7.31 (dm, 2H), 7.07 (dm, 2H), 4.83 (br., 2H), 3.95 (s, 3H), 3.57 (t, 4H), 3.45 (s, 2H), 2.35 (br., 4H)

1 ³ C-NMR (125 MHz, dmso-d6) d ppm 158, 154.7, 153.1, 142.9, 134.3, 130.4, 121.1, 117.3, 66.7, 62.3, 54.4, 53.6

Preparation R3bx: tert-butyl 2- [2- [4-(5-amino-6-methoxy-pyrimidin-4-yl)oxyphenyl] ethyl] piperidine- 1-carboxylate

Using General Procedure 2 starting from Preparation R2bx as reagent, Preparation R3bx was obtained. HRMS calculated for C23H32N4O4 : 428.2424; found 429.2486 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 7.73 (s, 1H), 7.23 (m, 2H), 7.02 (m, 2H), 4.81 (s, 2H), 4.15 (m, 1H), 3.95 (s, 3H), 3.86/2.8 (m+m, 2H), 2.54/2.44 (m+m, 2H), 1.93/1.72 (m+m, 2H), 1.64-1.19 (m, 6H), 1.38 (s, 3H).

1 ³ C-NMR (125 MHz, dmso-d6) d ppm 142.9, 129.6, 121.4, 54.4, 50.2, 38.7, 31.9, 31.8, 28.6

Preparation R3bv: tert-butyl 2-[3-(5-amino-6-methoxy-pyrimidin-4-yl)oxyphenyl] morpholine-4-carboxylate

Using General Procedure 2 starting from Preparation R2by as reagent, Preparation R3by was obtained. HRMS calculated for C ₂₀ H ₂₆ N ₄ O ₅ : 402.1903; found 403.197 ((M+H) ⁺ form).

1H-NMR (400 MHz, dmso-d6) d ppm 7.76 (s, 1H), 7.39 (t, 1H), 7.2 (dm, 1H), 7.12 (t, 1H), 7.08 (dm, 1H), 4.86 (brs, 2H), 4.43 (dd, 1H), 4.00-2.62 (brm, 4H), 3.96 (s, 3H), 3.94/3.54 (m+m, 2H), 1.41 (s, 9H).

1 ³ C-NMR (100 MHz, dmso-d6) d ppm 142.9, 142.9, 129.9, 122.9, 120.8, 119.1, 76.7, 66.3, 54.5

Preparation R3bz: tert-butyl N-[(lR)-l-[4-(5-amino-6-methoxy-pyrimidin-4- yl)oxyphenyl] -2,2,2-trifluoro-ethyl] carbamate

Using General Procedure 2 starting from Preparation R2bz as reagent, Preparation R3bz was obtained. HRMS calculated for C ₁₈ H ₂₁ F ₃ N ₄ O ₄ : 414.1515; found 415.1578 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 8.39 (d, 1H), 7.76 (s, 1H), 7.59 (m, 2H), 7.16 (m, 2H), 5.44 (m, 1H), 4.88 (brs, 2H), 3.96 (s, 3H), 1.41 (s, 9H)

1 ³ C-NMR (125 MHz, dmso-d6) d ppm 142.9, 130.2, 121.3, 55.3, 54.5, 28.5

Preparation R3ca: 2- [4-(5-amino-6-methoxy-pyrimidin-4-yl)oxyphenyl] acetonitrile Using General Procedure 3 starting from Preparation R2ca as reagent, Preparation R3ca was obtained. HRMS calculated for C ₁₃ H ₁₂ N ₄ O ₂ : 256.096; found 257.1034 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 7.74 (s, 1H), 7.37 (m, 2H), 7.15 (m, 2H), 4.87 (s, 2H), 4.04 (s, 2H), 3.95 (s, 3H)

¹³ C-NMR (125 MHz, dmso-d6) d ppm 158.1, 154.6, 153.5, 142.8, 129.7, 127.8, 122, 119.8, 54.4, 22.2

Preparation R3cb: [5-(5-amino-6-methoxy-pyrimidin-4-yl)oxy-2-fluoro- phenyl] methanol

Using General Procedure 2 starting from Preparation R2cb as reagent,

Preparation R3cb was obtained. HRMS calculated for C ₁₂ H ₁₂ FN ₃ O ₃ : 265.0863; found 266.0935 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 7.75 (s, 1H), 7.18 (dt, 1H), 7.17 (t, 1H), 7.07 (ddd, 1H), 5.35 (t, 1H), 4.86 (s, 2H), 4.55 (d, 2H), 3.95 (s, 3H).

¹³ C-NMR (125 MHz, dmso-d6) d ppm 158, 156.5, 154.9, 150, 142.8, 130.9, 121.4, 121.4, 117.3, 116, 57.1, 54.4

Preparation R3cc: 4-(3-amino-4-fluoro-phenoxy)-6-methoxy-pyrimidin-5-amine

Using General Procedure 2 starting from Preparation R2cc as reagent, Preparation R3cc was obtained. HRMS calculated for C ₁₁ H ₁₁ FN ₄ O ₂ : 250.0866; found 251.0938 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 7.75 (s, 1H), 6.96 (dd, 1H), 6.48 (dd, 1H), 6.23 (ddd, 1H), 5.26 (s, 2H), 4.78 (s, 2H), 3.94 (s, 3H)

¹³ C-NMR (125 MHz, dmso-d6) d ppm 157.9, 155, 150.5, 148, 143, 137.6, 117.1, 115.4, 108.9, 108.1, 54.4

Preparation R3cd: 4-(4-isopropyl-3-methoxy-phenoxy)-6-methoxy-pyrimidin-5-amin e Using General Procedure 2 starting from Preparation R2cd as reagent,

Preparation R3cd was obtained. HRMS calculated for C ₁₅ H ₁₉ N ₃ O ₃ : 289.1426; found 289.14174 (M ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 7.75 (s, 1H), 7.17 (d, 1H), 6.74 (d, 1H), 6.64 (dd, 1H), 4.8 (s, 2H), 3.95 (s, 3H), 3.75 (s, 3H), 3.21 (m, 1H), 1.16 (d, 6H)

¹³ C-NMR (125 MHz, dmso-d6) d ppm 157.9, 157.4, 155, 153, 143, 132.5, 126.4, 117.1, 113, 104.9, 56, 55.4, 26.4, 23.1 Preparation R3ce: tert-butyl 2-[4-(5-amino-6-methoxy-pyrimidin-4- yl)oxyphenyl] piperidine- 1-carboxylate

Using General Procedure 2 starting from Preparation R2ce as reagent,

Preparation R3ce was obtained. HRMS calculated for C ₂₁ H ₂₈ N ₄ O ₄ : 400.2111; found 345.1564 ((M+H-C ₄ H _S ) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 7.75 (s, 1H), 7.2 (m, 2H), 7.12 (m, 2H), 5.28 (brd, 1H), 4.84 (s, 2H), 3.95 (s, 3H), 3.94/2.71 (m+m, 2H), 1.4 (s, 9H)

¹³ C-NMR (125 MHz, dmso-d6) d ppm 142.9, 127.7, 121.5, 54.4, 52.9, 40.3, 28.5

Preparation R4a: 5-amino-4-phenoxy-lH-pyrimidin-6-one

Using General Procedure 4 starting from Preparation R3a as reagent, Preparation R4a was obtained. HRMS calculated for C ₁₀ H ₉ N ₃ O ₂ : 203.0695; found 204.077 ((M+H) ⁺ form). 1H-NMR (500 MHz, dmso-d6) d ppm 12.45 (brs, 1H), 7.5 (s, 1H), 7.35 (m, 2H), 7.11 (m, 1H), 7.02 (m, 2H), 4.6 (s, 2H).

¹³ C-NMR (125 MHz, dmso-d6) d ppm 159.3, 147.3, 135.7, 129.8, 123.8, 121.7, 119.7.

Preparation R4b: 5-amino-4-(2-fluorophenoxy)-lH-pyrimidin-6-one hydrochloride Using General Procedure 4 starting from Preparation R3b as reagent, Preparation R4b was obtained. HRMS calculated for C ₁₀ H ₈ FN ₃ O ₂ : 221.0601; found 222.0673 ((M+H) ⁺ form). 1H-NMR (500 MHz, dmso-d6) d ppm 13.12 (brs, 1H), 7.88 (s, 1H), 7.37 (m, 1H), 7.3 (m, 1H), 7.28 (m, 1H), 7.24 (m, 1H)

¹³ C-NMR (125 MHz, dmso-d6) d ppm 159.3, 155.3, 154.4, 143.8, 140.4, 127.2, 125.6, 124.1, 117.2.

Preparation R4c: 5-amino-4-(4-methoxyphenoxy)-lH-pyrimidin-6-one hydrochloride Using General Procedure 4 starting from Preparation R3c as reagent, Preparation R4c was obtained. HRMS calculated for C ₁₁ H ₁₁ N ₃ O ₃ : 233.08; found 234.08709 ((M+H) ⁺ form). 1H-NMR (400 MHz, dmso-d6) d ppm 13.04 (brs, 1H), 7.9 (s, 1H), 7.07 (m, 2H), 6.95 (m, 2H), 3.75 (s, 3H).

¹³ C-NMR (125 MHz, dmso-d6) d ppm 159.4, 156.8, 156.8, 146.8, 144.5, 122.5, 114.9, 55.9.

Preparation R4d: 5-amino-4-(3-methoxyphenoxy)-lH-pyrimidin-6-one hydrochloride Using General Procedure 4 starting from Preparation R3d as reagent, Preparation R4d was obtained. HRMS calculated for C ₁₁ H ₁₁ N ₃ O ₃ : 233.08; found 234.6871 ((M+H) ⁺ form). 1H-NMR (500 MHz, dmso-d6) d ppm 13.05 (br., 1H), 7.89 (s, 1H), 7.3 (t, 1H), 7.16 (br., 2H), 6.79 (dd, 1H), 6.71 (t, 1H), 6.69 (dd, 1H), 3.74 (s, 3H).

¹³ C-NMR (125 MHz, dmso-d6) d ppm 160.7, 159.5, 155.4, 154.8, 143.8, 130.4, 113.1, 110.8, 107.2, 55.8.

Preparation R4e: 5-amino-4-(4-fluorophenoxy)-lH-pyrimidin-6-one hydrochloride Using General Procedure 4 starting from Preparation R3e as reagent, Preparation R4e was obtained. HRMS calculated for C ₁₀ H ₈ FN ₃ O ₂ : 221.0601; found 222.0669 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 7.87 (s, 1H), 7.2 (m, 2H), 7.2 (m, 2H).

¹³ C-NMR (125 MHz, dmso-d6) d ppm 160.7, 159.5, 158.2, 149.8, 143.4, 122.9, 116.6.

Preparation R4f: 5-amino-4-(3-fluorophenoxy)-lH-pyrimidin-6-one hydrochloride Using General Procedure 4 starting from Preparation R3f as reagent, Preparation R4f was obtained. HRMS calculated for C ₁₀ H ₈ FN ₃ O ₂ : 221.0601; found 222.0672 ((M+H) ⁺ form). 1H-NMR (500 MHz, dmso-d6) d ppm 13.01 (br., 1H), 7.85 (s, 1H), 7.43 (m, 1H), 7.43 (br., 2H), 7.07-7.01 (m, 1H), 7.07-7.01 (m, 1H), 6.98 (m, 1H).

¹³ C-NMR (125 MHz, dmso-d6) d ppm 162.9, 159.5, 155.1, 153.4, 142.5, 131.2, 116.8, 111.7, 108.5.

Preparation R4g: 5-amino-4-(3,5-dimethoxyphenoxy)-lH-pyrimidin-6-one

hydrochloride

Using General Procedure 4 starting from Preparation R3g as reagent, Preparation R4g was obtained. HRMS calculated for C ₁₂ H ₁₃ N ₃ O ₄ : 263.0906; found 263.0977 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 12.91 (brs, 1H), 7.82 (s, 1H), 6.34 (t, 1H), 6.27 (d, 2H), 3.72 (s, 6H).

¹³ C-NMR (125 MHz, dmso-d6) d ppm 161.4, 159.5, 155.8, 153.5, 142.1, 99.4, 96.9, 55.9.

Preparation R4h: 5-amino-4-(3,5-difluorophenoxy)-lH-pyrimidin-6-one

hydrochloride

Using General Procedure 4 starting from Preparation R3h as reagent, Preparation R4h was obtained. HRMS calculated for C ₁₀ H ₇ F ₂ N ₃ O ₂ : 239.0506; found 240.0576 ((M+H) ⁺ form).

1H-NMR (400 MHz, dmso-d6) d ppm 12.96 (br., 1H), 7.81 (s, 1H), 7.07 (m, 1H), 6.93 (m, 2H).

¹³ C-NMR (125 MHz, dmso-d6) d ppm 163, 159.6, 156.2, 151.3, 141.3, 104.5, 100.2.

Preparation R4i: 5-(methylamino)-4-phenoxy-lH-pyrimidin-6-one hydrochloride Using General Procedure 4 starting from Preparation R3i as reagent, Preparation R4i was obtained. HRMS calculated for C ₁₁ H ₁₁ N ₃ O ₂ : 217.0851; found 218.0924 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 13.27 (brs, 1H), 8.04 (s, 1H), 7.42 (m, 2H), 7.24 (m, 1H), 7.18 (m, 2H), 2.87 (s, 3H)

¹³ C-NMR (125 MHz, dmso-d6) d ppm 159.4, 157.2, 153.5, 146.7, 130.1, 125.5, 121.2, 112.1, 34.3. Preparation R4i: 5-amino-4-(4-chlorophenoxy)-lH-pyrimidin-6-one hydrochloride Using General Procedure 4 starting from Preparation R3j as reagent, Preparation R4j was obtained. HRMS calculated for C10H8CIN3O2: 237.0305; found 238.0379 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 12.92 (brs, 1H), 7.8 (s, 1H), 7.44 (m, 2H), 7.14 (m, 2H).

¹³ C-NMR (125 MHz, dmso-d6) d ppm 159.4, 153, 152.9, 141.8, 129.8, 128.8, 122.5.

Preparation R4k: 5-amino-4-(4-chloro-3-methoxy-phenoxy)-lH-pyrimidin-6-one hydrochloride

Using General Procedure 4 starting from Preparation R3k as reagent, Preparation R4k was obtained. HRMS calculated for C1 1H10CIN3O3: 267.0411; found 268.0481 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 12.87 (brs, 1H), 7.78 (s, 1H), 7.4 (d, 1H), 6.86 (d, 1H), 6.68 (dd, 1H), 3.82 (s, 3H).

¹³ C-NMR (125 MHz, dmso-d6) d ppm 141.1, 130.3, 113.2, 106.2, 56.8.

Preparation R41: 5-amino-4-(3-chlorophenoxy)-lH-pyrimidin-6-one

Using General Procedure 4 starting from Preparation R31 as reagent, Preparation R41 was obtained. HRMS calculated for C10H8CIN3O2: 237.0305; found 238.0376 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 12.97 (br., 1H), 7.83 (s, 1H), 7.42 (t, 1H), 7.26 (dm, 1H), 7.26 (dm, 1H), 7.23 (t, 1H).

¹³ C-NMR (125 MHz, dmso-d6) d ppm 159.5, 154.9, 152.8, 142, 133.8, 131.4, 124.8, 120.8, 119.4.

Preparation R4n: 5-amino-4-(l,3-benzodioxol-5-yloxy)-lH-pyrimidin-6-one hydrochloride

Using General Procedure 4 starting from Preparation R3n as reagent, Preparation R4n was obtained. HRMS calculated for C1 1H9N3O4: 247.0593; found 248.0666 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 12.79 (brs, 1H), 7.74 (s, 1H), 6.89 (d, 1H), 6.77 (d, 1H), 6.55 (dd, 1H), 6.04 (s, 2H).

¹³ C-NMR (125 MHz, dmso-d6) d ppm 140.9, 113.3, 108.4, 103.5, 102.

Preparation R4o: 5-amino-4-(3-hydroxy-5-methoxy-phenoxy)-lH-pyrimidin-6-one Using General Procedure 4 starting from Preparation R3o as reagent, Preparation R4o was obtained. HRMS calculated for C ₁₁ H ₁₁ N ₃ O ₄ : 249.075; found 250.08193 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 12.44 (brs, 1H), 9.52 (s, 1H), 7.52 (s, 1H), 6.08 (t, 1H), 6.05 (t, 1H), 5.98 (t, 1H), 4.56 (s, 2H), 3.66 (s, 3H).

¹³ C-NMR (125 MHz, dmso-d6) d ppm 161.4, 159.4, 159.4, 157, 146.9, 135.6, 122.9, 99.1, 96.9, 96.7, 55.6.

Preparation R4p: 5-amino-4-(4-fluoro-3-methoxy-phenoxy)-lH-pyrimidin-6-one hydrochloride

Using General Procedure 4 starting from Preparation R3p as reagent, Preparation R4p was obtained. HRMS calculated for C ₁₁ H ₁₀ FN ₃ O ₃ : 251.0706; found 252.0779 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 12.79 (br., 1H), 7.75 (s, 1H), 7.2 (dd, 1H), 6.97 (dd, 1H), 6.64 (ddd, 1H), 5.91 (br., 2H), 3.8 (s, 3H)

¹³ C-NMR (125 MHz, dmso-d6) d ppm 159.4, 152.3, 150.6, 148.9, 148, 140.5, 116.2,

112.3, 107.3, 56.7 Preparation R4q: 4-phenoxy-5-(2,2,2-trifluoroethylamino)-lH-pyrimidin-6-one

Using General Procedure 4 starting from Preparation R3q as reagent, Preparation R4q was obtained. HRMS calculated for C ₁₂ H ₁₀ F ₃ N ₃ O ₂ : 285.0725; found 286.0801 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 12.64 (br., 1H), 7.64 (s, 1H), 7.37 (m, 2H), 7.15 (tm, 1H), 7.03 (m, 2H), 5.24 (br., 1H), 4.09 (brq, 2H).

¹³ C-NMR (125 MHz, dmso-d6) d ppm 159.8, 154.5, 150.1, 138.7, 130, 126.1, 124.4,

120.3, 119.5, 44.8.

Preparation R4r: 5-amino-4-[3-(trifhioromethoxy)phenoxy]-lH-pyrimidin-6-one hydrochloride

Using General Procedure 4 starting from Preparation R3r as reagent, Preparation R4r was obtained. HRMS calculated for C ₁₁ H ₈ F ₃ N ₃ O ₃ : 287.0518; found 288.0592 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 12.81 (brs, 1H), 7.73 (s, 1H), 7.51 (t, 1H), 7.17 (dm, 1H), 7.14 (dm, 1H), 7.14 (m, 1H).

¹³ C-NMR (125 MHz, dmso-d6) d ppm 159.5, 155.5, 150.5, 149.2, 139.9, 121.5, 121.3, 119.3, 116.8, 113.3.

Preparation R4s: 5-amino-4-(3-methylphenoxy)-lH-pyrimidin-6-one hydrochloride Using General Procedure 4 starting from Preparation R3s as reagent, Preparation R4s was obtained. HRMS calculated for C ₁₁ H ₁₁ N ₃ O ₂ : 217.0851; found 218.0922 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 13.06 (brs, 1H), 7.89 (s, 1H), 7.27 (t, 1H), 7.02 (dm, 1H), 6.93 (m, 1H), 6.91 (dm, 1H), 2.3 (s, 3H).

¹³ C-NMR (125 MHz, dmso-d6) d ppm 159.4, 155.6, 153.7, 143.9, 139.7, 129.7, 125.8, 121.5, 118.1, 21.3, 0.

Preparation R4t: 5-amino-4-(3-bromophenoxy)-lH-pyrimidin-6-one

Using General Procedure 4 starting from Preparation R3t as reagent, Preparation R4t was obtained. HRMS calculated for CioFFBrbbCh: 280.98; found 281.98762 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 12.49 (brs, 1H), 7.53 (s, 1H), 7.31 (m, 1H), 7.31 (m, 1H), 7.24 (m, 1H), 7.06 (m, 1H), 4.71 (brs, 2H).

¹³ C-NMR (125 MHz, dmso-d6) d ppm 159.4, 146.3, 135.7, 131.6, 126.6, 122.3, 118.6.

Preparation R4u: 5-amino-6- [3-(pentafhioro^ ⁶ -sulfanyl)phenoxy] pyrimidin-4(3//)- one hydrochloride

Using General Procedure 4 starting from Preparation R3u as reagent, Preparation R4u was obtained. HRMS calculated for C ₁₀ H ₈ F ₅ N ₃ O ₂ S: 329.0257; found 330.0321 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 12.77 (brs, 1H), 7.92 (m, 1H), 7.71 (m, 1H), 7.7 (s, 1H), 7.63 (m, 1H), 7.41 (dm, 1H)

¹³ C-NMR (125 MHz, dmso-d6) d ppm 159.5, 149.7, 139.1, 130.9, 124.3, 121.7, 117.9.

Preparation R4v: 5-amino-4-[3-(trifluoromethyl)phenoxy]-lH-pyrimidin-6-one hydrochloride

Using General Procedure 4 starting from Preparation R3v as reagent, Preparation R4v was obtained. HRMS calculated for C ₁₁ H ₈ F ₃ N ₃ O ₂ : 271.0569; found 272.0634 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 12.73 (brs, 1H), 7.67 (s, 1H), 7.61 (t, 1H), 7.51 (dm, 1H), 7.42 (m, 1H), 7.39 (dm, 1H).

1 ³ C-NMR (125 MHz, dmso-d6) d ppm 159.4, 155.1, 148.9, 138.3, 131.3, 130.6, 124.1, 120.8, 116.7.

Preparation R4w: 5-amino-4-[4-(hydroxymethyl)phenoxy]-lH-pyrimidin-6-one

Using General Procedure 4 starting from Preparation R3w as reagent, Preparation R4w was obtained. HRMS calculated for C ₁₁ H ₁₁ N ₃ O ₃ : 233.08; found 234.0878 ((M+H) ⁺ form).

1H-NMR (400 MHz, dmso-d6) d ppm 13 (brs, 1H), 7.85 (s, 1H), 7.33 (d, 2H), 7.07 (d, 2H), 4.48 (s, 2H)

¹³ C-NMR (125 MHz, dmso-d6) d ppm 159.4, 155.1, 152.4, 143.2, 139.5, 128.1, 120.8, 62.8 Preparation R4z: 4-[(5-amino-6-oxo-lH-pyrimidin-4-yl)oxy]benzonitrile

Using General Procedure 4 starting from Preparation R3z as reagent, Preparation R4z was obtained. HRMS calculated for C ₁₁ H ₈ N ₄ O ₂ : 228.0647; found 229.0718 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 12.54 (s, 1H), 7.82 (dm, 2H), 7.55 (s, 1H), 7.18 (dm, 2H), 4.93 (s, 2H).

¹³ C-NMR (125 MHz, dmso-d6) d ppm 159.5, 159.1, 145.1, 135.6, 134.5, 123.3, 119.7, 119.3, 105.8.

Preparation R4aa: 3- [(5-amino-6-oxo- lH-pyrimidin-4-yl)oxy] benzonitrile hydrochloride

Using General Procedure 4 starting from Preparation R3aa as reagent, Preparation R4aa was obtained. HRMS calculated for C ₁₁ H ₈ N ₄ O ₂ : 228.0647; found 229.072 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 12.9 (brs, 1H), 7.77 (s, 1H), 7.65 (dm, 1H), 7.65 (m, 1H), 7.6 (t, 1H), 7.47 (m, 1H).

¹³ C-NMR (125 MHz, dmso-d6) d ppm 159.5, 154.6, 151.2, 140.8, 131.4, 128.5, 125.6, 123.8, 118.6, 112.6.

Preparation R4ab: tert-butyl 7-[(5-amino-6-oxo-lH-pyrimidin-4-yl)oxy]-3,4-dihydro- lH-isoquinoline-2-carboxylate

Using General Procedure 4 starting from Preparation R3ab as reagent, 5-amino-4- (l,2,3,4-tetrahydroisoquinolin-7-yloxy)-lH-pyrimidin-6-one, hydrochloride was formed. The resulted crude product was reacted using General Procedure 6 to give Preparation R4ab. HRMS calculated for C ₁₈ H ₂₂ N ₄ O ₄ : 358.1641; found 359.1717 ((M+H)+ form).

1H-NMR (500 MHz, dmso-d6) d ppm 12.43 (s, 1H), 7.49 (s, 1H), 7.12 (d, 1H), 6.85 (d, 1H), 6.84 (dd, 1H), 4.55 (s, 2H), 4.45 (s, 2H), 3.54 (t, 2H), 2.73 (t, 2H), 1.42 (s, 9H) ³ C-NMR (125 MHz, dmso-d6) d ppm 159.3, 154.4, 153.4, 147.7, 135.8, 135.2, 130, 130, 121.4, 118.3, 117.4, 79.7, 45.5, 41.7, 28.6, 28

Preparation R4ac: methyl 3-[(5-amino-6-oxo-lH-pyrimidin-4-yl)oxy]benzoate

Using General Procedure 4 starting from Preparation R3ac as reagent, Preparation R4ac was obtained. HRMS calculated for C ₁₂ H ₁₁ N ₃ O ₄ : 261.075; found 262.0825 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 12.51 (brs, 1H), 7.71 (dm, 1H), 7.53 (s, 1H), 7.52 (m, 1H), 7.51 (t, 1H), 7.35 (dm, 1H), 4.73 (s, 2H), 3.84 (s, 3H).

¹³ C-NMR (125 MHz, dmso-d6) d ppm 166.2, 159.4, 155.5, 146.6, 135.7, 131.3, 130.6, 124.6, 124.5, 122.2, 119.7, 52.8.

Preparation R4ad: 5-amino-4-[3-(hydroxymethyl)phenoxy]-lH-pyrimidin-6-one

Using General Procedure 4 starting from Preparation R3ad as reagent, Preparation R4ad was obtained. HRMS calculated for C ₁₁ H ₁₁ N ₃ O ₃ : 233.08; found 234.0875 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 12.14 (brs, 1H), 7.5 (s, 1H), 7.28 (t, 1H), 7.04 (dm, 1H), 6.96 (t, 1H), 6.88 (dm, 1H), 5.25 (brt, 1H), 4.58 (s, 2H), 4.47 (brd, 2H).

1 ³ C-NMR (125 MHz, dmso-d6) d ppm 159.3, 147.4, 135.7, 129.5, 121.7, 121.7, 117.9, 117.4, 62.9.

Preparation R4ae: 5-amino-4-[4-(3-hydroxypropyl)phenoxy]-lH-pyrimidin-6-one hydrochloride

Using General Procedure 4 starting from Preparation R3ae as reagent, Preparation R4ae was obtained. HRMS calculated for C ₁₃ H ₁₅ N ₃ O ₃ : 261.1113; found 262.1184 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 7.9 (s, 1H), 7.21 (d, 2H), 7.02 (d, 2H), 3.4 (t, 2H), 2.6 (m, 2H), 1.7 (m, 2H).

¹³ C-NMR (125 MHz, dmso-d6) d ppm 151.6, 143.1, 139.1, 129.7, 121, 60.6, 34.8, 31.4. Preparation R4af: 5-amino-4-phenylsulfanyl-lH-pyrimidin-6-one hydrochloride

Using General Procedure 4 starting from Preparation R3af as reagent,

Preparation R4af was obtained. HRMS calculated for C ₁₀ H ₉ N ₃ OS: 219.0466; found 220.0537 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 7.96 (s, 1H), 7.36-7.23 (m, 5H).

1 ³ C-NMR (125 MHz, dmso-d6) d ppm 156.3, 137.7, 133.5, 123.8.

Preparation R4ag: tert-butyl 6-[(5-amino-6-oxo-lH-pyrimidin-4-yl)oxy]-3,4-dihydro- lH-isoquinoline-2-carboxylate

Using General Procedure 4 starting from Preparation R3ag as reagent, 5-amino-4- (l,2,3,4-tetrahydroisoquinolin-6-yloxy)-lH-pyrimidin-6-one hydrochloride salt was formed. The resulted crude product was reacted using General Procedure 6 to give Preparation R4ag. HRMS calculated for C ₁₈ H ₂₂ N ₄ O ₄ : 358.1641; found 359.1713 ((M+H) ⁺ form).

1H-NMR (400 MHz, dmso-d6) d ppm 12.46 (brs, 1H), 7.48 (s, 1H), 7.13 (d, 1H), 6.85 (dd, 1H), 6.82 (d, 1H), 4.55 (brs, 2H), 4.45 (s, 2H), 3.52 (t, 2H), 2.74 (t, 2H), 1.42 (s, 9H). ¹³ C-NMR (125 MHz, dmso-d6) d ppm 159.4, 147.6, 135.8, 127.6, 119.5, 118, 45.2, 41.3, 28.7, 28.6.

Preparation R4ah: tert-butyl 5-[(5-amino-6-oxo-lH-pyrimidin-4-yl)oxy]isoindoline-2- carboxylate

Using General Procedure 4 starting from Preparation R3ah as reagent, 5-amino-4- isoindolin-5-yloxy-lH-pyrimidin-6-one hydrochloride was formed. The resulted crude product was reacted using General Procedure 6 to give Preparation R4ah. HRMS calculated for C ₁₇ H ₂₀ N ₄ O ₄ : 344.1485; found 345.1555 ((M+H) ⁺ form).

1H-NMR (400 MHz, dmso-d6) d ppm 12.45 (brs, 1H), 7.49 (d, 1H), 7.28/7.27 (d, 1H), 7 (d, 1H), 6.95/6.93 (dd, 1H), 4.6-4.5 (brs, 4H), 4.57 (brs, 2H), 1.45 (s, 9H).

¹³ C-NMR (125 MHz, dmso-d6) d ppm 159.4, 147.7, 135.9, 124, 119.3, 114.4, 28.6.

Preparation R4ai: 5-amino-4-[4-(2-hydroxyethoxy)phenoxy]-lH-pyrimidin-6-one hydrochloride

Using General Procedure 4 starting from Preparation R3ai as reagent, Preparation R4ai was obtained. HRMS calculated for C ₁₂ H ₁₃ N ₃ O ₄ : 263.0906; found 264.0975 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 13.12 (brs, 1H), 7.94 (s, 1H), 7.07 (m, 2H), 6.95 (m, 2H), 3.97 (t, 2H), 3.7 (t, 2H).

¹³ C-NMR (125 MHz, dmso-d6) d ppm 159.4, 157.6, 156.3, 146.6, 145.3, 122.5, 115.5, 70.4, 60.

Preparation R4ai : tert-butyl 2-[4-[(5-amino-6-oxo-lH-pyrimidin-4- yl)oxy]phenyl]pyrrolidine-l-carboxylate

Using General Procedure 4 starting from Preparation R3aj as reagent, 5-amino-4-(4- pyrrolidin-2-ylphenoxy)-lH-pyrimidin-6-one hydrochloride was formed. The resulted crude product was reacted using General Procedure 6 to give Preparation R4aj. HRMS calculated for C ₂₀ H ₂₆ N ₄ O ₄ : 372.1797; found 373.1872 ((M+H) ⁺ form).

1H-NMR (400 MHz, dmso-d6) d ppm 12.45 (s, 1H), 7.5 (s, 1H), 7.14 (dm, 2H), 6.98 (dm, 2H), 4.82/4.71 (m, 1H), 4.58 (s, 2H), 3.55-3.41 (m, 2H), 2.27/1.7 (m+m, 2H), 1.82 (m, 2H), 1.39/1.15 (s, 9H). ¹³ C-NMR (100 MHz, dmso-d6) d ppm 159.5, 154, 147.3, 140.5, 135.7, 126.9, 119.6, 60.7/60.2, 47.4/47.2, 36.1/34.9, 28.7/28.3, 23.4/23.1

Preparation R4al: 5-amino-4-(lH-indazol-6-yloxy)-lH-pyrimidin-6-one

hydrochloride

Using General Procedure 4 starting from Preparation R3al as reagent, Preparation R4al was obtained. HRMS calculated for C ₁₁ H ₉ N ₅ O ₂ : 243.0756; found 244.0833 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 13.2 (brs, 1H), 9.36 (brs, 2H), 8.1 (d, 1H), 8.02 (d, 1H), 7.79 (d, 1H), 7.32 (d, 1H), 6.95 (dd, 1H).

1 ³ C-NMR (125 MHz, dmso-d6) d ppm 146.7, 133.9, 121.8, 115.8, 102.1.

Preparation R4am: 5-amino-4-[4-(2-hydroxyethyl)phenoxy]-lH-pyrimidin-6-one hydrochloride

Using General Procedure 4 starting from Preparation R3am as reagent,

Preparation R4am was obtained. HRMS calculated for C ₁₂ H ₁₃ N ₃ O ₃ : 247.0957; found 248.103 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 12.97 (brs, 1H), 7.86 (s, 1H), 7.23 (m, 2H), 7.01 (m, 2H), 3.59 (t, 2H), 2.71 (t, 2H).

¹³ C-NMR (125 MHz, dmso-d6) d ppm 143.4, 130.3, 120.8, 62.6, 38.7.

Preparation R4an: 5-amino-4-[4-(2,2,2-trifluoroethyl)phenoxy]-lH-pyrimidin-6-o ne hydrochloride

Using General Procedure 4 starting from Preparation R3an as reagent,

Preparation R4an was obtained. HRMS calculated for C ₁₂ H ₁₀ F ₃ N ₃ O ₂ : 285.0725; found 286.0800 ((M+H) ⁺ form).

1H-NMR(400 MHz, dmso-d6) d ppm 12.8 (br., 1H), 7.73 (s, 1H), 7.36 (dm, 2H), 7.09 (dm, 2H), 3.64 (q, 2H)

¹³ C-NMR (125 MHz, dmso-d6) d ppm 159.4, 154.1, 151.9, 140.4, 131.9, 127.3, 126.6, 120.5, 38.2

Preparation R4ao: 5-amino-4-[4-(2,2-difluoroethyl)phenoxy]-lH-pyrimidin-6-one hydrochloride

Using General Procedure 4 starting from Preparation R3ao as reagent, Preparation R4ao was obtained. HRMS calculated for C ₁₂ H ₁₁ F ₂ N ₃ O ₂ : 267.0819; found 268.0895 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 12.9 (brs, 1H), 7.8 (s, 1H), 7.31 (m, 2H), 7.07 (m, 2H), 6.24 (tt, 1H), 3.17 (td, 2H)

¹³ C-NMR (125 MHz, dmso-d6) d ppm 142.1, 131.5, 120.8, 117.5, 39.3

Preparation R4ap: 5-amino-4-[4-(2-fhioroethyl)phenoxy]-lH-pyrimidin-6-one hydrochloride

Using General Procedure 4 starting from Preparation R3ap as reagent,

Preparation R4ap was obtained. HRMS calculated for C ₁₂ H ₁₂ FN ₃ O ₂ : 249.0914; found

250.0988 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 13.03 (br., 1H), 7.89 (s, 1H), 7.29 (dm, 2H), 7.06 (dm, 2H), 4.64 (dt, 2H), 2.97 (dt, 2H).

1 ³ C-NMR (125 MHz, dmso-d6) d ppm 159.4, 155.8, 152.3, 143.9, 134.4, 130.5, 121.1, 84.4, 35.8

Preparation R4aq: 5-amino-4-[4-fluoro-3-(trifluoromethoxy)phenoxy]-lH-pyrimidi n- 6-one hydrochloride

Using General Procedure 4 starting from Preparation R3aq as reagent, Preparation R4aq was obtained. HRMS calculated for C ₁₁ H ₇ F ₄ N ₃ O ₃ : 305.0424; found

306.0501 ((M+H) ⁺ form).

1H-NMR (400 MHz, dmso-d6) d ppm 12.84 (br., 1H), 7.73 (s, 1H), 7.54 (dd, 1H), 7.41 (dm, 1H), 7.22 (ddd, 1H)

¹³ C-NMR (125 MHz, dmso-d6) d ppm 159.4, 150.8, 150.6, 140, 135.5, 121.3, 118.3, 116.6 Preparation R4ar: 5-amino-4-(4-fluoro-3-hydroxy-phenoxy)-lH-pyrimidin-6-one

Preparation R3p was dissolved in abs. DCM (5 mL) and cooled to 0 °C, then 1M boron tribromide (2.0 eq.) was added. It was stirred at 0 °C for 1 hour, then it was allowed warm to r.t. After 40 hours, the solid compound was filtered off (180 mg), it was purified by Hanbon preparative HPLC (C18 Silica, Gemini NX 5pm, 0.02 % HCOOH-MeCN, gradient method 5-90 %) to give Preparation R4ar. HRMS calculated for C ₁₀ H ₈ FN ₃ O ₃ : 237.055; found 238.0618 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 12.45/10 (brs, 2H), 7.51 (s, 1H), 7.08 (dd, 1H), 6.6 (dd, 1H), 6.44 (m, 1H), 4.59 (brs, 2H)

1 ³ C-NMR (125 MHz, dmso-d6) d ppm 159.3, 151.2, 148, 147.4, 145.7, 135.7, 121.5,

116.4, 110.1, 109.3

Preparation R4as: 5-amino-4-(4-chloro-3-ethyl-phenoxy)-lH-pyrimidin-6-one

Using General Procedure 4 starting from Preparation R3as as reagent, Preparation R4as was obtained. HRMS calculated for C ₁₂ H ₁₂ CIN ₃ O ₂ : 265.0618; found 266.0691 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 12.46 (brs, 1H), 7.51 (s, 1H), 7.36 (d, 1H), 7.04 (d, 1H), 6.88 (dd, 1H), 4.64 (s, 2H), 2.67 (q, 2H), 1.15 (t, 3H).

¹³ C-NMR (125 MHz, dmso-d6) d ppm 135.7, 130.2, 121, 118.9, 26.6, 14.4.

Preparation R4at: 5-amino-4-(3-benzyloxyphenoxy)-lH-pyrimidin-6-one

hydrochloride

Using General Procedure 4 starting from Preparation R3at as reagent, Preparation R4at was obtained. HRMS calculated for C ₁₇ H ₁₅ N ₃ O ₃ : 309.1113; found 310.1182 ((M+H) ⁺ form).

1H-NMR (400 MHz, dmso-d6) d ppm 12.94 (brs, 1H), 7.83 (s, 1H), 7.44 (dm, 2H), 7.4 (tm, 2H), 7.34 (tm, 1H), 7.29 (t, 1H), 6.85 (dd, 1H), 6.78 (t, 1H), 6.69 (dd, 1H), 5.1 (s, 2H).

¹³ C-NMR (125 MHz, dmso-d6) d ppm 159.8, 159.5, 155.1, 142.3, 137.3, 130.4, 128.9,

128.4, 128.3, 113, 111.3, 107.7, 69.9.

Preparation R4au: 4-[(5-amino-6-oxo-lH-pyrimidin-4-yl)oxy]benzaldehyde

Using General Procedure 4 starting from Preparation R3au as reagent, Preparation R4au was obtained. HRMS calculated for C _{1 1} H ₉ N ₃ O ₃ : 231.0644; found 232.0714 ((M+H) ⁺ form).

1H-NMR (400 MHz, dmso-d6) d ppm 12.55 (brs, 1H), 9.94 (s, 1H), 7.92 (d, 2H), 7.57 (s, 1H), 7.21 (d, 2H), 4.82 (brs, 2H).

¹³ C-NMR (125 MHz, dmso-d6) d ppm 192.1, 159.6, 131.9, 119.2. Preparation R4az: tert-butyl 2-[3-[[5-(tert-butoxycarbonylamino)-6-oxo-lH- pyrimidin-4-yl] oxy] phenyl] piperidine- 1-carboxylate

Using General Procedure 4 starting from Preparation R3az as reagent, 5-amino-4-[3-(2- piperidyl)phenoxy]-lH-pyrimidin-6-one hydrochloride was formed. The resulted crude product was reacted using General Procedure 6 to give Preparation R4az. HRMS calculated for C25H34N4O6: 486.2478; found 487.2547 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 12.72 (brs, 1H), 8.04 (s, 1H), 7.97 (s, 1H), 7.38 (t, 1H), 7.03 (dd, 1H), 6.95 (dd, 1H), 6.85 (dd, 1H), 5.26 (d, 1H), 3.91/2.68 (d+t, 2H), 2.26/1.76 (d+t, 2H), 1.54/1.24 (d+dd, 2H), 1.53/1.38 (d+t, 2H), 1.38 (s, 9H), 1.37 (s, 9H). ¹³ C-NMR (125 MHz, dmso-d6) d ppm 163.2, 161.6, 155, 154.3, 154.1, 147.8, 142.5,

130.1, 123, 120.4, 119.7, 119.4, 79.4, 78.9, 53, 40.2, 28.5, 28.5, 28.3, 25.3, 19.4

Preparation R4bc: 5-amino-4-(2-hydroxyindan-5-yl)oxy-lH-pyrimidin-6-one

Using General Procedure 4 starting from Preparation R3bc as reagent,

Preparation R4bc was obtained. HRMS calculated for C13H13N3O3: 259.0957; found 260.1027 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 13.02 (br., 1H), 7.89 (s, 1H), 7.2 (d, 1H), 6.95 (d, 1H), 6.87 (dd, lH), 4.5l (m, 1H)

¹³ C-NMR (125 MHz, dmso-d6) d ppm 159.4, 156.3, 152.3, 144.3, 143.7, 138.6, 125.6,

119.2, 117.7, 72, 42.7, 41.9

Preparation R4bf: 5-amino-4-[3-(l-hydroxy-l-methyl-ethyl)phenoxy]-lH-pyrimidin - 6-one

Using General Procedure 4 starting from Preparation R3bf as reagent,

Preparation R4bf was obtained. HRMS calculated for C ₁₃ H ₁₅ N ₃ O ₃ : 261.1113; found 262.1186 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 12.44 (brs, 1H), 7.5 (s, 1H), 7.25 (t, 1H), 7.17 (dm, 1H), 7.14 (t, 1H), 6.82 (dm, 1H), 5.04 (s, 1H), 4.57 (s, 2H), 1.4 (s, 6H)

¹³ C-NMR (125 MHz, dmso-d6) d ppm 159.5, 155, 153, 147.8, 135.8, 129, 121.6, 120.2,

117.3, 116.1, 71, 32.3 Preparation R4bg: 4-[(5-amino-6-oxo-lH-pyrimidin-4-yl)oxy]-2-fluoro-benzonitri le hydrochloride

Using General Procedure 4 starting from Preparation R3bg as reagent,

Preparation R4bg was obtained. HRMS calculated for C11H7FN4O2: 246.0553; found 247.0629 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 12.81 (brs, 1H), 7.92 (t, 1H), 7.7 (s, 1H), 7.39 (brs, 2H), 7.32 (dd, 1H), 7.1 (dd, 1H).

¹³ C-NMR (125 MHz, dmso-d6) d ppm 163.9, 160.5, 159.7, 147.4, 138.4, 135.2, 116.4,

114.5, 107.8, 95. Preparation R4bh: 4- [(5-amino-6-oxo- lH-pyrimidin-4-yl)oxy] -2-chloro-benzonitrile hydrochloride

Using General Procedure 4 starting from Preparation R3bh as reagent,

Preparation R4bh was obtained. HRMS calculated for C11H7CIN4O2: 262.0258; found 263.0335 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 12.83 (brs, 1H), 7.98 (d, 1H), 7.72 (s, 1H), 7.51 (d, 1H), 7.49 (br„ 2H), 7.24 (dd, 1H).

¹³ C-NMR (125 MHz, dmso-d6) d ppm 159.6, 159.2, 147.9, 138.9, 137, 136.3, 120.8, 119,

116.5, 107.1.

Preparation R4bi: 3- [4- [(5-amino-6-oxo- lH-pyrimidin-4- yl)oxy] phenyl] propanenitrile hydrochloride

Using General Procedure 4 starting from Preparation R3bj as reagent,

Preparation R4bj was obtained. HRMS calculated for C13H12N4O2: 256.096; found 257.103 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 12.89 (brs, 1H), 7.8 (s, 1H), 7.3 (d, 2H), 7.06 (d, 2H), 2.87 (t, 2H), 2.81 (t, 2H).

¹³ C-NMR (125 MHz, dmso-d6) d ppm 159.4, 152.8, 141.7, 135.4, 130, 120.7, 30.3, 18.8.

Preparation R4bk: 4-[(5-amino-6-oxo-lH-pyrimidin-4-yl)oxy]-3-chloro-benzonitri le Using General Procedure 4 starting from Preparation R3bk as reagent,

Preparation R4bk was obtained. HRMS calculated for C11H7CIN4O2: 262.0258; found 263.0330 ((M+H) ⁺ form).

1H-NMR (400 MHz, dmso-d6) d ppm 12.57 (br., 1H), 8.18 (d, 1H), 7.8 (dd, 1H), 7.51 (s, 1H), 7.25 (d, 1H), 4.84 (s, 2H)

¹³ C-NMR (125 MHz, dmso-d6) d ppm 159.4, 154.9, 145.5, 135.7, 134.6, 133.1, 125.7, 122.4, 121.9, 118, 107.7

Preparation R4bm: tert-butyl N-[l-[4-[(5-amino-6-oxo-lH-pyrimidin-4- yl)oxy] phenyl] ethyl] carbamate

Using General Procedure 4 starting from Preparation R3bm as reagent, 5-amino-4-[4- (l-aminoethyl)phenoxy]-lH-pyrimidin-6-one hydrochloride was formed. The resulted crude product was reacted using General Procedure 6 to give Preparation R4bm. HRMS calculated for C ₁₇ H ₂₂ N ₄ O ₄ : 346.1641; found 347.1716 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 12.16 (brs, 1H), 7.48 (s, 1H), 7.37 (d, 1H), 7.24 (d, 2H), 6.94 (d, 2H), 4.59 (qn, 1H), 4.49 (s, 2H), 1.36 (s, 9H), 1.28 (d, 3H)

¹³ C-NMR (125 MHz, dmso-d6) d ppm 160, 155.3, 153.9, 147.9, 141, 136.6, 127.2, 119.6, 78.1, 49.5, 28.7, 23.5

Preparation R4bn: tert-butyl N-[l-[4-[(5-amino-6-oxo-lH-pyrimidin-4- yl)oxy] phenyl] propyl] carbamate

Using General Procedure 4 starting from Preparation R3bn as reagent, 5-amino-4-[4-(l- aminopropyl)phenoxy]-lH-pyrimidin-6-one hydrochloride was formed. The resulted crude product was reacted using General Procedure 6 to give Preparation R4bn. HRMS calculated for C ₁₈ H ₂₄ N ₄ O ₄ : 360.1797; found 361.1866 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 12.32 (br., 1H), 7.49 (s, 1H), 7.32 (d, 1H), 7.23 (d, 2H), 6.95 (d, 2H), 4.57 (s, 2H), 4.33 (m, 1H), 1.6 (m, 2H), 1.36 (s, 9H), 0.81 (t, 3H) ¹³ C-NMR (125 MHz, dmso-d6) d ppm 159.3, 155.6, 153.7, 147.6, 140, 135.7, 127.8, 121.4, 119.5, 78, 55.9, 30, 28.7, 11.6

Preparation R4bq: 5-amino-4-(3-pyridyloxy)-lH-pyrimidin-6-one

Using General Procedure 4 starting from Preparation R3bq as reagent, Preparation R4bq was obtained. HRMS calculated for C ₉ H ₈ N ₄ O ₂ : 204.0647; found 205.07216 ((M+H) ⁺ form). Preparation R4bs: 5-amino-4-(lH-pyrrolo[3,2-b]pyridin-6-yloxy)-lH-pyrimidin-6- one, hydrochloride

Using General Procedure 4 starting from Preparation R3bs as reagent, Preparation R4bs was obtained. HRMS calculated for C ₁₁ H ₉ N ₅ O ₂ : 243.0756; found 244.083 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 12.82 (br., 1H), 12.75 (s, 1H), 8.76 (d, 1H), 8.44 (dd, 1H), 8.19 (t, 1H), 7.68 (s, 1H), 6.85 (m, 1H)

¹³ C-NMR (125 MHz, dmso-d6) d ppm 159.4/149.7, 145.7, 138.5, 137.4, 134.6, 132.4, 129.1, 120.5, 97 Preparation R4bt: 5-amino-4-(3-benzyloxy-4-chloro-phenoxy)-lH-pyrimidin-6-one Using General Procedure 4 starting from Preparation R3bt as reagent,

Preparation R4bt was obtained. HRMS calculated for C ₁₇ H ₁₄ CIN ₃ O ₃ : 343.0724; found 344.0792 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 13.03 (brs, 1H), 7.84 (s, 1H), 7.49-7.31 (m, 5H), 7.44 (d, 1H), 7.09 (d, 1H), 6.73 (dd, 1H), 5.18 (s, 2H)

¹³ C-NMR (125 MHz, dmso-d6) d ppm 142.8, 130.5, 113.9, 107.8, 70.7

Preparation R4bu: 5-amino-4-(3-benzyloxy-4-methyl-phenoxy)-lH-pyrimidin-6-one Using General Procedure 4 starting from Preparation R3bu as reagent,

Preparation R4bu was obtained. HRMS calculated for C ₁₈ H ₁₇ N ₃ O ₃ : 323.127; found 324.1338 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 7.87 (s, 1H), 7.48-7.29 (m, 5H), 13.04 (brs, 1H), 7.15 (dm, 1H), 6.85 (d, 1H), 6.61 (dd, 1H), 5.05 (s, 2H), 2.18 (brs, 3H)

¹³ C-NMR (125 MHz, dmso-d6) d ppm 144, 130.9, 112.8, 105.8, 69.8, 16.1

Preparation R4bv: tert-butyl 4- [2- [4- [(5-amino-6-oxo- lH-pyrimidin-4-yl)oxy] phenyl] ethyl] piperidine- 1-carboxylate

Using General Procedure 4 starting from Preparation R3bv as reagent, 5-amino-4-[4-[2- (4-piperidyl)ethyl]phenoxy]-lH-pyrimidin-6-one hydrochloride was formed. The resulted crude product was reacted using General Procedure 6 to give Preparation R4bv. HRMS calculated for C ₂₂ H ₃₀ N ₄ O ₄ : 414.2267; found 415.23350 ((M+H) ⁺ form).

1H-NMR (400 MHz, dmso-d6) d ppm 12.42 (brs, 1H), 7.48 (s, 1H), 7.16 (m, 2H), 6.92 (m, 2H), 4.54 (s, 2H), 3.92/2.66 (brd+brs, 4H), 2.57 (t, 2H), 1.68/0.99 (m+m, 4H), 1.49 (m, 2H), 1.38 (s, 9H), 1.38 (m, 1H).

¹³ C-NMR (100 MHz, dmso-d6) d ppm 135.7, 129.5, 119.8, 43.9, 38.5, 35.2, 32.1, 31.8, 28.5

Preparation R4bw: 5-amino-4-[4-(morpholinomethyl)phenoxy]-lH-pyrimidin-6-one Using General Procedure 4 starting from Preparation R3bw as reagent, Preparation R4bw was obtained. HRMS calculated for C ₁₅ H ₁₈ N ₄ O ₃ : 302.1379; found 303.1450 ((M+H) ⁺ form).

1H-NMR (400 MHz, dmso-d6) d ppm 12.88 (brs, 1H), 11.53 (brs, 1H), 7.76 (s, 1H), 7.64 (m, 2H), 7.16 (m, 2H), 4.3 (d, 2H), 3.83/3.82 (m+m, 4H), 3.19/3.06 (m+m, 4H)

¹³ C-NMR (100 MHz, dmso-d6) d ppm 140.6, 133.4, 120.4, 63.5, 58.7, 50.9 Preparation R4bx: tert-butyl 2-[2-[4-[(5-amino-6-oxo-lH-pyrimidin-4- yl)oxy]phenyl]ethyl]piperidine-l-carboxylate

Using General Procedure 4 starting from Preparation R3bx as reagent, 5-amino-4-[4-[2- (2-piperidyl)ethyl]phenoxy]-lH-pyrimidin-6-one hydrochloride was formed. The resulted crude product was reacted using General Procedure 6 to give Preparation R4bx. HRMS calculated for C22H30N4O4: 414.2267; found 415.23386 ((M+H) ⁺ form).

1H-NMR (400 MHz, dmso-d6) d ppm 12.46 (br., 1H), 7.48 (s, 1H), 7.18 (dm, 2H), 6.93 (dm, 2H), 4.54 (br., 2H), 4.14 (br., 1H), 3.85/2.79 (brd+brt, 2H), 2.53/2.42 (m+m, 2H), 1.91/1.7 (m+m, 2H), 1.60-1.44 (br., 2H), 1.57/1.49 (br.+br„ 2H), 1.56/1.26 (br.+br„ 2H), 1.38 (s, 9H).

¹³ C-NMR (100 MHz, dmso-d6) d ppm 159.3, 154.6, 153.1, 147.8, 137.4, 135.7, 129.5, 119.8, 78.8, 50.1, 38.7, 31.8, 31.8, 28.6, 28.5, 25.8, 19

Preparation R4bv: tert-butyl 2-[3-[(5-amino-6-oxo-lH-pyrimidin-4-yl)oxy]phenyl] morpholine-4-carboxylate Using General Procedure 4 starting from Preparation R3by as reagent, 5-amino-4-(3- morpholin-2-ylphenoxy)-lH-pyrimidin-6-one hydrochloride was formed. The resulted crude product was reacted using General Procedure 6 to give Preparation R4by. HRMS calculated for C ₁₉ H ₂₄ N ₄ O ₅ : 388.1747; found 389.1813 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 12.46 (brs, 1H), 7.51 (s, 1H), 7.34 (t, 1H), 7.12 (dd, 1H), 7.02 (t, 1H), 6.97 (dd, 1H), 4.62 (brs, 2H), 4.4 (dd, 1H), 3.93/3.53 (brd+td, 2H), 3.88/2.77 (br.+br., 2H), 3.76/2.96 (br.+br„ 2H), 1.41 (s, 9H).

¹³ C-NMR (125 MHz, dmso-d6) d ppm 159.4, 155.3, 154.3, 146.9, 141.6, 135.7, 129.9, 121.9, 121.7, 119.2, 117.4, 79.9, 76.9, 66.5, 49.6, 43.1, 28.5 Preparation R4bz: tert-butyl N-[(lR)-l-[4-[(5-amino-6-oxo-lH-pyrimidin-4-yl)oxy] phenyl] -2,2,2-trifluoro-ethyl] carbamate

Using General Procedure 4 starting from Preparation R3bz as reagent, 5-amino-4-[4- [(lR)-l-amino-2,2,2-trifluoro-ethyl]phenoxy]-lH-pyrimidin-6- one was formed. The resulted crude product was reacted using General Procedure 6 to give Preparation R4bz. HRMS calculated for C ₁₇ H ₁₉ F ₃ N ₄ O ₄ : 400.1358; found 401.1424 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 12.46 (s, 1H), 8.36 (d, 1H), 7.54 (m, 2H), 7.5 (s, 1H), 7.04 (m, 2H), 5.39 (m, 1H), 4.64 (s, 2H), 1.41 (s, 3H)

¹³ C-NMR (125 MHz, dmso-d6) d ppm 159.4, 146.8, 135.7, 130.1, 119.5, 55.3, 28.5

Preparation R4ca: 2- [4- [(5-amino-6-oxo- lH-pyrimidin-4-yl)oxy] phenyl] acetonitrile Using General Procedure 4 starting from Preparation R3ca as reagent, Preparation R4ca was obtained. HRMS calculated for C ₁₂ H ₁₀ N ₄ O ₂ : 242.0804; found 243.0878 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 12.45 (brs, 1H), 7.49 (s, 1H), 7.32 (d, 2H), 7.05 (d, 2H), 4.62 (s, 2H), 4 (s, 2H)

1 ³ C-NMR (125 MHz, dmso-d6) d ppm 159.4, 154.6, 147.3, 135.7, 129.6, 126.7, 121.7, 120.3, 119.9, 22.2

Preparation R4cb: 5-amino-4-[4-fluoro-3-(hydroxymethyl)phenoxy]-lH-pyrimidin-6 - one Using General Procedure 4 starting from Preparation R3cb as reagent, Preparation R4cb was obtained. HRMS calculated for C1 1H10FN3O3: 251.0706; found 252.0779 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 12.99 (br., 1H), 7.86 (s, 1H), 7.19 (d, 1H), 7.18 (t, 1H), 7.04 (dm, 1H), 4.54 (s, 2H)

¹³ C-NMR (125 MHz, dmso-d6) d ppm 159.4, 156.5, 154.9, 149.8, 143.1, 131, 121, 120.9, 116, 56.8

Preparation R4cc: 5-amino-4-(3-amino-4-fluoro-phenoxy)-lH-pyrimidin-6-one

Using General Procedure 4 starting from Preparation R3cb as reagent, it was purified by Hanbon preparative HPLC,Cl8 Silica, Gemini NX 5 pm, 5 mM NH ₄ HC03-MeCN using gradient method 5-90 %. Solvent was evaporated under reduced pressure to give Preparation R4cb. HRMS calculated for C10H9FN4O2: 236.071; found 237.0782 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 12.42 (brs, 1H), 7.5 (s, 1H), 6.91 (t, 1H), 6.39 (dd, 1H), 6.14 (dm, 1H), 5.21 (s, 2H), 4.53 (s, 2H)

¹³ C-NMR (125 MHz, dmso-d6) d ppm 159.3, 151.6, 147.8, 147.5, 137.5, 135.7, 121.4, 115.3, 107.3, 106.6

Preparation R4cd: 5-amino-4-(3-hydroxy-4-isopropyl-phenoxy)-lH-pyrimidin-6-one Preparation R3cd (159 mg, 0.55 mmol) was dissolved in abs. DCM (5 mL) and cooled to 0 °C, then 1M boron tribromide (3.0 eq.) was added. It was stirred at 0 °C for 1 hour, then it was allowed warm to r.t. After 20 hours, the reaction mixture was cooled to 0 °C and poured to crashed ice and sat. NaHCCU was added. It was extracted with ethyl acetate several times. Combined organic phases were dried over magnesium sulfate and evaporated to give Preparation R4cd. HRMS calculated for C13H15N3O3: 261.1113; found 262.1183 ((M+H)+ form).

1H-NMR (500 MHz, dmso-d6) d ppm 12.44 (s, 1H), 9.38 (s, 1H), 7.51 (s, 1H), 7.03 (d, 1H), 6.43 (d, 1H), 6.41 (dd, 1H), 3.13 (m, 1H), 1.13 (d, 6H)

¹³ C-NMR (125 MHz, dmso-d6) d ppm 159.3, 155.4, 153.6, 147.9, 136, 130, 126.6, 110.1, 106.5, 26.4, 23.1 Preparation R4ce: tert-butyl 2-[4-[(5-amino-6-oxo-lH-pyrimidin-4- yl)oxy] phenyl] piperidine- 1-carboxylate

Using General Procedure 4 starting from Preparation R3ce as reagent, 5-amino-4-[4-(2- piperidyl)phenoxy]-lH-pyrimidin-6-one hydrochloride was formed. The resulted crude product was reacted using General Procedure 6 to give Preparation R4ce. HRMS calculated for C ₂₀ H ₂₆ N ₄ O ₄ : 386.1954; found 387.2018 ((M+H) ⁺ form).

1H-NMR (500 MHz, dmso-d6) d ppm 12.44 (brs, 1H), 7.5 (s, 1H), 7.14 (m, 2H), 7.02 (m, 2H), 5.26 (dd, 1H), 4.59 (s, 2H), 3.92/2.69 (m+m, 2H), 2.27/1.75 (m+m, 2H), 1.4 (s, 9H) ¹³ C-NMR (125 MHz, dmso-d6) d ppm 135.7, 127.7, 119.8, 52.8, 40.1, 28.5, 28.4

Preparation R5a: [(lR,2R)-4,4-difluoro-2-phenyl-cyclohexyl]-(2-oxa-6- azaspiro [2.5] octan-6-yl)methanone

Step 1: ( lR,2R)-4,4-difluoro-2-phenyl-cyclohexanecarboxylic acid.

2-trimethylsilyloxy-4-phenyl-l, 3-butadiene (synthesized according to Tetrahedron 2001, 57, 6311-6327; 1.0 eq.) and ethyl propiolate (1.0 eq.) were placed in a sealed tube into anhydrous toluene. The reaction mixture was heated to 150 °C and it was stirred at this temperature overnight. Then the toluene was evaporated by reduced pressure and the residue was dissolved in a mixture of THF, water, and cc. sulfuric acid (3 eq.). The mixture was stirred for 1 hour at 25 °C. Reaction mixture was diluted with water (150 ml) and the product was isolated by extraction with DEE. The organic layer was dried and concentrated. Crude product was used without further purification.

The unsaturated cyclohexenone derivative was placed in a flask and dissolved in cyclo hexene. The reaction mixture was refluxed overnight in the presence 0.05 eq. 10 % Pd/C. After 16 hours, the Pd/C was filtered off through Celite pad. The saturated crude product was refluxed in methanol in the presence sodium ethoxide to give ethyl trans-4- oxo-2-phenyl-cyclohexanecarboxylate.

Ethyl trans-4-oxo-2-phenyl-cyclohexanecarboxylate was dissolved in DCM, then DAST was added (5.0 eq.). After 1 hour, water and DCM was added, then layers were separated. Organic layer was dried and evaporated. The residue was purified by flash chromatography (hexane:EEO). The enantiomers were separated by chiral chromatography to give ethyl (lR,2R)-4,4-difluoro-2-phenyl-cyclohexanecarboxylate and ethyl (lS,2S)-4,4-difluoro-2- phenyl-cyclohexanecarboxylate.

Ethyl (lR,2R)-4,4-difluoro-2-phenyl-cyclohexanecarboxylate was dissolved in ethanol and water (1 :1) and lithium hydroxide hydrate (4.0 eq.) was added. It was heated and stirred at 80 °C for 17 hours. Then the ethanol was evaporated under reduced pressure and 1N HC1 was added till solid compound was formed, which was filtered off to give (lR,2R)-4,4- difluoro-2-phenyl-cyclohexanecarboxylic acid. HRMS calculated for C ₁₃ H ₁₄ F ₂ O ₂ : 240.0962; found 258.1302 [(M+NH ₄ ) ⁺ form]

1H-NMR (500 MHz, dmso-d6) d ppm 12.06 (s, 1H), 7.34-7.16 (m, 5H), 2.95 (m, 1H), 2.73 (m, 1H), 2.24-2.00 (m, 2H), 2.20-1.93 (m, 2H), 2.05/1.68 (m+m, 2H)

¹³ C-NMR (125 MHz, dmso-d6) d ppm 47.5, 43.3, 40.2, 32.3, 26.6

Step 2: l-[(lR,2R)-4,4-difluoro-2-phenyl-cyclohexanecarbonyl]piperid in-4-one

4-Piperidone hydrochloride hydrate (3.14 g, 20.5 mmol), HBTU (11.66 g, 30.74 mmol), (lR,2R)-4,4-difluoro-2-phenyl-cyclohexanecarboxylic acid. (4.92 g, 20.5 mmol) and NN- diisopropylethylamine (13.26 g, 17.8 ml, 102.5 mmol) were dissolved in MeCN (50 mL) and stirred at r.t. for 5 hours. After evaporation, the residue was dissolved in DCM and it was washed with 1N NaOH and then with 1N HC1 and then with water. Organic layer was dried (MgS0 ₄ ) and evaporated. DIPO was added, solid compound was formed, which was filtered off to give the product of the title.

HRMS calculated for C ₁₈ H ₂₁ F ₂ NO ₂ : 321.154; found 322.1611 [(M+H)+ form]

1H-NMR (500 MHz, MSM-d6) d ppm 7.31-7.14 (m, 5H), 3.86-3.16 (m, 4H), 3.31 (m, 1H), 3.09 (m, 1H), 2.3/2.12 (m+m, 2H), 2.23-1.41 (m, 4H), 2.18-1.97 (m, 2H), 1.88/1.77 (m+m, 2H)

¹³ C-NMR (125 MHz, MSM-d6) d ppm 43.8, 43.1, 39.3, 32.4, 26.7 Step 3: Preparation R5a

l-[(lR,2R)-4,4-difluoro-2-phenyl-cyclohexanecarbonyl]pipe ridin-4-one (2.0 g, 6.2 mmol, 1.0 eq.) and trimethylsulfoxonium- iodide (3.4 g, 15.5 mmol, 2.5 eq.) was charged into a round bottom flask and dissolved/suspended in MeCN (10 ml) and MTBE (10 ml). NaOH (0.62 g, 15.5 mmol, 2.5 eq.) was dissolved in water (1.3 ml) and the obtained solution was added to the mixture and stirred at 60 °C for 6 hours. After the reaction completed, the reaction mixture was filtered through C elite, and washed with MTBE (3 x 4 ml). Water (15 ml) was added to the solution, layers were separated, and the aqueous layer was extracted with MTBE (2 x 4 ml). Combined organic layers were dried over MgS0 ₄ and after filtration evaporated to give Preparation R5a. HRMS calculated for C ₁₉ H ₂₃ F ₂ NO ₂ : 335.1697; found 336.1779 [(M+H)+ form]

1H-NMR (500 MHz, MSM-d6) d ppm 7.4-7 (m, 5H), 3.85-2.9 (m, 4H), 3.28 (m, 1H), 3.07 (brm, 1H), 2.59-2.5 (m, 2H), 2.36-2.05 (m, 2H), 2.17-1.96 (m, 2H), 1.83/1.74 5 (dm+tm, 2H), 1.38-0.79 (m, 4H).

¹³ C-NMR (125 MHz, MSM-d6) d ppm 57.4/57, 53.4/53, 43.7, 42.8, 39.4, 32.4, 26.7 Preparation R5b: (8,8-difluoro-2-oxa-6-azaspiro [2.5] octan-6-yl)- [(lR,2R)-4,4- difluoro-2-phenyl-cyclohexyl]methanone

Step 1: (3 ,3-difluoro-4, 4-dihydroxy- 1-piperidyl)- [ ( lR,2R)-4,4-difluoro-2-phenyl - cyclohexyl] methanone

3.3-difluoropiperidine-4,4-diol hydrochloride (740 mg, 3.903 mmol), 3-(ethyliminomethyleneamino)-N,N-dimethyl-propan-l -amine, hydrochloride (1 : 1)

(2992 mg, 15.613 mmol, 4.0 eq.) and (lR,2R)-4,4-difluoro-2-phenyl- cyclohexanecarboxylic acid (1031 mg, 4.2935 mmol) were dissolved in pyridine (10 mL) and stirred at r.t. for 23 hours. The mixture was purified by preparative HPLC (on C-18 Gemini-NX 5 pm column, 5 mM NH ₄ HCO ₃ aqueous solution - MeCN, gradient). The solvents were removed under reduced pressure to give the product of the title.

Step 2: Preparation R5b

3.3-difluoro-4,4-dihydroxy-l-piperidyl)-[(lR,2R)-4,4-difluor o-2-phenyl-cyclohexyl] methanone (200 mg, 0.5328 mmol, 1.0 eq.) and trimethylsulfoxonium-iodide (293 mg, 1.332 mmol, 2.5 eq.) was charged into a round bottom flask and dissolved/suspended in MeCN (2 ml) and MTBE (2 ml). NaOH (53 mg, 1.332 mmol, 2.5 eq.) was dissolved in water (0.4 ml) and the obtained solution was added to the mixture and stirred at 60 °C for 2 hours. After the reaction completed, the reaction mixture was cooled down to r.t., MTBE (2 ml) and water (2 ml) were added to the solution, layers were separated, and the aqueous layer was extracted with MTBE (3 x 3 ml). Combined organic layers were dried over MgS0 ₄ and after filtration evaporated to give Preparation R5b. HRMS calculated for C19H21F4NO2: 371.1508; 371.15063 [M ⁺ form]

1H-NMR (400/500 MHz, dmso-d6) d ppm 7.33-7.11 (m, 5H), 4.24-3.35 (m, 2H), 3.78-3.07 (m, 2H), 2.29-1.98 (m, 2H), 2.11-1.98 (m, 2H), 1.93-1.52 (m, 2H), 1.71-1.20 (m, 2H), 3.47/3.4 (m/m, 1H), 3.07 (m, 1H).

¹³ C-NMR (400/500 MHz, dmso-d6) d ppm 172.8, 142.5, 124.1, 117.2, 57.1, 50/46.3, 49.9, 43.6/43.5, 43/39.5, 42.6/41.8, 40.1, 32.3, 30.5/29.7, 26.8

Preparation R5c: [tr ans-5,5-difluoro-2-phenyl-cyclohexyl] -(2-oxa-6- azaspiro [2.5] octan-6-yl)methanone

A mixture of cinnamic acid, 1 ,4-hydroquinone (catalytic amount) were suspended in 1 ,4-butadiene (20 wt% in toluene), and the resulted mixture was heated together in a sealed tube or microwave vial at 200 °C for 2 hours. After being cooled to r.t., the sealed tube was cooled in an ice/water bath. Solid compound was formed which was filtered off, and it was washed with cold toluene three times and dried in air, then in vacuum, to afford trans-6- phenylcyclohex-3-ene- 1 -carboxylic acid.

A part of this product was dissolved in chloroform and cooled to 0 °C. Bromotrimethylsilane (1.0 eq.) in chloroform and MSM was added dropwise to the cooled solution. Then, diisopropylethylamine (1.0 eq.) was added dropwise at 0 °C to the mixture. It was stirred for 15 minutes at 0 °C, was warmed up to r.t., then it was refluxed overnight. Reaction mixture was diluted with EEO, and washed with water, 10 % HC1 solution, water and finally with brine. The organic layer was dried (MgS0 ₄ ) and evaporated. The isolated product was used without further purification.

The isolated product was dissolved in methanol and freshly prepared sodium methoxide (1.0 eq.) was added and the mixture was stirred at 40 °C for 16 hours. The mixture was then treated with 0.5M HC1 solution, and methanol was evaporated. The residue was dissolved in EEO and washed with water and the layers were separated. The aqueous layer was extracted with additional EEO, and the combined organic layers were washed with water, 5 % Na ₂ C03 and brine, and dried (Na ₂ S0 ₄ ) to give methyl trans-5-oxo-2-phenyl- cyclohexanecarboxylate as a crude product.

Methyl trans-5-oxo-2-phenyl-cyclohexanecarboxylate was dissolved in DCM, then DAST was added (5.0 eq.). After 1 hour, water and DCM was added, then layers were separated. Organic layer was dried and evaporated. The residue was purified by flash chromatography (hexane:EEO).

Then the product obtained from the previous step was dissolved with isopropyl alcohol and 10 cc. HC1 (5.0 eq.) was added. It was heated and stirred at 90 °C for 4 days, then the solid compound was filtered off and it was purified by preparative HPLC (on C-18 Gemini-NX 5 pm column, 0.02 % HCOOH aqueous solution - MeCN, gradient) to give trans-5,5- difluoro-2-phenyl-cyclohexanecarboxylic acid.

Using Steps 6 and 7 of General Procedure 8 and starting from trans-4,4-difluoro-2-(3- thienyl)cyclohexanecarboxylic acid, Preparation R5c was obtained. HRMS calculated for C ₁₉ H ₂₃ F ₂ NO ₂ : 335.1697; 336.1771 [(M+H) ⁺ form]

1H-NMR (500 MHz, dmso-d6) d ppm 7.37-7.05 (m, 5H), 3.86-2.88 (m, 4H), 3.29 (m, 1H), 2.91 (m, 1H), 2.55 (m, 2H), 2.21-1.76 (m, 6H), 1.38-0.72 (m, 4H)

¹³ C-NMR (125 MHz, dmso-d6) d ppm 170.7, 143.2, 124.3, 57.3/57, 53.4/53, 45.3/45.2, 42/41.9

Preparation R5d: [trans-4,4-difluoro-2-pyrrol- 1 -yl-cyclohexyl] -(2-oxa-6- azaspiro [2.5] octan-6-yl)methanone

Ethyl trans-2-(tert-butoxycarbonylamino)-4-oxo-cyclohexanecarboxyl ate was synthesized by literature method ( Molecules 2015, 20(12), 21094-21102).

XtalFluor-E® (1.5 eq.) was suspended in DCM. Et ₃ N.3HF (2.0 eq.) was added in 10 minutes followed by Et ₃ N (1.0 eq.) in 20 minutes. The suspension was dissolved totally. Ethyl (lR,2R)-2-(tert-butoxycarbonylamino)-4-oxo-cyclohexanecarbox ylate (1.0 eq.) dissolved in DCM and it was added in 40 minutes to the solution. After stirring 20 hours at r.t., the mixture was neutralized with KHC0 ₃ (10 % in water). Phases were separated and the organic phase was extracted with brine. The combined aqueous phase was extracted with DCM. The combined organic phase was washed with brine dried with MgS0 ₄ and concentrated under vacuum to give ethyl trans-2-(tert-butoxycarbonylamino)-4,4-difluoro- cyclohexanecarboxylate.

Ethyl trans-2-(tert-butoxycarbonylamino)-4,4-difluoro-cyclohexanec arboxylate was dissolved in DCM and TFA (4.0 eq.) was added. It was stirred at r.t. for 4 hours. Then it was washed with sat. NaHCCf _. the organic phase was dried over MgS0 ₄ and concentrated under vacuum to give ethyl trans-2-amino-4,4-difluoro-cyclohexanecarboxylate. Ethyl trans-2-amino-4,4-difluoro-cyclohexanecarboxylate (1.0 eq.) and 2,5- dimethoxytetrahydrofuran (1.0 eq.) and acetic acid (4.5 eq.) were heated at 80 °C for 2 hours, then it was evaporated under reduced pressure. It was dissolved in EtOAc and extracted with sat. NaHCCh. The organic phase was dried over MgS0 ₄ and concentrated under vacuum. It was purified by flash chromatography (hexane: EtOAc = 9:1) to give ethyl trans-4,4-difluoro-2-pyrrol- 1 -yl-cyclohexanecarboxylate.

The ethyl trans-4,4-difluoro-2-pyrrol-l -yl-cyclohexanecarboxylate was dissolved in the mixture of ethanol and water (5: 1, v/v) and lithium hydroxide hydrate (5.0 eq.) was added. It was stirred at 50 °C for 3 hours. Then the ethanol was evaporated under reduced pressure, 1N HC1 was added till pH 1. Solid compound was formed, which was filtered off to give trans-4,4-difluoro-2-pyrrol-l-yl-cyclohexanecarboxylic acid.

Starting from trans-4,4-difluoro-2-pyrrol-l-yl-cyclohexanecarboxylic acid using Steps 6 and 7 of General procedure 8, Preparation R5d was obtained. HRMS calculated for C ₁₇ H ₂₂ F ₂ N ₂ O ₂ : 324.1649; 325.1717 [(M+H) ⁺ form]

1H-NMR (500 MHz, dmso-d6) d ppm 6.79 (m, 2H), 5.96 (m, 2H), 4.32 (m, 1H), 3.93-2.93 (m, 4H), 3.5 (m, 1H), 2.65-2.28 (m, 2H), 2.59 (m, 2H), 2.17-1.93 (m, 2H), 1.84/1.64 (m+m, 2H), 1.43-1.06 (m, 4H).

¹³ C-NMR (125 MHz, dmso-d6) d ppm 170.9, 119.9/119.8, 108/107.9, 57.4/57.3, 57.1, 53.4/53.1, 43.5/43.4, 39.8/39.6, 31.9, 25

Preparation R5e: [tr ans-4,4-difluoro-2-(2-pyridyl)cyclohexyl] -(2-oxa-6- azaspiro [2.5] octan-6-yl)methanone

Using General Procedure 8 and starting from pyridine-2-carbaldehyde, Preparation

R5e was obtained. HRMS calculated for C ₁₈ H ₂₂ F ₂ N ₂ O ₂ : 336.1649; found 337.1717 ((M+H) ⁺ form).

Preparation R5g: [trans-4,4-difluoro-2-(5-methyl-3-thienyl)cyclohexyl]-(2-oxa -6- azaspiro [2.5] octan-6-yl)methanone

Using General Procedure 8 and starting from 5-methylthiophene-3-carbaldehyde, Preparation R5g was obtained. HRMS calculated for C ₁₈ H ₂₃ F ₂ NO ₂ S: 355.1418; found 356.149 ((M+H) ⁺ form). Preparation R5i: [trans-2-(l-ethylpyrazol-4-yl)-4,4-difluoro-cyclohexyl]-(2-o xa-6- azaspiro [2.5] octan-6-yl)methanone

Using Step 1 of General Procedure 8 and starting from 1 -ethyl- l//-pyrazole-4- carbaldehyde, (£')-4-(l -ethyl- lf/-pyrazol-4-yl)but-3-en-2-one was obtained.

It was dissolved in DCM and DBU (1.3 eq.) was added. Then, TMSC1 (1.2 eq.) was added dropwise at 0 °C. The solution was stirred for 2 hours at 40 °C then cooled and washed with NaHCCf solution 3 times. The organic layer was dried over MgS0 ₄ , then the solvent was evaporated under reduced pressure.

(E)- 1 -cthyl-4-(3-((trimcthylsilyl)oxy)buta- 1 ,3-dicn- 1 -yl )- 1 /7-pyrazolc was used without further purification according to Steps 3 to 7 of General Procedure 8 to give

Preparation R5i. HRMS calculated for C18H25F2N3O2: 353.1915; found 354.1979 ((M+H) ⁺ form).

Preparation R5k: [tr ans-4,4-difluoro-2-(2-furyl)cyclohexyl] -(2-oxa-6- azaspiro [2.5] octan-6-yl)methanone

Using General Procedure 8 and starting from furan-2-carbaldehyde, Preparation R5k was obtained. HRMS calculated for C17H21F2NO3: 325.149; found 326.1558 ((M+H) ⁺ form).

Preparation R51: [tr ans-4,4-difluoro-2-(3-thienyl)cyclohexyl] -(2-oxa-6- azaspiro [2.5] octan-6-yl)methanone

Using General Procedure 8 and starting from 3-thiophenecarboxaldehyde,

Preparation R51 was obtained. HRMS calculated for C ₁₇ H ₂₁ F ₂ NO ₂ S: 341.1261; found 342.1329 ((M+H) ⁺ form).

EXAMPLES

The following Examples illustrate the invention but do not limit it in any way. 5-amino-3-({l-[(l/?,2/?)-4,4-difluoro-2-phenylcyclohexane-l- carbonyl]-4- hydroxypiperidin-4-yl}methyl)-6-phenoxypyrimidin-4(3//)-one (EXAMPLE 1)

Using General Procedure 5 starting from Preparation R4a and Preparation R5a as reagents, EXAMPLE 1 was obtained. HRMS calculated for C29H32N4O4F2: 538.2391; found 539.2465 ((M+H) ⁺ form). 5-amino-3-({l-[(l/?,2/?)-4,4-difluoro-2-phenylcyclohexane-l- carbonyl]-4- hydroxypiperidin-4-yl}methyl)-6-(2-fluorophenoxy)pyrimidin-4 (3//)-one

(EXAMPLE 2)

Using General Procedure 5 starting from Preparation R4b and Preparation R5a as reagents, EXAMPLE 2 was obtained. HRMS calculated for C29H31N4O4F3 : 556.2297; found 557.2362 ((M+H) ⁺ form). 5-amino-3-({l-[(l/?,2/?)-4,4-difluoro-2-phenylcyclohexane-l- carbonyl]-4- hydroxypiperidin-4-yl}methyl)-6-(4-methoxyphenoxy)pyrimidin- 4(3//)-one

(EXAMPLE 3)

Using General Procedure 5 starting from Preparation R4c and Preparation R5a as reagents, EXAMPLE 3 was obtained. HRMS calculated for C30H34N4O5F2 : 568.2498; found 569.257 ((M+H) ⁺ form). 5-amino-3-({l-[(l/?,2/?)-4,4-difluoro-2-phenylcyclohexane-l- carbonyl]-4- hydroxypiperidin-4-yl}methyl)-6-(3-methoxyphenoxy)pyrimidin- 4(3//)-one

(EXAMPLE 4)

Using General Procedure 5 starting from Preparation R4d and Preparation R5a as reagents, EXAMPLE 4 was obtained. HRMS calculated for C30H34N4O5F2 : 568.2498; found 569.257 ((M+H) ⁺ form). 5-amino-3-({l-[(l/?,2/?)-4,4-difluoro-2-phenylcyclohexane-l- carbonyl]-4- hydroxypiperidin-4-yl}methyl)-6-(4-fluorophenoxy)pyrimidin-4 (3//)-one (EXAMPLE 5)

Using General Procedure 5 starting from Preparation R4e and Preparation R5a as reagents, EXAMPLE 5 was obtained. HRMS calculated for C29H31N4O4F3: 556.2297; found 557.237 ((M+H) ⁺ form). 5-amino-3-({l-[(l/?,2/?)-4,4-difluoro-2-phenylcyclohexane-l- carbonyl]-4- hydroxypiperidin-4-yl}methyl)-6-(3-fluorophenoxy)pyrimidin-4 (3//)-one

(EXAMPLE 6)

Using General Procedure 5 starting from Preparation R4f and Preparation R5a as reagents, EXAMPLE 6 was obtained. HRMS calculated for C29H31N4O4F3 : 556.2297; found 557.2361 ((M+H) ⁺ form). 5-amino-3-({l-[(l/?,2/?)-4,4-difluoro-2-phenylcyclohexane-l- carbonyl]-4- hydroxypiperidin-4-yl}methyl)-6-(3,5-dimethoxyphenoxy)pyrimi din-4(3//)-one

(EXAMPLE 7)

Using General Procedure 5 starting from Preparation R4g and Preparation R5a as reagents, EXAMPLE 7 was obtained. HRMS calculated for C31H36N4O6F2: 598.2603; found 599.267 ((M+H) ⁺ form).

^■ 5-amino-6-(3,5-difluorophenoxy)-3-({l-[(l/?,2/?)-4,4-difluor o-2-phenylcyclohexane- 1 -carbonyl ]-4-hydroxypiperidin-4-yl}methyl)pyrimidin-4(3//)-one (EXAMPLE 8)

Using General Procedure 5 starting from Preparation R4h and Preparation R5a as reagents, EXAMPLE 8 was obtained. HRMS calculated for C29H30N4O4F4 : 574.2203; found 575.2277 ((M+H) ⁺ form). 3-({l-[(l/?,2/?)-4,4-difluoro-2-phenylcyclohexane-l-carbonyl ]-4-hydroxypiperidin-4- yl}methyl)-5-(methylamino)-6-phenoxypyrimidin-4(3//)-one (EXAMPLE 9)

Using General Procedure 5 starting from Preparation R4i and Preparation R5a as reagents, EXAMPLE 9 was obtained. HRMS calculated for C30H34N4O4F2 : 552.2548; found 553.2618 ((M+H) ⁺ form).

^■ 5-amino-3-[[(4R)-l-[(lR,2R)-4,4-difluoro-2-phenyl-cyclohexan ecarbonyl]-3,3- difluoro-4-hydroxy-4-piperidyl] methyl] -6-phenoxy-pyrimidin-4-one (EXAMPLE 10) Using General Procedure 5 starting from Preparation R4a and Preparation R5b as reagents, EXAMPLE 10 was obtained. HRMS calculated for C29H30N4O4F4 : 574.2203; found 575.2276 ((M+H) ⁺ form). ^■ 5-amino-6-(4-chlorophenoxy)-3-({l-[(l/?,2/?)-4,4-difluoro-2- phenylcyclohexane-l- carbonyl] -4-hydroxypiperidin-4-yl} methyl)pyrimidin-4(3//)-one (EXAMPLE 11)

Using General Procedure 5 starting from Preparation R4j and Preparation R5a as reagents, EXAMPLE 11 was obtained. HRMS calculated for C29H31N4O4F2CI: 572.2002; found 573.2069 ((M+H) ⁺ form). 5-amino-6-(4-chloro-3-methoxy-phenoxy)-3-({l-[(l/?,2/?)-4,4- difluoro-2- phenylcyclohexane- 1 -carbonyl ]-4-hydroxypiperidin-4-yl}methyl)pyrimidin-4(3//)-one

(EXAMPLE 12)

Using General Procedure 5 starting from Preparation R4k and Preparation R5a as reagents, EXAMPLE 12 was obtained. HRMS calculated for C30H33N4O5F2CI: 602.2108; found 603.2183 ((M+H) ⁺ form).

^■ 5-amino-6-(3-chlorophenoxy)-3-({l-[(l/?,2/?)-4,4-difluoro-2- phenylcyclohexane-l- carbonyl]-4-hydroxypiperidin-4-yl}methyl)pyrimidin-4(3//)-on e (EXAMPLE 13)

Using General Procedure 5 starting from Preparation R41 and Preparation R5a as reagents, EXAMPLE 13 was obtained. HRMS calculated for C29H31N4O4F2CI: 572.2002; found 573.2079 ((M+H) ⁺ form).

^■ 5-amino-6- [(2H- 1 ,3-benzodioxol-5-yl)oxy] -3-({ 1- [(1/f ,2R)-4,4-difluoro-2- phenylcyclohexane- 1 -carbonyl ]-4-hydroxypiperidin-4-yl}methyl)pyrimidin-4(3//)-one (EXAMPLE 14)

Using General Procedure 5 starting from Preparation R4n and Preparation R5a as reagents, EXAMPLE 14 was obtained. HRMS calculated for C30H32N4O6F2: 582.229; found 583.2378 ((M+H) ⁺ form). 5-amino-3-({l-[(l/?,2/?)-4,4-difluoro-2-phenylcyclohexane-l- carbonyl]-4- hydroxypiperidin-4-yl}methyl)-6-(3-hydroxy-5-methoxyphenoxy) pyrimidin-4(3//)- one (EXAMPLE 15)

Using General Procedure 5 starting from Preparation R4o and Preparation R5a as reagents, EXAMPLE 15 was obtained. HRMS calculated for C30H34N4O6F2: 584.2446; found 585.2524 ((M+H) ⁺ form). 5-amino-3-({l-[(l/?,2/?)-4,4-difluoro-2-phenylcyclohexane-l- carbonyl]-4- hydroxypiperidin-4-yl}methyl)-6-(4-fluoro-3-methoxyphenoxy)p yrimidin-4(3//)-one

(EXAMPLE 16)

Using General Procedure 5 starting from Preparation R4p and Preparation R5a as reagents, EXAMPLE 16 was obtained. HRMS calculated for C30H33N4O5F3 : 586.2403; found 587.2468 ((M+H) ⁺ form). 3-({l-[(l/?,2/?)-4,4-difluoro-2-phenylcyclohexane-l-carbonyl ]-4-hydroxypiperidin-4- yl}methyl)-6-phenoxy-5-[(2,2,2-trifluoroethyl)amino]pyrimidi n-4(3 )-one

(EXAMPLE 17)

Using General Procedure 5 starting from Preparation R4q and Preparation R5a as reagents, EXAMPLE 17 was obtained. HRMS calculated for C31H33N4O4F5 : 620.2422; found 621.2493 ((M+H) ⁺ form). 5-amino-3-({l-[(l/?,2/?)-4,4-difluoro-2-phenylcyclohexane-l- carbonyl]-4- hydroxypiperidin-4-yl}methyl)-6-[3-(trifluoromethoxy)phenoxy ]pyrimidin-4(3//)-one (EXAMPLE 18)

Using General Procedure 5 starting from Preparation R4r and Preparation R5a as reagents, EXAMPLE 18 was obtained. HRMS calculated for C30H31N4O5F5 : 622.2214; found 623.2286 ((M+H) ⁺ form). 5-amino-3-({l-[(l/?,2/?)-4,4-difluoro-2-phenylcyclohexane-l- carbonyl]-4- hydroxypiperidin-4-yl}methyl)-6-(3-methylphenoxy)pyrimidin-4 (3//)-one

(EXAMPLE 19)

Using General Procedure 5 starting from Preparation R4s and Preparation R5a as reagents, EXAMPLE 19 was obtained. HRMS calculated for C30H34N4O4F2 : 552.2548; found 553.2625 ((M+H) ⁺ form).

^■ 5-amino-6-(3-bromophenoxy)-3-({l-[(l/?,2/?)-4,4-difluoro-2-p henylcyclohexane-l- carbonyl] -4-hydroxypiperidin-4-yl} methyl)pyrimidin-4(3//)-one (EXAMPLE 20)

Using General Procedure 5 starting from Preparation R4t and Preparation R5a as reagents, EXAMPLE 20 was obtained. HRMS calculated for C ₂₉ H _3i N ₄ 0 ₄ F ₂ Br: 616.1497; found 617.1568 ((M+H) ⁺ form). 5-amino-3-({l-[(l/?,2/?)-4,4-difluoro-2-phenylcyclohexane-l- carbonyl]-4- hydroxypiperidin-4-yl}methyl)-6-|3-(pentafluoro^ ⁶ -sulfanyl)phenoxy]pyrimidin- 4(3//)-one (EXAMPLE 21)

Using General Procedure 5 starting from Preparation R4u and Preparation R5a as reagents, EXAMPLE 21 was obtained. HRMS calculated for C ₂₉ H _3i N ₄ 0 ₄ F ₇ S: 664.1954; found 665.2018 ((M+H) ⁺ form). 5-amino-3-({l-[(l/?,2/?)-4,4-difluoro-2-phenylcyclohexane-l- carbonyl]-4- hydroxypiperidin-4-yl}methyl)-6-|3-(trifluoromethyl)phenoxy] pyrimidin-4(3//)-one (EXAMPLE 22)

Using General Procedure 5 starting from Preparation R4v and Preparation R5a as reagents, EXAMPLE 22 was obtained. HRMS calculated for C30H3 1N4O4F5: 606.2266; found 607.2339 ((M+H) ⁺ form). 5-amino-3-({l-[(l/?,2/?)-4,4-difluoro-2-phenylcyclohexane-l- carbonyl]-4- hydroxypiperidin-4-yl}methyl)-6-[4-(hydroxymethyl)phenoxy]py rimidin-4(3//)-one (EXAMPLE 23)

Using General Procedure 5 starting from Preparation R4w and Preparation R5a as reagents, EXAMPLE 23 was obtained. HRMS calculated for C3oH3 ₄ F ₂ N ₄ 05: 568.2498; found 569.2559 ((M+H) ⁺ form). 4-{[5-amino-l-({l-[(l/?,2/?)-4,4-difluoro-2-phenylcyclohexan e-l-carbonyl]-4- hydroxypiperidin-4-yl}methyl)-6-oxo-l,6-dihydropyrimidin-4-y l]oxy}benzonitrile (EXAMPLE 24) Using General Procedure 5 starting from Preparation R4z and Preparation R5a as reagents, EXAMPLE 24 was obtained. HRMS calculated for C30H31F2N5O4: 563.2344; found 564.2421 ((M+H) ⁺ form). 3-{[5-amino-l-({l-[(l/?,2/?)-4,4-difluoro-2-phenylcyclohexan e-l-carbonyl]-4- hydroxypiperidin-4-yl}methyl)-6-oxo-l,6-dihydropyrimidin-4-y l]oxy}benzonitrile (EXAMPLE 25)

Using General Procedure 5 starting from Preparation R4aa and Preparation R5a as reagents, EXAMPLE 25 was obtained. HRMS calculated for C30H31F2N5O4: 563.2344; found 564.24 ((M+H) ⁺ form). 5-amino-3-({l-[(l/?,2/?)-4,4-difluoro-2-phenylcyclohexane-l- carbonyl]-4- hydroxypiperidin-4-yl}methyl)-6-[(l,2,3,4-tetrahydroisoquino lin-7-yl)oxy]pyrimidin- 4(3//)-one, hydrochloride (EXAMPLE 26)

Using General Procedure 5 starting from Preparation R4ab and Preparation R5a as reagents, tert-butyl 7-[5-amino- 1 -[[ 1 -[(lR,2R)-4,4-difluoro-2-phenyl-cyclo hexane carbonyl]-4-hydroxy-4-piperidyl]methyl]-6-oxo-pyrimidin-4-yl ]oxy-3, 4-dihydro- 1H- isoquinoline-2-carboxylate was formed. The resulted Boc-protected crude product was reacted using General Procedure 7 to give EXAMPLE 26 as HC1 salt. HRMS calculated for C ₃₂ H ₃₇ F ₂ N ₅ O ₄ : 593.2814; found 594.2883 ((M+H) ⁺ form). methyl 3-{[5-amino-l-({l-[(l/?,2/?)-4,4-difluoro-2-phenylcyclohexan e-l-carbonyl]-4- hydroxypiperidin-4-yl}methyl)-6-oxo-l,6-dihydropyrimidin-4-y l]oxy}benzoate

(EXAMPLE 27)

Using General Procedure 5 starting from Preparation R4ac and Preparation R5a as reagents, EXAMPLE 27 was obtained. HRMS calculated for C31H34F2N4O6: 596.2446; found 597.252 ((M+H) ⁺ form). 5-amino-3-({l-[(l/?,2/?)-4,4-difluoro-2-phenylcyclohexane-l- carbonyl]-4- hydroxypiperidin-4-yl}methyl)-6-[3-(hydroxymethyl)phenoxy]py rimidin-4(3//)-one (EXAMPLE 28)

Using General Procedure 5 starting from Preparation R4ad and Preparation R5a as reagents, EXAMPLE 28 was obtained. HRMS calculated for C30H34F2N4O5 : 568.2498; found 569.2563 ((M+H) ⁺ form). 5-amino-3-({l-[(l/?,2/?)-4,4-difluoro-2-phenylcyclohexane-l- carbonyl]-4- hydroxypiperidin-4-yl}methyl)-6-[4-(3-hydroxypropyl)phenoxy] pyrimidin-4(3//)-one (EXAMPLE 29)

Using General Procedure 5 starting from Preparation R4ae and Preparation R5a as reagents, EXAMPLE 29 was obtained. HRMS calculated for C32H38F2N4O5: 596.281; found 597.2878 ((M+H) ⁺ form). 5-amino-3-({l-[(l/?,2/?)-4,4-difluoro-2-phenylcyclohexane-l- carbonyl]-4- hydroxypiperidin-4-yl}methyl)-6-(phenylsulfanyl)pyrimidin-4( 3//)-one (EXAMPLE 30) Using General Procedure 5 starting from Preparation R4af and Preparation R5a as reagents, EXAMPLE 30 was obtained. HRMS calculated for C29H32F2N4O3S : 554.2163; found 555.2232 ((M+H) ⁺ form). 5-amino-3-({l-[(l/?,2/?)-4,4-difluoro-2-phenylcyclohexane-l- carbonyl]-4- hydroxypiperidin-4-yl}methyl)-6-[(l,2,3,4-tetrahydroisoquino lin-6-yl)oxy]pyrimidin- 4(3//)-one (EXAMPLE 31)

Using General Procedure 5 starting from Preparation R4ag and Preparation R5a as reagents tert-butyl 6-[5-amino- 1 -[[ 1 -[(lR,2R)-4,4-difluoro-2-phenyl-cyclo hexane carbonyl]-4-hydroxy-4-piperidyl]methyl]-6-oxo-pyrimidin-4-yl ]oxy-3, 4-dihydro- 1H- isoquinoline-2-carboxylate was formed. The resulted Boc-protected crude product was reacted using General Procedure 7 to give EXAMPLE 31. HRMS calculated for C32H37F2N5O4 : 593.2814; found 594.2885 ((M+H) ⁺ form). 5-amino-3-({l-[(l/?,2/?)-4,4-difluoro-2-phenylcyclohexane-l- carbonyl]-4- hydroxypiperidin-4-yl}methyl)-6-[(2, 3-dihydro- l//-isoindol-5-yl)oxy]pyrimidin- 4(3//)-one (EXAMPLE 32)

Using General Procedure 5 starting from Preparation R4ah and Preparation R5a as reagents, tert-butyl 5-[5-amino- 1 -[[ 1 -[(lR,2R)-4,4-difluoro-2-phenyl-cyclo hexane carbonyl]-4-hydroxy-4-piperidyl]methyl]-6-oxo-pyrimidin-4-yl ]oxyisoindo line-2- carboxylate was formed. The resulted Boc-protected crude product was reacted using General Procedure 7 to give EXAMPLE 32. HRMS calculated for C31H35F2N5O4: 579.2657; found 580.2717 ((M+H) ⁺ form). 5-amino-3-({l-[(l/?,2/?)-4,4-difluoro-2-phenylcyclohexane-l- carbonyl]-4- hydroxypiperidin-4-yl}methyl)-6-[4-(2-hydroxyethoxy)phenoxy] pyrimidin-4(3//)-one (EXAMPLE 33)

Using General Procedure 5 starting from Preparation R4ai and Preparation R5a as reagents, EXAMPLE 33 was obtained. HRMS calculated for C31H36F2N4O6: 598.2603; found 599.2676 ((M+H) ⁺ form). 5-amino-3-({l-[(l/?,2/?)-4,4-difluoro-2-phenylcyclohexane-l- carbonyl]-4- hydroxypiperidin-4-yl}methyl)-6-[4-(pyrrolidin-2-yl)phenoxy] pyrimidin-4(3//)-one (EXAMPLE 34)

Using General Procedure 5 starting from Preparation R4aj and Preparation R5a as reagents, tert-butyl 2-[4-[5-amino- 1 -[[ 1 -[(lR,2R)-4,4-difluoro-2-phenyl-cyclo hexane carbonyl]-4-hydroxy-4-piperidyl]methyl]-6-oxo-pyrimidin-4-yl ]oxyphenyl]pyrrolidine- 1 - carboxylate was formed. The resulted Boc-protected crude product was reacted using General Procedure 7 to give EXAMPLE 34. HRMS calculated for C33H39F2N5O4 : 607.297; found 608.3026 ((M+H) ⁺ form). 5-amino-3-({l-[(l/?,2/?)-4,4-difluoro-2-phenylcyclohexane-l- carbonyl]-4- hydroxypiperidin-4-yl}methyl)-6-[(l//-indazol-6-yl)oxy]pyrim idin-4(3//)-one

(EXAMPLE 35)

Using General Procedure 5 starting from Preparation R4al and Preparation R5a as reagents, EXAMPLE 35 was obtained. HRMS calculated for C30H32F2N6O4: 578.2453; found 579.2525 ((M+H) ⁺ form). 5-amino-3-({l-[(l/?,2/?)-4,4-difluoro-2-phenylcyclohexane-l- carbonyl]-4- hydroxypiperidin-4-yl}methyl)-6-[4-(2-hydroxyethyl)phenoxy]p yrimidin-4(3//)-one (EXAMPLE 36)

Using General Procedure 5 starting from Preparation R4am and Preparation R5a as reagents, EXAMPLE 36 was obtained. HRMS calculated for C31H36F2N4O5: 582.2654; found 583.2725 ((M+H) ⁺ form). 5-amino-3-({l-[(l/?,2/?)-4,4-difluoro-2-phenylcyclohexane-l- carbonyl]-4- hydroxypiperidin-4-yl}methyl)-6-[4-(2,2,2-trifluoroethyl)phe noxy]pyrimidin-4(3//)- one (EXAMPLE 37)

Using General Procedure 5 starting from Preparation R4an and Preparation R5a as reagents, EXAMPLE 37 was obtained. HRMS calculated for C31H33F5N4O4 : 620.2422; found 621.2493 ((M+H) ⁺ form). 5-amino-6-[4-(2,2-difluoroethyl)phenoxy]-3-({l-[(l/?,2/?)-4, 4-difluoro-2- phenylcyclohexane- 1 -carbonyl ]-4-hydroxypiperidin-4-yl}methyl)pyrimidin-4(3//)-one (EXAMPLE 38)

Using General Procedure 5 starting from Preparation R4ao and Preparation R5a as reagents, EXAMPLE 38 was obtained. HRMS calculated for C31H34F4N4O4 : 602.2516; found 603.2594 ((M+H) ⁺ form). 5-amino-3-({l-[(l/?,2/?)-4,4-difluoro-2-phenylcyclohexane-l- carbonyl]-4- hydroxypiperidin-4-yl}methyl)-6-[4-(2-fluoroethyl)phenoxy]py rimidin-4(3//)-one (EXAMPLE 39)

Using General Procedure 5 starting from Preparation R4ap and Preparation R5a as reagents, EXAMPLE 39 was obtained. HRMS calculated for C31H35F3N4O4 : 584.261; found 585.2689 ((M+H) ⁺ form). 5-amino-3-({l-[(l/?,2/?)-4,4-difluoro-2-phenylcyclohexane-l- carbonyl]-4- hydroxypiperidin-4-yl}methyl)-6-[4-fluoro-3-(trifluoromethox y)phenoxy]pyrimidin- 4(3//)-one (EXAMPLE 40)

Using General Procedure 5 starting from Preparation R4aq and Preparation R5a as reagents, EXAMPLE 40 was obtained. HRMS calculated for C30H30F6N4O5: 640.212; found 641.2183 ((M+H) ⁺ form). 5-amino-3-({l-[(l/?,2/?)-4,4-difluoro-2-phenylcyclohexane-l- carbonyl]-4- hydroxypiperidin-4-yl}methyl)-6-(4-fluoro-3-hydroxyphenoxy)p yrimidin-4(3//)-one

(EXAMPLE 41)

Using General Procedure 5 starting from Preparation R4ar and Preparation R5a as reagents, EXAMPLE 41 was obtained. HRMS calculated for C29H31F3N4O5 : 572.2247; found 573.2319 ((M+H) ⁺ form). 5-amino-6-(4-chloro-3-ethylphenoxy)-3-({l-[(l/?,2/?)-4,4-dif luoro-2- phenylcyclohexane- 1 -carbonyl ]-4-hydroxypiperidin-4-yl}methyl)pyrimidin-4(3//)-one (EXAMPLE 42)

Using General Procedure 5 starting from Preparation R4as and Preparation R5a as reagents, EXAMPLE 42 was obtained. HRMS calculated for C31H35CIF2N4O4 : 600.2315; found 601.2385 ((M+H) ⁺ form). 5-amino-6-[3-(benzyloxy)phenoxy]-3-({l-[(l/f,2R)-4,4-difluor o-2- phenylcyclohexane- 1 -carbonyl ]-4-hydroxypiperidin-4-yl}methyl)pyrimidin-4(3//)-one (EXAMPLE 43)

Using General Procedure 5 starting from Preparation R4at and Preparation R5a as reagents, EXAMPLE 43 was obtained. HRMS calculated for C36H38F2N4O5: 644.281; found 645.2891 ((M+H) ⁺ form). 4-{[5-amino-l-({l-[(l/?,2/?)-4,4-difluoro-2-phenylcyclohexan e-l-carbonyl]-4- hydroxypiperidin-4-yl}methyl)-6-oxo-l,6-dihydropyrimidin-4-y l]oxy}benzaldehyde (EXAMPLE 44)

Using General Procedure 5 starting from Preparation R4au and Preparation R5a as reagents, EXAMPLE 44 was obtained. HRMS calculated for C30H32F2N4O5: 566.2341; found 567.2407 ((M+H) ⁺ form).

^■ 5-amino-3-({l-[(l/?,2/?)-4,4-difluoro-2-phenylcyclohexane-l- carbonyl]-3,3-difluoro- 4-hydroxypiperidin-4-yl}methyl)-6-(4-fluorophenoxy)pyrimidin -4(3//)-one

(EXAMPLE 45)

Using General Procedure 5 starting from Preparation R4e and Preparation R5b as reagents, EXAMPLE 45 was obtained. HRMS calculated for C29H29F5N4O4: 592.2109; found 593.2177 ((M+H) ⁺ form).

^■ 4-{[5-amino-l-({l-[(l/?,2/?)-4,4-difluoro-2-phenylcyclohexan e-l-carbonyl]-3,3- difluoro-4-hydroxypiperidin-4-yl}methyl)-6-oxo-l,6-dihydropy rimidin-4- yl]oxy}benzonitrile, racemic (EXAMPLE 46)

Using General Procedure 5 starting from Preparation R4z and Preparation R5b as reagents, EXAMPLE 46 was obtained.

1H-NMR (500 MHz, dmso-d ₆ ) d ppm 7.85 (m, 2H), 7.7/7.66 (s/s, 1H), 7.19 (m, 2H), 6.08/6.03 (s/s, 1H), 4.97/4.93 (s/s, 2H), 4.61/4.45/3.92/3.76 (d/d+d/d, 2H), 3.42/3.37 (td/td, 1H), 3.04 (m, 1H), 1.54/1.17 (m, 2H)

¹³ C-NMR (125 MHz, dmso-d ₆ ) d ppm 159.5/159.4, 159/158.9, 139.1/139, 134.6, 124.1, 120.1, 119.7, 119.3, 106, 47.5/47.2, 44/43.4, 42.4/41.9, 32.7/31.6, 26.5/26.4 5-amino-3-({l-[(l/?,2/?)-4,4-difluoro-2-phenylcyclohexane-l- carbonyl]-4- hydroxypiperidin-4-yl}methyl)-6-[3-(piperidin-2-yl)phenoxy]p yrimidin-4(3//)-one

(EXAMPLE 47)

Using General Procedure 5 starting from Preparation R4az and Preparation R5a as reagents, tert-butyl 2-[3-[5-amino- 1 -[[ 1 -[(lR,2R)-4,4-difluoro-2-phenyl-cyclo hexane carbonyl]-4-hydroxy-4-piperidyl]methyl]-6-oxo-pyrimidin-4-yl ]oxyphenyl]piperidine-l- carboxylate was formed. The resulted Boc-protected crude product was reacted using General Procedure 7 to give EXAMPLE 47. HRMS calculated for C34H41F2N5O4: 621.3127; found 622.3198 ((M+H) ⁺ form). 5-amino-3-({l-[(l/?,2/?)-4,4-difluoro-2-phenylcyclohexane-l- carbonyl]-4- hydroxypiperidin-4-yl}methyl)-6-[(2-hydroxy-2, 3-dihydro- l//-inden-5- yl)oxy]pyrimidin-4(3//)-one (EXAMPLE 48)

Using General Procedure 5 starting from Preparation R4bc and Preparation R5a as reagents, EXAMPLE 48 was obtained. HRMS calculated for C32H36F2N4O5: 594.2654; found 595.2722 ((M+H) ⁺ form). 5-amino-3-({l-[(l/?,2/?)-4,4-difluoro-2-phenylcyclohexane-l- carbonyl]-4- hydroxypiperidin-4-yl}methyl)-6-[3-(2-hydroxypropan-2-yl)phe noxy]pyrimidin- 4(3//)-one (EXAMPLE 49)

Using General Procedure 5 starting from Preparation R4bf and Preparation R5a as reagents, EXAMPLE 49 was obtained. HRMS calculated for C32H38F2N4O5: 596.281; found 619.2695 ((M+Na) ⁺ form). 4-{[5-amino-l-({l-[(l/?,2/?)-4,4-difluoro-2-phenylcyclohexan e-l-carbonyl]-4- hydroxypiperidin-4-yl}methyl)-6-oxo-l,6-dihydropyrimidin-4-y l]oxy}-2- fluorobenzonitrile (EXAMPLE 50)

Using General Procedure 5 starting from Preparation R4bg and Preparation R5a as reagents, EXAMPLE 50 was obtained. HRMS calculated for C30H30F3N5O4 : 581.225; found 582.2324 ((M+H) ⁺ form). 4-{[5-amino-l-({l-[(l/?,2/?)-4,4-difluoro-2-phenylcyclohexan e-l-carbonyl]-4- hydroxypiperidin-4-yl}methyl)-6-oxo-l,6-dihydropyrimidin-4-y l]oxy}-2- chlorobenzonitrile (EXAMPLE 51)

Using General Procedure 5 starting from Preparation R4bh and Preparation R5a as reagents, EXAMPLE 51 was obtained. HRMS calculated for C30H30CIF2N5O4 : 597.1954; found 598.2019 ((M+H) ⁺ form). 3-(4-{[5-amino-l-({l-[(l/?,2/?)-4,4-difluoro-2-phenylcyclohe xane-l-carbonyl]-4- hydroxypiperidin-4-yl}methyl)-6-oxo-l,6-dihydropyrimidin-4-y l]oxy}-2- chlorophenyl)propanenitrile (EXAMPLE 52)

Using General Procedure 5 starting from Preparation R4bj and Preparation R5a as reagents, EXAMPLE 52 was obtained. HRMS calculated for C32H35F2N5O4 : 591.2657; found 592.2728 ((M+H) ⁺ form). 4-{[5-amino-l-({l-[(l/?,2/?)-4,4-difluoro-2-phenylcyclohexan e-l-carbonyl]-4- hydroxypiperidin-4-yl}methyl)-6-oxo-l,6-dihydropyrimidin-4-y l]oxy}-3- chlorobenzonitrile (EXAMPLE 53)

Using General Procedure 5 starting from Preparation R4bk and Preparation R5a as reagents, EXAMPLE 53 was obtained. HRMS calculated for C30H30CIF2N5O4 : 597.1954; found 598.2031 ((M+H) ⁺ form). 5-amino-6-[4-(l-aminoethyl)phenoxy]-3-({l-[(l/?,2/?)-4,4-dif luoro-2- phenylcyclohexane- 1 -carbonyl ]-4-hydroxypiperidin-4-yl}methyl)pyrimidin-4(3//)- one, diastereoisomer 1 (EXAMPLE 54)

and

5-amino-6- [4-(l-aminoethyl)phenoxy] -3-({l- [(li? ,2/?)-4,4-difluoro-2- phenylcyclohexane- 1 -carbonyl ]-4-hydroxypiperidin-4-yl}methyl)pyrimidin-4(3//)- one, diastereoisomer 2 (EXAMPLE 55)

Using General Procedure 5 starting from Preparation R4bm and Preparation R5a as reagents, tert-butyl N-[ 1 -[4-[5-amino- 1 -[[ 1 -[(lR,2R)-4,4-difluoro-2-phenyl-cyclo hexane carbonyl]-4-hydroxy-4-piperidyl]methyl]-6-oxo-pyrimidin-4-yl ]oxyphenyl]ethyl] carbamate was formed. tert-Butyl N-[l-[4-[5-amino-l-[[l-[(lR,2R)-4,4-difluoro-2-phenyl- cyclohexanecarbonyl]-4-hydroxy-4-piperidyl]methyl]-6-oxo-pyr imidin-4-yl]oxyphenyl] ethyl] carbamate, diastereoisomer 1 and tert-butyl N-[l-[4-[5-amino-l-[[l-[(lR,2R)-4,4- difluoro-2-phenyl-cyclohexanecarbonyl]-4-hydroxy-4-piperidyl ]methyl]-6-oxo-pyrimidin- 4-yl]oxyphenyl]ethyl]carbamate, diastereoisomer 2 were obtained separately by chiral chromatography.

tert-Butyl N-[ 1 -[4-[5-amino- 1 -[[ 1 -[(lR,2R)-4,4-difluoro-2-phenyl-cyclohexanecarbonyl]- 4-hydroxy-4-piperidyl]methyl]-6-oxo-pyrimidin-4-yl]oxyphenyl ]ethyl]carbamate, diastereoisomer 1 was reacted using General Procedure 7 to give EXAMPLE 54.

tert-Butyl N-[ 1 -[4-[5-amino- 1 -[[ 1 -[(lR,2R)-4,4-difluoro-2-phenyl-cyclohexanecarbonyl]- 4-hydroxy-4-piperidyl]methyl]-6-oxo-pyrimidin-4-yl]oxyphenyl ]ethyl]carbamate, diastereoisomer 2 was reacted using General Procedure 7 to give EXAMPLE 55. HRMS calculated for C31H37F2N5O4 : 581.2814; found 582.2883 ((M+H) ⁺ form) for both diastereoisomers. 5-amino-6-[4-(l-aminopropyl)phenoxy]-3-({l-[(l/?,2/?)-4,4-di fluoro-2- phenylcyclohexane- 1 -carbonyl ]-4-hydroxypiperidin-4-yl}methyl)pyrimidin-4(3//)-one (EXAMPLE 56)

Using General Procedure 5 starting from Preparation R4bn and Preparation R5a as reagents, tert-butyl N-[ 1 -[4-[5-amino- 1 -[[ 1 -[(lR,2R)-4,4-difluoro-2-phenyl-cyclo hexane carbonyl]-4-hydroxy-4-piperidyl]methyl]-6-oxo-pyrimidin-4-yl ]oxyphenyl]propyl] carbamate was formed. The resulted Boc-protected crude product was reacted using General Procedure 7 to give EXAMPLE 56. HRMS calculated for C32H39F2N5O4: 595.297; found 596.3038 ((M+H) ⁺ form). 5-(benzylamino)-3-({l-[(l/?,2/?)-4,4-difluoro-2-phenylcycloh exane-l-carbonyl]-4- hydroxypiperidin-4-yl}methyl)-6-(4-fluorophenoxy)pyrimidin-4 (3//)-one

(EXAMPLE 57)

EXAMPLE 5 (100 mg, 0.1797 mmol), benzaldehyde (2.0 eq.), sodium triacetoxyborohydride (5.0 eq.), acetic acid (2.0 eq.) were dissolved in THF and heated and stirred at 70 °C for 2 days. The reaction mixture was purified by preparative LC (on C-18 Gemini-NX 5 pm column, 5 mM aqueous NH ₄ HC03-MeCN, gradient), then it was repurified by preparative LC (on C-18 Gemini-NX 5 pm column, 0.2 % aqueous formic acid solution-MeCN, gradient). Solvent was evaporated under reduced pressure to give EXAMPLE 57. HRMS calculated for C36H37F3N4O4: 646.2767; found 647.2839 ((M+H) ⁺ form). 4-{[5-amino-l-({l-[(l/?,2/?)-4,4-difluoro-2-phenylcyclohexan e-l-carbonyl]-4- hydroxypiperidin-4-yl}methyl)-6-oxo-l,6-dihydropyrimidin-4-y l]oxy}benzamide (EXAMPLE 58)

EXAMPLE 24 (80 mg, 0.1419 mmol), (lE)-acetaldehyde oxime (83.84 mg, 0.0865 mL, 1.419 mmol, 10 eq.), Cu ²⁺ on 4Ά molecular sieve (100 mg) were dissolved in methanol (3 mL) and l,4-dioxane (2 mL). The reaction mixture was then warmed up to 60 °C and stirred at that temperature for 3 days. The mixture was filtered, the filtrate was evaporated and purified by preparative LC (on C-18 Gemini-NX 5 pm column, 5 mM aqueous NH ₄ HC03-MeCN, gradient). Solvent was evaporated under reduced pressure to give EXAMPLE 58. HRMS calculated for C30H33F2N5O5: 581.245; found 582.2533 ((M+H) ⁺ form). 5-amino-6-[4-(aminomethyl)phenoxy]-3-({l-[(l/?,2/?)-4,4-difl uoro-2- phenylcyclohexane- 1 -carbonyl ]-4-hydroxypiperidin-4-yl}methyl)pyrimidin-4(3//)-one (EXAMPLE 59)

Autoclave was charged with EXAMPLE 24 (100 mg, 0.1774 mmol), Raney-nickel catalyst (100 mg) and 7N ammonia in methanol (5 mL) and l,4-dioxane (5 mL) and then placed under a nitrogen atmosphere. After that it was filled with 10 bar ¾ gas. The reaction mixture was stirred in autoclave at r.t. for 20 hours. The reaction mixture was removed from the autoclave and filtered. The filtrate was purified by preparative LC (on C-18 Gemini-NX 5 pm column, 5 mM aqueous NH ₄ HC03-MeCN, gradient). Solvent was evaporated under reduced pressure to give EXAMPLE 59. HRMS calculated for C30H35F2N5O4: 567.2657; found 568.2735 ((M+H) ⁺ form). 5-amino-3-({l-[(l/?,2/?)-4,4-difluoro-2-phenylcyclohexane-l- carbonyl]-4- hydroxypiperidin-4-yl}methyl)-6-{4-[(methylamino)methyl]phen oxy}pyrimidin- 4(3 )-one (EXAMPLE 60)

EXAMPLE 44 (80 mg, 0.1412 mmol), methylamine (2M in THF) (20 eq.), sodium triacetoxyborohydride (5.0 eq.), acetic acid (5.0 eq.) were dissolved in THF and stirred r.t. for 24 hours. The reaction mixture was evaporated, dissolved in DMF/methanol and it was purified by preparative LC (on C-18 Gemini-NX 5 pm column, 5 mM aqueous NH4HCO3- MeCN, gradient). Solvent was evaporated under reduced pressure to give EXAMPLE 60. HRMS calculated for C31H37F2N5O4: 581.2814; found 582.2878 ((M+H) ⁺ form). 5-amino-6-[3-(aminomethyl)phenoxy]-3-({l-[(l/?,2/?)-4,4-difl uoro-2- phenylcyclohexane- 1 -carbonyl ]-4-hydroxypiperidin-4-yl}methyl)pyrimidin-4(3//)-one

(EXAMPLE 61)

Autoclave was charged with EXAMPLE 25 (100 mg, 0.1774 mmol), Raney-nickel catalyst (150 mg) and 7N ammonia in methanol (5 mL) and l,4-dioxane (5 mL) and then placed under a nitrogen atmosphere. After that it was filled with 10 bar ¾ gas. The reaction mixture was stirred in autoclave at r.t. for 20 hours. The reaction mixture was removed from the autoclave and filtered. The filtrate was purified by preparative LC (on C-18 Gemini-NX 5 pm column, 5 mM aqueous NH ₄ HC03-MeCN, gradient). Solvent was evaporated under reduced pressure to give EXAMPLE 61. HRMS calculated for C30H35F2N5O4: 567.2657; found 568.2723 ((M+H) ⁺ form). 3-{[5-amino-l-({l-[(l/?,2/?)-4,4-difluoro-2-phenylcyclohexan e-l-carbonyl]-4- hydroxypiperidin-4-yl}methyl)-6-oxo-l,6-dihydropyrimidin-4-y l]oxy}benzamide (EXAMPLE 62)

EXAMPLE 25 (100 mg, 0.1774 mmol), (lE)-acetaldehyde oxime (104.8 mg, 0.108 mL, 1.774 mmol, 10 eq.), Cu ²⁺ on 4Ά molecular sieve (100 mg) were dissolved in methanol (3 mL) and l,4-dioxane (2 mL). The reaction mixture was then warmed up to 60 °C and stirred at that temperature for 70 hours. The mixture was filtered, the filtrate was evaporated and purified by preparative LC (on C-18 Gemini-NX 5 pm column, 5 mM aqueous MLHCCL-MeCN, gradient). Solvent was evaporated under reduced pressure to give EXAMPLE 62. HRMS calculated for C30H33L2N5O5: 581.245; found 582.2528 ((M+H) ⁺ form). 3-{[5-amino-l-({l-[(l/?,2/?)-4,4-difluoro-2-phenylcyclohexan e-l-carbonyl]-4- hydroxypiperidin-4-yl}methyl)-6-oxo-l,6-dihydropyrimidin-4-y l]oxy}benzoic acid (EXAMPLE 63)

EXAMPLE 27 (100 mg, 0.1676 mmol), lithium-hydroxide monohydrate (28.13 mg, 0.6705 mmol, 4.0 eq.) were stirred in methanol (3 ml) and water (3 ml) at r.t. for 15 hours. The mixture was partially evaporated and the aqueous residue was acidified with 1N HC1 (670 pL, aq.). The resulted precipitate was filtered off, washed with water and dried to give EXAMPLE 63. HRMS calculated for C ₃₀ H ₃₂ L ₂ N ₄ O ₆ : 582.229; found 583.2358 ((M+H) ⁺ form). 5-amino-3-({l-[(l/?,2/?)-4,4-difluoro-2-phenylcyclohexane-l- carbonyl]-4- hydroxypiperidin-4-yl}methyl)-6-(3-hydroxyphenoxy)pyrimidin- 4(3//)-one

(EXAMPLE 64)

Autoclave was charged with EXAMPLE 43 (138 mg, 0.2141 mmol) 10 % palladium on charcoal (30 mg) and methanol (10 mL), and then placed under a nitrogen atmosphere. After that it was filled with 10 bar ¾ gas. The reaction mixture was stirred in autoclave at r.t. for 20 hours. The catalyst was washed with methanol and filtered off. The mother liquor was purified by Hanbon prep HPLC,Cl8 Silica, Gemini NX 5 pm, 5 mM NH ₄ HC0 ₃ -MeCN using gradient method 5-90 %. Solvent was evaporated under reduced pressure to give EXAMPLE 64. HRMS calculated for C ₂₉ H ₃₂ L ₂ N ₄ O ₅ : 554.2341; found 555.2405 ((M+H) ⁺ form). 5-amino-6-[4-(aminomethyl)-3-fluorophenoxy]-3-({l-[(l/?,2/?) -4,4-difluoro-2- phenylcyclohexane- 1 -carbonyl ]-4-hydroxypiperidin-4-yl}methyl)pyrimidin-4(3//)-one (EXAMPLE 65)

Autoclave was charged with EXAMPLE 50 (60.8 mg, 0.105 mmol), Raney-nickel catalyst (60 mg) and 7N ammonia in methanol (5 mL) and l,4-dioxane (5 mL) and then placed under a nitrogen atmosphere. After that it was filled with 10 bar ¾ gas. The reaction mixture was stirred in autoclave at r.t. for 20 hours. The reaction mixture was removed from the autoclave and filtered. The filtrate was purified by preparative LC (on C-18 Gemini-NX 5 pm column, 5 mM aqueous NH ₄ HC03-MeCN, gradient). Solvent was evaporated under reduced pressure to give EXAMPLE 65. HRMS calculated for

C30H34F3N5O4: 585.2563; found 586.2627 ((M+H) ⁺ form). 5-amino-6-[4-(aminomethyl)-3-chlorophenoxy]-3-({l-[(l/f,2/f) -4,4-difluoro-2- phenylcyclohexane- 1 -carbonyl ]-4-hydroxypiperidin-4-yl}methyl)pyrimidin-4(3//)-one (EXAMPLE 66)

Autoclave was charged with EXAMPLE 51 (64.8 mg, 0.108 mmol), Raney-nickel catalyst (60 mg) and 7N ammonia in methanol (5 mL) and l,4-dioxane (5 mL) and then placed under a nitrogen atmosphere. After that it was filled with 10 bar ¾ gas. The reaction mixture was stirred in autoclave at r.t. for 20 hours. The reaction mixture was removed from the autoclave and filtered. The filtrate was purified by preparative LC (on C-18 Gemini-NX 5 pm column, 5 mM aqueous NLLHCCL-MeCN, gradient). Solvent was evaporated under reduced pressure to give EXAMPLE 66. HRMS calculated for

C30H34CIF2N5O4: 601.2267; found 602.2327 ((M+H) ⁺ form). 3-(4-{[5-amino-l-({l-[(l/?,2/?)-4,4-difluoro-2-phenylcyclohe xane-l-carbonyl]-4- hydroxypiperidin-4-yl}methyl)-6-oxo-l,6-dihydropyrimidin-4- yl]oxy}phenyl)propanamide (EXAMPLE 67)

EXAMPLE 52 (80 mg, 0.1352 mmol), (lE)-acetaldehyde oxime (79.88 mg, 0.0824 mL, 1.352 mmol 10 eq.), Cu ²⁺ on 4Ά molecular sieve (100 mg) were dissolved in methanol (3 mL) and l,4-dioxane (2 mL). The reaction mixture was stirred at r.t. for 4 days. The mixture was filtered, the filtrate was evaporated and purified by preparative LC (on C-18 Gemini-NX 5 pm column, 5 mM aqueous NH ₄ HC03-MeCN, gradient). Solvent was evaporated under reduced pressure to give EXAMPLE 67. HRMS calculated for C32H37F2N5O5: 609.2763; found 610.2832 ((M+H) ⁺ form). 5-amino-6-[4-(3-aminopropyl)phenoxy]-3-({l-[(l/?,2/?)-4,4-di fluoro-2- phenylcyclohexane- 1 -carbonyl ]-4-hydroxypiperidin-4-yl}methyl)pyrimidin-4(3//)-one (EXAMPLE 68)

Autoclave was charged with EXAMPLE 52 (80 mg, 0.1352 mmol), Raney-nickel catalyst (80 mg) and 7N ammonia in methanol (5 mL) and l,4-dioxane (5 mL) and then placed under a nitrogen atmosphere. After that it was filled with 10 bar ¾ gas. The reaction mixture was stirred in autoclave at r.t. for 20 hours. The reaction mixture was removed from the autoclave and filtered. The filtrate was purified by preparative LC (on C-18 Gemini-NX 5 pm column, 5 mM aqueous NH ₄ HC03-MeCN, gradient). Solvent was evaporated under reduced pressure to give EXAMPLE 68. HRMS calculated for C32H39F2N5O4: 595.297; found 596.3037 ((M+H) ⁺ form). 5-amino-6-[4-(aminomethyl)-2-chlorophenoxy]-3-({l-[(l/?,2/?) -4,4-difluoro-2- phenylcyclohexane- 1 -carbonyl ]-4-hydroxypiperidin-4-yl}methyl)pyrimidin-4(3//)-one

(EXAMPLE 69)

Autoclave was charged with EXAMPLE 53 (1.0 eq.), Raney-nickel catalyst (10 w/w%) and 7N ammonia in methanol (5 mL) and l,4-dioxane (5 mL) and then placed under a nitrogen atmosphere. After that it was filled with 10 bar ¾ gas. The reaction mixture was stirred in autoclave at r.t. for 20 hours. The reaction mixture was removed from the autoclave and filtered. The filtrate was purified by preparative LC (on C-18 Gemini-NX 5 pm column, 5 mM aqueous NH ₄ HC03-MeCN, gradient). Solvent was evaporated under reduced pressure to give EXAMPLE 69. HRMS calculated for C3oH3 ₄ ClF ₂ N50 ₄ : 601.2267; found 602.2335 ((M+H) ⁺ form). 5-amino-6-[4-(anilinomethyl)phenoxy]-3-({l-[(l/?,2/?)-4,4-di fluoro-2- phenylcyclohexane- 1 -carbonyl ]-4-hydroxypiperidin-4-yl}methyl)pyrimidin-4(3//)-one

(EXAMPLE 70)

EXAMPLE 44 (80 mg, 0.1412 mmol), aniline (65.7486 mg, 0.706 mmol, 5.0 eq.), sodium triacetoxyborohydride (149.63 mg, 0.706 mmol, 5.0 eq.), acetic acid (42.40 mg, 0.04041 mL, 0.706 mmol, 5.0 eq.) were dissolved in THF and stirred at r.t. for 24 hours. The reaction mixture was evaporated, dissolved in DMF/methanol and it was purified by preparative LC (on C-18 Gemini-NX 5 pm column, 5 mM aqueous NH ₄ HC0 ₃ -MeCN, gradient). Solvent was evaporated under reduced pressure to give EXAMPLE 70. HRMS calculated for C ₃₆ H ₃₉ F ₂ N ₅ O ₄ : 643.297; found 644.3038 ((M+H) ⁺ form).

^■ 4-{[5-amino-l-({(45)-l-[(l/f,2/f)-4,4-difluoro-2-phenylcyclo hexane-l-carbonyl]-3,3- difluoro-4-hydroxypiperidin-4-yl}methyl)-6-oxo-l,6-dihydropy rimidin-4- yl]oxy}benzonitrile (EXAMPLE 71)

and

4-{[5-amino-l-({(4/?)-l-[(l/?,2/?)-4,4-difluoro-2-phenylcycl ohexane-l-carbonyl]-3,3- difluoro-4-hydroxypiperidin-4-yl}methyl)-6-oxo-l,6-dihydropy rimidin-4- yl]oxy}benzonitrile (EXAMPLE 72)

Starting from EXAMPLE 46, EXAMPLE 71 and EXAMPLE 72 were obtained separately by chiral chromatography.

EXAMPLE 71:

1H-NMR (500 MHz, dmso-d6) d ppm 7.85 (m, 2H), 7.7/7.66 (s/s, 1H), 7.33-7.14 (m, 5H), 7.19 (m, 2H), 6.08/6.03 (s/s, 1H), 4.97/4.93 (s/s, 2H), 4.61/4.45/3.92/3.76 (d/d+d/d, 2H), 4.30-2.33 (m, 4H), 3.42/3.37 (td/td, 1H), 3.04 (m, 1H), 2.24-1.95 (m, 4H), 1.90-1.55 (m, 2H), 1.54/1.17 (m, 2H).

¹³ C-NMR (125 MHz, dmso-d6) d ppm 159.5/159.4, 159/158.9, 139.1/139, 134.6, 124.1, 120.1, 119.7, 119.3, 106, 47.5/47.2, 44/43.4, 42.4/41.9, 32.7/31.6, 26.5/26.4

EXAMPLE 72:

1H-NMR (500 MHz, dmso-d6) d ppm 7.85 (m, 2H), 7.71/7.7 (s/s, 1H), 7.29-7.15 (m, 5H), 7.19 (m, 2H), 6.08/6.06 (s/s, 1H), 4.95/4.91 (s/s, 2H), 4.49/4.41/3.89/3.86 (d/d+d/d, 2H), 4.38-2.68 (m, 4H), 3.45/3.35 (td/td, 1H), 3.05 (m, 1H) 1.96-1.44 (m, 4H), 1.90-1.55 (m, 2H), 1.75-1.14 (m, 2H).

¹³ C-NMR (125 MHz, dmso-d6) d ppm 159.5/159.4, 159, 139, 134.6, 124.1, 120.5, 119.7, 119.3, 106, 47.3/47.2, 43.5, 42.4/41.6, 32.9/31.7, 26.8/26.4

^■ 5-amino-3-({l-[(l/f,2/f)-4,4-difluoro-2-phenylcyclohexane-l- carbonyl]-4-hydroxy piperidin-4-yl}methyl)-6-(4-{[(2,2,2-trifluoroethyl)amino]me thyl}phenoxy)pyrimidin- 4(3//)-one (EXAMPLE 73)

and

7V-[(4-{[5-amino-l-({l-[(l/?,2/?)-4,4-difluoro-2-phenylcyclo hexane-l-carbonyl]-4- hydroxypiperidin-4-yl}methyl)-6-oxo-l,6-dihydropyrimidin-4-y l]oxy}phenyl)methyl]- 7V-(2,2,2-trifluoroethyl)formamide (EXAMPLE 74)

EXAMPLE 44 (0.158 mmol; 1.0 eq.), 2,2,2-trifluoroethanamine (5.0 eq.), sodium triacetoxyborohydride (5.0 eq.), acetic acid (5.0 eq.) were dissolved in THF and stirred r.t. for 3.5 hours. The reaction mixture was evaporated, dissolved in DMF and it was purified by preparative LC (on C-18 Gemini-NX 5 pm column, 5 mM aqueous NH ₄ HC0 ₃ -MeCN, gradient) and compounds were isolated separately. Solvent was evaporated under reduced pressure to give EXAMPLE 73 and EXAMPLE 74.

EXAMPLE 73: HRMS calculated for C ₃₂ H ₃₆ F ₅ N ₅ O ₄ : 649.2687; found 650.2753 ((M+H) ⁺ form).

EXAMPLE 74: HRMS calculated for C ₃₃ H ₃₆ F ₅ N ₅ O ₅ : 677.2637; found 678.2707 ((M+H) ⁺ form). 5-amino-6-{4-[(tef -butylamino)methyl]phenoxy}-3-({l-[(l/?,2/?)-4,4-difluoro-2- phenylcyclohexane- 1 -carbonyl ]-4-hydroxypiperidin-4-yl}methyl)pyrimidin-4(3//)-one

(EXAMPLE 75)

EXAMPLE 44 (0.158 mmol; 1.0 eq.), 2-methylpropan-2-amine (5.0 eq.), sodium triacetoxyborohydride (5.0 eq.), acetic acid (5.0 eq.) were dissolved in THF and stirred r.t. for 3.5 hours. The reaction mixture was evaporated, dissolved in DMF and it was purified by preparative LC (on C-18 Gemini-NX 5 pm column, 5 mM aqueous NH ₄ HC0 ₃ -MeCN, gradient). Solvent was evaporated under reduced pressure to give EXAMPLE 75. HRMS calculated for C ₃₄ H ₄₃ F ₂ N ₅ 0 ₄ : 623.3283; found 624.3346 ((M+H) ⁺ form). 5-amino-6-{4-[(benzylamino)methyl]phenoxy}-3-({l-[(l/?,2/?)- 4,4-difluoro-2- phenylcyclohexane- 1 -carbonyl ]-4-hydroxypiperidin-4-yl}methyl)pyrimidin-4(3//)-one (EXAMPLE 76)

EXAMPLE 44 (0.123 mmol; 1.0 eq.), benzylamine (5.0 eq.), sodium triacetoxyborohydride (5.0 eq.), acetic acid (5.0 eq.) were dissolved in THF and stirred r.t. for 70 hours. The reaction mixture was evaporated, dissolved in DMF/methanol and it was purified by preparative LC (on C-18 Gemini-NX 5 pm column, 5 mM aqueous NH ₄ HC03-MeCN, gradient). Solvent was evaporated under reduced pressure to give EXAMPLE 76. HRMS calculated for C37H41F2N5O4: 657.3127; found 658.3202 ((M+H) ⁺ form). 5-amino-6-{4-[(cyclopropylamino)methyl]phenoxy}-3-({l-[(l/?, 2/?)-4,4-difluoro-2- phenylcyclohexane- 1 -carbonyl ]-4-hydroxypiperidin-4-yl}methyl)pyrimidin-4(3//)-one

(EXAMPLE 77)

EXAMPLE 44 (0.158 mmol; 1.0 eq.), cyclopropylamine (5.0 eq.), sodium triacetoxyborohydride (5.0 eq.), acetic acid (5.0 eq.) were dissolved in THF and stirred r.t. for 24 hours. The reaction mixture was evaporated, dissolved in DMF/methanol and it was purified by preparative LC (on C-18 Gemini-NX 5 pm column, 5 mM aqueous NH4HCO3- MeCN, gradient). Solvent was evaporated under reduced pressure to give EXAMPLE 77. HRMS calculated for C33H39F2N5O4: 607.297; found 608.3039 ((M+H) ⁺ form).

^■ 5-amino-3-({(4S)-l-[(l/?,2/?)-4,4-difluoro-2-phenylcyclohexa ne-l-carbonyl]-3,3- difluoro-4-hydroxypiperidin-4-yl}methyl)-6-(4-fluorophenoxy) pyrimidin-4(3//)-one (EXAMPLE 78)

and

5-amino-3-({(4/?)-l-[(l/?,2/?)-4,4-difluoro-2-phenylcyclohex ane-l-carbonyl]-3,3- difluoro-4-hydroxypiperidin-4-yl}methyl)-6-(4-fluorophenoxy) pyrimidin-4(3//)-one

(EXAMPLE 79)

Starting from EXAMPLE 45, EXAMPLE 78 and EXAMPLE 79 were obtained separately by chiral chromatography.

EXAMPLE 78: HRMS calculated for C29H29F5N4O4: 592.2109; found 593.2182 ((M+H) ⁺ form).

EXAMPLE 79: HRMS calculated for C29H29F5N4O4: 592.2109; found 593.2177 ((M+H) ⁺ form). 4-{[5-amino-l-({l-[(l/?,2/?)-4,4-difluoro-2-phenylcyclohexan e-l-carbonyl]-4- hydroxypiperidin-4-yl}methyl)-6-oxo-l,6-dihydropyrimidin-4-y l]oxy}-2- chlorobenzamide (EXAMPLE 80)

EXAMPLE 51 (65 mg, 0.108 mmol), (lE)-acetaldehyde oxime (1.08 mmol, 10 eq.), Cu ²⁺ on 4Ά molecular sieve (80 mg) were dissolved in methanol (3 mL) and l,4-dioxane (2 mL). The reaction mixture was stirred at r.t. for 4 days. The mixture was filtered, the filtrate was evaporated and purified by preparative LC (on C-18 Gemini-NX 5 pm column, 5 mM aqueous NH ₄ HC03-MeCN, gradient). Solvent was evaporated under reduced pressure to give EXAMPLE 80. HRMS calculated for C30H32CIF2N5O5: 615.206; found 616.2129 ((M+H) ⁺ form). 4-{[5-amino-l-({l-[(l/?,2/?)-4,4-difluoro-2-phenylcyclohexan e-l-carbonyl]-4- hydroxypiperidin-4-yl}methyl)-6-oxo-l,6-dihydropyrimidin-4-y l]oxy}-2- fluorobenzamide (EXAMPLE 81)

EXAMPLE 50 (65 mg, 0.111 mmol), (lE)-acetaldehyde oxime (1.11 mmol, 10 eq.), Cu ²⁺ on 4A molecular sieve (80 mg) were dissolved in methanol (3 mL) and l,4-dioxane (2 mL). The reaction mixture was stirred at r.t. for 4 days. The mixture was filtered, the filtrate was evaporated and purified by preparative LC (on C-18 Gemini-NX 5 pm column, 5 mM aqueous MUHCCL-MeCN, gradient). Solvent was evaporated under reduced pressure to give EXAMPLE 81. HRMS calculated for C ₃₀ H ₃₂ L ₃ N ₅ O ₅ : 599.2355; 600.2428 ((M+H) ⁺ form). 5-amino-3-({l-[(l/?,2/?)-5,5-difluoro-2-phenylcyclohexane-l- carbonyl]-4- hydroxypiperidin-4-yl}methyl)-6-phenoxypyrimidin-4(3//)-one (EXAMPLE 82)

Using General Procedure 5 starting from Preparation R4a and Preparation R5c as reagents, EXAMPLE 82 was obtained. HRMS calculated for C29H32P2N4O4 : 538.2391; found 539.2468 ((M+H) ⁺ form). 5-amino-3-({l-[(l/?,2/?)-4,4-difluoro-2-(l//-pyrrol-l-yl)cyc lohexane-l-carbonyl]-4- hydroxypiperidin-4-yl}methyl)-6-phenoxypyrimidin-4(3//)-one (EXAMPLE 83)

Using General Procedure 5 starting from Preparation R4a and Preparation R5d as reagents, EXAMPLE 83 was obtained. HRMS calculated for C27H31P2N5O4: 527.2344;

found 528.2416 ((M+H) ⁺ form). 5-amino-3-({l-[(l,2-trans)-4,4-difluoro-2-phenylcyclohexane- l-carbonyl]-4- hydroxypiperidin-4-yl}methyl)-6-[(pyridin-3-yl)oxy]pyrimidin -4(3//)-one (EXAMPLE 84)

Using General Procedure 5 starting from Preparation R4bq and Preparation R5a as reagents, EXAMPLE 84 was obtained. HRMS calculated for C28H31F2N5O4: 539.2344; found 540.2425 ((M+H) ⁺ form). 5-amino-3-({l-[(l,2-trans)-4,4-difluoro-2-(pyridin-2-yl)cycl ohexane-l-carbonyl]-4- hydroxypiperidin-4-yl}methyl)-6-(4-fluorophenoxy)pyrimidin-4 (3//)-one

(EXAMPLE 85)

Using General Procedure 5 starting from Preparation R4e and Preparation R5e as reagents, EXAMPLE 85 was obtained. HRMS calculated for C28H30F3N5O4: 557.225; found 558.2321 ((M+H) ⁺ form).

^■ 5-amino-3-({l-[(l,2-trans)-4,4-difluoro-2-(5-methylthiophen- 3-yl)cyclohexane-l- carbonyl]-4-hydroxypiperidin-4-yl}methyl)-6-(4-fluorophenoxy )pyrimidin-4(3//)-one (EXAMPLE 86)

Using General Procedure 5 starting from Preparation R4e and Preparation R5g as reagents, EXAMPLE 86 was obtained. HRMS calculated for C28H31F3N4O4S: 576.2018; found 577.2091 ((M+H) ⁺ form).

^■ 5-amino-3-({l-[(l,2-trans)-2-(l-ethyl-l//-pyrazol-4-yl)-4,4- difluorocyclohexane-l- carbonyl]-4-hydroxypiperidin-4-yl}methyl)-6-(4-fluorophenoxy )pyrimidin-4(3//)-one (EXAMPLE 87)

Using General Procedure 5 starting from Preparation R4e and Preparation R5i as reagents, EXAMPLE 87 was obtained. HRMS calculated for C28H33F3N6O4: 574.2515; found 575.2586 ((M+H) ⁺ form). 5-amino-3-({l-[(l,2-trans)-4,4-difluoro-2-(furan-2-yl)cycloh exane-l-carbonyl]-4- hydroxypiperidin-4-yl}methyl)-6-(4-fluorophenoxy)pyrimidin-4 (3//)-one

(EXAMPLE 88)

Using General Procedure 5 starting from Preparation R4e and Preparation R5k as reagents, EXAMPLE 88 was obtained. HRMS calculated for C27H29F3N4O5 : 546.209; found 547.2164 ((M+H) ⁺ form). 5-amino-3-({l-[(l/?,2/?)-4,4-difluoro-2-(thiophen-3-yl)cyclo hexane-l-carbonyl]-4- hydroxypipendin-4-yl}methyl)-6-(4-fluorophenoxy)pynmidin-4(3 //)-one

(EXAMPLE 89)

Using General Procedure 5 starting from Preparation R4e and Preparation R51 as reagents, EXAMPLE 89 was obtained. HRMS calculated for C27H29F3N4O4S : 562.1862; found 563.1932 ((M+H) ⁺ form). 5-amino-6-[4-(aminomethyl)phenoxy]-3-({(45)-l-[(l/f,2/f)-4,4 -difluoro-2- phenylcyclohexane-l-carbonyl]-3,3-difluoro-4-hydroxypiperidi n-4- yl}methyl)pyrimidin-4(3//)-one (EXAMPLE 90)

Autoclave was charged with EXAMPLE 71 (50 mg, 0.083 mmol), Raney-nickel catalyst (100 mg) and 7N ammonia in methanol (5 mL) and l,4-dioxane (5 mL) and then placed under a nitrogen atmosphere. After that it was filled with 10 bar ¾ gas. The reaction mixture was stirred in autoclave at r.t. for 20 hours. The reaction mixture was removed from the autoclave and filtered. The filtrate was purified by preparative LC (on C-18 Gemini-NX 5 pm column, 0.2 % aqueous HCOOH-MeCN, gradient). Solvent was evaporated under reduced pressure to give EXAMPLE 90. HRMS calculated for C30H33F4N5O4: 603.2469; found 604.2530 ((M+H) ⁺ form).

General Procedures for Examples 91 to 103 and 122 to 177

All reagents obtained from commercial sources were used without further purification. Anhydrous solvents were obtained from commercial sources and used without further drying. Flash chromatography was performed with pre- packed silica gel cartridges (Strata SI-1 ; 61 A, Phenomenex, Cheshire UK or 1ST Flash II, 54Ά, Argonaut, Hengoed, UK) or by automated flash chromatography using a Combiflash R _f apparatus (Teledyne Isco Inc.) using RediSep R _f prepacked silica columns (Teledyne Isco Inc.) or SilaSep pre-packed columns (Silicycle Inc.). Thin layer chromatography was conducted with 5 x 10 cm plates coated with Merck Type 60 F ₂ 5 ₄ silica gel.

The compounds of the present invention were characterized by high performance liquid chromatography-mass spectroscopy (HPLC-MS) on either an Agilent HP 1200 Rapid Resolution Mass detector 6140 multimode source M/z range 150 to 1000 amu or an Agilent HP1100 Mass detector 1946D ESI source M/z range 150 to 1000 amu. The conditions and methods listed below are identical for both machines.

Column for 7.5 min run: GeminiNX, 5mhi, Cl 8, 30 x 2.1 mm (Phenomenex) or Zorbax Eclipse Plus, 3.5 pm, C18, 30 x 2.1 mm (Agilent). Temperature: 35 °C. Column for 3.75 min run: GeminiNX, 5pm, C 18, 30 x 2.1 mm (Phenomenex) or Zorbax Eclipse Plus, 3.5 pm, C18, 30 x 2.1 mm (Agilent). Temperature: 35 °C. Column for 1.9 min run: Kinetex, 2.5 pm, Cl 8, 50 x 2.1 mm (Phenomenex) or Accucore, 2.6 pm, C18, 50 x 2.1 mm. Temperature: 55 °C.

Mobile Phase: A - H ₂ 0 + 10 mmol / ammonium formate + 0.08 % (v/v) formic acid at pH ca 3.5.

B - 95 % Acetonitrile + 5 % A + 0.08 % (v/v) formic acid.

Injection Volume: 1 pL

Method A "Short" method gradient table, either positive (pos) or positive and negative (pos / neg) ionisation

Method B "Super Short" method gradient table, either positive (pos) or positive and negative (pos / neg) ionisation

Detection: UV detection at 230, 254 and 270 nm.

The compounds of the present invention were also characterized by Nuclear Magnetic Resonance (NMR). Analysis was performed with a Bruker DPX-400 spectrometer and proton NMR spectra were measured at 400 MHz. The spectral reference was the known chemical shift of the solvent. Proton NMR data is reported as follows: chemical shift (d) in ppm, followed by the multiplicity, where s = singlet, d = doublet, t = triplet, q = quartet, m = multiplet, dd = doublet of doublets, dt = doublet of triplets, dm = doublet of multiplets, ddd = doublet of double doublets, td = triplet of doublets, qd = quartet of doublets and br = broad, and finally the integration. Some compounds of the invention were purified by preparative HPLC. These were performed on a Waters FractionLynx MS autopurification system, with a Gemini® 5 pm Cl 8(2), 100 mm x 20 mm i.d. column from Phenomenex, running at a flow rate of 20 cm ³ . min ¹ with UV diode array detection (210-400 nm) and mass-directed collection. At pH 4: solvent A = 10 mM ammonium acetate in HPLC grade water + 0.08 % v/v formic acid. Solvent B = 95 % v/v HPLC grade acetonitrile + 5 % v/v solvent A + 0.08 % v/v formic acid.

At pH 9: solvent A = 10 mM ammonium acetate in HPLC grade water + 0.08 % v/v ammonia solution. Solvent B = 95 % v/v HPLC grade acetonitrile + 5 % v/v solvent A + 0.08 % v/v ammonia solution.

Some compounds of the invention were purified by preparative HPLC using a Teledyne ISCO ACCQPrep HP125, with a Gemini® 5 pm Cl8(2), 150 mm x 21 mm i.d. column from Phenomenex, running at a flow rate of 21 cm ³ . min ¹ with UV diode array detection (210-400 nm) and collection. The mass spectrometer was a Waters Micromass ZQ2000 spectrometer, operating in positive or negative ion electrospray ionisation modes, with a molecular weight scan range of 150 to 1000.

Some compounds of the present invention were characterised using an Agilent 1290 Infinity II series instrument connected to an Agilent TOF 6230 single quadrupole with an ESI source. High resolution mass spectra were recorded in positive-negative switching mode ionization unless otherwise stated. UV detection was by diode array detector at 230, 254 and 270 nm. Column: Thermo Accucore 2.6 pM Cl 8, 50 x 2 mm, at 55 °C column temperature. Buffer A: Water /l 0 mM ammonium formate / 0.04 % (v/v) formic acid pH=3.5. Buffer B: Acetonitrile / 5.3 % (v/v) A / 0.04 % (v/v) formic. (Injection volume: 1 pL).

IUPAC chemical names were generated using AutoNom Standard or using ChemAxon’s ‘Structure to Name’ (s2n) functionality within MarvinSketch or JChem for Excel (JChem versions 16.6.13 - 18.22.3). rel-5-amino-3-({l-[(lR,2R,4R)-4-ethynyl-4-hydroxy-2-phenyl-c yclohexanecarbonyl]- 4-hydroxypiperidin-4-yl}methyl)-6-(4-fluorophenoxy)-3,4-dihy dropyrimidin-4-one (EXAMPLE 91)

Step 1: rel-ethyl ( 1R,2R,4R) -4 -hydroxy -2 -phenyl -4 -[2 -(trimethylsilyl)ethynyl] cyclohexane - 1 -carboxylate and rel-ethyl (lR,2R,4S)-4-hydroxy-2-phenyl-4-[2-(trimethylsilyl)ethynylJ cyclohexane -1 -carboxylate

Following procedure described in Step 1 of EXAMPLE 96 and starting from rel-ethyl (lR,2R)-4-oxo-2-phenylcyclo hexane- 1 -carboxylate (500 mg, 2.03 mmol) and ethynyltrimethylsilane (219 mg, 2.23 mmol) instead of 2-picoline, the obtained residue was purified via flash chromatography using Heptane-20 % EtO Ac/Heptane (gradient) as eluent to afford:

First elute: rel-ethyl (lR,2R,4S)-4-hydroxy-2-phenyl-4-[2-(trimethylsilyl)ethynyl] cyclohexane- 1 -carboxylate as a colourless oil.

1H NMR (399 MHz, Chloroform-^) d 7.22-6.95 (m, 5H), 3.73 (q, J = 7.1 Hz, 2H), 3.10 (ddd, J = 13.0, 11.5, 3.6 Hz, 1H), 2.44 (td, j= 11.8, 3.4 Hz, 1H), 2.07-1.55 (m, 5H), 1.24- 0.96 (m, 2H), 0.80 (t, j= 7.1 Hz, 3H), 0.00 (s, 9H).

Second elute: rel-ethyl (lR,2R,4R)-4-hydroxy-2-phenyl-4-[2-(trimethylsilyl)ethynyl] cyclohexane- 1 -carboxylate as a colourless oil.

1H NMR (399 MHz, Chloroform-^) d 7.28-6.90 (m, 5H), 3.74 (qd, j = 7.1, 3.5 Hz, 2H), 3.04 (ddd, J = 13.0, 11.4, 3.2 Hz, 1H), 2.38 (td, j = 11.4, 4.6 Hz, 1H), 2.08-1.79 (m, 5H), 1.63 (t, j= 12.8 Hz, 1H), 1.51 (td, j= 12.5, 4.8 Hz, 1H), 0.82 (t, j= 7.1 Hz, 3H), 0.10 (s, 9H).

Step 2: rel-ethyl ( I R,2R,4R) -4 -ethynyl -4 -hydroxy -2 -pheny /cyclohexane -/ -carboxylate To a solution of rel-ethyl (lR,2R,4R)-4-hydroxy-2-phenyl-4-[2-(trimethylsilyl)ethynyl] cyclohexane- 1 -carboxylate (100 mg, 0.29 mmol) in THF (2 mF), TBAF (1M in THF, 1 mF, 1 mmol) was added dropwise at 0 °C under N ₂ . The reaction mixture was stirred at the same temperature for 10 minutes before allowed to warm to r.t. overnight. The mixture was diluted with EtO Ac (20mF) and brine (!5mF). The organic layer was separated, dried (MgS0 ₄ ) and evaporated in vacuo. The residue was purified via flash chromatography using Heptane-30 %EtO Ac/Heptane (gradient) as eluent to afford the desired product, rel-ethyl (lR,2R,4R)-4-ethynyl-4-hydroxy-2-phenylcyclo hexane- l-carboxylate as a colourless oil.

1H NMR (399 MHz, Chloroform-^) d 7.41-7.08 (m, 5H), 3.90 (q, J = 7.2 Hz, 2H), 3.21 (ddd, J = 12.9, 11.4, 3.3 Hz, 1H), 2.67 (s, 1H), 2.56 (td, j= 11.5, 4.3 Hz, 1H), 2.25 (s, 1H), 2.23-2.14 (m, 2H), 2.13-1.96 (m, 2H), 1.82 (t, j= 12.9 Hz, 1H), 1.70 (td, j= 12.7, 4.6 Hz, 1H), 0.96 (t, J = Ί l Hz, 3H).

Step 3: rel -(1 R,2R,4R) -4 -ethynyl -4 -hydroxy -2 -phenylcyclohexane -1 -carboxylic acid Starting from rel-ethyl (lR,2R,4R)-4-ethynyl-4-hydroxy-2-phenyl-cyclo hexane- 1- carboxylate (62 mg, 0.23 mmol) following procedure described in Step 2 of EXAMPLE 94, rel-(lR,2R,4R)-4-ethynyl-4-hydroxy-2-phenylcyclohexane-l -carboxylic acid was obtained as a yellow solid. The compound was used without further purification.

1H NMR (399 MHz, DMSO- ) d 11.92 (s, 1H), 7.44-7.00 (m, 5H), 5.67 (s, 1H), 3.48 (s, 1H), 3.01 (td, j= 12.4, 3.5 Hz, 1H), 2.04-1.42 (m, 7H).

Step 4: EXAMPLE 91

Following procedure described in Step 3 of EXAMPLE 94 and starting from re l-(lR,2R,4R)-4-ethynyl-4-hydroxy-2-phenyl-cyclo hexane- 1 -carboxylic acid (60 mg) and 5-amino-6-(4-fluorophenoxy)-3-[(4-hydroxypiperidin-4-yl)meth yl]pyrimidin-4-one (185 mg, 0.22 mmol), EXAMPLE 91 was obtained as a white solid.

LC/MS (Method B): RT = 1.01; m/z = 561 [M+H] ⁺

1H NMR (399 MHz, DMSO- ) d 7.59 (d, j= 24.3 Hz, 1H), 7.33-6.99 (m, 9H), 5.64 (d, J = 3.4 Hz, 1H), 4.81 (d, j = 10.9 Hz, 1H), 4.68 (d, j = 12.5 Hz, 2H), 3.99-3.78 (m, 2H), 3.74-3.58 (m, 2H), 3.45 (d, j = 2.4 Hz, 1H), 3.20-2.80 (m, 3H), 2.70-2.58 (m, 1H), 1.97- 1.56 (m, 5H), 1.47-1.04 (m, 3H), 0.76 (td, j= 12.8, 4.5 Hz, 1H), 0.62-0.49 (m, 1H).

HRMS (TOF, ESI) m/z: Calculated for C ₃₁ H ₃₃ FN ₄ O ₅ 560.2435, Found: 561.2538 [M+H] ⁺ rel-5-amino-3-[(l-{[(lR,2R,4S)-4-ethynyl-4-hydroxy-2-phenyl- cyclohexyl] carbonyl}- 4-hydroxypiperidin-4-yl)methyl] -6-(4-fluorophenoxy)pyrimidin-4-one (EXAMPLE 92) Step 1: rel-ethyl (lR,2R,4S)-4-ethynyl-4-hydroxy-2-phenyl-cyclohexane-l-carbox ylate Starting from rel-ethyl (lR,2R,4S)-4-hydroxy-2-phenyl-4-[2-(trimethylsilyl)ethynyl] cyclohexane- l-carboxylate (60 mg, 0.2 mmol) following procedure described in Step 2 of EXAMPLE 91, rel-ethyl (lR,2R,4S)-4-ethynyl-4-hydroxy-2-phenylcyclo hexane- 1- carboxylate was obtained as a colourless oil.

1H NMR (399 MHz, Chloroform-^) d 7.39-7.12 (m, 5H), 3.90 (q, J = 7.1 Hz, 2H), 3.28 (ddd, J = 13.0, 11.5, 3.6 Hz, 1H), 2.64-2.57 (m, 1H), 2.49 (s, 1H), 2.26-2.01 (m, 3H), 1.99- 1.76 (m, 3H), 1.30-1.24 (m, 1H), 0.96 (t, j= 7.1 Hz, 2H), 0.93-0.88 (m, 1H).

Step 2: rel-(lR,2R,4S)-4-ethynyl-4-hydroxy-2-phenyl-cyclohexane-l-ca rboxylic acid Starting from rel-ethyl (lR,2R,4S)-4-ethynyl-4-hydroxy-2-phenylcyclo hexane- 1- carboxylate (35 mg, 0.13 mmol) following procedure described in Step 2 of EXAMPLE 94, rel-(lR,2R,4S)-4-ethynyl-4-hydroxy-2-phenylcyclohexane-l -carboxylic acid was obtained as a yellow solid.

1H NMR (399 MHz, DMSO- ) d 11.80 (s, 1H), 7.29-7.15 (m, 5H), 5.43 (s, 1H), 3.38 (m, 1H), 3.08 (td, j= 12.4, 3.5 Hz, 1H), 2.60 (m, 1H), 1.96-1.70 (m, 6H).

Step 3: EXAMPLE 92

Starting from rel-( 1 R,2R,4S)-4-ethynyl-4-hydroxy-2-phenyl-cyclo hexane- 1 -carboxylic acid (27 mg, 0.11 mmol) and 5-amino-6-(4-fluorophenoxy)-3-[(4-hydroxypiperidin-4- yl)methyl]pyrimidin-4-one (37 mg, 0.11 mmol) following procedure described in Step 3 of EXAMPLE 94, EXAMPLE 92 was obtained as a white solid.

LC/MS (Method B): RT = 1.07; m/z = 561 [M+H] ⁺

1H NMR (399 MHz, DMSO- ) d 7.60 (d, j = 23.3 Hz, 1H), 7.33-7.03 (m, 9H), 5.37 (s, 1H), 4.94-4.57 (m, 3H), 3.99-3.57 (m, 4H), 3.28-2.82 (m, 3H), 2.71-2.57 (m, 1H), 2.00- 1.69 (m, 5H), 1.54-1.04 (m, 4H), 0.82-0.56 (m, 2H).

HRMS (TOF, ESI) m/z: Calculated for C ₃₁ H ₃₃ FN ₄ O ₅ 560.2435, Found: 561.2576 [M+H] ⁺ rel-5-amino-3-({l-[(lR,2R)-4-ethynyl-4-fluoro-2-phenyl-cyclo hexanecarbonyl]-4- hydroxypiperidin-4-yl}methyl)-6-(4-fluorophenoxy)-3,4-dihydr opyrimidin-4-one

(EXAMPLE 93) Step 1: rel-ethyl (IR,2R) -4-ethynyl-4-fluoro-2-phenylcyclohexane-l -carboxylate

To an ice cooled solution of rel-ethyl (lR,2R,4R)-4-ethynyl-4-hydroxy-2- phenylcyclo hexane- 1 -carboxylate (67 mg, 0.25 mmol) in DCM (2 mL), bis(2-methoxyethyl)amino sulphur trifluoride, (50 % solution in THF, 0.21 mL, 0.49 mmol) was added dropwise under N ₂ . After 5 minutes, the ice bath was removed and the reaction mixture was allowed to warm to r.t. over 2 hours. Cooled to 0 °C and quenched with sat. NaHCCf solution (10 mL). The reaction mixture was extracted with EtOAc (2 x 15 mL). The combined organic layer were dried (MgS0 ₄ ) and evaporated in vacuo. The residue was purified via flash chromatography using Heptane- 10 % EtO Ac/Heptane (gradient) as eluent to afford rel-ethyl (lR,2R)-4-ethynyl-4-fluoro-2-phenylcyclohexane-l -carboxylate as a white solid.

1H NMR (399 MHz, Chloroform-^) d 7.46-7.12 (m, 5H), 3.90 (qd, J = 7.1, 1.7 Hz, 2H), 3.30-3.08 (m, 1H), 2.71-2.52 (m, 2H), 2.49-2.27 (m, 2H), 2.21-1.64 (m, 4H), 0.96 (td, J = 7.1, 2.7 Hz, 3H).

Step 2: rel -(1R,2R) -4 -ethynyl -4 -fluoro -2 -phenylcyclohexane-1 -carboxylic acid

Starting from rel-ethyl (lR,2R)-4-ethynyl-4-fluoro-2-phenylcyclohexane-l -carboxylate (30 mg, 0.11 mmol) following procedure described in Step 2 of EXAMPLE 94, rel-(lR,2R)-4-ethynyl-4-fluoro-2-phenylcyclohexane-l -carboxylic acid was obtained as a colourless oil.

1H NMR (399 MHz, DMSO- ) d 11.97 (s, 1H), 7.43-7.01 (m, 5H), 3.57-3.14 (m, 4H), 3.12-2.56 (m, 2H), 2.30-1.41 (m, 3H)

Step 3: EXAMPLE 93

Starting from rel-(lR,2R)-4-ethynyl-4-fluoro-2-phenyl-cyclohexane-l -carboxylic acid (18 mg, 0.07 mmol) and 5-amino-6-(4-fluorophenoxy)-3-[(4-hydroxypiperidin-4-yl) methyl]pyrimidin-4-one (24 mg, 0.07 mmol) following procedure described in Step 3 of EXAMPLE 94, the obtained residue was purified via prep HPLC (Prep HPLC Column: Gemini pH 4 Dimensions: 21.1 mm x 150 mm 5 pm) to give EXAMPLE 93 as a white solid. LC/MS (Method B): RT = 1.177; m/z = 563 [M+H] ⁺

1H NMR (399 MHz, DMSO- ) d 7.60 (d, J= 22.4 Hz, 1H), 7.43-6.99 (m, 9H), 4.86 (d, J = 7.0 Hz, 1H), 4.68 (d, J = 14.0 Hz, 2H), 4.00-3.52 (m, 4H), 3.30-3.01 (m, 3H), 2.97-2.82 (m, 1H), 2.65 (td, J = 12.6, 2.5 Hz, 1H), 2.29-1.88 (m, 3H), 1.86-1.55 (m, 2H), 1.46-1.04 (m, 3H), 0.68 (m, 2H).

HRMS (TOF, ESI) m/z: Calculated for C31H32F2N4O4 562.2392, Found: 563.2528 [M+H] ⁺ rel-5-amino-3-({l-[(lR,2R,4R)-4-benzyl-4-hydroxy-2-phenyl-cy clohexanecarbonyl]- 4-hydroxypiperidin-4-yl}methyl)-6-(4-fluorophenoxy)-3,4-dihy dropyrimidin-4-one (EXAMPLE 94)

Step 1: r el -ethyl ( I R, 2 R,4R) -4 -benzyl -4 -hydroxy -2 -phenyl -cyclohexane -I -carboxylate and rel -( 1 R, 5R, 6S) -/ -benzyl -6 -phenyl -2 -oxabicyclo[ 3.2.2]nonan -3 -one

To a solution of benzylmagnesium chloride (0.89 mF, 1M solution in DEE, 0.89 mmol) in THF (2 mF) at 0 °C under N2, was added dropwise a solution of rel-ethyl (lR,2R)-4-oxo- 2-phenylcyclo hexane- 1 -carboxylate (200 mg, 0.81 mmol) in THF (4 mF). The mixture was stirred at the same temperature for 10 minutes before allowed to warm to r.t. over 1 hour. Saturated ammonium chloride solution (15 mF) was added and the aqueous layer was extracted with EtOAc (25 mF). The organic layer was separated, dried (MgSCF) and evaporated in vacuo. The residue was purified via flash chromatography using Heptane- 80 % EtO Ac/Heptane (gradient) as eluent to afford:

First elute: rel-(lR,5R,6S)-l-benzyl-6-phenyl-2-oxabicyclo[3.2.2]nonan-3- one as a colourless oil.

1H NMR (399 MHz, DMSO- ) d 7.45-7.18 (m, 10H), 3.45-3.37 (m, 1H), 3.05 (s, 2H), 2.20-2.02 (m, 3H), 1.96-1.84 (m, 1H), 1.73-1.48 (m, 3H)

FC/MS (Method B): RT = 1.36; m/z = 293 [M+H] ⁺

Second elute: rel-ethyl (lR,2R,4R)-4-benzyl-4-hydroxy-2-phenyl-cyclo hexane- 1 - carboxylate as a colourless oil.

1H NMR (399 MHz, DMSO- ) d 7.40-7.17 (m, 10H), 4.57 (s, 1H), 3.88 (q, J = 7.1 Hz, 2H), 3.03 (td, J = 11.9, 4.5 Hz, 1H), 2.98-2.87 (m, 2H), 2.68 (td, j = 11.7, 3.8 Hz, 1H),

1.95 (m, 1H), 1.86-1.68 (m, 2H), 1.65-1.47 (m, 3H), 0.92 (t , j= 7.1 Hz, 3H).

Step 2: reI-( I R, 2 R, 4 R) -4 -benzyl -4 -hydroxy -2 -phenyl -cyclohexane -I -carboxylic acid To a solution of rel-ethyl (lR,2R,4R)-4-benzyl-4-hydroxy-2-phenyl-cyclo hexane- 1- carboxylate (55 mg, 0.16 mmol) in methanol (0.5 mF) and THF (0.5 mF), sodium hydroxide (1M aq. solution, 0.49 mL, 0.49 mmol) was added and the reaction mixture stirred at 65 °C overnight. Allowed to cool to r.t., concentrated in vacuo, the residue was dissolved in water (10 mL), acidified to pH 4 with 1M HC1 and extracted with EtOAc (2 x 15 mL). The combined organic layer were dried (MgS0 ₄ ), evaporated in vacuo to afford re l-(lR,2R,4R)-4-benzyl-4-hydroxy-2-phenylcyclo hexane- 1 -carboxylic acid. The compound was used without further purification.

Step 3: EXAMPLE 94

To a solution of 5-amino-6-(4-fluorophenoxy)-3-[(4-hydroxypiperidin-4-yl)meth yl] pyrimidin-4-one (54 mg, 0.16 mmol) and rel-(lR,2R,4R)-4-benzyl-4-hydroxy-2- phenylcyclo hexane- 1 -carboxylic acid (50 mg) in acetonitrile (3 mL) was added triethylamine (0.04 mL, 0.32 mmol) followed by HATU (61 mg, 0.16 mmol) at r.t. under N ₂ . The reaction mixture was stirred for 2 hours and then concentrated in vacuo. The resultant residue was partitioned between EtOAc (25 mL) and sat. NaHC0 ₃ solution (15 mL). The organic layer was separated, dried (MgS0 ₄ ) and concentrated in vacuo. The residue was purified via flash chromatography using DCM-4 % MeOH/DCM (gradient) as eluent to afford EXAMPLE 94 as a white solid.

LC/MS (Method B): RT = 1.15; m/z = 627 [M+H] ⁺

1H NMR (399 MHz, DMSO-d6) d 7.60 (d, J = 24.2 Hz, 1H), 7.33-7.06 (m, 14H), 4.82 (d, J = 12.0 Hz, 1H), 4.68 (d, J = 11.9 Hz, 2H), 4.46 (d, J = 2.6 Hz, 1H), 4.02-3.56 (m, 5H), 3.22-2.80 (m, 4H), 2.74-2.62 (m, 1H), 1.83-1.07 (m, 8H), 0.87-0.74 (m, 1H), 0.68-0.55 (m,

1H).

HRMS (TOE, ESI) m/z: Calculated for C ₃₆ H ₃₉ FN ₄ 0 ₅ 626.2904, Found: 627.3001 [M+H] ⁺ rel-5-amino-3-({l-[(lR,2R,4S)-4-benzyl-4-hydroxy-2-phenyl-cy clohexanecarbonyl]- 4-hydroxypiperidin-4-yl}methyl)-6-(4-fluorophenoxy)-3,4-dihy dropyrimidin-4-one (EXAMPLE 95)

Step 1: reI-( IR,2R,4S) -4 -benzyl -4 -hydroxy -2 -phenyl cyclohexane -I -carboxylic acid

Starting from rel-(lR,5R,6S)-l-benzyl-6-phenyl-2-oxabicyclo[3.2.2]nonan-3- one (105 mg, 0.36 mmol) following procedure described in Step 2 of EXAMPLE 94, rel-(lR,2R,4S)-4- benzyl-4-hydroxy-2-phenylcyclo hexane- 1 -carboxylic acid was obtained as a yellow solid. The compound was used without further purification.

LC/MS (Method B): RT = 1.20; m/z = 309 [M+H] ⁺

Step 2: EXAMPLE 95

Starting from 5 -amino-6-(4-fluorophenoxy)-3 - [(4-hydroxypiperidin-4-yl)methyl] pyrimidin-4-one (120 mg, 0.36 mmol) and rel-(lR,2R,4S)-4-benzyl-4-hydroxy-2- phenylcyclo hexane- 1 -carboxylic acid (185 mg) following procedure described in Step 3 of EXAMPLE 94, the obtained residue was purified via prep HPLC (Prep HPLC Column: Gemini pH 4 Dimensions: 21.1 mm x 150 mm 5 pm) to give EXAMPLE 95 as a white solid. LC/MS (Method B): RT = 1.21; m/z = 627 [M+H] ⁺

1H NMR (399 MHz, DMSO- ) d 7.60 (d, J= 22.3 Hz, 1H), 7.29-7.05 (m, 14H), 4.81 (d, J = 11.7 Hz, 1H), 4.67 (d, J= 9.7 Hz, 2H), 4.30 (d, J= 9.8 Hz, 1H), 3.99-3.60 (m, 4H), 3.27- 2.81 (m, 3H), 2.73-2.56 (m, 3H), 1.97-1.78 (m, 1H), 1.66-0.98 (m, 8H), 0.82-0.65 (m, 1H). HRMS (TOF, ESI) m/z: Calculated for C36H39FN405 626.2904, Found: 627.3002 [M+H] ⁺ rel-5-amino-6-(4-fluorophenoxy)-3-({4-hydroxy-l-[(lR,2R,4R)- 4-hydroxy-2-phenyl- 4-[(pyridin-2-yl)methyl]cyclohexanecarbonyl]piperidin-4-yl}m ethyl)-3,4- dihydropyrimidin-4-one (EXAMPLE 96)

Step 1: rel-ethyl (1R,2R,4R) -4 -hydroxy -2 -phenyl -4 -[(pyridin -2 -yl)methyl] cyclohexane -1 - carboxylate and rel-ethyl (1 R,2R,4S) -4 -hydroxy -2 -phenyl -4 -[(pyridin -2 -yl)methyl] cyclohexane J -carboxylate

To a solution of 2-picoline (0.07 mL, 0.67 mmol) in THF (4 mL), n-butyl lithium (2.5M solution in hexanes, 0.26 mL, 0.64 mmol) was added dropwise under N ₂ at -78 °C. After 20 minutes, a solution of rel-ethyl (lR,2R)-4-oxo-2-phenylcyclohexane-l -carboxylate (150 mg, 0.61 mmol) in THF (2 mL) was added dropwise and stirring continued at -78 °C for 1 hour. The reaction mixture was allowed to warm to r.t. and quenched with aq. NH ₄ Cl solution (10 mL). The aqueous layer was extracted with EtOAc (20 mL), dried (MgS0 ₄ ) and concentrated in vacuo. The residue was purified via flash chromatography using heptane-25 % EtO Ac/Heptane (gradient) as eluent to afford: First elute: rel-ethyl (lR,2R,4R)-4-hydroxy-2-phenyl-4-[(pyridin-2-yl)methyl]

cyclohexane- l-carboxylate as a colourless oil.

LC/MS (Method B): RT = 1.18; m/z = 340 [M+H] ⁺

Second elute: rel-ethyl (lR,2R,4S)-4-hydroxy-2-phenyl-4-[(pyridin-2-yl)methyl] cyclohexane- l-carboxylate as a colourless oil.

LC/MS (Method B): RT = 1.18; m/z = 340 [M+H] ⁺

Step 2: rel-( 1 R, 2R, 4R) -4 -hydroxy -2 -phenyl -4 -[ (pyridin -2 -yl)methyl] cyclohexane -/ - carboxylic acid

Starting from rel-ethyl (lR,2R,4R)-4-hydroxy-2-phenyl-4-[(pyridin-2-yl)methyl] cyclohexane- l-carboxylate (25 mg, 0.07 mmol) following procedure described in Step 2 of

EXAMPLE 94, the reaction mixture was concentrated in vacuo to give rel-(lR,2R,4R)-4- hydroxy-2-phenyl-4- [(pyridin-2-yl)methyl]cyclo hexane- 1 -carboxylic acid. The compound was used without further purification.

LC/MS (Method B): RT = 0.70; m/z = 312 [M+H] ⁺ Step 3: EXAMPLE 96

Starting from 5 -amino-6-(4-fluorophenoxy)-3 - [(4-hydroxypiperidin-4-yl)methyl] pyrimidin-4-one (23 mg, 0.07 mmol) and rel-(lR,2R,4R)-4-hydroxy-2-phenyl-4-[(pyridin- 2-yl)methyl]cyclo hexane- 1 -carboxylic acid (45 mg) using Step 3 of EXAMPLE 94, EXAMPLE 96 was obtained as a white solid.

LC/MS (Method B): RT = 1.07; m/z = 628 [M+H] ⁺

1H NMR (399 MHz, DMSO- ) d 8.57-8.44 (m, 1H), 7.72 (tt, J= 7.7, 1.9 Hz, 1H), 7.60 (d, J= 23.8 Hz, 1H), 7.40 (ddt, J= 7.9, 2.1, 1.1 Hz, 1H), 7.31-7.02 (m, 10H), 5.08 (d, J= 16.2 Hz, 1H), 4.83 (d, J= 13.1 Hz, 1H), 4.68 (d, J= 11.4 Hz, 2H), 4.03-3.57 (m, 4H), 3.28-2.83 (m, 6H), 2.76-2.60 (m, 1H), 1.86-1.04 (m, 7H), 0.72 (ddt, J= 66.2, 12.8, 6.5 Hz, 2H). HRMS (TOF, ESI) m/z: Calculated for C ₃₅ H ₃₈ FN ₅ O ₅ 627.2857, Found: 628.2951 [M+H] ⁺ rel-5-amino-6-(4-fluorophenoxy)-3-[(4-hydroxy-l-{[(lR,2R,4S) -4-hydroxy-2-phenyl- 4-(pyridin-2-ylmethyl)cyclohexyl]carbonyl}piperidin-4-yl)met hyl]pyrimidin-4-one (EXAMPLE 97) Step 1: rel-(lR,2R,4S) -4 -hydroxy -2 -phenyl -4 -[ (pyridin -2 -yl) methyl ] cyclohexane -l - carboxylic acid

Starting from rel-ethyl (lR,2R,4S)-4-hydroxy-2-phenyl-4-[(pyridin-2-yl)methyl] cyclohexane- l-carboxylate (35 mg, 0.10 mmol) following procedure described in Step 2 of EXAMPLE 94, the reaction mixture was concentrated in vacuo to give rel-(lR,2R,4S)-4- hydroxy-2-phenyl-4- [(pyridin-2-yl)methyl]cyclo hexane- 1 -carboxylic acid. The compound was used without further purification.

LC/MS (Method B): RT = 0.74; m/z = 312 [M+H] ⁺

Step 2: EXAMPLE 97

Starting from 5-amino-6-(4-fluorophenoxy)-3-[(4-hydroxypiperidin-4-yl)meth yl] pyrimidin-4-one (33 mg, 0.10 mmol) and rel-(lR,2R,4S)-4-hydroxy-2-phenyl-4-[(pyridin- 2-yl)methyl]cyclo hexane- 1 -carboxylic acid (60 mg) using Step 3 of EXAMPLE 94, EXAMPLE 97 was obtained as a white solid.

LC/MS (Method B): RT = 1.08; m/z = 628 [M+H] ⁺

1H NMR (399 MHz, DMSO- ) 6 8.46 (dddd, J= 4.2, 3.1, 1.8, 0.8 Hz, 1H), 7.74-7.65 (m, 1H), 7.60 (d, J = 22.6 Hz, 1H), 7.32-7.05 (m, 11H), 4.84-4.74 (m, 2H), 4.68 (d, j = 10.5 Hz, 2H), 3.98-3.58 (m, 4H), 3.28-2.78 (m, 6H), 2.71-2.58 (m, 1H), 1.98-1.76 (m, 1H), 1.72-1.03 (m, 7H), 0.85-0.61 (m, 1H).

HRMS (TOF, ESI) m/z: Calculated for C ₃₅ H ₃₈ FN ₅ O ₅ 627.2857, Found: 628.2952 [M+H] ⁺ rel-5-amino-6-(4-fluorophenoxy)-3-[(4-hydroxy-l-{[(lR,2R,4R) -4-hydroxy-2- phenyl-4-(pyrazin-2-ylmethyl)cyclohexyl]carbonyl}piperidin-4 -yl)methyl]pyrimidin- 4-one (EXAMPLE 98)

Step 1: rel-ethyl (1R,2R,4R) -4 -hydroxy -2 -phenyl -4 -[(pyrazin -2 -yl)methyl] cyclohexane -1 - carboxylate

Starting from rel-ethyl (lR,2R)-4-oxo-2-phenylcyclohexane- l-carboxylate (700 mg, 2.84 mmol) and 2-methylpyrazine (0.24 mL, 2.58 mmol) following procedure described in Step 1 of EXAMPLE 96, the obtained residue was purified via flash chromatography using Heptane- 10 % EtO Ac/Heptane (gradient) as eluent to afford rel-ethyl (lR,2R,4R)-4- hydroxy-2-phenyl-4-[(pyrazin-2-yl)methyl]cyclo hexane- l-carboxylate. The compound was used without further purification.

LC/MS (Method B): RT = 1.09; m/z = 341 [M+H] ⁺

Step 2: rel-(lR,2R,4R)-4-hydroxy-2-phenyl-4-(pyrazin-2-ylmethyl)cycl ohexane-l- carboxylic acid

Starting from rel-ethyl (lR,2R,4R)-4-hydroxy-2-phenyl-4-[(pyrazin-2-yl)methyl] cyclohexane- l-carboxylate (136 mg, 0.4 mmol) following procedure described in Step 2 of EXAMPLE 94, the reaction mixture was concentrated in vacuo to give rel-(lR,2R,4R)-4- hydroxy-2-phenyl-4-(pyrazin-2-ylmethyl)cyclo hexane- 1 -carboxylic acid. The compound was used without further purification.

LC/MS (Method B): RT = 0.84; m/z = 313 [M+H] ⁺

Step 3: EXAMPLE 98

Starting from 5 -amino-6-(4-fluorophenoxy)-3 - [(4-hydroxypiperidin-4-yl)methyl] pyrimidin-4-one (107 mg, 0.32 mmol) and rel-(lR,2R,4R)-4-hydroxy-2-phenyl-4-(pyrazin- 2-ylmethyl)cyclo hexane- 1 -carboxylic acid (100 mg) following procedure described in Step 3 of EXAMPLE 94, the obtained residue was purified via flash chromatography using DCM-2 % MeOH/DCM (gradient) as eluent to give EXAMPLE 98 as a white solid.

LC/MS (Method B): RT = 1.00; m/z = 629 [M+H] ⁺

1H NMR (399 MHz, DMSO- ) d 8.63-8.52 (m, 2H), 8.46 (dd, J = 4.3, 2.6 Hz, 1H), 7.61 (d, J = 24.2 Hz, 1H), 7.34-7.04 (m, 9H), 4.88-4.75 (m, 2H), 4.68 (d, J = 11.7 Hz, 2H), 4.01-3.57 (m, 4H), 3.29-2.84 (m, 5H), 2.68 (t, J = 11.8 Hz, 1H), 1.90-1.07 (m, 8H), 0.82 (tt, J= 12.5, 4.3 Hz, 1H), 0.63 (t, J= 11.5 Hz, 1H).

HRMS (TOF, ESI) m/z: Calculated for C ₃₄ H ₃₇ FN ₆ O ₅ 628.2809, Found: 629.2979 [M+H] ⁺ rel-5-amino-6-(4-fluorophenoxy)-3-({l-[(lR,2R,4R)-4-[(4-fluo rophenyl)methyl]-4- hydroxy-2-phenylcyclohexanecarbonyl]-4-hydroxypiperidin-4-yl }methyl)-3,4- dihydropyrimidin-4-one (EXAMPLE 99) Step 1: rel-ethyl (lR,2R,4R)-4-[(4-fluorophenyl)methyl]-4-hydroxy-2-phenylcycl ohexane- 1-carboxylate and rel-( 1 R, 5R, 6S) -l-[(4 -fluorophenyl)methyl] -6 -phenyl -2 - oxabicyclo[3.2.2Jnonan-3 -one

Following procedure described in Step 1 of EXAMPLE 94 and starting from rel-ethyl (lR,2R)-4-oxo-2-phenylcyclo hexane- l-carboxylate (500 mg, 2.03 mmol) and bromo[(4- fluorophenyl)methyl]magnesium (1.94 mL, 1.15 M, 2.23 mmol) (prepared following procedure described in WO 2011/026349), the obtained residue was purified via flash chromatography using Heptane-50 % EtO Ac/Heptane (gradient) as eluent to afford:

First elute: rel-(lR,5R,6S)-l-[(4-fluorophenyl)methyl]-6-phenyl-2-oxabicy clo[3.2.2] nonan-3-one as a colourless oil.

1H NMR (399 MHz, DMSO-d ₆ ) d 7.40-7.24 (m, 7H), 7.19-7.13 (m, 2H), 3.43-3.37 (m, 1H), 3.04 (s, 2H), 2.50-2.47 (m, 1H), 2.16-2.03 (m, 2H), 1.93-1.85 (m, 1H), 1.71-1.48 (m, 3H)

Second elute: rel-ethyl (lR,2R,4R)-4-[(4-fluorophenyl)methyl]-4-hydroxy-2-phenyl cyclohexane- l-carboxylate as a colourless oil.

1H NMR (399 MHz, DMSO-d ₆ ) d 7.25-7.14 (m, 7H), 7.11-7.05 (m, 2H), 4.53 (s, 1H), 3.81 (q, J = 7.1 Hz, 2H), 2.99-2.81 (m, 3H), 2.65-2.57 (m, 1H), 1.01-1.84 (m, 1H), 1.79-1.60 (m, 2H), 1.55-1.42 (m, 3H), 0.85 (t, J = 7.1 Hz, 3H).

Step 2: rel-(lR,2R,4R)-4-[(4-fluorophenyl)methyl]-4-hydroxy-2-phenyl cyclohexane-l- carboxylic acid

Starting from rel-ethyl (lR,2R,4R)-4-[(4-fluorophenyl)methyl]-4-hydroxy-2-phenyl cyclohexane- l-carboxylate (105 mg, 0.29 mmol) following procedure described in Step 2 of EXAMPLE 94, rel-(lR,2R,4R)-4-[(4-fluorophenyl)methyl]-4-hydroxy-2-phenyl cyclohexane- 1 -carboxylic acid was obtained as a yellow oil. The compound was used without further purification.

LC/MS (Method B): RT = 1.07; m/z = 327 [M-H]

Step 3: EXAMPLE 99

Starting from 5 -amino-6-(4-fluorophenoxy)-3 - [(4-hydroxypiperidin-4-yl)methyl] pyrimidin-4-one (97 mg, 0.29 mmol) and rel-(lR,2R,4R)-4-[(4-fluorophenyl)methyl]-4- hydroxy-2-phenylcyclo hexane- 1 -carboxylic acid (95 mg) following procedure described in Step 3 of EXAMPLE 94, the residue was purified via flash chromatography using DCM- 6 % MeOH/DCM (gradient) as eluent to afford crude EXAMPLE 99. The residue was purified again via flash chromatography using EtOAc-2 % MeOH/EtOAc (gradient) as eluent to give EXAMPLE 99 as a white solid.

LC/MS (Method B): RT = 1.16; m/z = 645 [M+H] ⁺

1H NMR (399 MHz, DMSO-d ₆ ) d 7.60 (d, .7= 24.1 Hz, 1H), 7.37-7.03 (m, 13H), 4.83 (d, J = 12.4 Hz, 1H), 4.68 (d, J = 11.9 Hz, 2H), 4.50 (d, J = 2.7 Hz, 1H), 4.00-3.82 (m, 2H), 3.79-3.59 (m, 2H), 3.19-2.79 (m, 5H), 2.73-2.61 (m, 1H), 1.79-1.07 (m, 8H), 0.90-0.72 (m, 1H), 0.67-0.54 (m, 1H).

HRMS (TOF, ESI) m/z: Calculated for C ₃₆ H ₃₈ F ₂ N ₄ O ₅ 644.2810, Found: 645.2910 [M+H] ⁺ rel-5-amino-6-(4-fluorophenoxy)-3-[(l-{[(lR,2R,4S)-4-[(4-flu orophenyl)methyl]-4- hydroxy-2-phenylcyclohexyl]carbonyl}-4-hydroxypiperidin-4-yl )methyl]pyrimidin-4- one (EXAMPLE 100)

Step 1: rel-(lR,2R,4S)-4-[(4-fluorophenyl)methyl]-4-hydroxy-2-phenyl cyclohexane-l- carboxylic acid

Starting from rel-(lR,5R,6S)-l-[(4-fluorophenyl)methyl]-6-phenyl-2-oxabicy clo[3.2.2] nonan-3-one (70 mg, 0.23 mmol) following procedure described in Step 2 of EXAMPLE 94, rel-(lR,2R,4S)-4-[(4-fluorophenyl)methyl]-4-hydroxy-2-phenyl cyclohexane-l -carboxylic acid was obtained as a yellow oil. The compound was used without further purification. FC/MS (Method B): RT = 1.15; m/z = 327 [M-H]-

Step 2: EXAMPLE 100

Starting from 5 -amino-6-(4-fluorophenoxy)-3 - [(4-hydroxypiperidin-4-yl)methyl] pyrimidin-4-one (74 mg, 0.22 mmol) and rel-(lR,2R,4S)-4-[(4-fluorophenyl)methyl]-4- hydroxy-2-phenylcyclo hexane- 1 -carboxylic acid (182 mg) following procedure described in Step 3 of EXAMPLE 94, the obtained residue was purified via flash chromatography using EtOAc-2 % MeOH/EtOAc (gradient) as eluent to give crude EXAMPLE 100. The residue was purified via prep HPFC (Prep HPFC Column: Gemini pH 4 Dimensions: 21.1 mm x 150 mm 5 pm) to give EXAMPLE 100 as a white solid.

FC/MS (Method B): RT = 1.22; m/z = 645 [M+H] ⁺ 1H NMR (399 MHz, DMSO- ) d 7.60 (d, J= 22.3 Hz, 1H), 7.30-7.02 (m, 13H), 4.81 (d, J = 11.7 Hz, 1H), 4.67 (d, = 9.8 Hz, 2H), 4.3l (d, = 9.2 Hz, 1H), 3.98-3.78 (m, 2H), 3.75- 3.60 (m, 2H), 3.26-2.81 (m, 3H), 2.66 (d, j= 4.3 Hz, 3H), 1.87 (dt, j= 12.2, 5.8 Hz, 1H), 1.65-1.05 (m, 8H), 0.82-0.65 (m, 1H).

HRMS (TOF, ESI) m/z: Calculated for C ₃₆ H ₃₈ F ₂ N ₄ O ₅ , Found: 645.2983 [M+H] ⁺ rel-5-amino-6-(4-fluorophenoxy)-3-({4-hydroxy-l-[(lR,2R,4R)- 4-hydroxy-4-[(l- methyl-lH-imidazol-2-yl)methyl]-2-phenyl-cyclohexanecarbonyl ]piperidin-4-yl} methyl)-3,4-dihydropyrimidin-4-one (EXAMPLE 101)

Step 1: rel-ethyl ( I R,2R,4R) -4 -hydroxy -4 -[( / -111 ethyl - / H -in 1 idazo I -2 -yl)n 1 e thy I ] -2 -ph enyl - cyclohexane -1 -carboxylate

Using Step 1 of EXAMPLE 96 and starting from rel-ethyl (lR,2R)-4-oxo-2- phenylcyclo hexane- 1 -carboxylate (200 mg, 0.81 mmol, 1.0 eq.) and 1 ,2-dimethyl- 1H- imidazole (156 mg, 1.62 mmol) instead of 2-picoline, rel-ethyl (lR,2R,4R)-4-hydroxy-4- [(1 -methyl- lH-imidazol-2-yl)methyl]-2-phenyl-cyclohexane- 1 -carboxylate was obtained as a yellow oil.

FC/MS (Method B): RT = 1.10; m/z = 343 [M+H] ⁺

Step 2: rel -( 1 R, 2R, 4R) -4 -hydroxy -4-[(l -methyl -Hi-imidazol-2 -yl)methyl] -2 -phenyl- cyclohexane J -carboxylic acid

Starting from rel-ethyl (lR,2R,4R)-4-hydroxy-4-[(l-methyl-lH-imidazol-2-yl)methyl]-2 - phenylcyclo hexane- 1 -carboxylate (40 mg, 0.012 mmol) following procedure described in

Step 2 of EXAMPLE 94, (rel-(lR,2R,4R)-4-hydroxy-4-[(l-methyl-lH-imidazol-2- yl)methyl] -2-phenylcyclo hexane- 1 -carboxylic acid was obtained. The compound was used without further purification.

FC/MS (Method B): RT = 0.66; m/z = 315 [M+H] ⁺ Step 3: EXAMPLE 101

Starting from (rel-( 1 R,2R,4R)-4-hydroxy-4- [( 1 -methyl- 1 H-imidazol-2-yl)methyl] -2- phenylcyclo hexane- 1 -carboxylic acid (85 mg) and 5-amino-6-(4-fluorophenoxy)-3-[(4- hydroxypiperidin-4-yl)methyl]pyrimidin-4-one (39 mg, 0.12 mmol) following procedure described in Step 3 of EXAMPLE 94, EXAMPLE 101 was obtained as a white solid.

LC/MS (Method B): RT = 0.89; m/z = 631 [M+H] ⁺

1H NMR (399 MHz, DMSO-d ₆ ) d 7.60 (d, J = 24.5 Hz, 1H), 7.46 (d, J = 2.3 Hz, 1H), 7.37 (d, J = 4.4 Hz, 1H), 7.34-7.03 (m, 9H), 4.84 (d, j = 14.0 Hz, 1H), 4.68 (d, j = 11.8 Hz, 2H), 4.05-3.57 (m, 7H), 3.23-2.86 (m, 5H), 2.68 (tt, j = 12.9, 3.1 Hz, 1H), 1.88-1.07 (m, 9H), 0.82 (qd, J = 14.3, 13.1, 4.8 Hz, 1H), 0.57 (td, j= 13.1, 4.3 Hz, 1H).

HRMS (TOF, ESI) m/z: Calculated for C34H39FN6O5 630.2966, Found: 631.3098 [M+H] ⁺ rel-5-amino-6-(4-fluorophenoxy)-3-[(4-hydroxy-l-{[(lR,2R,4R) -4-hydroxy-2,4- diphenylcyclohexyl] carbonyl}piperidin-4-yl)methyl]pyrimidin-4-one (EXAMPLE 102)

Step 1: r el -ethyl ( l R,2R,4R)-4 -hydroxy -2, 4 -dipheny /cyclohexane -I -carboxylate and rel- (1R, 5R, 6S) -1, 6 -diphenyl -2 -oxabicyclo[ 3.2.2 ]nonan -3 -one

Starting from rel-ethyl (lR,2R)-4-oxo-2-phenylcyclohexane-l -carboxylate (500 mg, 2.03 mmol) and phenylmagnesium bromide (2.23 mL, 1M, 2.23 mmol) following procedure described in Step 1 of EXAMPLE 94, the obtained residue was purified via flash chromatography using Heptane-50 % EtO Ac/Heptane (gradient) as eluent to afford:

First elute: rel-(lR,5R,6S)-l,6-diphenyl-2-oxabicyclo[3.2.2]nonan-3-one as a white solid. LC/MS (Method B): RT = 1.30; m/z = 279 [M+H] ⁺

Second elute: rel-ethyl (lR,2R,4R)-4-hydroxy-2,4-diphenylcyclo hexane- 1 -carboxylate as a colourless oil.

1H NMR (399 MHz, DMSO-de) d 7.60-7.52 (m, 2H), 7.43 (dd, J = 8.4, 6.9 Hz, 2H), 7.36- 7.24 (m, 3H), 7.27-7.14 (m, 3H), 5.08 (s, 1H), 3.73 (qd, J = 7.1, 1.7 Hz, 2H), 2.79-2.52 (m, 3H), 2.46 (dt, J = 13.2, 2.8 Hz, 1H), 1.99-1.87 (m, 2H), 1.81 (td, J = 13.6, 3.8 Hz, 1H), 1.47-1.32 (m, 1H), 0.79 (t, J = 7.1 Hz, 3H).

Step 2: rel-(lR,2R,4R)-4-hydroxy-2,4-diphenylcyclohexane-l-carboxyli c acid

Starting from rel-ethyl (lR,2R,4R)-4-hydroxy-2,4-diphenylcyclo hexane- 1 -carboxylate (70 mg, 0.22 mmol) following procedure described in Step 2 of EXAMPLE 94, rel- (lR,2R,4R)-4-hydroxy-2,4-diphenylcyclo hexane- 1 -carboxylic acid was obtained. The compound was used without further purification. 1H NMR (399 MHz, DMSO-d ₆ ) d 11.85 (s, 1H), 7.60-7.53 (m, 2H), 7.47-7.38 (m, 2H), 7.35-7.24 (m, 3H), 7.19 (ddd, J = 7.9, 6.9, 1.1 Hz, 3H), 5.05 (s, 1H), 2.76-2.62 (m, 2H), 2.62-2.44 (m, 2H), 2.03-1.73 (m, 3H), 1.39 (m, 1H).

Step 3: EXAMPLE 102

Starting from 5 -amino-6-(4-fluorophenoxy)-3 - [(4-hydroxypiperidin-4-yl)methyl] pyrimidin-4-one (68 mg, 0.20 mmol) and rel-(lR,2R,4R)-4-hydroxy-2,4- dipheny ley clo hexane- 1 -carboxylic acid (60 mg) following procedure described in Step 3 of EXAMPLE 94, the obtained residue was purified via flash chromatography using DCM-5 % MeOH/DCM (gradient) as eluent to give EXAMPLE 102 as a white solid.

LC/MS (Method B): RT = 1.11; m/z = 613 [M+H] ⁺

1H NMR (399 MHz, DMSO- ) d 7.68-7.49 (m, 3H), 7.42 (td, J = 7.6, 3.3 Hz, 2H), 7.34- 7.05 (m, 10H), 5.02 (d, J = 2.0 Hz, 1H), 4.80 (d, J = 13.4 Hz, 1H), 4.67 (d, J = 11.4 Hz, 2H), 3.97-3.58 (m, 4H), 3.23-2.85 (m, 2H), 2.83-2.71 (m, 1H), 2.66-2.56 (m, 1H), 2.49- 2.39 (m, 1H), 2.11-1.78 (m, 3H), 1.75-1.61 (m, 1H), 1.41 (q, J= 13.9, 13.4 Hz, 1H), 1.31- 1.02 (m, 2H), 0.76 (td, J= 12.8, 4.5 Hz, 1H), 0.59 (td, J= 12.9, 4.3 Hz, 1H).

HRMS (TOF, ESI) m/z: Calculated for C35H37FN4O5 612.2748, Found: 613.2908 [M+H] ⁺ rel-5-amino-6-(4-fluorophenoxy)-3-[(4-hydroxy-l-{[(lR,2R,4S) -4-hydroxy-2,4- diphenylcyclohexyl] carbonyl}piperidin-4-yl)methyl]pyrimidin-4-one (EXAMPLE 103)

Step 1: rel-(lR,2R,4S)-4-hydroxy-2,4-diphenylcyclohexane-l-carboxyli c acid

Starting from rel-(lR,5R,6S)-l,6-diphenyl-2-oxabicyclo[3.2.2]nonan-3-one (360 mg, 1.29 mmol) following procedure described in Step 2 of EXAMPLE 94, rel-(lR,2R,4S)-4- hydroxy-2, 4-diphenylcy clo hexane- 1 -carboxylic acid was obtained. The compound was used without further purification.

LC/MS (Method B): RT = 1.11; m/z = 295 [M-H]-

Step 2: EXAMPLE 103

Starting from re l-(lR,2R,4S)-4-hydroxy-2,4-diphenylcyclo hexane- 1 -carboxylic acid (100 mg, 0.34 mmol) and 5-amino-6-(4-fluorophenoxy)-3-[(4-hydroxypiperidin-4- yl)methyl]pyrimidin-4-one (113 mg, 0.34 mmol) following procedure described in Step 3 of EXAMPLE 94, the obtained residue was purified via flash chromatography using EtOAc- 1.6 % MeOH/EtOAc (gradient) as eluent to give EXAMPLE 103 as a white solid.

LC/MS (Method B): RT = 1.19; m/z = 595 [other

1H NMR (399 MHz, DMSO- ) d 7.67-7.51 (m, 3H), 7.36-7.05 (m, 12H), 4.97 (d, J = 9.2 Hz, 1H), 4.83 (d, J = 10.7 Hz, 1H), 4.68 (d, J = 12.6 Hz, 2H), 4.01-3.64 (m, 4H), 3.42 (td, J = 12.7, 11.9, 3.4 Hz, 1H), 3.29-2.93 (m, 2H), 2.70 (m, 1H), 2.19-1.92 (m, 3H), 1.79-1.06 (m, 6H), 0.86-0.69 (m, 1H).

HRMS (TOF, ESI) m/z: Calculated for C35H37FN4O5 612.2748, Found: 613.2925 [M+H] ⁺

^■ 5-amino-3-({(45)-l-[(l/?,2/?)-4,4-difluoro-2-phenylcyclohexa ne-l-carbonyl]-3,3- difluoro-4-hydroxypipendin-4-yl}methyl)-6-(3-hydroxyphenoxy) pynmidin-4(3//)-one (EXAMPLE 104)

and

5-amino-3-({(4/?)-l-[(l/?,2/?)-4,4-difluoro-2-phenylcyclohex ane-l-carbonyl]-3,3- difluoro-4-hydroxypiperidin-4-yl}methyl)-6-(3-hydroxyphenoxy )pyrimidin-4(3//)-one (EXAMPLE 105)

Using General Procedure 5 starting from Preparation R4at and Preparation R5b,

5-amino-6-[3-(benzyloxy)phenoxy]-3-({l -[(17?, 27?)-4,4-difluoro-2-phenylcyclo hexane- 1- carbonyl]-3,3-difluoro-4-hydroxypiperidin-4-yl}methyl)pyrimi din-4(377)-one was obtained. It was separated by chiral chromatography to give 5-amino-6-[3- (benzyloxy)phenoxy]-3-( {(4 S)- 1 -[(17?, 27?)-4,4-difluoro-2-phenylcyclo hexane- 1 -carbonyl]-

3.3-difluoro-4-hydroxypiperidin-4-yl}methyl)pyrimidin-4(3 77)-one and 5-amino-6-[3- (benzyloxy)phenoxy]-3-( {(47?)- l-[(l7?,27?)-4, 4-difluoro-2-phenylcyclo hexane- l-carbonyl]-

3.3-difluoro-4-hydroxypiperidin-4-yl}methyl)pyrimidin-4(3 77)-one.

Autoclave was charged with 5-amino-6-[3-(benzyloxy)phenoxy]-3-({(4S)-l-[(l7?,27?)-4,4- difluoro-2-phenylcyclohexane-l-carbonyl]-3,3-difluoro-4-hydr oxypiperidin-4-yl} methyl)pyrimidin-4(377)-one (83 mg, 0.1219 mmol) 10 % palladium on charcoal (17 mg) and methanol (5 mL), and then placed under a nitrogen atmosphere. After that, it was filled with 10 bar H ₂ gas. The reaction mixture was stirred in autoclave at r.t. for 19 hours. The catalyst was washed with methanol and filtered off. The mother liquor was purified by Hanbon prep HPLC, Cl 8 Silica, Gemini NX 5 pm, 5 mM NH ₄ HC03-MeCN using gradient method 5-90 %. Solvent was evaporated under reduced pressure to give EXAMPLE 104. HRMS calculated for C29H30F4N4O5: 590.2152; found 591.2228 ((M+H) ⁺ form).

Autoclave was charged with 5-amino-6-[3-(benzyloxy)phenoxy]-3-({(47?)-l-[(l7?,27?)-4,4- difluoro-2-phenylcyclohexane-l-carbonyl]-3,3-difluoro-4-hydr oxypiperidin-4-yl} methyl )pyri midi n-4(3/7)-onc (55 mg, 0.081 mmol) 10 % palladium on charcoal (12 mg) and methanol (5 mL), and then placed under a nitrogen atmosphere. After that it was filled with 10 bar ¾ gas. The reaction mixture was stirred in autoclave at r.t. for 19 hours. The catalyst was washed with methanol and filtered off. The mother liquor was purified by Hanbon prep HPLC, Cl 8 Silica, Gemini NX 5 pm, 5 mM MUHCCL-MeCN using gradient method 5-90 %. Solvent was evaporated under reduced pressure to give EXAMPLE 105. HRMS calculated for C29H30F4N4O5: 590.2152; found 591.2234 ((M+H) ⁺ form). 5-amino-3-({l-[(l/?,2/?)-4,4-difluoro-2-phenylcyclohexane-l- carbonyl]-4- hydroxypiperidin-4-yl}methyl)-6- |(l//-pyrrolo [3,2 -b] pyridin-6-yl)oxy] pyrimidin- 4(3//)-one (EXAMPLE 106)

Using General Procedure 5 starting from Preparation R4bs and Preparation R5a as reagents, EXAMPLE 106 was obtained. HRMS calculated for C30H32F2N6O4: 578.2453; found 579.252 ((M+H) ⁺ form). 4-{[5-amino-l-({l-[(l/?,2/?)-4,4-difluoro-2-phenylcyclohexan e-l-carbonyl]-4- hydroxypiperidin-4-yl}methyl)-6-oxo-l,6-dihydropyrimidin-4-y l]oxy}-3- chlorobenzamide (EXAMPLE 107)

EXAMPLE 53 (100 mg, 0.1672 mmol), (lE)-acetaldehyde oxime (98.77 mg, 0.102 mL, 1.352 mmol 10 eq.), Cu ²⁺ on 4Ά molecular sieve (100 mg) were dissolved in methanol (3 mL) and l,4-dioxane (2 mL). The reaction mixture was stirred at 60°C for 18 hours. The mixture was filtered, the filtrate was evaporated and purified by preparative LC (on C-18 Gemini-NX 5 pm column, 5 mM aqueous NH ₄ HC03-MeCN, gradient). Solvent was evaporated under reduced pressure to give EXAMPLE 107. HRMS calculated for C30H32CIL2N5O5: 615.206; found 616.2129 ((M+H) ⁺ form). 5-amino-3-({l-[(l/?,2/?)-4,4-difluoro-2-phenylcyclohexane-l- carbonyl]-4- hydroxypiperidin-4-yl}methyl)-6-{4-[(dimethylamino)methyl]ph enoxy}pyrimidin- 4(3//)-one (EXAMPLE 108)

EXAMPLE 44 (100 mg, 0.1765 mmol), dimethylamine (2M in THF) (5.0 eq.), sodium triacetoxyborohydride (5.0 eq.), acetic acid (5.0 eq.) were dissolved in THF and stirred r.t. for 24 hours. The reaction mixture was diluted with water and it was purified by preparative LC (on C-18 Gemini-NX 5 pm column, 5 mM aqueous NH ₄ HC03-MeCN, gradient). Solvent was evaporated under reduced pressure to give EXAMPLE 108. HRMS calculated for C32H39F2N5O4: 595.297; found 596.3035 ((M+H) ⁺ form). ^■ 5-amino-3-({(45)-l-[(l/f,2/f)-4,4-difluoro-2-phenylcyclohexa ne-l-carbonyl]-3,3- difluoro-4-hydroxypiperidin-4-yl}methyl)-6-(4-fluoro-3-hydro xyphenoxy)pyrimidin- 4(3//)-one (EXAMPLE 109)

Using General Procedure 5 starting from Preparation R4ar and Preparation R5b as reagents, after chiral separation, EXAMPLE 109 was obtained. HRMS calculated for C29H29F5N4O5: 608.2058; found 609.2125 ((M+H) ⁺ form). 5-amino-6-(4-chloro-3-hydroxyphenoxy)-3-({l-[(l/?,2/?)-4,4-d ifluoro-2- phenylcyclohexane- 1 -carbonyl ]-4-hydroxypiperidin-4-yl}methyl)pyrimidin-4(3//)-one (EXAMPLE 110)

Using General Procedure 5 starting from Preparation R4bt and Preparation R5a as reagents, to give 5-amino-6-(3-benzyloxy-4-chloro-phenoxy)-3-[[l-[(lR,2R)-4,4- difluoro- 2-phenyl-cyclohexanecarbonyl]-4-hydroxy-4-piperidyl]methyl]p yrimidin-4-one as a crude product. Autoclave was charged with 5-amino-6-(3-benzyloxy-4-chloro-phenoxy)-3-[[l- [(lR,2R)-4,4-difluoro-2-phenyl-cyclohexanecarbonyl]-4-hydrox y-4-piperidyl]methyl] pyrimidin-4-one (93 mg, 0.137 mmol) 10 % palladium on charcoal (15 mg) and l,4-dioxane (3 mL), and then placed under a nitrogen atmosphere. After that it was filled with 10 bar ¾ gas. The reaction mixture was stirred in autoclave at r.t. for 21 hours. The catalyst was washed with methanol and filtered off. The mother liquor was purified by Hanbon preparative HPLC, Cl 8 Silica, Gemini NX 5 pm, 5 mM MUHCCU-MeCN using gradient method 5-90 %. Solvent was evaporated under reduced pressure to give EXAMPLE 110. HRMS calculated for C29H31CIF2N4O5: 588.1951; found 589.2011 ((M+H) ⁺ form). 5-amino-3-({l-[(l/?,2/?)-4,4-difluoro-2-phenylcyclohexane-l- carbonyl]-4- hydroxypiperidin-4-yl}methyl)-6-(3-hydroxy-4-methylphenoxy)p yrimidin-4(3//)-one (EXAMPLE 111)

Using General Procedure 5 starting from Preparation R4bu and Preparation R5a as reagents, to give 5-amino-6-(3-benzyloxy-4-methyl-phenoxy)-3-[[l-[(lR,2R)-4,4- difluoro- 2-phenyl-cyclohexanecarbonyl]-4-hydroxy-4-piperidyl]methyl]p yrimidin-4-one as a crude product. Autoclave was charged with 5-amino-6-(3-benzyloxy-4-methyl-phenoxy)-3-[[l- [(lR,2R)-4,4-difluoro-2-phenyl-cyclohexanecarbonyl]-4-hydrox y-4-piperidyl]methyl] pyrimidin-4-one (85 mg, 0.129 mmol) 10 % palladium on charcoal (14 mg) and l,4-dioxane (3 mL), and then placed under a nitrogen atmosphere. After that it was filled with 10 bar ¾ gas. The reaction mixture was stirred in autoclave at r.t. for 21 hours. The catalyst was washed with methanol and filtered off. The mother liquor was purified by Hanbon HPLC, Cl 8 Silica, Gemini NX 5 pm, 5 mM MLHCCL-MeCN using gradient method 5-90 %. Solvent was evaporated under reduced pressure to give EXAMPLE 111. HRMS calculated for C30H34F2N4O5: 568.2498; found 569.2569 ((M+H) ⁺ form). 5-amino-3-({l-[(l/f,2/f)-4,4-difluoro-2-phenylcyclohexane-l- carbonyl]-4- hydroxypiperidin-4-yl}methyl)-6-{4-[2-(piperidin-4-yl)ethyl] phenoxy}pyrimidin- 4(3//)-one (EXAMPLE 112)

Using General Procedure 5 starting from Preparation R4bv and Preparation R5a as reagents, tert-butyl 4-[2-[4-[5-amino-l-[[l-[(lR,2R)-4,4-difluoro-2-phenyl- cyclohexanecarbonyl]-4-hydroxy-4-piperidyl]methyl]-6-oxo-pyr imidin-4-yl]oxyphenyl] ethyl]piperidine-l-carboxylate was formed. The resulted Boc-protected crude product was reacted using General Procedure 7. It was purified by Hanbon preparative HPLC, C18 Silica, Gemini NX 5 pm, 5 mM NH ₄ HC03-MeCN using gradient method 5-90 %. Solvent was evaporated under reduced pressure to give to EXAMPLE 112. HRMS calculated for C36H45F2N5O4: 649.3439; found 650.3496 ((M+H) ⁺ form). 5-amino-3-({l-[(l/?,2/?)-4,4-difluoro-2-phenylcyclohexane-l- carbonyl]-4- hydroxypiperidin-4-yl}methyl)-6-{4-[(morpholin-4-yl)methyl]p henoxy}pyrimidin- 4(3//)-one (EXAMPLE 113)

Using General Procedure 5 starting from Preparation R4bw and Preparation R5a as reagents, EXAMPLE 113 was obtained. HRMS calculated for C34H41F2N5O5: 637.3076; found 638.31482 ((M+H) ⁺ form). 5-amino-3-({l-[(l/?,2/?)-4,4-difluoro-2-phenylcyclohexane-l- carbonyl]-4- hydroxypiperidin-4-yl}methyl)-6-{4-[2-(piperidin-2-yl)ethyl] phenoxy}pyrimidin- 4(3//)-one (EXAMPLE 114)

Using General Procedure 5 starting from Preparation R4bx and Preparation R5a as reagents, tert-butyl 2-[2-[4-[5-amino-l-[[l-[(lR,2R)-4,4-difluoro-2-phenyl- cyclohexanecarbonyl]-4-hydroxy-4-piperidyl]methyl]-6-oxo-pyr imidin-4-yl]oxyphenyl] ethyl]piperidine-l-carboxylate was formed. The resulted Boc-protected crude product was reacted using General Procedure 7. It was purified by Hanbon preparative HPLC, C18 Silica, Gemini NX 5 pm, 5 mM NH ₄ HC03-MeCN using gradient method 5-90 %. Solvent was evaporated under reduced pressure to give to EXAMPLE 114. HRMS calculated for C36H45F2N5O4: 649.3439; found 650.3505 ((M+H) ⁺ form). 5-amino-3-({l-[(l/?,2/?)-4,4-difluoro-2-phenylcyclohexane-l- carbonyl]-4- hydroxypiperidin-4-yl}methyl)-6-[3-(morpholin-2-yl)phenoxy]p yrimidin-4(3//)-one (EXAMPLE 115)

Using General Procedure 5 starting from Preparation R4by and Preparation R5a as reagents, tert-butyl 2- [3 - [5 -amino- 1 - [ [ 1 - [( 1 R,2R)-4,4-difluoro-2-phenyl- cyclohexanecarbonyl]-4-hydroxy-4-piperidyl]methyl]-6-oxo-pyr imidin-4-yl]oxyphenyl] morpholine-4-carboxylate was formed. The resulted Boc-protected crude product was reacted using General Procedure 7. It was purified by Hanbon preparative HPLC, C18 Silica, Gemini NX 5 pm, 5 mM NH ₄ HC03-MeCN using gradient method 5-90 %. Solvent was evaporated under reduced pressure to give to EXAMPLE 115. HRMS calculated for C33H39F2N5O5: 623.2919; found 624.2990 ((M+H) ⁺ form). 5-amino-6-{4-[(l/?)-l-amino-2,2,2-trifluoroethyl]phenoxy}-3- ({l-[(l/?,2/?)-4,4- difluoro-2-phenylcyclohexane-l-carbonyl]-4-hydroxypiperidin- 4- yl}methyl)pyrimidin-4(3//)-one (EXAMPLE 116)

Using General Procedure 5 starting from Preparation R4bz and Preparation R5a as reagents, tert-butyl N-[(l R)- 1 -[4-[5-amino- 1 -[[ l-[(lR,2R)-4,4-difluoro-2-phenyl- cyclohexanecarbonyl]-4-hydroxy-4-piperidyl]methyl]-6-oxo-pyr imidin-4-yl]oxyphenyl]- 2, 2, 2-trifluoro-ethyl] carbamate was formed. The resulted Boc-protected crude product was reacted using General Procedure 7. It was purified by Hanbon preparative HPLC, C18 Silica, Gemini NX 5 pm, 5 mM NH ₄ HC03-MeCN using gradient method 5-90 %. Solvent was evaporated under reduced pressure to give to EXAMPLE 116. HRMS calculated for C31H34F5N5O4: 635.2531; found 636.26 ((M+H) ⁺ form). (4-{[5-amino-l-({l-[(l/?,2/?)-4,4-difluoro-2-phenylcyclohexa ne-l-carbonyl]-4- hydroxypiperidin-4-yl}methyl)-6-oxo-l,6-dihydropyrimidin-4- yl]oxy}phenyl)acetonitrile (EXAMPLE 117)

Using General Procedure 5 starting from Preparation R4ca and Preparation R5a as reagents, EXAMPLE 117 was obtained. HRMS calculated for C31H33F2N5O4 : 577.2501; found 578.2567 ((M+H) ⁺ form). 5-amino-3-({l-[(l/?,2/?)-4,4-difluoro-2-phenylcyclohexane-l- carbonyl]-4- hydroxypiperidin-4-yl}methyl)-6-[4-fluoro-3-(hydroxymethyl)p henoxy]pyrimidin- 4(3//)-one (EXAMPLE 118)

Using General Procedure 5 starting from Preparation R4cb and Preparation R5a as reagents, EXAMPLE 118 was obtained. HRMS calculated for C30H33F3N4O5 : 586.2403; found 587.2473 ((M+H) ⁺ form). 5-amino-6-(3-amino-4-fluorophenoxy)-3-({l-[(l/?,2/?)-4,4-dif luoro-2- phenylcyclohexane- 1 -carbonyl ]-4-hydroxypiperidin-4-yl}methyl)pyrimidin-4(3//)-one (EXAMPLE 119)

Using General Procedure 5 starting from Preparation R4cc and Preparation R5a as reagents, EXAMPLE 119 was obtained. HRMS calculated for C29H32F3N5O4 : 571.2407; found 572.2477 ((M+H) ⁺ form). 5-amino-3-({l-[(l/?,2/?)-4,4-difluoro-2-phenylcyclohexane-l- carbonyl]-4- hydroxypiperidin-4-yl}methyl)-6-[3-hydroxy-4-(propan-2-yl)ph enoxy]pyrimidin- 4(3//)-one (EXAMPLE 120)

Using General Procedure 5 starting from Preparation R4cd and Preparation R5a as reagents, EXAMPLE 120 was obtained. HRMS calculated for C32H38F2N4O5: 596.281; found 597.2883 ((M+H) ⁺ form). 5-amino-3-({l-[(l/f,2/f)-4,4-difluoro-2-phenylcyclohexane-l- carbonyl]-4- hydroxypiperidin-4-yl}methyl)-6-[4-(piperidin-2-yl)phenoxy]p yrimidin-4(3//)-one (EXAMPLE 121)

Using General Procedure 5 starting from Preparation R4ce and Preparation R5a as reagents, tert-butyl 2-[4-[5-amino- 1 -[[ 1 -[(lR,2R)-4,4-difluoro-2-phenyl-cyclo hexane carbonyl]-4-hydroxy-4-piperidyl]methyl]-6-oxo-pyrimidin-4-yl ]oxyphenyl]piperidine-l- carboxylate was formed. The resulted Boc-protected crude product was reacted using General Procedure 7 and the crude was purified by Hanbon preparative HPLC, C18 Silica, Gemini NX 5 pm, 5 mM NH ₄ HC03-MeCN using gradient method 5-90 %. Solvent was evaporated under reduced pressure to give to EXAMPLE 121. HRMS calculated for C34H41F2N5O4: 621.3127; found 622.3203 ((M+H) ⁺ form). 5-amino-3-({l-[(lR,2R,4S)-4-ethynyl-4-fluoro-2-phenylcyclohe xanecarbonyl]-4- hydroxypiperidin-4-yl}methyl)-6-(4-fluorophenoxy)-3,4-dihydr opyrimidin-4-one (EXAMPLE 122)

and

5-amino-3-({l-[(lR,2R,4R)-4-ethynyl-4-fluoro-2-phenylcyclohe xanecarbonyl]-4- hydroxypiperidin-4-yl}methyl)-6-(4-fluorophenoxy)-3,4-dihydr opyrimidin-4-one (EXAMPLE 123)

Step 1: Ethyl (1R,2R) -4 -oxo -2 -phenylcyclohexane-1 -carboxylate (El) and ethyl ( JS,2S) -4 - oxo -2 -phenylcydohexane -I -carboxylate (E2)

The enantiomers of rel-ethyl (lR,2R)-4-oxo-2-phenylcyclohexane-l -carboxylate were separated via chiral chromatography (Column: IA, Eluents: heptane / DCM). The enantiomer eluting earlier was collected as El with 99.8 % ee and the enantiomer eluting later was collected as E2 with 99.9 % ee.

Step 2: Ethyl ( I R,2R, 4Rj -4 -hydroxy -2 -phenyl -4 -[2 -( trimethylsilyljethynyl ] cyclohexane -I - carboxylate

To a solution of diisopropylamine (0.4 mL, 2.84 mmol, 1.4 eq.) in THF (10 mL), was added n-butyl lithium (2.5M in hexane, 1.15 mL, 2.74 mmol, 1.35 eq.) dropwise at -78 °C under nitrogen. The reaction mixture was stirred for 10 minutes before adding (trimethylsilyl)acetylene (0.37 mL, 2.64 mmol, 1.3 eq.) in THF (2 mL) dropwise. After 5 minutes, a solution of El (500 mg, 2.03 mmol) in THF (3 mL) was added dropwise and stirring continued at -78 °C for 4 hours. The reaction mixture was quenched with aq. NH ₄ Cl solution (10 mL). The aqueous layer was extracted with EtOAc (20 mL), dried (MgS0 ₄ ) and concentrated in vacuo. The residue was purified via flash chromatography using Heptane- 15 % EtO Ac/Heptane (gradient) as eluent to afford ethyl (lR,2R,4R)-4- hydroxy-2-phenyl-4-[2-(trimethylsilyl)ethynyl]cyclo hexane- 1 -carboxylate as a colourless oil. The compound was used without further purification.

1H NMR (399 MHz, Chloroform-^) d 7.21-7.01 (m, 5H), 3.83-3.66 (m, 2H), 3.04 (ddd, J = 12.9, 11.4, 3.2 Hz, 1H), 2.42-2.32 (m, 1H), 2.02-1.78 (m, 4H), 1.63 (t, J = 12.8 Hz, 1H), 1.51 (td, J= 12.5, 4.9 Hz, 1H), 0.82 (td, j= 7.1, 2.3 Hz, 3H), 0.10 (s, 9H).

Step 3: Ethyl ( I R,2R, 4R) -4 -ethynyl -4 -hydroxy -2 -pheny /cyclohexane -I -carboxylate

Starting from ethyl (li?,27?,47?)-4-hydroxy-2-phenyl-4-[2-(trimethylsilyl)ethyny l] cyclohexane- 1 -carboxylate (970 mg, 2.82 mmol) following procedure described in Step 2 of EXAMPLE 91, the obtained residue was purified via flash chromatography using Heptane-40 % EtO Ac/Heptane (gradient) as eluent to afford ethyl (li?,27?,47?)-4-ethynyl-4- hydroxy-2-phenylcyclo hexane- 1 -carboxylate as a colourless oil.

1H NMR (399 MHz, Chloroform-^) d 7.37-7.13 (m, 5H), 3.90 (q, J = 7.1 Hz, 2H), 3.21 (ddd, J = 13.0, 11.5, 3.3 Hz, 1H), 2.67 (s, 1H), 2.56 (td, j = 11.5, 4.4 Hz, 1H), 2.28-2.13 (m, 2H), 2.12-1.96 (m, 2H), 1.82 (t, j = 12.9 Hz, 1H), 1.70 (td, j = 12.7, 4.6 Hz, 1H), 0.96 (t, j= l.\ Hz, 3H).

Step 4: Ethyl ( I R, 2 R) -4 -ethynyl -4 -fluoro -2 -pheny /cyclohexane -I -carboxylate To a solution of triethylamine trihydrofluoride (0.74 mL, 4.55 mmol, 2.0 eq.) in DCM (12 mL), was added triethylamine (0.32 mL, 2.28 mmol, 1.0 eq.) at -78 °C under nitrogen. XtalFluor-M® (830 mg, 3.41 mmol, 1.5 eq.) and a solution of ethyl (lR,2R,4R)-4-ethynyl- 4-hydroxy-2-phenylcyclohexane-l-carboxylate (620 mg, 2.28 mmol, 1.0 eq.) in DCM (12 mL) were then added sequentially. The reaction mixture was stirred at the same temperature for 1 hour before being allowed to warm to r.t. overnight. The mixture was quenched with 5 % aq. NaHCCL solution (40 mL) and stirred for 15 minutes. DCM (50 mL) was added and the organic layer was separated, dried (MgS0 ₄ ) and evaporated in vacuo. The residue was purified via flash chromatography using Heptane-5 % EtOAc/Heptane (gradient) as eluent to afford the ethyl (lR,2R)-4-ethynyl-4-fluoro-2- phenylcyclohexane-l-carboxylate as a colourless oil.

1H NMR (399 MHz, Chloroform-^) d 7.38-7.11 (m, 5H), 3.90 (qd, J = 7.1, 1.6 Hz, 2H), 3.21 (tdd, J= 16.9, 12.4, 3.3 Hz, 1H), 2.90-2.52 (m, 2H), 2.50-2.30 (m, 2H), 2.25-1.69 (m, 4H), 0.96 (td, J= 7.1, 2.8 Hz, 3H).

Step 5: ( 1 R, 2 R) -4 -ethynyl -4 -fluoro -2 -pheny /cyclohexane -/ -carboxylic acid

To a solution of ethyl (lR,2R)-4-ethynyl-4-fluoro-2-phenylcyclohexane-l-carboxylate (385 mg, 1.4 mmol) in THF (4 mL), methanol (2 mL) and water (1 mL), was added lithium hydroxide monohydrate (353 mg, 8.42 mmol, 6.0 eq.) and the mixture was stirred at r.t. for 72 hours. The reaction mixture was concentrated in vacuo, water (10 mL) was added and the mixture was acidified to pH 3 using 1 2N HC1 (7 mL). The aqueous layer was extracted with EtOAc (50 mL), dried (MgS0 ₄ ) and evaporated in vacuo to afford (lR,2R)-4-ethynyl- 4-fluoro-2-phenylcyclo hexane- 1 -carboxylic acid as a colourless oil. The compound was used without further purification.

1H NMR (399 MHz, DMSO- ) d 12.01 (s, 1H), 7.38-7.07 (m, 5H), 4.13-3.84 (m, 1H), 2.97 (ddd, J = 11.6, 8.9, 4.7 Hz, 1H), 2.84-2.59 (m, 1H), 2.27-1.82 (m, 5H), 1.82-1.63 (m, 1H).

Step 6: EXAMPLE 122 and EXAMPLE 123

Starting from (lR,2R)-4-ethynyl-4-fluoro-2-phenylcyclohexane-l -carboxylic acid (350 mg, 1.42 mmol) and 5-amino-6-(4-fluorophenoxy)-3-[(4-hydroxypiperidin-4-yl) methyl]pyrimidin-4-one (475 mg, 1.42 mmol) following procedure described in Step 3 of EXAMPLE 94, the obtained residue was purified via flash chromatography using DCM-5 % MeOH/DCM (gradient) as eluent to afford the products a mixture of diastereoisomers. Final purification via prep HPLC (Prep HPLC Column: Gemini pH 4 Dimensions: 21.1 mm x 150 mm 5 pm) gave:

First elute: EXAMPLE 122 as a white solid.

LC/MS (Method B): RT = 1.18; m/z = 563 [M+H] ⁺

1H NMR (399 MHz, DMSO- ) d 7.59 (m, 1H), 7.35-7.13 (m, 7H), 7.09 (ddd, J= 9.1, 4.6, 2.3 Hz, 2H), 4.82 (d, J = 7.3 Hz, 1H), 4.69 (d, J= 14.1 Hz, 2H), 3.99-3.58 (m, 5H), 3.33- 3.02 (m, 3H), 2.97-2.57 (m, 1H), 2.28-1.88 (m, 4H), 1.85-1.53 (m, 2H), 1.49-1.06 (m, 3H), 0.68 (dtd, J= 44.2, 12.9, 4.4 Hz, 1H).

HRMS (TOF, ESI) m/z: Calculated for C31H32F2N4O4 562.2392, Found: 563.2490 [M+H] ⁺ Second elute: EXAMPLE 123 as a white solid.

LC/MS (Method B): RT = 1.19; m/z = 563 [M+H] ⁺

1H NMR (399 MHz, DMSO- ) d 7.59 (m, 1H), 7.39-6.99 (m, 9H), 4.81 (d, J = 7.2 Hz, 1H), 4.69 (d, J = 14.6 Hz, 2H), 4.09-3.77 (m, 3H), 3.75-3.57 (m, 2H), 3.26-3.01 (m, 3H),

2.92-2.56 (m, 1H), 2.35-1.89 (m, 4H), 1.80 (d, J = 14.3 Hz, 2H), 1.50-1.05 (m, 3H), 0.64 (dtd, J= 81.7, 13.0, 4.4 Hz, 1H).

HRMS (TOF, ESI) m/z: Calculated for C31H32F2N4O4 562.2392, Found: 563.2507 [M+H] ⁺ rel-5-amino-3-[(l-{[(lR,2R)-4-(2-cyclopropylethynyl)-4-fluor o-2- phenylcyclohexyl]carbonyl}-4-hydroxypiperidin-4-yl)methyl]-6 -(4- fluorophenoxy)pyrimidin-4-one (EXAMPLE 124)

Step 1: rel-ethyl (lR,2R,4R)-4-(2-cyclopropylethynyl)-4-hydroxy-2-phenylcycloh exane-l- carboxylate

Starting from rel-ethyl (lR,2R)-4-oxo-2-phenylcyclo hexane- 1 -carboxylate (500 mg, 2.03 mmol) and ethynylcyclopropane (0.22 ml, 2.64 mmol, 1.3 eq.) following procedure described in Step 2 of EXAMPLES 122 and 123, the obtained residue was purified via flash chromatography using Heptane-25 % EtOAc/Heptane (gradient) as eluent to afford rel- ethyl ( 1 R,2R,4R)-4-(2-cyclopropylethynyl)-4-hydroxy-2-phenylcyclo hexane- 1 -carboxylate as a colourless oil. 1H NMR (399 MHz, Chloroform-^/) d 7.34-7.25 (m, 2H), 7.25-7.17 (m, 3H), 3.90 (q, J = 7.1 Hz, 2H), 3.16 (ddd, J = 13.0, 11.5, 3.3 Hz, 1H), 2.53 (td, J = 11.5, 4.4 Hz, 1H), 2.16- 1.87 (m, 4H), 1.78 (t , J= 12.8 Hz, 1H), 1.71-1.61 (m, 1H), 1.41-1.24 (m, 1H), 0.96 (t , J = 7.1 Hz, 3H), 0.91-0.72 (m, 4H).

Step 2: rel-ethyl (lR,2R)-4-(2-cyclopropylethynyl)-4-fluoro-2-phenylcyclohexan e-l- carboxylate

Starting from rel-ethyl (lR,2R,4R)-4-(2-cyclopropylethynyl)-4-hydroxy-2-phenyl cyclohexane- l-carboxylate (233 mg, 0.96 mmol) following procedure described in Step 4 of EXAMPLES 122 and 123, rel-ethyl (lR,2R)-4-(2-cyclopropylethynyl)-4-fluoro-2- phenylcyclo hexane- l-carboxylate (157 mg, 0.5 mmol, 78%) was obtained as a colourless oil.

1H NMR (399 MHz, Chloroform-^/) d 7.35-7.25 (m, 2H), 7.27-7.17 (m, 3H), 3.90 (qd, J = 7.1, 3.8 Hz, 2H), 3.26-3.09 (m, 1H), 2.68-2.51 (m, 1H), 2.43-2.21 (m, 2H), 2.15-1.68 (m, 4H), 1.42-1.27 (m, 1H), 0.96 (t, J= 7.1 Hz, 3H), 0.92-0.69 (m, 5H).

Step 3: reI-( I R, 2 R)-4-(2-cyc/opropy/ethyny/)-4 fluoro-2-pheny /cyclohexane- 1 -carboxylic acid

Starting from rel-ethyl (lR,2R,4R)-4-(2-cyclopropylethynyl)-4-hydroxy-2-phenyl cyclohexane- l-carboxylate (255 mg, 0.81 mmol) following procedure described in Step 5 of EXAMPLES 122 and 123, rel-(lR,2R)-4-(2-cyclopropylethynyl)-4-fluoro-2- phenylcyclo hexane- 1 -carboxylic acid was obtained as a colourless oil. The compound was used without further purification.

LC/MS (Method B): RT = 1.29; m/z = 285 [M-H]-

Step 4: EXAMPLE 124

Starting from 5 -amino-6-(4-fluorophenoxy)-3 - [(4-hydroxypiperidin-4-yl)methyl] pyrimidin-4-one (140 mg, 0.42 mmol) and rel-(lR,2R)-4-(2-cyclopropylethynyl)-4-fluoro- 2 -phenylcyclo hexane- 1 -carboxylic acid (274 mg) following procedure described in Step 3 of EXAMPLE 94, the obtained residue was purified via flash chromatography using Hexane- 100 % EtO Ac/Hexane (gradient) as eluent to give the crude product as a white solid. Final purification via prep HPLC (Prep HPLC Column: Gemini pH 4 Dimensions: 21.1 mm x 150 mm 5 pm) afforded the desired product as a white solid.

LC/MS (Method B): RT = 1.28; m/z = 603 [M+H] ⁺

1H NMR (399 MHz, DMSO- ) d 7.65-7.53 (m, 1H), 7.34-7.13 (m, 7H), 7.09 (ddd, J = 9.0, 4.6, 2.1 Hz, 2H), 4.82 (d, J = 8.0 Hz, 1H), 4.69 (d, J = 13.9 Hz, 2H), 4.01-3.77 (m, 2H), 3.76-3.56 (m, 2H), 3.33-2.98 (m, 3H), 2.95-2.57 (m, 1H), 2.22-1.82 (m, 4H), 1.81- 1.53 (m, 2H), 1.52-1.03 (m, 4H), 0.94-0.47 (m, 5H).

HRMS (TOF, ESI) m/z: Calculated for C34H36F2N4O4 602.2705 Found: 603.2729 [M+H] ⁺ rel-5-amino-3-[(l-{[(lR,2R)-4-fluoro-2-phenyl-4-(prop-l-yn-l - yl)cyclohexyl]carbonyl}-4-hydroxypiperidin-4-yl)methyl]-6-(4 - fluorophenoxy)pyrimidin-4-one (EXAMPLE 125)

Step 1: rel-ethyl (lR,2R,4R)-4-hydroxy-2-phenyl-4-(prop-l-yn-l-yl)cyclohexane- l- carboxylate

Starting from rel-ethyl (lR,2R)-4-oxo-2-phenylcyclo hexane- 1 -carboxylate (500 mg, 2.03 mmol) and propyne (2.64 mL, 1M in THF, 2.64 mmol, 1.3 eq.), following procedure described in Step 2 of EXAMPLES 122 and 123, the obtained residue was purified via flash chromatography using Heptane-30 % EtO Ac/Heptane (gradient) as eluent to afford rel- ethyl (lR,2R,4R)-4-hydroxy-2-phenyl-4-(prop-l-yn-l-yl)cyclo hexane- 1 -carboxylate as a colourless oil.

1H NMR (399 MHz, Chloroform-^/) d 7.35-7.14 (m, 5H), 3.90 (q, J = 7.1 Hz, 2H), 3.17 (ddd, J = 12.9, 11.4, 3.3 Hz, 1H), 2.54 (td, J = 11.4, 4.6 Hz, 1H), 2.25-1.96 (m, 4H), 1.95 (s, 1H), 1.78 (t, J= 12.8 Hz, 1H), 1.72-1.60 (m, 3H), 0.95 (t , J= 7.1 Hz, 3H).

Step 2: rel-ethyl (lR,2R)-4-fluoro-2-phenyl-4-(prop-l-yn-l-yl)cyclohexane-l-ca rboxylate Starting from rel-ethyl (lR,2R,4R)-4-hydroxy-2-phenyl-4-(prop-l-yn-l-yl)cyclo hexane- 1- carboxylate (360 mg, 1.26 mmol) following procedure described in Step 4 of EXAMPLES 122 and 123, rel-ethyl (lR,2R)-4-fluoro-2-phenyl-4-(prop-l-yn-l- yl)cyclo hexane- 1 -carboxylate was obtained as a colourless oil. 1H NMR (399 MHz, Chloroform-^) d 7.36-7.15 (m, 5H), 3.90 (qd, J = 7.1, 2.5 Hz, 2H), 3.28-3.08 (m, 1H), 2.68-2.51 (m, 1H), 2.44-2.23 (m, 2H), 2.17-1.69 (m, 7H), 0.96 (td, J =

7.1, 3.8 Hz, 3H).

Step 3: rel-(lR,2R)-4-fluoro-2-phenyl-4-(prop-l-yn-l-yl)cyclohexane- l-carboxylic acid Starting from rel-ethyl (lR,2R)-4-fluoro-2-phenyl-4-(prop-l-yn-l-yl)cyclo hexane- 1- carboxylate (280 mg, 0.97 mmol) following procedure described in Step 5 of EXAMPLES 122 and 123, rel-(lR,2R)-4-fluoro-2-phenyl-4-(prop-l-yn-l-yl)cyclo hexane- 1- carboxylic acid was obtained as a colourless oil. The compound was used without further purification.

LC/MS (Method B): RT = 1.20; m/z = 259 [M-H]-

1H NMR (399 MHz, DMSO- ) d 11.97 (s, 1H), 7.34-7.15 (m, 5H), 3.03-2.92 (m, 1H), 2.80-2.60 (m, 1H), 2.13-1.83 (m, 8H), 1.76 (m, 1H)

Step 4: EXAMPLE 125

Starting from 5 -amino-6-(4-fluorophenoxy)-3 - [(4-hydroxypiperidin-4-yl)methyl] pyrimidin-4-one (154 mg, 0.46 mmol) and rel-(lR,2R)-4-fluoro-2-phenyl-4-(prop-l-yn-l- yl)cyclo hexane- 1 -carboxylic acid (120 mg) following procedure described in Step 3 of EXAMPLE 94, the obtained residue was purified via flash chromatography using DCM-5 % MeOH/DCM (gradient) as eluent to give the crude product as a white solid. Final purification via prep HPLC (Prep HPLC Column: Gemini pH 4 Dimensions: 21.1 mm x 150 mm 5 pm) afforded the desired product as a white solid.

LC/MS (Method B): RT = 1.22; m/z = 577 [M+H] ⁺

1H NMR (399 MHz, DMSO- ) d 7.64-7.54 (m, 1H), 7.35-7.13 (m, 7H), 7.09 (ddd, J =

9.1, 4.6, 2.3 Hz, 2H), 4.82 (d, J = 8.2 Hz, 1H), 4.69 (d, J = 14.0 Hz, 2H), 3.99-3.56 (m, 4H), 3.30-3.00 (m, 3H), 2.95-2.55 (m, 1H), 2.25-2.00 (m, 3H), 2.00-1.91 (m, 2H), 1.87 (dd, J = 6.0, 2.6 Hz, 1H), 1.60 (t, j = 14.9 Hz, 2H), 1.48-1.24 (m, 1H), 1.12 (d, j = 13.0 Hz, 2H), 0.73 (dq, J= 12.1, 5.8, 4.9 Hz, 1H), 0.57 (q, j= 12.1, 11.3 Hz, 1H).

HRMS (TOF, ESI) m/z: Calculated for C32H34F2N4O4 576.2548, Found: 577.2656 [M+H] ⁺ rel-5-amino-3-[(l-{[(lR,2R,4S)-4-fluoro-2-phenyl-4-(pyridin- 2- ylmethyl)cyclohexyl]carbonyl}-4-hydroxypiperidin-4-yl)methyl ]-6-(4- fluorophenoxy)pyrimidin-4-one (EXAMPLE 126)

Step 1: rel-ethyl (I R,2R, 4S) -4 -fluoro -2 -phenyl -4 -[( py riel in -2 -y l ) methyl ] cyclohexane -/ - carboxylate

Starting from rel-ethyl (lR,2R)-4-hydroxy-2-phenyl-4-[(pyridin-2-yl)methyl]cyclo hexane- 1 -carboxylate (obtained according to Step 1 of EXAMPLE 96; 230 mg, 0.68 mmol) following procedure described in Step 4 of EXAMPLES 122 and 123, rel-ethyl (lR,2R,4S)- 4-fluoro-2-phenyl-4-[(pyridin-2-yl)methyl]cyclohexane-l -carboxylate was obtained as a colourless oil.

1H NMR (399 MHz, Chloroform-^) d 8.53 (ddd, J= 4.9, 1.9, 0.9 Hz, 1H), 7.64 (td, J= 7.7, 1.8 Hz, 1H), 7.35-7.11 (m, 7H), 3.87 (q, J= 7.1 Hz, 2H), 3.29-3.05 (m, 2H), 2.64-2.48 (m, 1H), 2.15-1.87 (m, 4H), 1.82-1.53 (m, 2H), 0.94 (t , J= 7.1 Hz, 3H).

Step 2: rel-(lR,2R,4S)-4-fluoro-2-phenyl-4-(pyridin-2-ylmethyl)cyclo hexane-l-carboxylic acid

Starting from rel-ethyl (lR,2R)-4-fluoro-2-phenyl-4-(prop-l-yn-l-yl)cyclo hexane- 1- carboxylate (41 mg, 0.12 mmol) following procedure described in Step 5 of EXAMPLES 122 and 123, rel-(lR,2R,4S)-4-fluoro-2-phenyl-4-(pyridin-2-ylmethyl) cyclohexane- 1 -carboxylic acid was obtained as an off- white solid. The compound was used without further purification.

LC/MS (Method B): RT = 0.92; m/z = 314 [M+H] ⁺

Step 3: EXAMPLE 126

Starting from 5 -amino-6-(4-fluorophenoxy)-3 - [(4-hydroxypiperidin-4-yl)methyl] pyrimidin-4-one (37 mg, 0.11 mmol) and rel-(lR,2R,4S)-4-fluoro-2-phenyl-4-(pyridin-2- y lmethyl)cyclo hexane- 1 -carboxylic acid (35 mg) following procedure described in Step 3 of EXAMPLE 94, the obtained residue was purified via flash chromatography using EtOAc- 10 % MeOH/EtOAc (gradient) as eluent to give the crude product as a colourless oil. Final purification via prep HPLC (Prep HPLC Column: Gemini pH 4 Dimensions: 21.1 mm x 150 mm 5 pm) afforded the desired product as a yellow solid. LC/MS (Method B): RT = 1.08; m/z = 630 [M+H] ⁺

1H NMR (399 MHz, DMSO- ) d 8.49 (ddd, J= 4.9, 1.9, 1.0 Hz, 1H), 7.72 (tt, J= 7.7, 1.6 Hz, 1H), 7.59 (m, 1H), 7.35-7.04 (m, 11H), 4.81 (d, = 8.4 Hz, 1H), 4.68 (d, J= 11.7 Hz, 2H), 3.98-3.60 (m, 4H), 3.23-2.82 (m, 4H), 2.73-2.56 (m, 1H), 1.97-1.50 (m, 6H), 1.48- 1.05 (m, 4H), 0.80-0.59 (m, 1H).

HRMS (TOF, ESI) m/z: Calculated for C35H37F2N5O4 629.2814, Found: 630.2876 [M+H] ⁺ rel-5-amino-3-[(l-{[(lR,2R)-4-fluoro-4-methyl-2-phenylcycloh exyl]carbonyl}-4- hydroxypiperidin-4-yl)methyl] -6-(4-fluorophenoxy)pyrimidin-4-one (EXAMPLE 127)

Step 1: rel-ethyl ( lR,2R,4S)-4-hydroxy-4-methyl-2-phenylcyclohexane-l-carboxyla te and rel-ethyl ( JR , 2R, 4R)-4-hydroxy-4-methyl-2-phenylcyclohexane-l-carboxylate

To a N ₂ flushed flask containing cerium(III) chloride (840.59 mg, 3.41 mmol, 2.8 eq.), anhydrous THF (6 mF) was added and the suspension cooled to 0 °C. Methylmagnesium bromide solution (1.14 mF, 3M in THF, 3.41 mmol, 2.8 eq.) was then added slowly dropwise. After addition was complete, the mixture was stirred at 0 °C for 90 minutes. rel-ethyl (lR,2R)-4-oxo-2-phenylcyclohexane-l-carboxylate (300 mg, 1.22 mmol, 1.0 eq.) dissolved in THF (2 mF) was then added dropwise and stirred for 2 hours. The reaction mixture was poured onto ice/water and acetic acid was added (0.2 mF). The mixture was extracted EtOAc (30 mF), dried (MgS0 ₄ ) and evaporated in vacuo to afford a crude oil. The residue was purified via flash chromatography using heptane-69 % EtO Ac/Heptane (gradient) as eluent to afford:

First elute: rel-ethyl ( 1 R,2R,4S)-4-hydroxy-4-methyl-2-phenylcyclohexane- 1 -carboxylate 1H NMR (399 MHz, DMSO- ) d 7.33-7.06 (m, 5H), 4.28 (s, 1H), 3.78 (q, J = 7.1 Hz, 2H), 3.12 (td, j= 12.0, 3.9 Hz, 1H), 2.51 (d, j= 1.9 Hz, 1H), 1.97-1.79 (m, 1H), 1.73-1.33 (m, 5H), 1.13 (s, 3H), 0.85 (t, j= 7.1 Hz, 3H).

Second elute: rel-ethyl (lR,2R,4R)-4-hydroxy-4-methyl-2-phenylcyclohexane-l- carboxylate

1H NMR (399 MHz, DMSO- ) d 7.33-7.10 (m, 5H), 4.54 (s, 1H), 3.79 (q, J = 7.1 Hz, 2H), 2.78 (ddd, J = 11.5, 9.6, 7.0 Hz, 1H), 2.51 (d, J = 1.9 Hz, 1H), 1.95-1.83 (m, 1H), 1.68-1.37 (m, 5H),l27 1.24 (s, 3H), 0.84 (t, j= 7.1 Hz, 3H). Step 2: rel-ethyl (lR,2R)-4-fluoro-4-methyl-2-phenylcyclohexane-l-carboxylate

Starting from rel-ethyl (lR,2R)-4-hydroxy-4-methyl-2-phenylcyclo hexane- l-carboxylate (192 mg, 0.73 mmol) following the procedure described in Step 4 of EXAMPLES 122 and 123, rel-ethyl (lR,2R)-4-fluoro-4-methyl-2-phenylcyclo hexane- l-carboxylate was obtained as a colourless oil.

1H NMR (399 MHz, Chloroform-^) d 7.35-7.26 (m, 3H), 7.26-7.17 (m, 2H), 3.95-3.84 (m, 2H), 3.33-2.83 (m, 1H), 2.67-2.49 (m, 1H), 2.20-1.62 (m, 5H), 1.57-1.46 (m, 1H), 1.40 (d, J= 21.1 Hz, 3H), 0.96 (dt, J= 7.8, 7.1 Hz, 3H).

Step 3: rel-(lR,2R)-4-fluoro-4-methyl-2-phenylcyclohexane-l-carboxyl ic acid

Starting from rel-ethyl (lR,2R)-4-fluoro-4-methyl-2-phenylcyclo hexane- l-carboxylate (100 mg, 0.38 mmol) following procedure described in Step 5 of EXAMPLES 122 and 123, re l-(lR,2R)-4-fluoro-4-methyl-2-phenylcyclo hexane- 1 -carboxylic acid was obtained as a colourless oil. The compound was used without further purification.

1H NMR (399 MHz, DMSO- ) d 11.97 (s, 1H), 7.44-6.91 (m, 5H), 3.09-2.52 (m, 2H), 2.04-1.56 (m, 6H), 1.55-1.27 (m, 3H)

Step 3: EXAMPLE 127

Starting from 5 -amino-6-(4-fluorophenoxy)-3 - [(4-hydroxypiperidin-4-yl)methyl] pyrimidin-4-one (67 mg, 0.2 mmol) and rel-(lR,2R)-4-fluoro-4-methyl-2- phenylcyclo hexane- 1 -carboxylic acid (95 mg) following procedure described in Step 3 of EXAMPLE 94, the obtained residue was purified via flash chromatography using DCM-5 % MeOH/DCM (gradient) as eluent to give the desired product as a white solid.

LC/MS (Method B): RT = 1.19; m/z = 553 [M+H] ⁺

1H NMR (399 MHz, DMSO-d ₆ ) d 7.59 (m, 1H), 7.34-7.05 (m, 9H), 4.81 (dd, J = 9.0, 2.5 Hz, 1H), 4.68 (d, J = 12.7 Hz, 2H), 4.00-3.78 (m, 2H), 3.77-3.56 (m, 2H), 3.15-3.02 (m, 2H), 2.92 (t , J= 13.6 Hz, 1H), 2.72-2.58 (m, 1H), 2.18-1.01 (m, 12H), 0.82-0.46 (m, 1H).

HRMS (TOF, ESI) m/z: Calculated for C30H34F2N4O4 552.2548, Found: 553.2574 [M+H] ⁺ 5-amino-3-[(l-{[(lS,2S,4R)-4-ethynyl-4-fluoro-2-phenylcycloh exyl]carbonyl}-4- hydroxypiperidin-4-yl)methyl] -6-(4-fluorophenoxy)pyrimidin-4-one (EXAMPLE 128) and 5-amino-3-[(l-{[(lS,2S,4S)-4-ethynyl-4-fluoro-2-phenylcycloh exyl]carbonyl}-4- hydroxypiperidin-4-yl)methyl] -6-(4-fluorophenoxy)pyrimidin-4-one (EXAMPLE 129)

Step 1: ethyl ( I S, 2 S, 4R)-4-hydroxy-2-pheny 1-4- [2-(trimethy Isi/y Ijethy yl] cyclohexane- 1 - carboxylate and ethyl ( lS,2S,4S)-4-hydroxy-2-phenyl-4-[2 - (trimethylsilyl)ethynyl] cyclohexane- 1-carboxy late

Starting from ethyl (lS,2S)-4-oxo-2-phenylcyclohexane-l-carboxylate (2.0 g, 8.12 mmol) and ethynyltrimethylsilane (1.24 ml, 8.93 mmol) following procedure described in Step 2 of EXAMPLES 122 and 123, the obtained residue was purified via flash chromatography using Heptane- 14 % EtO Ac/Heptane (gradient) as eluent to afford:

First elute: ethyl (1 S,2S,4R)-4-hydroxy-2-phenyl-4-[2-(trimethylsilyl)ethynyl]

cyclohexane- 1 -carboxylate obtained as a colourless oil.

1H NMR (399 MHz, Chloroform-^) d 7.31-6.92 (m, 5H), 3.73 (q, J = 7.1 Hz, 2H), 3.10 (ddd, J = 13.0, 11.6, 3.7 Hz, 1H), 2.44 (td, j = 11.7, 3.4 Hz, 1H), 2.09-1.56 (m, 6H), 1.12 (t, j= 7.1 Hz, 1H), 0.90-0.65 (m, 3H), 0.00 (s, 9H).

Second elute: ethyl (1 S,2S,4S)-4-hydroxy-2-phenyl-4-[2-(trimethylsilyl)ethynyl] cyclohexane- 1 -carboxylate obtained as a colourless oil. The compound was used without further purification.

1H NMR (399 MHz, Chloroform-^/) d 7.23-6.96 (m, 5H), 3.86-3.63 (m, 2H), 3.04 (ddd, j = 13.0, 11.5, 3.2 Hz, 1H), 2.50-2.26 (m, 1H), 2.09-1.77 (m, 4H), 1.63 (t, j = 12.8 Hz, 1H), 1.12 (t, j= 7.1 Hz, 1H), 0.82 (td, j= 7.1, 2.3 Hz, 3H), 0.10 (s, 9H).

Step 2: ethyl (lS,2S)-4-ethynyl-4-hydroxy-2-phenylcyclohexane-l-carboxylat e

Starting from ethyl (lS,2S)-4-hydroxy-2-phenyl-4-[2-(trimethylsilyl)ethynyl]cycl ohexane- 1 -carboxylate (2.05 g, 5.95 mmol) following procedure described in Step 2 of EXAMPLE 91, the obtained residue was purified via flash chromatography using Heptane- 30 % EtO Ac/Heptane (gradient) as eluent to afford ethyl (lS,2S)-4-ethynyl-4-hydroxy-2- phenylcyclo hexane- 1 -carboxylate as a pale yellow oil. The compound was used without further purification.

1H NMR (399 MHz, Chloroform-^/) d 7.44-7.14 (m, 5H), 4.02-3.80 (m, 2H), 3.21 (ddd, j = 13.0, 11.5, 3.3 Hz, 1H), 2.69-2.43 (m, 2H), 2.37-1.76 (m, 4H), 1.70 (td, j = 12.7, 4.5 Hz, 1H), 1.28 (t, j= 7.1 Hz, 1H), 1.04-0.80 (m, 3H). Step 3: ethyl (lS,2S)-4-ethynyl-4-fluoro-2-phenylcyclohexane-l-carboxylate Starting from ethyl (lS,2S)-4-ethynyl-4-hydroxy-2-phenylcyclohexane-l-carboxylat e (890 mg) following procedure described in Step 4 of EXAMPLES 122 and 123, ethyl (lS,2S)-4-ethynyl-4-fluoro-2-phenylcyclohexane-l-carboxylate was obtained as a colourless oil.

LC/MS (Method B): RT = 1.22; m/z = 275 [M+H] ⁺

Step 4: ( lS,2S)-4-ethynyl-4-fluoro-2-phenylcyclohexane-l-carboxylic acid

Starting from ethyl (lS,2S)-4-ethynyl-4-fluoro-2-phenylcyclohexane-l-carboxylate (300 mg, 1.09 mmol) following procedure described in Step 5 of EXAMPLES 122 and 123, (lS,2S)-4-ethynyl-4-fluoro-2-phenylcyclohexane-l-carboxylic acid was obtained as a colourless oil. The compound was used without further purification.

LC/MS (Method B): RT = 1.15; m/z = 245 [M-H]-

Step 5: EXAMPLE 128 and EXAMPLE 129

Starting from (lS,2S)-4-ethynyl-4-fluoro-2-phenylcyclohexane-l-carboxylic acid (100 mg) and 5-amino-6-(4-fluorophenoxy)-3-[(4-hydroxypiperidin-4-yl)meth yl]pyrimidin-4-one

(136 mg, 0.41 mmol) following procedure described in Step 3 of EXAMPLE 94, the obtained residue was purified via flash chromatography using DCM-5 % MeOH/DCM (gradient) as eluent to afford the products a mixture of diastereoisomers. Final purification via prep HPLC (Prep HPLC Column: Gemini pH 4 Dimensions: 21.1 mm x 150 mm 5 pm) gave:

First elute: EXAMPLE 128 as a white solid.

LC/MS (Method B): RT = 1.18; m/z = 563 [M+H] ⁺

1H NMR (399 MHz, DMSO- ) d 7.60 (m, 1H), 7.35-7.13 (m, 7H), 7.09 (ddd, J= 9.1, 4.6, 2.3 Hz, 2H), 4.83 (d, J = 7.3 Hz, 1H), 4.69 (d, J= 14.1 Hz, 2H), 3.99-3.78 (m, 3H), 3.77- 3.55 (m, 2H), 3.30-3.01 (m, 3H), 2.96-2.57 (m, 1H), 2.35-1.87 (m, 4H), 1.85-1.54 (m, 2H),

1.49-1.03 (m, 3H), 0.67 (dtd, J= 44.5, 13.0, 4.4 Hz, 1H).

HRMS (TOF, ESI) m/z: Calculated for C ₃₁ H ₃₂ F ₂ N ₄ O ₄ 562.2392, Found: 563.2404 [M+H] ⁺ Second elute: EXAMPLE 129 as a white solid.

LC/MS (Method B): RT = 1.19; m/z = 563 [M+H] ⁺ 1H NMR (399 MHz, DMSO- ) d 7.59 (m, 1H), 7.37-7.14 (m, 7H), 7.09 (ddd, J= 9.1, 4.6, 2.2 Hz, 2H), 4.84 (d, J= 7.1 Hz, 1H), 4.69 (d, J= 14.7 Hz, 2H), 4.06 (dd, J= 5.3, 3.3 Hz, 1H), 3.99-3.77 (m, 2H), 3.75-3.56 (m, 2H), 3.27-3.03 (m, 3H), 2.91-2.57 (m, 1H), 2.28- 1.90 (m, 4H), 1.79-1.59 (m, 2H), 1.49-1.03 (m, 3H), 0.63 (dtd, J= 81.5, 12.7, 4.2 Hz, 1H). HRMS (TOF, ESI) m/z: Calculated for C ₃₁ H ₃₂ F ₂ N ₄ O ₄ 562.2392, Found: 563.2402 [M+H] ⁺

^■ 5-amino-3-[(l-{[(lR,2R,4R)-4-fluoro-2-phenyl-4-[2-(pyridin-3 - yl)ethynyl] cyclohexyl] carbonyl}-4-hydroxypiperidin-4-yl)methyl] -6-(4- fluorophenoxy)pyrimidin-4-one (EXAMPLE 130)

Step 1: ethyl ( I R, 2 R, 4R)-4-hydroxy-2-phenyl-4- [2-(pyridin-3-yl)ethynyl] cyclohexane- 1 - carboxylate

Starting from ethyl (lR,2R)-4-oxo-2-phenylcyclo hexane- 1 -carboxylate (400 mg, 1.62 mmol) and 3-ethynylpyridine, (218 mg, 2.11 mmol, 1.3 eq.), following procedure described in Step 2 of EXAMPLES 122 and 123, the obtained residue was purified via flash chromatography using Heptane-78 % EtO Ac/Heptane (gradient) as eluent to afford ethyl (lR,2R,4R)-4-hydroxy-2-phenyl-4-[2-(pyridin-3-yl)ethynyl]cyc lohexane-l -carboxylate as a white foam.

FC/MS (Method B): RT = 1.15; m/z = 350 [M+H] ⁺

Step 2: ethyl ( lR,2R)-4-fluoro-2-phenyl-4-[2-(pyridin-3-yl)ethynyl]cyclohex ane-l - carboxylate

Starting from ethyl (lR,2R,4R)-4-hydroxy-2-phenyl-4-[2-(pyridin-3-yl)ethynyl] cyclohexane- 1 -carboxylate (420 mg, 1.2 mmol) following procedure described in Step 4 of EXAMPLES 122 and 123, ethyl (lR,2R)-4-fluoro-2-phenyl-4-[2-(pyridin-3-yl)ethynyl] cyclohexane- 1 -carboxylate was obtained as a colourless oil.

FC/MS (Method B): RT = 1.35; m/z = 352 [M+H] ⁺ Step 3: ( I R, 2 R)-4 fiuoro-2-phenyl-4-[2-(pyridin-3-yl)ethynyl] cyclohexane- 1 -carboxylic acid

Starting from ethyl (lR,2R)-4-fluoro-2-phenyl-4-[2-(pyridin-3-yl)ethynyl]cyclohe xane-l- carboxylate (330 mg, 0.94 mmol) following procedure described in Step 5 of EXAMPLES 122 and 123, (lR,2R)-4-fluoro-2-phenyl-4-[2-(pyridin-3-yl)ethynyl] cyclohexane- 1 -carboxylic acid was obtained as a white solid. The compound was used without further purification.

LC/MS (Method B): RT = 1.01; m/z = 342 [M+H] ⁺

Step 4: EXAMPLE 130

Starting from 5 -amino-6-(4-fluorophenoxy)-3 - [(4-hydroxypiperidin-4-yl)methyl] pyrimidin-4-one (110 mg, 0.33 mmol) and (lR,2R)-4-fluoro-2-phenyl-4-[2-(pyridin-3- yl)ethynyl]cyclo hexane- 1 -carboxylic acid (152 mg) following procedure described in Step 3 of EXAMPLE 94, the obtained residue was purified via flash chromatography using DCM-5 % MeOH/DCM (gradient) as eluent to give the crude product as a white solid. Final purification via prep HPLC (Prep HPLC Column: Gemini pH 4 Dimensions: 21.1 mm x 150 mm 5 pm) afforded the desired product as a white solid.

LC/MS (Method B): RT = 1.08; m/z = 640 [M+H] ⁺

1H NMR (399 MHz, DMSO- ) d 8.80-8.74 (m, 1H), 8.66 (dt, J = 4.9, 1.5 Hz, 1H), 8.01 (ddd, J = 7.8, 3.5, 1.7 Hz, 1H), 7.59 (m, 1H), 7.54-7.48 (m, 1H), 7.37-7.14 (m, 7H), 7.09 (ddd, j = 9.2, 4.6, 2.4 Hz, 2H), 4.82 (d, j = 7.5 Hz, 1H), 4.69 (d, j = 14.3 Hz, 2H), 4.02- 3.78 (m, 2H), 3.77-3.58 (m, 3H), 3.31-3.08 (m, 2H), 2.98-2.56 (m, 1H), 2.40-2.01 (m, 4H), 1.87 (s, 2H), 1.54-1.03 (m, 2H), 0.76 (td, j= 12.5, 4.2 Hz, 1H), 0.57 (td, j= 13.0, 4.3 Hz, 1H).

HRMS (TOF, ESI) m/z: Calculated for C ₃₆ H ₃₅ F ₂ N ₅ O ₄ 639.2657, Found: 640.2765 [M+H] ⁺ 5-amino-3-[(l-{[(lR,2R,4S)-4-fluoro-2-phenyl-4-[2-(pyridin-2 - yl)ethynyl] cyclohexyl] carbonyl}-4-hydroxypiperidin-4-yl)methyl] -6-(4- fluorophenoxy)pyrimidin-4-one (EXAMPLE 131)

and

5-amino-3- [(l-{ [(lR,2R,4R)-4-fluoro-2-phenyl-4- [2-(pyridin-2- yl)ethynyl] cyclohexyl] carbonyl}-4-hydroxypiperidin-4-yl)methyl] -6-(4- fluorophenoxy)pyrimidin-4-one (EXAMPLE 132)

Step 1: ethyl (lR,2R)-4-hydroxy-2-phenyl-4-[2-(pyridin-2-yl)ethynyl]cycloh exane-l- carboxylate Starting from ethyl (lR,2R)-4-oxo-2-phenylcyclo hexane- l-carboxylate (400 mg, 1.62 mmol) and 2-ethynylpyridine (0.21 mL, 2.11 mmol, 1.3 eq.) following procedure described in Step 2 of EXAMPLES 122 and 123, the obtained residue was purified via flash chromatography using Heptane-63 % EtO Ac/Heptane (gradient) as eluent to afford ethyl (lR,2R)-4-hydroxy-2-phenyl-4-[2-(pyridin-2-yl)ethynyl]cycloh exane-l-carboxylate as a brown foam.

LC/MS (Method B): RT = 1.15; m/z 350 [M+H] ⁺

Step 2: ethyl ( lR,2R)-4-fluoro-2-phenyl-4-[2-(pyridin-2-yl)ethynyl]cyclohex ane-l - carboxylate

Starting from ethyl (lR,2R)-4-hydroxy-2-phenyl-4-[2-(pyridin-2-yl)ethynyl]cycloh exane- 1 -carboxylate (480 mg, 1.37 mmol) following procedure described in Step 4 of EXAMPLES 122 and 123, ethyl (lR,2R)-4-fluoro-2-phenyl-4-[2-(pyridin-2- yl)ethynyl] cyclohexane- l-carboxylate was obtained as a colourless oil. The compound was used without further purification.

LC/MS (Method B): RT = 1.34; m/z 352 [M+H] ⁺

Step 3: ( I R, 2 R)-4 fluoro-2-pheny/-4-[2-(pyridin-2-y/)ethyny/] cyclohexane- 1 -carboxylic acid

Starting from ethyl (lR,2R)-4-fluoro-2-phenyl-4-[2-(pyridin-2-yl)ethynyl]cyclohe xane-l- carboxylate (360 mg) following procedure described in Step 5 of EXAMPLES 122 and 123, (lR,2R)-4-fluoro-2-phenyl-4-[2-(pyridin-2-yl)ethynyl]cyclohe xane-l-carboxylic acid was obtained as a yellow oil. The compound was used without further purification.

LC/MS (Method B): RT = 1.13 and 1.14; m/z = 324 [M+H] ⁺

Step 4: EXAMPLE 131 and EXAMPLE 132

To a mixture of (lR,2R)-4-fluoro-2-phenyl-4-[2-(pyridin-2-yl)ethynyl]cyclohe xane-l- carboxylic acid (180 mg) and 5-amino-6-(4-fluorophenoxy)-3-[(4-hydroxypiperidin-4- yl)methyl]pyrimidin-4-one (112 mg, 0.33 mmol) in acetonitrile (4 mL), triethylamine (0.14 mL, 1 mmol, 3.0 eq.) and l-hydroxybenzotriazole hydrate (56.26 mg, 0.37 mmol, 1.1 eq.) were added. After 1 minute, l-(3-dimethylaminopropyl)-3-ethyl-carbodiimide hydrochloride (70.43 mg, 0.37 mmol, 1.1 eq.) was added and the resulting yellow solution was stirred overnight. The reaction mixture was concentrated in vacuo and the residue was partitioned between EtOAc (25 mL) and sat. NaHCCh solution (20 mL). The organic layer was separated, dried (MgS0 ₄ ) and evaporated in vacuo to afford a crude oil. The residue was purified via flash chromatography using DCM-5 % MeOH/DCM (gradient) as eluent to afford the products a mixture of diastereoisomers. Final purification via prep HPLC (Prep HPLC Column: Gemini pH4 Dimensions: 21.1 mm x 150 mm 5 pm) gave:

First elute: EXAMPLE 131 as a white solid.

LC/MS (Method B): RT = 1.19; m/z = 640 [M+H] ⁺

1H NMR (399 MHz, DMSO- ) d 8.59 (ddd, J = 4.9, 1.7, 1.0 Hz, 1H), 7.89-7.75 (m, 1H), 7.66-7.48 (m, 2H), 7.44 (ddt, J = 7.5, 4.9, 1.2 Hz, 1H), 7.40-7.14 (m, 7H), 7.10 (ddq, J = 6.9, 4.6, 2.2 Hz, 2H), 4.83 (d, J = 6.9 Hz, 1H), 4.69 (d, J = 14.3 Hz, 2H), 4.03-3.49 (m, 4H), 3.33-2.55 (m, 4H), 2.45-2.01 (m, 3H), 1.92-1.59 (m, 2H), 1.51-0.97 (m, 3H), 0.68 (dtd, J= 50.8, 12.7, 4.3 Hz, 2H).

HRMS (TOF, ESI) m/z: Calculated for C36H35F2N5O4 639.2657, Found: 640.2683 [M+H] ⁺ Second elute: EXAMPLE 132 as a white solid.

LC/MS (Method B): RT = 1.22; m/z = 640 [M+H] ⁺

1H NMR (399 MHz, DMSO- ) d 8.64 (ddd, J = 4.7, 1.8, 1.0 Hz, 1H), 7.96-7.81 (m, 1H), 7.67 (ddt, J= 7.9, 2.3, 1.1 Hz, 1H), 7.59 (m, 1H), 7.49 (ddt, J= 7.6, 4.9, 1.3 Hz, 1H), 7.37- 7.15 (m, 7H), 7.09 (ddd, J = 9.1, 4.7, 2.4 Hz, 2H), 4.82 (d, J = 6.9 Hz, 1H), 4.69 (d, J = 14.8 Hz, 2H), 4.01-3.78 (m, 2H), 3.77-3.56 (m, 2H), 3.31-3.06 (m, 3H), 2.95-2.59 (m, 1H), 2.40-1.99 (m, 4H), 1.88 (d, J= 14.6 Hz, 2H), 1.52-1.03 (m, 2H), 0.76 (td, J= 13.0, 4.4 Hz, 1H), 0.56 (dd, J= 13.0, 9.1 Hz, 1H).

HRMS (TOF, ESI) m/z: Calculated for C36H35F2N5O4 639.2657, Found: 640.2672 [M+H] ⁺ 5-amino-3-[(l-{[(lR,2R,4R)-4-fluoro-4-[2-(5-fluoropyridin-2- yl)ethynyl]-2- phenylcyclohexyl]carbonyl}-4-hydroxypiperidin-4-yl)methyl]-6 -(4- fluorophenoxy)pyrimidin-4-one (EXAMPLE 133)

Step 1: (lR,2R)-4-oxo-2-phenylcyclohexane-l -carboxylic acid

Starting from ethyl (lR,2R)-4-oxo-2-phenylcyclohexane-l-carboxylate (2.27 g, 9.22 mmol, 1.0 eq.) following procedure described in Step 5 of EXAMPLES 122 and 123, (lR,2R)-4-oxo-2-phenylcyclo hexane- 1 -carboxylic acid was obtained as a yellow solid. LC/MS (Method B): RT = 0.84; m/z = 217 [M-H]-

Step 2: tert-butyl ( lR,2R)-4-oxo-2-phenylcyclohexane- l-carboxylate

To a solution of (lR,2R)-4-oxo-2-phenylcyclo hexane- 1 -carboxylic acid (1.43 g, 6.55 mmol, 1.0 eq.) and tert-butanol (1.84 mL, 19.66 mmol, 3 eq.) in DCM (40 mL), was added a solution of dicyclohexylcarbodiimide (1.57 ml, 7.21 mmol, 1.1 eq.) in DCM (16 mL) at 0 °C dropwise followed by DMAP (800 mg, 6.55 mmol, 1.0 eq.). The reaction mixture was stirred at the same temperature for 30 minutes before being allowed to warm to r.t. overnight. Diethyl ether (50 mL) was added and the suspension was filtered through a pad of celite, washed with diethyl ether. The filtrate was concentrated in vacuo to afford a crude solid. Purification via flash chromatography using Heptane-33 % EtO Ac/Heptane (gradient) as eluent afforded the desired product as a white solid.

1H NMR (399 MHz, Chloroform-^) d 7.34 (ddd, J = 8.9, 6.5, 0.9 Hz, 2H), 7.29-7.18 (m, 3H), 3.23 (ddd, J = 12.0, 10.9, 5.2 Hz, 1H), 2.98-2.87 (m, 1H), 2.68-2.42 (m, 4H), 2.32 (ddt, J= 13.1, 5.9, 3.4 Hz, 1H), 2.03 (tdd, j= 13.3, 11.7, 5.0 Hz, 1H), 1.18 (s, 9H). Step 3: tert-butyl ( lR,2R)-4-[2-(5-fluoropyridin-2-yl)ethynyl]-4-hydroxy-2 - phenylcyclohexane-l-carboxylate

Starting from tert-butyl (lR,2R)-4-oxo-2-phenylcyclo hexane- l-carboxylate (300 mg, 1.09 mmol) and 2-ethynyl-5-fluoropyridine (172 mg, 1.42 mmol, 1.3 eq.) following procedure described in Step 2 of EXAMPLES 122 and 123, the obtained residue was purified via flash chromatography using Heptane-30 % EtO Ac/Heptane (gradient) as eluent to afford the desired product as a colourless oil.

LC/MS (Method B): RT = 1.32; m/z = 396 [M+H] ⁺

Step 4: tert-butyl ( lR,2R,4R)-4-fluoro-4-[2-(5-fluoropyridin-2-yl)ethynyl]-2 - phenylcyclohexane- l-carboxylate and tert-butyl ( 1 R,2R,4S)-4-fluoro-4-[2-(5 - fluoropyridin-2-yl)ethynyl]-2-phenylcyclohexane- l-carboxylate

Starting from tert-butyl (lR,2R)-4-[2-(5-fluoropyridin-2-yl)ethynyl]-4-hydroxy-2- phenylcyclo hexane- l-carboxylate (272 mg, 0.69 mmol) following procedure described in Step 4 of EXAMPLES 122 and 123, the obtained residue was purified via flash chromatography using Heptane- 10 % EtO Ac/Heptane (gradient) as eluent to afford: First elute: tert-butyl (lR,2R,4R)-4-fluoro-4-[2-(5-fluoropyridin-2-yl)ethynyl]-2-ph enyl cyclohexane- l-carboxylate obtained as a colourless oil. The compound was used without further purification

LC/MS (Method B): RT = 1.46; m/z = 398 [M+H] ⁺

Second elute: tert-butyl (lR,2R,4S)-4-fluoro-4-[2-(5-fluoropyridin-2-yl)ethynyl]-2- phenylcyclo hexane- l-carboxylate obtained as a colourless oil.

LC/MS (Method B): RT = 1.47; m/z = 398 [M+H] ⁺

Step 5: (lR,2R,4R)-4-fluoro-4-[2-(5-fluoropyridin-2-yl)ethynyl]-2-ph enylcyclohexane-l- carboxylic acid

To a solution of tert-butyl (lR,2R,4R)-4-fluoro-4-[2-(5-fluoropyridin-2-yl)ethynyl]-2- phenylcyclo hexane- l-carboxylate (100 mg, 0.25 mmol) in DCM (2 mL), TFA (2 mL) was added slowly at 0 °C under nitrogen. The mixture was allowed to warm to r.t. over 2 hours. The reaction mixture was concentrated in vacuo. The residue was partitioned between DCM (25 mL) and water (25 mL). The organic layer was separated, dried (MgS0 ₄ ) and evaporated in vacuo to afford (lR,2R,4R)-4-fluoro-4-[2-(5-fluoropyridin-2-yl)ethynyl]-2- phenylcyclo hexane- 1 -carboxylic acid as an off- white solid. The compound was used without further purification.

LC/MS (Method B): RT = 1.18; m/z = 342 [M+H] ⁺

Step 6: EXAMPLE 133

Starting from 5 -amino-6-(4-fluorophenoxy)-3 - [(4-hydroxypiperidin-4-yl)methyl] pyrimidin-4-one (75 mg, 0.23 mmol) and (lR,2R,4R)-4-fluoro-4-[2-(5-fluoropyridin-2- yl)ethynyl]-2-phenylcyclo hexane- 1 -carboxylic acid (70 mg) following procedure described in Step 3 of EXAMPLE 94, the obtained residue was purified via flash chromatography using Heptane- 100 % EtOAc (gradient) as eluent to give the crude product as a colourless oil. Final purification via prep HPLC (Prep HPLC Column: Gemini pH 4 Dimensions: 21.1 mm x 150 mm 5 pm) afforded the desired product as a beige solid.

LC/MS (Method B): RT = 1.25; m/z = 658 [M+H] ⁺

1H NMR (399 MHz, DMSO- ) d 8.66 (dd, J= 2.8, 1.8 Hz, 1H), 7.86 (tdd, J= 8.6, 3.0, 1.5 Hz, 1H), 7.82-7.74 (m, 1H), 7.60 (m, 1H), 7.40-7.14 (m, 7H), 7.09 (ddd, J = 9.2, 4.6, 2.4 Hz, 2H), 4.82 (s, 3H), 4.00-3.56 (m, 4H), 3.30-2.96 (m, 3H), 2.95-2.58 (m, 1H), 2.40-2.02 (m, 4H), 1.96-1.70 (m, 2H), 1.51-0.97 (m, 2H), 0.76 (td, J = 12.8, 4.5 Hz, 1H), 0.56 (td, J = 13.4, 4.7 Hz, 1H).

HRMS (TOF, ESI) m/z: Calculated for C ₃₆ H ₃₄ F ₃ N ₅ O ₄ 657.2563, Found: 658.2665 [M+H] ⁺ 5-amino-3-[(l-{[(lR,2R,4S)-4-fluoro-4-[2-(5-fluoropyridin-2- yl)ethynyl]-2- phenylcyclohexyl]carbonyl}-4-hydroxypiperidin-4-yl)methyl]-6 -(4- fluorophenoxy)pyrimidin-4-one (EXAMPLE 134)

Step 1: (lR,2R,4S)-4-fluoro-4-[2-(5-fluoropyridin-2-yl)ethynyl]-2-ph enylcyclohexane-l- carboxylic acid

Starting from tert-butyl (lR,2R,4S)-4-fluoro-4-[2-(5-fluoropyridin-2-yl)ethynyl]-2-ph enyl cyclohexane- l-carboxylate (98 mg, 0.25 mmol, 1.0 eq.) following procedure described in Step 5 of EXAMPLE 133, (lR,2R,4S)-4-fluoro-4-[2-(5-fluoropyridin-2-yl)ethynyl]-2- phenylcyclo hexane- 1 -carboxylic acid (84 mg) was obtained as an off- white solid. The compound was used without further purification.

FC/MS (Method B): RT = 1.073; m/z = 342 [M+H] ⁺

Step 2: EXAMPLE 134

Starting from 5 -amino-6-(4-fluorophenoxy)-3 - [(4-hydroxypiperidin-4-yl)methyl] pyrimidin-4-one (83 mg, 0.25 mmol) and (lR,2R,4S)-4-fluoro-4-[2-(5-fluoropyridin-2- yl)ethynyl]-2-phenylcyclo hexane- 1 -carboxylic acid (84 mg) following procedure described in Step 3 of EXAMPLE 94, the obtained residue was purified via flash chromatography (Cl 8) using 10 % to 100 % acetonitrile/water (gradient) as eluent to afford EXAMPLE 134 as a white solid.

FC/MS (Method B): RT = 1.23; m/z = 638 [M-HF] ⁺

1H NMR (399 MHz, DMSO-d ₆ ) d 8.60 (m, 1H), 7.81 (tdd, J = 8.6, 3.0, 1.6 Hz, 1H), 7.69 (ddd, J = 8.8, 4.6, 2.7 Hz, 1H), 7.61 (m, 1H), 7.36-7.18 (m, 7H), 7.11-7.07 (m, 2H), 4.83 (m, 1H), 4.70 (m, 2H), 3.97-3.62 (m, 4H), 3.33-3.11 (m, 3H), 2.94-2.63 (m, 1H), 2.41-2.07 (m, 4H), 1.84-1.65 (m, 2H), 1.47-1.11 (m, 3H), 0.78-0.58 (m, 1H).

HRMS (TOF, ESI) m/z: Calculated for C ₃₆ H ₃₄ F ₃ N ₅ O ₄ 657.2563, Found: 658.2652 [M+H] ⁺ 5-amino-3-({l-[(lR,2R,4R)-4-fluoro-2-phenyl-4-(2- phenylethynyl)cyclohexanecarbonyl]-4-hydroxypiperidin-4-yl}m ethyl)-6-(4- fluorophenoxy)-3,4-dihydropyrimidin-4-one (EXAMPLE 135)

and

5-amino-3-({l-[(lR,2R,4S)-4-fluoro-2-phenyl-4-(2- phenylethynyl)cyclohexanecarbonyl]-4-hydroxypiperidin-4-yl}m ethyl)-6-(4- fluorophenoxy)-3,4-dihydropyrimidin-4-one (EXAMPLE 136)

To a solution of 5-amino-3-({l-[(lR,2R)-4-ethynyl-4-fluoro-2-phenylcyclohexan e carbonyl]-4-hydroxypiperidin-4-yl}methyl)-6-(4-fluorophenoxy )-3,4-dihydropyrimidin-4- one (110 mg, 0.2 mmol, 1.0 eq.) in THF (2 mL) was added copper(I) iodide (33 mg, 0.02 mmol, 0.08 eq.) and bis(triphenylphosphine)palladium(II) dichloride (5.5 mg, 0.01 mmol, 0.04 eq.). The reaction mixture was degassed under nitrogen for 5 minutes before adding triethylamine (0.04 mL, 0.29 mmol, 1.5 eq.) followed by iodobenzene (0.03 mL, 0.29 mmol, 1.5 eq.). The reaction mixture was stirred at r.t. for 1 hour. The mixture was partitioned between EtOAc (20 mL) and brine (20 mL). The organic layer was separated, dried (MgS0 ₄ ) and evaporated in vacuo to afford a crude brown oil. The residue was purified via flash chromatography using DCM-4.5 % MeOH/DCM (gradient) as eluent to give:

First elute: EXAMPLE 135 obtained as a yellow oil.

LC/MS (Method B): RT = 1.22; m/z = 639 [M+H] ⁺

1H NMR (399 MHz, DMSO- ) d 7.66-7.41 (m, 6H), 7.34-7.18 (m, 7H), 7.11-7.07 (m, 2H) 4.94-4.49 (m, 3H), 4.05-3.53 (m, 4H), 3.17 (m, 2H), 2.70 (s, 1H), 2.39-1.99 (m, 4H), 1.86 (d, J= 9.1 Hz, 2H), 1.52-1.02 (m, 3H), 0.77 (dt, J= 12.7, 6.2 Hz, 1H), 0.66-0.41 (m, 1H). Second elute: EXAMPLE 136 obtained as a brown oil.

LC/MS (Method B): RT = 1.22; m/z = 619 [M-HF]+

1H NMR (399 MHz, DMSO- ) d d 7.66-7.40 (m, 6H), 7.33-7.17 (m, 7H), 7.12-7.08 (m, 2H), 4.77 (dd, J = 49.4, 5.7 Hz, 3H), 4.11-3.53 (m, 4H), 3.18 (dt, j = 27.8, 11.8 Hz, 2H), 2.99-2.59 (m, 1H), 2.41-1.93 (m, 4H), 1.74 (dt, j= 51.7, 12.9 Hz, 2H), 1.50-1.01 (m, 3H), 0.92-0.48 (m, 2H). 5-amino-3-({l-[(lR,2R,4S)-4-fluoro-2-phenyl-4-[2-(pyrazin-2- yl)ethynyl]cyclohexanecarbonyl]-4-hydroxypiperidin-4-yl}meth yl)-6-(4- fluorophenoxy)-3,4-dihydropyrimidin-4-one (EXAMPLE 137)

and

5-amino-3-({l-[(lR,2R,4R)-4-fluoro-2-phenyl-4-[2-(pyrazin -2- yl)ethynyl]cyclohexanecarbonyl]-4-hydroxypiperidin-4-yl}meth yl)-6-(4- fluorophenoxy)-3,4-dihydropyrimidin-4-one (EXAMPLE 138)

Step 1: ethyl ( 1R,2R) -4 -hydroxy -2 -phenyl -4 -[2 -(pyrazin -2 -yl)ethynyl] cyclohexane -1 - carboxylate

Starting from ethyl (lR,2R)-4-oxo-2-phenylcyclo hexane- l-carboxylate (400 mg, 1.62 mmol) and 2-ethynylpyrazine (220 mg, 2.11 mmol) following procedure described in Step 2 of EXAMPLES 122 and 123, the obtained residue was purified via flash chromatography using Heptane-20 % EtO Ac/Heptane (gradient) as eluent to afford ethyl (lR,2R)-4-hydroxy-2-phenyl-4-[2-(pyrazin-2-yl)ethynyl]cyclo hexane- 1 -carboxylate as a colourless oil.

LC/MS (Method B): RT = 1.096; m/z = 351 [M+H] ⁺

Step 2: ethyl ( I R,2R) -4 -fluoro -2 -phenyl -4 -[2 -( pyrazin -2 -yl) ethynyl ] cyclohexane -I - carboxylate

Starting from ethyl (lR,2R)-4-hydroxy-2-phenyl-4-[2-(pyrazin-2-yl)ethynyl]cyclo hexane- l-carboxylate (476 mg, 1.36 mmol) following procedure described in Step 4 of EXAMPLES 122 and 123, the obtained residue was purified via flash chromatography using Heptane-20 % EtO Ac/Heptane (gradient) as eluent to afford ethyl (lR,2R)-4-fluoro-2- phenyl-4-[2-(pyrazin-2-yl)ethynyl]cyclo hexane- l-carboxylate as colourless oil.

LC/MS (Method B): RT = 1.317; m/z = 353 [M+H] ⁺ Step 3: ( 1R,2R) -4 -fluoro -2 -phenyl -4 -[2 -(pyrazin -2 -yl) ethynyl] cyclohexane -7 -carboxylic acid

Starting from ethyl (lR,2R)-4-fluoro-2-phenyl-4-[2-(pyrazin-2-yl)ethynyl]cyclo hexane- 1- carboxylate (129 mg, 0.37 mmol) following procedure described in Step 5 of EXAMPLES 122 and 123, (lR,2R)-4-fluoro-2-phenyl-4-[2-(pyrazin-2-yl)ethynyl] cyclohexane- 1 -carboxylic acid was obtained as a colourless oil. The compound was used without further purification.

LC/MS (Method B): RT = 1.069; m/z = 323 [M-H] ⁺

Step 4: EXAMPLE 137 and EXAMPLE 138

Starting from (lR,2R)-4-fluoro-2-phenyl-4-[2-(pyrazin-2-yl)ethynyl]cyclo hexane- 1- carboxylic acid (115 mg) and 5-amino-6-(4-fluorophenoxy)-3-[(4-hydroxypiperidin-4- yl)methyl]pyrimidin-4-one (79 mg, 0.24 mmol) following procedure described in Step 3 of EXAMPLE 94, the obtained residue was purified via prep HPLC (Prep HPLC Column: Gemini pH 7.4 Dimensions: 21.1 mm x 150 mm 5 pm) to give:

First elute: EXAMPLE 137 as a white solid.

LC/MS (Method B): RT = 1.155; m/z = 621 [M-HF] ⁺

1H NMR (399 MHz, DMSO- ) d 8.82 (m, 1H), 8.77-8.66 (m, 2H), 7.60 (m, 1H), 7.34- 7.18 (m, 7H), 7.10-7.07 (m, 2H), 4.84 (s, 1H), 4.68 (m, 2H), 3.97-3.82 (m, 2H), 3.76-3.63 (m, 2H), 3.31-2.88 (m, 3H), 2.72-2.61 (m, 1H), 2.45-2.10 (m, 4H), 1.85-1.67 (m, 2H), 1.47-1.12 (m, 3H), 0.78-0.58 (m, 1H).

Second elute: EXAMPLE 138 as a white solid.

LC/MS (Method B): RT = 1.176; m/z = 641 [M-H] ⁺

1H NMR (399 MHz, DMSO- ) d 8.91 (m, 1H), 8.75-8.72 (m, 2H), 7.59 (m, 1H), 7.35- 7.18 (m, 7H), 7.11-7.07 (m, 2H), 4.82 (m, 1H), 4.69 (m, 2H), 3.96-3.82 (m, 2H), 3.74-3.61 (m, 2H), 3.32-2.86 (m, 3H), 2.66 (m, 1H), 2.36-2.11 (m, 4H), 1.90-1.82 (m, 2H), 1.47-1.11

(m, 3H), 0.79-0.53 (m, 1H). 5-amino-6-(4-fluorophenoxy)-3-[(4-hydroxy-l-{[(lR,2R,4R)-4-m ethoxy-2-phenyl-4- [2-(pyrimidin-5-yl)ethynyl] cyclohexyl] carbonyl}piperidin-4-yl)methyl] pyrimidin-4- one (EXAMPLE 139) Step 1: Ethyl ( lR,2R)-4-hydroxy-2-phenyl-4-[2-(pyrimidin-5-yl)ethynyl]cyclo hexane-l - carboxylate

Starting from El (400 mg, 1.62 mmol) and 5-ethynylpyrimidine (220 mg, 2.11 mmol), following procedure described in Step 2 of EXAMPLES 122 and 123, the obtained residue was purified via flash chromatography using Heptane- 100 % EtOAc (gradient) as eluent to afford ethyl (lR,2R)-4-hydroxy-2-phenyl-4-[2-(pyrimidin-5-yl)ethynyl]cycl ohexane-l- carboxylate as an white oil.

LC/MS (Method B): RT = 1.10; m/z = 351 [M+H] ⁺

Step 2: Ethyl ( lR,2R)-4-fluoro-2-phenyl-4-[2-(pyrimidin-5-yl)ethynyl]cycloh exane-l - carboxylate

Starting from ethyl (lR,2R)-4-hydroxy-2-phenyl-4-[2-(pyrimidin-5-yl)ethynyl] cyclohexane- 1 -carboxylate (410 mg, 1.17 mmol) following procedure described in Step 4 of EXAMPLES 122 and 123, the residue was purified via flash chromatography using Heptane-30 % EtO Ac/Heptane (gradient) as eluent to afford ethyl (lR,2R)-4-fluoro-2- phenyl-4-[2-(pyrimidin-5-yl)ethynyl]cyclo hexane- 1 -carboxylate as a colourless oil.

LC/MS (Method B): RT = 1.31; m/z = 353 [M+H] ⁺

Step 3: (lR,2R)-4-methoxy-2-phenyl-4- [2-(pyrimidin-5-yl)ethynyl] cyclohexane- 1- carboxylic acid

To a solution of ethyl (lR,2R)-4-fluoro-2-phenyl-4-[2-(pyrimidin-5-yl)ethynyl] cyclohexane- 1 -carboxylate (100 mg, 0.28 mmol) in methanol (3.75 mL) and water (1.25 mL) was added at r.t. 50 % (w/w) sodium hydroxide (0.25 mL). The reaction mixture was stirred at r.t. for 71 hours. The reaction mixture was concentrated in vacuo, diluted with water (30 mL) and extracted with diethyl ether (2 x 30 mL). The aqueous layer was acidified to pH 2 with 2N HC1 and extracted with EtO Ac (3 x 50 mL). The organic layers were combined, dried (MgS0 ₄ ) and evaporated to afford (lR,2R)-4-methoxy-2-phenyl-4- [2-(pyrimidin-5-yl)ethynyl]cyclo hexane- 1 -carboxylic acid as a yellow solid. The compound was used without further purification.

LC/MS (Method B): RT = 1.05; m/z = 337 [M+H] ⁺

Step 4: EXAMPLE 139

Starting from 5-amino-6-(4-fluorophenoxy)-3-[(4-hydroxypiperidin-4-yl)meth yl] pyrimidin-4-one (56 mg, 0.17 mmol) and (lR,2R)-4-methoxy-2-phenyl-4-[2-(pyrimidin-5- yl)ethynyl]cyclo hexane- 1 -carboxylic acid (56 mg, 0.17 mmol) following procedure described in Step 3 of EXAMPLE 94, the obtained residue was purified via flash chromatography using DCM-5 % MeOH/DCM (gradient) as eluent to give the crude product as a white solid. Final purification via prep HPLC (Prep HPLC Column: Gemini pH 4 Dimensions: 21.1 mm x 150 mm 5 pm) afforded the desired product as a white solid. LC/MS (Method B): RT = 1.14; m/z = 653 [M+H] ⁺

1H NMR (399 MHz, DMSO-d6) d 9.23 (d, J = 1.3 Hz, 1H), 9.02 (d, J = 3.1 Hz, 2H), 7.60 (m, 1H), 7.40-7.14 (m, 7H), 7.13-7.04 (m, 2H), 4.82 (d, J = 7.5 Hz, 1H), 4.69 (d, J = 14.3

Hz, 2H), 4.01-3.59 (m, 4H), 3.38 (d, J = 2.5 Hz, 3H), 3.27-3.05 (m, 3H), 2.76-2.58 (m, 1H), 2.29-2.09 (m, 2H), 1.97-1.66 (m, 4H), 1.51-1.03 (m, 3H), 0.88-0.49 (m, 1H).

^■ 5-amino-3-({l-[(lR,2R,4S)-4-fluoro-2-phenyl-4-[2-(pyrimidin- 5- yl)ethynyl]cyclohexanecarbonyl]-4-hydroxypiperidin-4-yl}meth yl)-6-(4- fluorophenoxy)-3,4-dihydropyrimidin-4-one (EXAMPLE 140)

Step 1: tert-butyl ( I R,2R) -4 -hydroxy -2 -phenyl -4 -[2 -( pyrimidin -5 -yl) ethynyl ] cyclohexane -/ - carboxylate

Starting from tert-butyl (lR,2R)-4-oxo-2-phenylcyclohexane-l -carboxylate (300 mg, 1.09 mmol) and 5-ethynylpyrimidine (148 mg, 1.42 mmol) following procedure described in Step 2 of EXAMPLES 122 and 123, the obtained residue was purified via flash chromatography using Heptane-40 % EtOAc/Heptane (gradient) as eluent to afford tert-butyl (lR,2R)-4-hydroxy-2-phenyl-4-[2-(pyrimidin-5-yl)ethynyl]cycl ohexane- 1 - carboxylate as a white solid.

LC/MS (Method B): RT = 1.217; m/z = 379 [M+H] ⁺ Step 2: tert-butyl (1R,2R,4R) -4 -fluoro -2 -phenyl -4 -[2 -(pyrimidin -5 -yl) ethynyl] cyclohexane - 1 -carboxylate and tert -butyl ( JR , 2R, 4S) -4 -fluoro -2 -phenyl -4 -[ 2 -(pyrimidin -5 - yl) ethynyl] cyclohexane -1 -carboxylate

Starting from tert-butyl (lR,2R)-4-hydroxy-2-phenyl-4-[2-(pyrimidin-5-yl)ethynyl] cyclohexane- 1 -carboxylate (233 mg, 0.62 mmol) following procedure described in Step 4 of EXAMPLES 122 and 123, the obtained residue was purified via flash chromatography using Heptane-50 % EtOAc/Heptane (gradient) as eluent to afford:

First elute: tert-butyl (lR,2R,4R)-4-fluoro-2-phenyl-4-[2-(pyrimidin-5- yl)ethynyl]cyclo hexane- 1 -carboxylate as a white solid.

LC/MS (Method B): RT = 1.404; m/z = 381 [M+H] ⁺ Second elute: tert-butyl (lR,2R,4S)-4-fluoro-2-phenyl-4-[2-(pyrimidin-5- yl)ethynyl]cyclohexane-l-carboxylate as a white solid.

LC/MS (Method B): RT = 1.411; m/z = 381 [M+H] ⁺

Step 3: ( 1R,2R,4S ) -4 -fluoro -2 -phenyl -4 -[2 -(pyrimidin -5 -yl)ethynyl] cyclohexane -1 - carboxylic acid

Starting from tert-butyl (lR,2R,4S)-4-fluoro-2-phenyl-4-[2-(pyrimidin-5-yl)ethynyl] cyclohexane- l-carboxylate (85 mg, 0.22 mmol) following procedure described in Step 5 of EXAMPLE 133, (lR,2R,4S)-4-fluoro-2-phenyl-4-[2-(pyrimidin-5-yl)ethynyl]cy clo hexane- 1 -carboxylic acid was obtained as a white solid.

LC/MS (Method B): RT = 1.068; m/z = 323 [M-H]-

Step 4: EXAMPLE 140

Starting from (lR,2R,4S)-4-fluoro-2-phenyl-4-[2-(pyrimidin-5-yl)ethynyl]cy clohexane- 1 - carboxylic acid (67 mg, 0.21 mmol) and 5-amino-6-(4-fluorophenoxy)-3-[(4- hydroxypiperidin-4-yl)methyl]pyrimidin-4-one (69 mg, 0.21 mmol) following procedure described in Step 3 of EXAMPLE 94, the obtained residue was purified via flash chromatography using water- 100 % MeCN/water (gradient) as eluent to afford EXAMPLE 140 as a white solid.

LC/MS (Method B): RT = 1.151; m/z = 621 [M-HF+H] ⁺

1H NMR (399 MHz, DMSO- ) 9.22 (s, 1H), 8.96 (m, 2H), 7.65-7.57 (m, 1H), 7.34-7.16 (m, 7H), 7.12-7.08 (m, 2H), 4.83 (m, 1H), 4.69 (m, 2H), 3.97-3.63 (m, 4H), 3.27-2.90 (m,

3H), 2.70-2.64 (m, 1H), 2.42-2.09 (m, 4H), 1.85-1.67 (m, 2H), 1.47-1.12 (m, 3H), 0.76- 0.64 (m, 1H).

HRMS (TOF, ESI) m/z: Calculated for C35H34F2N6O4 640.2610, Found: 641.2699 [M+H] ⁺ 5-amino-3-[(l-{[(lR,2R,4R)-4-fluoro-2-phenyl-4-[2-(pyrimidin -2- yl)ethynyl] cyclohexyl] carbonyl}-4-hydroxypiperidin-4-yl)methyl]-6-(4- fluorophenoxy)pyrimidin-4-one (EXAMPLE 141),

5-amino-3- [(l-{ [(lR,2R,4S)-4-fluoro-2-phenyl-4- [2-(pyrimidin-2- yl)ethynyl] cyclohexyl] carbonyl}-4-hydroxypiperidin-4-yl)methyl] -6-(4- fluorophenoxy)pyrimidin-4-one (EXAMPLE 142) and

5-amino-6-(4-fluorophenoxy)-3- [(4-hydroxy- 1- { [(1 R,6R)-6-phenyl-4- [2-(pyrimidin-2- yl)ethynyl]cyclohex-3-en-l-yl]carbonyl}piperidin-4-yl)methyl ]pyrimidin-4-one (EXAMPLE 143) Step 1: tert-butyl ( lR,2R)-4-[2-(5-fluoropyridin-2-yl)ethynyl]-4-hydroxy-2 - phenylcyclohexane-l-carboxylate

Starting from tert- butyl (lR,2R)-4-oxo-2-phenylcyclo hexane- l-carboxylate (600 mg, 2.19 mmol) and 2-ethynylpyrimidine (296 mg, 2.84 mmol, 1.3 eq.) following procedure described in Step 2 of EXAMPLES 122 and 123, the obtained residue was purified via flash chromatography using Heptane-65 % EtO Ac/Heptane (gradient) as eluent to give:

First elute: tert- butyl (lR,2R,4S)-4-hydroxy-2-phenyl-4-[2-(pyrimidin-2- yl)ethynyl]cyclo hexane- l-carboxylate obtained as a white solid.

LC/MS (Method B): RT = 1.233; m/z = 379 [M+H] ⁺

Second elute: tert- butyl (lR,2R,4R)-4-hydroxy-2-phenyl-4-[2-(pyrimidin-2- yl)ethynyl]cyclo hexane- l-carboxylate obtained as a colourless oil.

LC/MS (Method B): RT = 1.205; m/z = 379 [M+H] ⁺

Step 2: tert-butyl ( lR,2R)-4-fluoro-2-phenyl-4-[2-(pyrimidin-2-yl)ethynyl]cycloh exane-l - carboxylate

Starting from tert- butyl (lR,2R,4R)-4-hydroxy-2-phenyl-4-[2-(pyrimidin-2-yl)ethynyl] cyclohexane- l-carboxylate (220 mg, 0.58 mmol) following procedure described in Step 4 of EXAMPLES 122 and 123, the obtained residue was purified via flash chromatography using Heptane-35 % EtO Ac/Heptane (gradient) as eluent to afford tert- butyl (lR,2R)-4- fluoro-2-phenyl-4-[2-(pyrimidin-2-yl)ethynyl]cyclohexane- l-carboxylate as a yellow oil. LC/MS (Method B): RT = 1.376; m/z = 381 [M+H] ⁺ Step 3: ( I R, 2 R)-4-fluoro-2-phenyl-4-[2-(pyrimidin-2-yl)ethynyl] cyclohexane- 1 -carboxylic acid

Starting from tert- butyl (lR,2R)-4-fluoro-2-phenyl-4-[2-(pyrimidin-2-yl)ethynyl] cyclohexane- l-carboxylate (150 mg, 0.39 mmol) following procedure described in Step 5 of EXAMPLE 133, (1 R,2R)-4-fluoro-2-phenyl-4-[2-(pyrimidin-2-yl)ethynyl]cyclo hexane- 1 - carboxylic acid was obtained as a yellow oil. The compound was used without further purification.

LC/MS (Method B): RT = 1.02; m/z = 325 [M+H] ⁺

Step 4: EXAMPLES 141, 142 and 143

Starting from 5 -amino-6-(4-fluorophenoxy)-3 - [(4-hydroxypiperidin-4-yl)methyl] pyrimidin-4-one (127 mg, 0.38 mmol) and (lR,2R)-4-fluoro-2-phenyl-4-[2-(pyrimidin-2- yl)ethynyl]cyclo hexane- 1 -carboxylic acid (190 mg) following procedure described in Step 3 of EXAMPLE 94, the obtained residue was purified via flash chromatography using DCM-5 % MeOH (gradient) as eluent to give the still impure product as colourless oil. Final purification was performed via prep HPLC Prep (HPLC Column: Gemini pH4 Dimensions: 21.1 mm x 150 mm 5 pm) to afford the desired products.

First elute: EXAMPLE 143 as a white solid.

LC/MS (Method 1290): RT = 0.93; m/z = 621 [M+H] ⁺

1H NMR (399 MHz, DMSO- ) d 8.79 (m, 2H), 7.63-7.59 (m, 1H), 7.47 (t, 1H), 7.33-7.18 (m, 7H), 7.12-7.07 (m, 2H), 6.49 (m, 1H), 4.86 (m, 1H), 4.69 (m, 2H), 3.94-3.68 (m, 4H), 3.47-3.35 (m, 1H), 3.18-2.93 (m, 2H), 2.7-2.54 (m, 2H), 2.40 (m, 3H), 1.46-1.13 (m, 3H), 0.93-0.64 (m, 1H).

HRMS (TOF, ESI) m/z: Calculated for C35H33FN6O4 620.2547, Found: 621.2659 [M+H] ⁺ Second elute: EXAMPLE 142 as a white solid.

LC/MS (Method 1290): RT = 0.94; m/z = 641 [M+H] ⁺

1H NMR (399 MHz, DMSO- ) d 8.83 (m, 2H), 7.63-7.54 (m, 2H), 7.37-7.15 (m, 7H), 7.11-7.07 (m, 2H), 4.86 (m, 1H), 4.69 (m, 2H), 3.97-3.62 (m, 4H), 3.27-2.87 (m, 3H), 2.66 (m, 1H), 2.43-2.10 (m, 4H), 1.84-1.66 (m, 2H), 1.45-1.11 (m, 3H), 0.78-0.57 (m, 1H) HRMS (TOF, ESI) m/z: Calculated for C35H34F2N6O4 640.261, Found: 641.2705 [M+H] ⁺ Third elute: EXAMPLE 141 as a white solid.

LC/MS (Method 1290): RT = 0.96; m/z = 641 [M+H] ⁺

1H NMR (399 MHz, DMSO- ) d 8.87 (m, 2H), 7.62-7.56 (m, 2H), 7.35-7.15 (m, 7H), 7.11-7.07 (m, 2H), 4.82 (m, 1H), 4.69 (m, 2H), 3.96-3.61 (m, 4H), 3.31-2.85 (m, 3H), 2.65 (m, 1H), 2.36-2.10 (m, 4H), 1.92-1.80 (m, 2H), 1.46-1.11 (m, 3H), 0.78-0.53 (m, 1H) HRMS (TOF, ESI) m/z: Calculated for C35H34F2N6O4 640.261, Found: 641.2613 [M+H] ^{+ ■} 5-amino-3-({l-[(lR,2R,4R)-4-fluoro-2-phenyl-4-[2-(pyrimidin- 5- yl)ethynyl]cyclohexanecarbonyl]-4-hydroxypiperidin-4-yl}meth yl)-6-(4- fluorophenoxy)-3,4-dihydropyrimidin-4-one (EXAMPLE 144)

Step 1: ( JR , 2R, 4R) -4 -fluoro -2 -phenyl -4 -[ 2 -(pyrimidin -5 -yl)ethynyl] cyclohexane -I - carboxylic acid

Starting from tert-butyl (lR,2R,4R)-4-fluoro-2-phenyl-4-[2-(pyrimidin-5-yl)ethynyl] cyclohexane- l-carboxylate (68 mg, 0.18 mmol) following procedure described in Step 5 of EXAMPLE 133, (lR,2R,4R)-4-fluoro-2-phenyl-4-[2-(pyrimidin-5-yl)ethynyl]cy clo hexane- 1 -carboxylic acid was obtained as a white solid.

LC/MS (Method B): RT = 1.099; m/z = 323 [M-H] ⁺

Step 2: EXAMPLE 144

Starting from (lR,2R,4R)-4-fluoro-2-phenyl-4-[2-(pyrimidin-5-yl)ethynyl]cy clohexane- 1 - carboxylic acid (46 mg, 0.14 mmol) and 5-amino-6-(4-fluorophenoxy)-3-[(4- hydroxypiperidin-4-yl)methyl]pyrimidin-4-one (47 mg, 0.14 mmol) following procedure described in Step 3 of EXAMPLE 94, the obtained residue was purified via prep HPLC Prep (HPLC Column: Gemini pH4 Dimensions: 21.1 mm x 150 mm 5 pm) to afford EXAMPLE 144 as a white solid.

LC/MS (Method B): RT = 1.175; m/z = 641 [M+H] ⁺

1H NMR (399 MHz, DMSO- ) 9.27 (s, 1H), 9.06 (m, 2H), 7.65-7.57 (m, 1H), 7.34-7.17 (m, 7H), 7.12-7.07 (m, 2H), 4.82 (m, 1H), 4.69 (m, 2H), 3.97-3.61 (m, 4H), 3.32-2.87 (m,

3H), 2.68-2.52 (m, 1H), 2.33-2.09 (m, 4H), 1.87 (m, 2H), 1.47-1.11 (m, 3H), 0.79-0.55 (m, 1H).

HRMS (TOF, ESI) m/z: Calculated for C ₃₅ H ₃₄ F ₂ N ₆ O ₄ 640.2610, Found: 641.2627 [M+H] ⁺

^■ 5-amino-3-[(l-{[(lR,2R,4R)-4-fluoro-2-phenyl-4-[2-(pyridazin -3- yl)ethynyl] cyclohexyl] carbonyl}-4-hydroxypiperidin-4-yl)methyl]-6-(4- fluorophenoxy)pyrimidin-4-one (EXAMPLE 145)

Step 1: tert-butyl ( lR,2R)-4-hydroxy-2-phenyl-4-[2-(pyridazin-3-yl)ethynyl]cyclo hexane-l - carboxylate Starting from tert-butyl (lR,2R)-4-oxo-2-phenylcyclo hexane- l-carboxylate (400 mg, 1.46 mmol) and 3-ethynylpyridazine, (197 mg, 1.9 mmol, 1.3 eq.) following procedure described in Step 2 of EXAMPLES 122 and 123, the obtained residue was purified via flash chromatography using Heptane- 88 %EtO Ac/Heptane (gradient) as eluent to give tert-butyl (lR,2R)-4-hydroxy-2-phenyl-4-[2-(pyridazin-3-yl)ethynyl]cycl ohexane-l-carboxylate as a yellow solid.

LC/MS (Method B): RT = 1.18; m/z = 379 [M+H] ⁺

Step 2: tert-butyl ( lR,2R)-4-fluoro-2-phenyl-4-[2-(pyridazin-3-yl)ethynyl]cycloh exane-l - carboxylate

Starting from tert-butyl (lR,2R)-4-hydroxy-2-phenyl-4-[2-(pyridazin-3-yl)ethynyl] cyclohexane- l-carboxylate (260 mg, 0.69 mmol) following procedure described in Step 4 of EXAMPLES 122 and 123, the obtained residue was purified via flash chromatography using Heptane-93 % EtO Ac/Heptane (gradient) as eluent to afford tert-butyl (lR,2R)-4- fluoro-2-phenyl-4-[2-(pyridazin-3-yl)ethynyl]cyclohexane- l-carboxylate as a yellow foam. LC/MS (Method B): RT = 1.15; m/z = 381 [M+H] ⁺

Step 3: (lR,2R)-4-fluoro-2-phenyl-4-[2-(pyridazin-3-yl)ethynyl] cyclohexane- 1 -carboxylic acid

Starting from tert-butyl (lR,2R)-4-fluoro-2-phenyl-4-[2-(pyridazin-3-yl)ethynyl] cyclohexane- l-carboxylate (90 mg, 0.24 mmol) following procedure described in Step 5 of EXAMPLE 133, (lR,2R)-4-fluoro-2-phenyl-4-[2-(pyridazin-3-yl)ethynyl]cyclo hexane-l- carboxylic acid was obtained as a yellow oil. The compound was used without further purification.

LC/MS (Method B): RT = 0.987; m/z = 325 [M+H] ⁺

Step 4: EXAMPLE 145

Starting from 5-amino-6-(4-fluorophenoxy)-3-[(4-hydroxypiperidin-4-yl)meth yl] pyrimidin-4-one (123 mg, 0.37 mmol) and (lR,2R)-4-fluoro-2-phenyl-4-[2-(pyridazin-3- yl)ethynyl]cyclo hexane- 1 -carboxylic acid (170 mg) following procedure described in Step 3 of EXAMPLE 94, the obtained residue was purified via flash chromatography using DCM-6 % MeOH (gradient) as eluent to give the still impure product as colourless oil. Final purification was performed via prep HPLC Prep (HPLC Column: Gemini pH4 Dimensions: 21.1 mm x 150 mm 5 pm) to afford EXAMPLE 145 as a white solid.

LC/MS (Method B): RT = 1.13; m/z = 641 [M+H] ⁺

1H NMR (399 MHz, DMSO- ) d 9.31 (dt, J= 5.l, 1.6 Hz, 1H), 7.99 (ddd, J= 8.5, 3.2, 1.7 Hz, 1H), 7.82 (ddd, J = 8.5, 5.1, 1.5 Hz, 1H), 7.62-7.57 (m, 1H), 7.35-7.17 (m, 7H), 7.12- 7.07 (m, 2H), 4.82 (m, 1H), 4.68 (m, 2H), 3.96-3.61 (m, 4H), 3.31-2.87 (m, 3H), 2.65 (m, 1H), 2.40-2.12 (m, 4H), 1.89 (m, 2H), 1.47-1.11 (m, 3H), 0.79-0.55 (m, 1H).

HRMS (TOF, ESI) m/z: Calculated for C35H34F2N6O4 640.2610, Found: 641.2684 [M+H] ⁺ 5-amino-6-(4-fluorophenoxy)-3-[(4-hydroxy-l-{[(lR,2R,4R)-4-m ethoxy-2-phenyl-4- [2-(pyridazin-3-yl)ethynyl] cyclohexyl] carbonyl}piperidin-4-yl)methyl] pyrimidin-4- one (EXAMPLE 146)

and

5-amino-6-(4-fluorophenoxy)-3-[(4-hydroxy-l-{[(lR,2R,4S)-4-m ethoxy-2-phenyl-4-[2- (pyridazin-3-yl)ethynyl] cyclohexyl] carbonyl}piperidin-4-yl)methyl] pyrimidin-4-one (EXAMPLE 147)

Step 1: tert-butyl ( lR,2R)-4-methoxy-2-phenyl-4-[2-(pyridazin-3-yl)ethynyl]cyclo hexane-l - carboxylate

To a solution of tert- butyl (lR,2R)-4-hydroxy-2-phenyl-4-[2-(pyridazin-3-yl)ethynyl] cyclohexane- 1 -carboxylate (100 mg, 0.26 mmol, 1 eq.) in DMF (3 mL) at 0°C under nitrogen, sodium hydride (13 mg, 0.53 mmol, 2 eq.) was added. The mixture stirred for 10 minutes before adding iodomethane (0.02 mL, 0.26 mmol, 1 eq.). After 10 minutes the reaction mixture was allowed to warm to r.t. over 1 hour. Aq. NH ₄ CI solution was added (15 mL) and extracted with EtOAc (2 x 20 mL). The combined organic layer were washed with brine (3 x 20 mL), dried over MgSCL and evaporated in vacuo to afford a crude oil (200 mg). This residue was purified via flash chromatography using Heptane-60 % EtOAc

(gradient) as eluent to give tert-butyl (lR,2R)-4-methoxy-2-phenyl-4-[2-(pyridazin-3- yl)ethynyl]cyclo hexane- 1 -carboxylate as a brown oil.

LC/MS (Method B): RT = 1.11; m/z = 393 [M+H] ⁺ Step 2: (lR,2R)-4-methoxy-2-phenyl-4-[2-(pyridazin-3-yl)ethynyl] cyclohexane- 1- carboxylic acid

Starting from tert-butyl (lR,2R)-4-methoxy-2-phenyl-4-[2-(pyridazin-3-yl)ethynyl] cyclohexane- l-carboxylate (80 mg, 0.2 mmol) following procedure described in Step 5 of EXAMPLE 133, (lR,2R)-4-methoxy-2-phenyl-4-[2-(pyridazin-3-yl)ethynyl]cycl ohexane-l- carboxylic acid was obtained as a yellow oil. The compound was used without further purification.

LC/MS (Method B): RT = 0.80; m/z = 337 [M+H] ⁺

Step 3: EXAMPLES 146 and 147

Starting from 5 -amino-6-(4-fluorophenoxy)-3 - [(4-hydroxypiperidin-4-yl)methyl] pyrimidin-4-one (60 mg, 0.18 mmol) and (lR,2R)-4-methoxy-2-phenyl-4-[2-(pyridazin-3- yl)ethynyl]cyclo hexane- 1 -carboxylic acid (60 mg, 1 eq.) following procedure described in Step 3 of EXAMPLE 94, the obtained residue was purified via flash chromatography using DCM-5 % MeOH (gradient) as eluent to give the still impure product as colourless oil. Final purification was performed via prep HPLC Prep (HPLC Column: Gemini pH4 Dimensions: 21.1 mm x 150 mm 5 pm) to afford:

First elute: EXAMPLE 147 as a white solid.

LC/MS (Method B): RT = 1.08; m/z = 653 [M+H] ⁺

1H NMR (399 MHz, DMSO- ) d 9.28 (dt, J = 5.1, 1.6 Hz, 1H), 7.94 (ddd, J = 8.5, 2.8, 1.7 Hz, 1H), 7.79 (ddd, J = 8.5, 5.0, 1.3 Hz, 1H), 7.63-7.57 (m, 1H), 7.33-7.16 (m, 7H), 7.11- 7.07 (m, 2H), 4.82 (m, 1H), 4.68 (m, 2H), 3.96-3.61 (m, 4H), 3.41 (m, 3H), 3.25-2.89 (m, 3H), 2.67 (m, 1H), 2.22 (m, 2H), 1.97-1.74 (m, 4H), 1.46-1.11 (m, 3H), 0.80-0.55 (m, 1H) HRMS (TOF, ESI) m/z: Calculated for CseHsyFNeOs 652.2809, Found: 653.2886 [M+H] ⁺ Second elute: EXAMPLE 146 as a white solid

LC/MS (Method B): RT = 1.11; m/z = 653 [M+H] ⁺

1H NMR (399 MHz, DMSO- ) 9.15 (dt, J = 5.0, 1.6 Hz, 1H), Ί.Ί6 (ddd, J = 8.5, 3.2, 1.7 Hz, 1H), 7.66 (ddd, J = 8.5, 5.0, 1.8 Hz, 1H) 7.57-7.51 (m, 1H), 7.25-7.09 (m, 7H), 7.05- 7.00 (m, 2H), 4.80 (m, 2H), 3.89-3.53 (m, 4H), 3.41 (m, 3H), 3.17-2.83 (m, 4H), 2.58 (m, 1H), 2.22-1.86 (m, 5H), 1.68 (m, 1H), 1.54-1.06 (m, 3H), 0.73-0.50 (m, 1H)

HRMS (TOF, ESI) m/z: Calculated for CseHsyFNeOs 652.2809, Found: 653.2889 [M+H] ⁺ 5-amino-3-({l-[(lR,2R,4R)-4-fluoro-4-[2-(3-methylpyrazin-2-y l)ethynyl]-2- phenylcyclohexanecarbonyl]-4-hydroxypiperidin-4-yl}methyl)-6 -(4-fluorophenoxy)- 3,4-dihydropyrimidin-4-one (EXAMPLE 148)

Step 1: tert-butyl (lR,2R) -4-hydroxy-4-[2-(3-methylpyrazin-2-yl)ethynyl] -2- phenylcyclohexane-l -carboxylate

Starting from tert-butyl (lR,2R)-4-oxo-2-phenylcyclohexane-l -carboxylate (300 mg, 1.09 mmol) and 2-ethynyl-3-methylpyrazine (167.93 mg, 1.42 mmol) following procedure described in Step 2 of EXAMPLES 122 and 123, the obtained residue was purified via flash chromatography using Heptane-60 % EtO Ac/Heptane (gradient) as eluent to afford tert- butyl ( 1 R,2R)-4-hydroxy-4- [2-(3 -methylpyrazin-2-yl)ethynyl] -2-phenylcyclo hexane- 1 - carboxylate as a yellow oil.

LC/MS (Method B): RT = 1.247; m/z = 393 [M+H] ⁺

Step 2: tert-butyl ( lR,2R)-4-fluoro-4-[2-(3-methylpyrazin-2-yl)ethynyl]-2 - phenylcyclohexane-l -carboxylate

Starting from tert-butyl (lR,2R)-4-hydroxy-4-[2-(3-methylpyrazin-2-yl)ethynyl]-2- phenylcyclo hexane- 1 -carboxylate (252 mg, 0.64 mmol) following procedure described in Step 4 of EXAMPLES 122 and 123, the obtained residue was purified via flash chromatography using Heptane-30 % EtO Ac/Heptane (gradient) as eluent to afford tert-butyl ( 1 R,2R)-4-fluoro-4- [2-(3 -methylpyrazin-2-yl)ethynyl] -2-phenylcyclo hexane- 1 - carboxylate as an oil.

LC/MS (Method B): RT = 1.427; m/z = 395 [M+H] ⁺

Step 3: (lR,2R)-4 -fluoro -4 -[2 -(3 -methylpyrazin -2 -yl)ethynyl] -2 -phenylcyclohexane -/ - carboxylic acid

Starting from tert-butyl (lR,2R)-4-fluoro-4-[2-(3-methylpyrazin-2-yl)ethynyl]-2- phenylcyclohexane-l -carboxylate (47 mg, 0.12 mmol) following procedure described in Step 5 of EXAMPLE 133, (lR,2R)-4-fluoro-4-[2-(3-methylpyrazin-2-yl)ethynyl]-2- phenylcyclo hexane- 1 -carboxylic acid was obtained as a yellow oil. The compound was used without further purification.

LC/MS (Method B): RT = 1.12; m/z = 339 [M-H] ⁺ Step 4: EXAMPLE 148

Starting from ( 1 R,2R)-4-fluoro-4- [2-(3 -methylpyrazin-2-yl)ethynyl] -2-phenylcyclohexane- l-carboxylic acid (150 mg) and 5-amino-6-(4-fluorophenoxy)-3-[(4-hydroxypiperidin-4- yl)methyl]pyrimidin-4-one (148 mg, 0.44 mmol) following procedure described in Step 3 of EXAMPLE 94, the obtained residue was purified via prep HPLC Prep (HPLC Column: Gemini pH4 Dimensions: 21.1 mm x 150 mm 5 pm) to afford EXAMPLE 148 as a white solid.

LC/MS (Method B): RT = 1.203; m/z = 655 [M+H] ⁺

1H NMR (399 MHz, DMSO- ) 8.59 (m, 1H), 8.56 (m, 1H), 7.62-7.56 (m, 1H), 7.35-7.18 (m, 7H), 7.11-7.09 (m, 2H), 4.82 (m, 1H), 4.67 (m, 2H), 3.96-3.59 (m, 4H), 3.27-2.85 (m,

3H), 2.74 (s, 3H), 2.66 (m, 1H), 2.35-2.10 (m, 4H), 1.89 (m, 2H), 1.47-1.11 (m, 3H), 0.74- 0.56 (m, 1H).

HRMS (TOF, ESI) m/z: Calculated for CseHseFzNeCF 654.2766, Found: 655.2849 [M+H] ⁺ 5-amino-3-[(l-{[(lR,2R,4R)-4-fluoro-4-[2-(l-methylimidazol-2 -yl)ethynyl]-2- phenylcyclohexyl]carbonyl}-4-hydroxypiperidin-4-yl)methyl]-6 -(4- fluorophenoxy)pyrimidin-4-one (EXAMPLE 149)

Step 1: tert-butyl ( lR,2R)-4-hydroxy-4-[2-(l-methylimidazol-2-yl)ethynyl]-2 - phenylcyclohexane-l-carboxylate

Starting from tert-butyl (lR,2R)-4-oxo-2-phenylcyclo hexane- l-carboxylate (400 mg, 1.46 mmol) and 2-ethynyl-l -methyl- lH-imidazole (201 mg, 1.9 mmol, 1.3 eq.) following procedure described in Step 2 of EXAMPLES 122 and 123, the obtained residue was purified via flash chromatography using DCM-5 % MeOH/DCM (gradient) as eluent to give tert-butyl ( 1 R,2R)-4-hydroxy-4- [2-( 1 -methylimidazo l-2-yl)ethynyl] -2- phenylcyclo hexane- l-carboxylate as a white solid.

FC/MS (Method B): RT = 1.122; m/z = 381 [M+H] ⁺

Step 2: tert-butyl ( lR,2R,4S)-4-fluoro-4-[2-(l-methylimidazol-2-yl)ethynyl]-2 - phenylcyclohexane- l-carboxylate (XX) and tert-butyl (lR,2R,4R)-4-fluoro-4-[2-(l- methylimidazol-2-yl)ethynyl]-2-phenylcyclohexane- l-carboxylate Starting from tert-butyl (lR,2R)-4-hydroxy-4-[2-(l-methylimidazol-2-yl)ethynyl]-2- phenylcyclohexane-l-carboxylate (380 mg, 1.00 mmol) following procedure described in Step 4 of EXAMPLES 122 and 123, the obtained residue was purified via flash chromatography using Heptane-58 % EtO Ac/Heptane (gradient) as eluent to afford:

First elute: tert-butyl (lR,2R,4R)-4-fluoro-4-[2-(l-methylimidazol-2-yl)ethynyl]-2- phenylcyclo hexane- 1 -carboxylate

LC/MS (Method B): RT = 1.32; m/z = 383 [M+H] ⁺

Second elute: tert-butyl (lR,2R,4S)-4-fluoro-4-[2-(l-methylimidazol-2-yl)ethynyl]-2- phenylcyclo hexane- 1 -carboxylate

LC/MS (Method B): RT = 1.33; m/z = 383 [M+H] ⁺

Step 3: (lR,2R,4R)-4-fluoro-4-[2-(l-methylimidazol-2-yl)ethynyl]-2-p henylcyclohexane-l- carboxylic acid

Starting from tert-butyl (lR,2R,4R)-4-fluoro-4-[2-(l-methylimidazol-2-yl)ethynyl]-2- phenylcyclo hexane- 1 -carboxylate (65 mg, 0.17 mmol) following procedure described in Step 5 of EXAMPLE 133, (lR,2R,4R)-4-fluoro-4-[2-(l-methylimidazol-2-yl)ethynyl]-2- phenylcyclo hexane- 1 -carboxylic acid was obtained as a yellow oil. The compound was used without further purification.

LC/MS (Method B): RT = 1.003; m/z = 327 [M+H] ⁺

Step 4: EXAMPLE 149

Starting from 5 -amino-6-(4-fluorophenoxy)-3 - [(4-hydroxypiperidin-4-yl)methyl] pyrimidin-4-one (92 mg, 0.28 mmol) and (lR,2R,4R)-4-fluoro-4-[2-(l-methylimidazol-2- yl)ethynyl]-2-phenylcyclo hexane- 1 -carboxylic acid (90 mg) following procedure described in Step 3 of EXAMPLE 94, the obtained residue was purified via prep HPLC Prep (HPLC Column: Gemini pH4 Dimensions: 21.1 mm x 150 mm 5 pm) to afford EXAMPLE 149 as a white solid.

LC/MS (Method B): RT = 1.11; m/z = 643 [M+H] ⁺

1H NMR (399 MHz, DMSO- ) d 7.55-7.50 (m, 1H), 7.33 (s, 1H), 7.27-6.94 (m, 10H), 4.75 (m, 3H), 3.89-3.77 (m, 2H), 3.72 (s, 3H), 3.65-3.52 (m, 2H), 3.24-2.77 (m, 3H), 2.62- 2.54 (m, 1H), 2.30-2.00 (m, 4H), 1.84-1.73 (m, 2H), 1.39-1.03 (m, 3H), 0.71-0.42 (m, 1H). HRMS (TOF, ESI) m/z: Calculated for C35H36F2N6O4 642.2766, Found: 643.2808 [M+H] ⁺ 5-amino-3-({l-[(lR,2R,4S)-4-fluoro-4-[2-(5-methylpyrazin-2-y l)ethynyl]-2- phenylcyclohexanecarbonyl]-4-hydroxypiperidin-4-yl}methyl)-6 -(4-fluorophenoxy)- 3,4-dihydropyrimidin-4-one (EXAMPLE 150)

and

5-amino-3-({l-[(lR,2R,4R)-4-fluoro-4-[2-(5-methylpyrazin- 2-yl)ethynyl]-2- phenylcyclohexanecarbonyl]-4-hydroxypiperidin-4-yl}methyl)-6 -(4-fluorophenoxy)- 3,4-dihydropyrimidin-4-one (EXAMPLE 151)

Step 1: tert-butyl (lR,2R) -4-hydroxy-4-[2-(5-methylpyrazin-2-yl)ethynyl] -2- ph enyl eye I o h ex a n e - / -carboxylate

Starting from tert-butyl (lR,2R)-4-oxo-2-phenylcyclohexane-l -carboxylate (300 mg, 1.09 mmol) and 2-ethynyl-5-methylpyrazine (168 mg, 1.42 mmol, 1.3 eq.) following procedure described in Step 2 of EXAMPLES 122 and 123, the obtained residue was purified via flash chromatography using Heptane-60 % EtOAc/Heptane (gradient) as eluent to afford tert-butyl (lR,2R)-4-hydroxy-4-[2-(5-methylpyrazin-2-yl)ethynyl]-2- phenylcyclo hexane- 1 -carboxylate as an off- white solid.

LC/MS (Method B): RT = 1.26; m/z = 393 [M+H] ⁺

Step 2: tert-butyl (lR,2R) -4-fluoro-4-[2-(5-methylpyrazin-2-yl)ethynyl] -2- ph enyl eye l o h ex a n e - / -carboxylate

Starting from tert-butyl (lR,2R)-4-hydroxy-4-[2-(5-methylpyrazin-2-yl)ethynyl]-2- phenylcyclo hexane- 1 -carboxylate (185 mg, 0.47 mmol) following procedure described in Step 4 of EXAMPLES 122 and 123, the obtained residue was purified via flash chromatography using Heptane-60 % EtOAc/Heptane (gradient) as eluent to afford tert- butyl (lR,2R)-4-fluoro-4-[2-(5-methylpyrazin-2-yl)ethynyl]-2-pheny lcyclohexane- 1 - carboxylate as an oil.

LC/MS (Method B): RT = 1.437; m/z = 395 [M+H] ⁺

Step 3: (lR,2R)-4 -fluoro -4 -[2 -(5 -methylpyrazin -2 -yl)ethynyl] -2 -phenylcyclohexane -/ - carboxylic acid Starting from tert-butyl (lR,2R)-4-fluoro-4-[2-(5-methylpyrazin-2-yl)ethynyl]-2- phenylcyclohexane-l-carboxylate (147 mg, 0.37 mmol) following procedure described in Step 5 of EXAMPLE 133, (lR,2R)-4-fluoro-4-[2-(5-methylpyrazin-2-yl)ethynyl]-2- phenylcyclo hexane- 1 -carboxylic acid was obtained as a yellow oil. The compound was used without further purification.

LC/MS (Method B): RT = 1.136; m/z = 339 [M+H] ⁺

Step 4: 5 EXAMPLES 150 and 151

Starting from ( 1 R,2R)-4-fluoro-4- [2-(5 -methylpyrazin-2-yl)ethynyl] -2-phenylcyclohexane- 1 -carboxylic acid (144 mg)and 5-amino-6-(4-fluorophenoxy)-3-[(4-hydroxypiperidin-4- yl)methyl]pyrimidin-4-one (142 mg, 0.44 mmol) following procedure described in Step 3 of EXAMPLE 94, the obtained residue was purified via prep HPLC Prep (HPLC Column: Gemini pH4 Dimensions: 21.1 mm x 150 mm 5 pm) to give:

First elute: EXAMPLE 150 as a white solid.

LC/MS (Method B): RT = 1.198; m/z = 635 [M-HF] ⁺

1H NMR (399 MHz, DMSO- ) 8.68 (m, 1H), 8.59 (m, 1H), 7.63-7.57 (m, 1H), 7.33-7.17 (m, 7H), 7.12-7.07 (m, 2H), 4.82 (m, 1H), 4.68 (m, 2H), 3.97-3.62 (m, 4H), 3.28-2.88 (m, 3H), 2.67 (m, 1H), 2.53 (s, 3H), 2.46-2.08 (m, 4H), 1.87-1.65 (m, 2H), 1.47-1.11 (m, 3H), 0.79-0.57 (m, 1H).

HRMS (TOF, ESI) m/z: Calculated for CseHseFzNeCL 654.2766, Found: 655.2818 [M+H] ⁺ Second elute: EXAMPLE 151 as a white solid.

LC/MS (Method B): RT = 1.216; m/z = 655 [M+H] ⁺

1H NMR (399 MHz, DMSO- ) 8.76 (m, 1H), 8.64 (m, 1H), 7.62-7.56 (m, 1H), 7.35-7.17 (m, 7H), 7.12-7.07 (m, 2H), 4.82 (m, 1H), 4.68 (m, 2H), 3.96-3.61 (m, 4H), 3.29-2.85 (m, 3H), 2.66 (m, 1H), 2.57 (s, 3H), 2.34-2.08 (m, 4H), 1.86 (m, 2H), 1.47-1.11 (m, 3H), 0.78- 0.53 (m, 1H).

HRMS (TOF, ESI) m/z: Calculated for C ₃₆ H ₃₆ F ₂ N ₆ O ₄ 654.2766, Found: 655.2809 [M+H] ⁺ 5-amino-3-[(l-{[(lR,2R,4S)-4-fluoro-4-[2-(l-methylimidazol-2 -yl)ethynyl]-2- phenylcyclohexyl]carbonyl}-4-hydroxypiperidin-4-yl)methyl]-6 -(4- fluorophenoxy)pyrimidin-4-one (EXAMPLE 152) Step 1: (lR,2R,4S)-4-fluoro-4-[2-(l-methylimidazol-2-yl)ethynyl]-2-p henylcyclohexane-l- carboxylic acid

Starting from tert-butyl (lR,2R,4S)-4-fluoro-4-[2-(l-methylimidazol-2-yl)ethynyl]-2- phenylcyclohexane-l-carboxylate (190 mg, 0.50 mmol) following procedure described in Step 5 of EXAMPLE 133, (lR,2R,4S)-4-fluoro-4-[2-(l-methylimidazol-2-yl)ethynyl]-2- phenylcyclo hexane- 1 -carboxylic acid was obtained as a yellow oil. The compound was used without further purification.

LC/MS (Method B): RT = 0.77; m/z = 327 [M+H] ⁺

Step 2: EXAMPLE 152

Starting from 5-amino-6-(4-fluorophenoxy)-3-[(4-hydroxypiperidin-4-yl)meth yl] pyrimidin-4-one (195 mg, 0.98 mmol) and (lR,2R,4S)-4-fluoro-4-[2-(l-methylimidazol-2- yl)ethynyl]-2-phenylcyclohexane-l -carboxylic acid (190 mg) following procedure described in Step 3 of EXAMPLE 94, the obtained residue was purified via flash chromatography using DCM-3 % MeOH (gradient) as eluent to give the still impure product as colourless oil. Final purification was performed via prep HPLC Prep (HPLC Column: Gemini pH4 Dimensions: 21.1 mm x 150 mm 5 pm) to afford EXAMPLE 152 as a white solid.

LC/MS (Method B): RT = 1.088; m/z = 643 [M+H] ⁺

1H NMR (399 MHz, DMSO- ) d 7.55-7.50 (m, 1H), 7.26-7.08 (m, 8H), 7.04-7.00 (m, 2H), 6.91 (m, 1H), 4.76 (m, 1H), 4.60 (m, 2H), 3.90-3.55 (m, 5H), 3.41-2.82 (m, 5H),

2.62-2.51 (m, 1H), 2.20-1.98 (m, 4H), 1.84-1.53 (m, 2H), 1.43-0.97 (m, 3H), 0.70-0.55 (m, 1H).

HRMS (TOF, ESI) m/z: Calculated for C ₃₅ H ₃₆ F ₂ N ₆ O ₄ 642.2766, Found: 643.281 [M+H] ⁺ 5-amino-3-({l-[(lR,2R,4R)-4-[2-(3-chloropyrazin-2-yl)ethynyl ]-4-fluoro-2- phenylcyclohexanecarbonyl]-4-hydroxypiperidin-4-yl}methyl)-6 -(4-fluorophenoxy)- 3,4-dihydropyrimidin-4-one (EXAMPLE 153)

Step 1: tert-butyl (1R,2R) -4-[2 -(3 -chloropyrazin-2 -yl)ethynyl] -4-hydroxy-2 - ph enyl eye I o h ex a n e - / -carboxylate Starting from tert-butyl (lR,2R)-4-oxo-2-phenylcyclohexane-l-carboxylate (300 mg, 1.09 mmol) and 2-chloro-3-ethynylpyrazine (196.96 mg, 1.42 mmol) following procedure described in Step 2 of EXAMPLES 122 and 123, the obtained residue was purified via flash chromatography using Heptane-40 % EtO Ac/Heptane (gradient) as eluent to afford tert- butyl (lR,2R)-4-[2-(3-chloropyrazin-2-yl)ethynyl]-4-hydroxy-2-phen ylcyclohexane- 1 - carboxylate as a yellow foam.

1H NMR (399 MHz, Chloroform-d) 8.44 (d, J = 2.5 Hz, 1H), 8.27 (d, J = 2.5 Hz, 1H), 7.26-7.09 (m, 5H), 3.22 (ddd, J = 13.1, 11.4, 3.3 Hz, 1H), 2.49-2.42 (m, 1H), 2.38 (s, 1H), 2.28-2.23 (m, 2H), 2.07-2.01 (m, 2H), 1.91-1.67 (m, 2H), 1.25-1.15 (m, 1H), 1.07 (s, 9H). Step 2: tert-butyl (1R,2R) -4-[2 -(3 -chloropyrazin-2 -yl)ethynyl] -4-fluoro-2- ph enyl eye l o h ex a n e - / -carboxylate

Starting from tert-butyl (lR,2R)-4-[2-(3-chloropyrazin-2-yl)ethynyl]-4-hydroxy-2- phenylcyclo hexane- 1 -carboxylate (196 mg, 0.47 mmol) following procedure described in Step 4 of EXAMPLES 122 and 123, the obtained residue was purified via flash chromatography using Heptane-60 % EtO Ac/Heptane (gradient) as eluent to afford tert- butyl ( 1 R,2R)-4- [2-(3 -chloropyrazin-2-yl)ethynyl] -4-fluoro-2-phenylcyclo hexane- 1 - carboxylate as an oil.

LC/MS (Method B): RT = 1.471; m/z = 394 Others

Step 3: ( 1R,2R ) -4 -[2 -(3 -chloropyrazin -2 -yl)ethynyl] -4 -fluoro -2 -phenylcyclohexane -1 - carboxylic acid

Starting from tert-butyl (lR,2R)-4-[2-(3-chloropyrazin-2-yl)ethynyl]-4-fluoro-2- phenylcyclo hexane- 1 -carboxylate (121 mg, 0.29 mmol) following procedure described in Step 5 of EXAMPLE 133, (lR,2R)-4-fluoro-4-[2-(3-methylpyrazin-2-yl)ethynyl]-2- phenylcyclo hexane- 1 -carboxylic acid was obtained as a yellow oil. The compound was used without further purification.

LC/MS (Method B): RT = 1.185; m/z = 357 [M-H]-

Step 4: EXAMPLE 153

Starting from ( 1 R,2R)-4-fluoro-4- [2-(3 -methylpyrazin-2-yl)ethynyl] -2-phenylcyclohexane- 1 -carboxylic acid (123 mg) and 5-amino-6-(4-fluorophenoxy)-3-[(4-hydroxypiperidin-4- yl)methyl]pyrimidin-4-one (14 mg, 0.34 mmol) following procedure described in Step 3 of EXAMPLE 94, the obtained residue was purified via prep HPLC Prep (HPLC Column: Gemini pH4 Dimensions: 21.1 mm x 150 mm 5 pm) to afford EXAMPLE 153 as a white solid.

LC/MS (Method B): RT = 1.258; m/z = 675 [M+H] ⁺

1H NMR (399 MHz, DMSO- ) 8.75 (t, J = 2.3 Hz, 1H), 8.61 (t, J = 2.1 Hz, 1H), 7.62-7.57 (m, 1H), 7.35-7.17 (m, 7H), 7.12-7.07 (m, 2H), 4.82 (m, 1H), 4.69 (m, 2H), 3.95-3.61 (m, 4H), 3.31-2.86 (m, 3H), 2.66 (m, 1H), 2.42-2.13 (m, 4H), 1.89 (m, 2H), 1.47-1.10 (m, 3H), 0.78 -056 (m, 1H).

HRMS (TOF, ESI) m/z: Calculated for C35H33CIF2N6O4 674.222, Found: 675.2265 [M+H] ⁺ 5-amino-3-({l-[(lR,2R,4R)-4-fluoro-4-[2-(3-methoxypyrazin-2- yl)ethynyl]-2- phenylcyclohexanecarbonyl]-4-hydroxypiperidin-4-yl}methyl)-6 -(4-fluorophenoxy)- 3,4-dihydropyrimidin-4-one (EXAMPLE 154) Step 1: tert-butyl (lR,2R) -4-hydroxy-4-[2-(3-methoxypyrazin-2-yl)ethynylJ -2- ph enyl eye I o h ex a n e - / -carboxylate

Starting from tert-butyl (lR,2R)-4-oxo-2-phenylcyclohexane-l -carboxylate (300 mg, 1.09 mmol) and 2-ethynyl-3-methoxypyrazine (191 mg, 1.42 mmol) following procedure described in Step 2 of EXAMPLES 122 and 123, the obtained residue was purified via flash chromatography using Heptane-60 % EtO Ac/Heptane (gradient) as eluent to afford tert- butyl ( 1 R,2R)-4-hydroxy-4- [2-(3 -methoxypyrazin-2-yl)ethynyl] -2-phenylcyclo hexane- 1 - carboxylate as an off- white solid.

FC/MS (Method B): RT = 1.318; m/z = 409 [M+H] ⁺ r

Step 2: tert-butyl (lR,2R) -4-fluoro-4-[2-(3-methoxypyrazin-2-yl)ethynyl] -2- ph enyl eye l o h ex a n e - / -carboxylate

Starting from tert-butyl (lR,2R)-4-hydroxy-4-[2-(3-methoxypyrazin-2-yl)ethynyl]-2- phenylcyclo hexane- 1 -carboxylate (230 mg, 0.56 mmol) following procedure described in Step 4 of EXAMPLES 122 and 123, the obtained residue was purified via flash chromatography using Heptane-30 % EtO Ac/Heptane (gradient) as eluent to afford tert- butyl (lR,2R)-4-fluoro-4-[2-(3-methoxypyrazin-2-yl)ethynyl]-2-phen ylcyclohexane- 1 - carboxylate as an oil.

LC/MS (Method B): RT = 1.488; m/z = 411 [M+H] ⁺

Step 3: (lR,2R)-4 -fluoro -4 -[2 -(3 -methoxypyrazin -2 -yl)ethynyl] -2 -phenylcyclohexane -/ - carboxylic acid

Starting from tert-butyl (lR,2R)-4-fluoro-4-[2-(3-methoxypyrazin-2-yl)ethynyl]-2- phenylcyclo hexane- 1 -carboxylate (113 mg, 0.28 mmol) following procedure described in Step 5 of EXAMPLE 133, (lR,2R)-4-fluoro-4-[2-(3-methoxypyrazin-2-yl)ethynyl]-2- phenylcyclo hexane- 1 -carboxylic acid was obtained as a yellow oil. The compound was used without further purification.

LC/MS (Method B): RT = 1.17; m/z = 355 [M+H] ⁺

Step 4: EXAMPLE 154

Starting from ( 1 R,2R)-4-fluoro-4- [2-(3 -methoxypyrazin-2-yl)ethynyl] -2- phenylcyclo hexane- 1 -carboxylic acid (110 mg) and 5-amino-6-(4-fluorophenoxy)-3-[(4- hydroxypiperidin-4-yl)methyl]pyrimidin-4-one (106 mg, 0.32 mmol) following procedure described in Step 3 of EXAMPLE 94, the obtained residue was purified via prep HPLC Prep (HPLC Column: Gemini pH4 Dimensions: 21.1 mm x 150 mm 5 pm) to afford EXAMPLE 154 as a white solid.

LC/MS (Method B): RT = 1.06; m/z = 671 [M+H] ⁺

1H NMR (399 MHz, DMSO- ) 8.32 (dd, J = 2.7, 1.7 Hz, 1H), 8.29 (dd, J = 2.7, 1.9 Hz, 1H), 7.62-7.57 (m, 1H), 7.35-7.16 (m, 7H), 7.12-7.07 (m, 2H), 4.83 (s, 1H), 4.68 (m, 2H), 4.04 (s, 3H), 3.96-3.82 (m, 2H), 3.75-3.61 (m, 2H), 3.26-2.87 (m, 3H), 2.65 (m, 1H), 2.36- 2.10 (m, 4H), 1.88 (m, 2H), 1.47-1.11 (m, 3H), 0.78-0.56 (m, 1H).

HRMS (TOF, ESI) m/z: Calculated for CseHseFzNeOs 670.2715, Found: 671.2759 [M+H] ⁺ 5-amino-3-[(l-{[(lR,2R,4R)-4-ethynyl-4-methoxy-2-phenylcyclo hexyl]carbonyl}-4- hydroxypiperidin-4-yl)methyl] -6-(4-fluorophenoxy)pyrimidin-4-one (EXAMPLE 155)

Step 1: tert-butyl ( I R, 2 Rj -4 -hydroxy -2 -phenyl -4 -[2 -( triniethylsilyljethynyl ] cyclohexane -/ - carboxylate Starting from tert-butyl (lR,2R)-4-oxo-2-phenylcyclohexane-l-carboxylate (500 mg, 1.82 mmol) and ethynyltrimethylsilane (233 mg, 2.37 mmol) following procedure described in Step 2 of EXAMPLES 122 and 123, the obtained residue was purified via flash chromatography using Heptane-20 % EtO Ac/Heptane (gradient) as eluent to afford tert- butyl ( 1 R,2R)-4-hydroxy-2-phenyl-4- [2-(trimethylsilyl)ethynyl]cyclo hexane- 1 -carboxylate as an off-white solid.

1H NMR (399 MHz, DMSO- ) d 7.11-6.94 (m, 5H), 5.42 (s, 1H), 2.87-2.74 (m, 1H), 2.57-2.34 (m, 1H), 2.23 (td, J = 11.6, 3.8 Hz, 1H), 2.10-1.92 (m, 1H), 1.69-1.51 (m, 3H), 1.47-1.29 (m, 1H), 0.87 (s, 9H), 0.00 (s, 9H). Step 2: tert-butyl ( lR,2R)-4-ethynyl-4-methoxy-2-phenylcyclohexane-l-carboxylate

Starting from tert-butyl (lR,2R)-4-hydroxy-2-phenyl-4-[2-(trimethylsilyl)ethynyl] cyclohexane- 1 -carboxylate (525 mg, 0.78 mmol) following procedure described in Step 1 of EXAMPLES 146 and 147, tert-butyl (lR,2R)-4-ethynyl-4-methoxy-2- phenylcyclo hexane- 1 -carboxylate was obtained as a white solid.

1H NMR (399 MHz, DMSO- ) d 7.30-7.18 (m, 5H), 3.71 (s, 1H), 3.28 (s, 3H), 2.94 (ddd, J = 13.0, 11.5, 3.4 Hz, 1H), 2.56 (dd, J = 11.8, 3.6 Hz, 1H), 2.10-1.88 (m, 3H), 1.82-1.48 (m, 3H), 1.08 (s, 9H).

Step 3: (lR,2R)-4-ethynyl-4-methoxy-2-phenylcyclohexane-l -carboxylic acid

Starting from tert-butyl (lR,2R)-4-ethynyl-4-methoxy-2-phenylcyclo hexane- 1 -carboxylate (110 mg, 0.35 mmol) following procedure described in Step 5 of EXAMPLE 133, (lR,2R)-

4-ethynyl-4-methoxy-2-phenylcyclo hexane- 1 -carboxylic acid was obtained as a colourless oil. The compound was used without further purification.

LC/MS (Method B): RT = 1.08; m/z = 257 [M-H]-

Step 4: EXAMPLE 155

Starting from 5-amino-6-(4-fluorophenoxy)-3-[(4-hydroxypiperidin-4-yl)meth yl] pyrimidin-4-one (131 mg, 0.39 mmol) and (lR,2R)-4-ethynyl-4-methoxy-2- phenylcyclo hexane- 1 -carboxylic acid (92 mg) following procedure described in Step 3 of EXAMPLE 94, the obtained residue was purified via flash chromatography using DCM-5 % MeOH (gradient) as eluent to give the still impure product as colourless oil. Final purification was performed via flash chromatography using Heptane- 100 % EtOAc (gradient) as eluent to afford EXAMPLE 155 as a white solid.

LC/MS (Method B): RT = 1.17; m/z = 575 [M+H] ⁺

1H NMR (399 MHz, DMSO- ) d 7.62-7.56 (m, 1H), 7.34-7.05 (m, 9H), 4.81 (m, 1H), 4.68 (d, 2H), 3.96-3.81 (m, 2H), 3.71-3.60 (m, 3H), 3.29 (s, 3H), 3.17-2.85 (m, 3H), 2.68-

2.62 (m, 1H), 2.11-1.95 (m, 2H), 1.90-1.54 (m, 4H), 1.48-1.05 (m, 3H), 0.76-0.54 (m, 1H). HRMS (TOF, ESI) m/z: Calculated for C32H35FN4O5 574.2591, Found: 575.2646 [M+H] ⁺ 5-amino-6-(4-fluorophenoxy)-3-({4-hydroxy-l-[(lR,2R,4R)-4-me thoxy-2-phenyl-4- [2-(pyrazin-2-yl)ethynyl]cyclohexanecarbonyl]piperidin-4-yl} methyl)-3,4- dihydropyrimidin-4-one (EXAMPLE 156)

Step 1: tert-butyl ( 1R,2R) -4 -hydroxy -2 -phenyl -4 -[2 -(pyrazin -2 -yl)ethynyl] cyclohexane -1 - carboxylate

Starting from tert-butyl (lR,2R)-4-oxo-2-phenylcyclohexane-l-carboxylate (300 mg, 1.09 mmol) and 2-ethynylpyrazine (148 mg, 1.42 mmol) following procedure described in Step 2 of EXAMPLES 122 and 123, the obtained residue was purified via flash chromatography using Heptane-60 % EtO Ac/Heptane (gradient) as eluent to afford tert- butyl ( 1 R,2R)-4-hydroxy-2-phenyl-4- [2-(pyrazin-2-yl)ethynyl]cyclo hexane- 1 -carboxylate as a white solid.

LC/MS (Method B): RT = 1.230; m/z = 379 [M+H] ⁺ Step 2: tert-butyl ( 1R,2R) -4 -methoxy -2 -phenyl -4 -[2 -(pyrazin -2 -yl)ethynyl] cyclohexane -1 - carboxylate

Starting from tert-butyl (lR,2R)-4-hydroxy-2-phenyl-4-[2-(pyrazin-2-yl)ethynyl] cyclohexane- 1 -carboxylate (293 mg, 0.77 mmol) following procedure described in Step 1 of EXAMPLES 146 and 147, the obtained residue was purified via flash chromatography using Heptane-30 % EtOAc/Heptane (gradient) as eluent to afford tert-butyl (lR,2R)-4- methoxy-2-phenyl-4-[2-(pyrazin-2-yl)ethynyl]cyclohexane-l -carboxylate as an oil.

LC/MS (Method B): RT = 1.39; m/z = 393 [M+H] ⁺ Step 3: (lR,2R)-4 -methoxy -2 -phenyl -4 -[ 2 -(pyrazin -2 -yl)ethynyl] cyclohexane -1 -carboxylic acid

Starting from tert-butyl (lR,2R)-4-methoxy-2-phenyl-4-[2-(pyrazin-2-yl)ethynyl] cyclohexane- l-carboxylate (223 mg, 0.57 mmol) following procedure described in Step 5 of EXAMPLE 133, (lR,2R)-4-methoxy-2-phenyl-4-[2-(pyrazin-2-yl)ethynyl]cycloh exane- 1 -carboxylic acid was obtained as a yellow oil. The compound was used without further purification.

LC/MS (Method B): RT = 1.061; m/z = 337 [M+H] ⁺

Step 4: EXAMPLE 156

Starting from (lR,2R)-4-methoxy-2-phenyl-4-[2-(pyrazin-2-yl)ethynyl]cyclo hexane- 1- carboxylic acid (193 mg) and 5-amino-6-(4-fluorophenoxy)-3-[(4-hydroxypiperidin-4- yl)methyl]pyrimidin-4-one (192 mg, 0.57 mmol) following procedure described in Step 3 of EXAMPLE 94, the obtained residue was purified via flash chromatography using water- 100 % MeCN/water (gradient) as eluent to afford EXAMPLE 156 as a white solid.

LC/MS (Method B): RT = 1.162; m/z = 653 [M+H] ⁺

1H NMR (399 MHz, DMSO- ) 8.87 (m, 1H), 8.71 (m, 1H), 8.69 (m, 1H), 7.62-7.56 (m, 1H), 7.33-7.14 (m, 7H), 7.12-7.07 (m, 2H), 4.82 (m, 1H), 4.68 (m, 2H), 3.96-3.62 (m, 4H), 3.40 (s, 3H), 3.23-2.88 (m, 3H), 2.66 (m, 1H), 2.21 (m, 2H), 1.95-1.72 (m, 4H), 1.45-1.11 (m, 3H), 0.81-0.56 (m, 1H).

HRMS (TOF, ESI) m/z: Calculated for CseHsyFNeOs 652.2809, Found: 653.2857 [M+H] ⁺ 5-amino-3-({l-[(lR,2R,4R)-4-fluoro-4-[2-(4-fluoropyridin-2-y l)ethynyl]-2- phenylcyclohexanecarbonyl]-4-hydroxypiperidin-4-yl}methyl)-6 -(4-fluorophenoxy)- 3,4-dihydropyrimidin-4-one (EXAMPLE 157)

Step 1: tert-butyl (lR,2R) -4-[2-(4 -fluoropyridin -2 -yl) ethynyl ] -4 -hydroxy -2 - ph enyl eye I o h ex a n e - / -carboxylate

Starting from tert-butyl (lR,2R)-4-oxo-2-phenylcyclohexane- l-carboxylate (348 mg, 1.27 mmol) and 2-ethynyl-4-fluoropyridine (148 mg, 1.42 mmol) following procedure described in Step 2 of EXAMPLES 122 and 123, the obtained residue was purified via flash chromatography using Heptane-50 % EtO Ac/Heptane (gradient) as eluent to afford tert- butyl ( 1 R,2R)-4- [2-(4-fluoropyridin-2-yl)ethynyl] -4-hydroxy-2-phenylcyclo hexane- 1 - carboxylate as a white solid.

LC/MS (Method B): RT = 1.310; m/z = 396 [M+H] ⁺

Step 2: tert-butyl (lR,2R,4R) -4fluoro-4-[2-(4fluoropyridin-2-yl)ethynyl]-2- phenylcyclohexane -/ -carboxylate and tert -butyl ( IR , 2R, 4S) -4 -fluoro -4-[2-(4- fluoropyridin -2 -yl)ethynyl] -2 -phenylcyclohexane -/ -carboxylate

Starting from tert-butyl (lR,2R)-4-[2-(4-fluoropyridin-2-yl)ethynyl]-4-hydroxy-2- phenylcyclo hexane- 1 -carboxylate (200 mg, 0.51 mmol) following procedure described in Step 4 of EXAMPLES 122 and 123, the obtained residue was purified via flash chromatography using Heptane-25 % EtO Ac/Heptane (gradient) as eluent to afford:

First elute: tert-butyl (lR,2R,4R)-4-fluoro-4-[2-(4-fluoropyridin-2-yl)ethynyl]-2- phenylcyclo hexane- 1 -carboxylate as a gum.

LC/MS (Method B): RT = 1.470; m/z = 398 [M+H] ⁺

Second elute: tert-butyl (lR,2R,4S)-4-fluoro-4-[2-(4-fluoropyridin-2-yl)ethynyl]-2- phenylcyclohexane- 1 -carboxylate as a gum.

LC/MS (Method B): RT = 1.480; m/z = 398 [M+H] ⁺

Step 3: (1R, 2R, 4R) -4 -fluoro -4 -[2 -(4 -fluoropyridin -2 -yl)ethynyl] -2 -phenylcyclohexane -/ - carboxylic acid

Starting from tert-butyl (lR,2R,4R)-4-fluoro-4-[2-(4-fluoropyridin-2-yl)ethynyl]-2- phenylcyclohexane- 1 -carboxylate (73 mg, 0.19 mmol) following procedure described in Step 5 of EXAMPLE 133, (lR,2R,4R)-4-fluoro-4-[2-(4-fluoropyridin-2-yl)ethynyl]-2- phenylcyclo hexane- 1 -carboxylic acid was obtained as a white solid.

LC/MS (Method B): RT = 1.190; m/z = 342 [M-H]

Step 4: EXAMPLE 157

Starting from ((lR,2R,4R)-4-fluoro-4-[2-(4-fluoropyridin-2-yl)ethynyl]-2- phenylcyclo hexane- 1 -carboxylic acid (55 mg, 0.161 mmol) and 5-amino-6-(4- fluorophenoxy)-3-[(4-hydroxypiperidin-4-yl)methyl]pyrimidin- 4-one (54 mg, 0.161 mmol) following procedure described in Step 3 of EXAMPLE 94, the obtained residue was purified via flash chromatography using DCM-10 % MeOH/DCM (gradient) as eluent to afford EXAMPLE 157 as a white solid.

LC/MS (Method B): RT = 1.07; m/z = 658 [M+H] ⁺

1H NMR (399 MHz, DMSO- ) 8.68 (m, 1H), 7.70 (m, 1H), 7.62-7.57 (m, 1H), 7.47 (m, 1H), 7.34-7.18 (m, 7H), 7.11-7.08 (m, 2H), 4.82 (m, 1H), 4.70 (m, 2H), 3.96-3.60 (m, 4H),

3.28-2.86 (m, 3H), 2.66 (m, 1H), 2.37-2.06 (m, 4H), 1.85 (m, 2H), 1.46-1.12 (m, 3H), 0.78-0.52 (m, 1H). 5-amino-3-({l-[(lR,2R,4S)-4-fluoro-4-[2-(4-fluoropyridin-2-y l)ethynyl]-2- phenylcyclohexanecarbonyl]-4-hydroxypiperidin-4-yl}methyl)-6 -(4-fluorophenoxy)- 3,4-dihydropyrimidin-4-one (EXAMPLE 158)

Step 1: ( 1R,2R,4S ) -4 -fluoro -4 -[2 -( 4 -fluoropyridin -2 -yl) ethynyl ] -2 -pheny /cyclohexane -/ - carboxylic acid

Starting from tert-butyl (lR,2R,4S)-4-fluoro-4-[2-(4-fluoropyridin-2-yl)ethynyl]-2- phenylcyclohexane-l-carboxylate (69 mg, 0.17 mmol) following procedure described in Step 5 of EXAMPLE 133, (lR,2R,4S)-4-fluoro-4-[2-(4-fluoropyridin-2-yl)ethynyl]-2- phenylcyclo hexane- 1 -carboxylic acid was obtained as a white solid.

LC/MS (Method B): RT = 1.180; m/z = 342 [M-H]-

Step 2: EXAMPLE 158

Starting from ((lR,2R,4S)-4-fluoro-4-[2-(4-fluoropyridin-2-yl)ethynyl]-2- phenylcyclo hexane- 1 -carboxylic acid (55 mg, 0.161 mmol) and 5-amino-6-(4- fluorophenoxy)-3-[(4-hydroxypiperidin-4-yl)methyl]pyrimidin- 4-one (54 mg, 0.161 mmol) following procedure described in Step 3 of EXAMPLE 94, the obtained residue was purified via flash chromatography using DCM-10 % MeOH/DCM (gradient) as eluent to afford EXAMPLE 158 as a white solid.

LC/MS (Method B): RT = 1.04; m/z = 638 [M-HF] ⁺

1H NMR (399 MHz, DMSO- ) 8.62 (m, 1H), 7.62-7.57 (m, 2H), 7.43 (m, 1H), 7.34-7.17 (m, 7H), 7.12-7.07 (m, 2H), 4.82 (m, 1H), 4.69 (m, 2H), 3.96-3.61 (m, 4H), 3.29-2.86 (m, 3H), 2.67 (m, 1H), 2.41-2.05 (m, 4H), 1.84-1.66 (m, 2H), 1.46-1.10 (m, 3H), 0.78-0.58 (m, 1H). HRMS (TOF, ESI) m/z: Calculated for C ₃₆ H ₃₄ F ₃ N ₅ O ₄ 657.2563, Found: 658.2644 [M+H] ⁺ 5-amino-6-(4-fluorophenoxy)-3-[(4-hydroxy-l-{[(lR,2R,4R)-4-m ethoxy-4-[2-(l- methylimidazol-2-yl)ethynyl]-2-phenylcyclohexyl]carbonyl}pip eridin-4- yl)methyl]pyrimidin-4-one (EXAMPLE 159)

and

5-amino-6-(4-fluorophenoxy)-3-[(4-hydroxy-l-{[(lR,2R,4S)-4-m ethoxy-4-[2-(l- methylimidazol-2-yl)ethynyl]-2-phenylcyclohexyl]carbonyl}pip eridin-4- yl)methyl]pyrimidin-4-one (EXAMPLE 160)

Step 1: tert-butyl ( lR,2R)-4-methoxy-4-[2-(l-methylimidazol-2-yl)ethynyl]-2 - phenylcyclohexane-l-carboxylate

Starting from tert-butyl (lR,2R)-4-hydroxy-4-[2-(l-methyl-lH-imidazol-2-yl)ethynyl]-2 - phenylcyclohexane-l-carboxylate (100 mg, 0.26 mmol) following procedure described in Step 1 of EXAMPLES 146 and 147, tert-butyl (lR,2R)-4-methoxy-4-[2-(l-methylimidazol- 2-yl)ethynyl]-2-phenylcyclohexane-l-carboxylate was obtained as a brown oil.

FC/MS (Method B): RT = 1.28; m/z = 395 [M+H] ⁺

Step 2 (lR,2R)-4-methoxy-4-[2-(l-methylimidazol-2-yl)ethynyl]-2-phe nylcyclohexane-l- carboxylic acid

Starting from tert-butyl (lR,2R)-4-methoxy-4-[2-(l-methylimidazol-2-yl)ethynyl]-2- phenylcyclohexane-l-carboxylate (95 mg, 0.24 mmol) following procedure described in Step 5 of EXAMPLE 133, (lR,2R)-4-methoxy-4-[2-(l-methylimidazol-2-yl)ethynyl]-2- phenylcyclo hexane- 1 -carboxylic acid was obtained as a yellow oil. The compound was used without further purification.

FC/MS (Method B): RT = 0.919; m/z = 339 [M+H] ⁺

Step 3: EXAMPLES 159 and 160

Starting from 5-amino-6-(4-fluorophenoxy)-3-[(4-hydroxypiperidin-4-yl)meth yl] pyrimidin-4-one (145 mg, 0.43 mmol) and (lR,2R)-4-methoxy-4-[2-(l-methylimidazol-2- yl)ethynyl]-2-phenylcyclo hexane- 1 -carboxylic acid (98 mg) following procedure described in Step 3 of EXAMPLE 94, the obtained residue was purified via flash chromatography using DCM-10 % MeOH (gradient) as eluent to give the still impure product as colourless oil. Final purification was performed via prep HPLC Prep (HPLC Column: Gemini pH9 Dimensions: 21.1 mm x 150 mm 5 pm) to afford:

First elute: EXAMPLE 160 as a white solid.

LC/MS (Method B): RT = 0.850; m/z = 655 [M+H] ⁺

1H NMR (399 MHz, DMSO-d6) d 7.56-7.50 (m, 1H), 7.29-7.07 (m, 8H), 7.02 (m, 2H), 6.87 (m, 1H), 4.78 (m, 1H), 4.61 (m, 2H), 3.89-3.55 (m, 7H), 3.30 (s, 3H), 3.21-2.79 (m, 3H), 2.53 (m, 1H), 2.18-1.82 (m, 4H), 1.78-1.44 (m, 2H), 1.35-1.04 (m, 3H), 0.68-0.53 (m, 1H).

HRMS (TOF, ESI) m/z: Calculated for CseHsgFNeOs 654.2966, Found: 655.3045 [M+H] ⁺ Second elute: EXAMPLE 159 as a white solid.

LC/MS (Method B): RT = 0.866; m/z = 655 [M+H] ⁺

1H NMR (399 MHz, DMSO-d6) d 7.55-7.49 (m, 1H), 7.26-7.06 (m, 8H), 7.03-6.99 (m, 2H), 6.91 (m, 1H), 4.74 (m, 1H), 4.59 (m, 2H), 3.88-3.52 (m, 7H), 3.30 (s, 3H), 3.16-2.78 (m, 3H), 2.57 (m, 1H), 2.10 (m, 2H), 1.88-1.62 (m, 4H), 1.38-1.02 (m, 3H), 0.73-0.44 (m, 1H).

HRMS (TOF, ESI) m/z: Calculated for CseHsgFNeOs 654.2966, Found: 655.3048 [M+H] ⁺ 5-amino-3-[(l-{[(lR,2R,4R)-4-[2-(6-aminopyridin-2-yl)ethynyl ]-4-fluoro-2- phenylcyclohexyl]carbonyl}-4-hydroxypiperidin-4-yl)methyl]-6 -(4- fluorophenoxy)pyrimidin-4-one (EXAMPLE 161)

Step 1: tert-butyl ( lR,2R)-4-(2-{6-[bis(tert-butoxycarbonyl)amino]pyridin-2-yl}e thynyl)-4 - hydroxy-2-phenylcyclohexane-l-carboxylate

Starting from tert-butyl (lR,2R)-4-oxo-2-phenylcyclo hexane- l-carboxylate (500 mg, 1.82 mmol) and tert-butyl N-[(tert-butoxy)carbonyl]-N-(6-ethynylpyridin-2-yl)carbamate (754 mg, 2.37 mmol, 1.3 eq.) following procedure described in Step 2 of EXAMPLES 122 and 123, the obtained residue was purified via flash chromatography using Heptane 34 % EtO Ac/Heptane (gradient) as eluent to give tert-butyl (lR,2R)-4-(2-{6-[bis(tert- butoxycarbonyl)amino]pyridin-2-yl} ethynyl)-4-hydroxy-2-phenylcyclo hexane- 1 - carboxylate as a white solid.

LC/MS (Method B): RT = 1.35; m/z = 593 [M+H] ⁺ Step 2 tert-butyl (lR,2R)-4-(2-{6-[bis(tert-butoxycarbonyl)amino]pyridin-2-yl} ethynyl)-4- fluoro-2-phenylcyclohexane-l-carboxylate

Starting from tert-butyl (lR,2R)-4-(2-{6-[bis(tert-butoxycarbonyl)amino]pyridin-2- yl}ethynyl)-4-hydroxy-2-phenylcyclo hexane- l-carboxylate (545 mg, 0.92 mmol) following procedure described in Step 4 of EXAMPLES 122 and 123, the obtained residue was purified via flash chromatography using Heptane- 18 % EtO Ac/Heptane (gradient) as eluent to afford tert-butyl (lR,2R)-4-(2-{6-[bis(tert-butoxycarbonyl)amino]pyridin-2- yl}ethynyl)-4-fluoro-2-phenylcyclo hexane- l-carboxylate as a colourless oil. The compound was used without further purification.

LC/MS (Method B): RT = 1.44; m/z = 595 [M+H] ⁺

Step 3: (1R, 2R)-4-[ 2-(6-aminopyridin-2-yl)ethynyl]-4-fluoro-2-phenylcyclohexane -l- carboxylic acid

Starting from tert-butyl (lR,2R)-4-(2-{6-[bis(tert-butoxycarbonyl)amino]pyridin-2- yl}ethynyl)-4-fluoro-2-phenylcyclo hexane- l-carboxylate (520 mg) following procedure described in Step 5 of EXAMPLE 133, (lR,2R)-4-[2-(6-aminopyridin-2-yl)ethynyl]-4- fluoro-2-phenylcyclo hexane- 1 -carboxylic acid (350 mg) was obtained as a white foam. The compound was used without further purification.

LC/MS (Method B): RT = 0.818; m/z = 339 [M+H] ⁺

Step 4: EXAMPLE 161

Starting from 5-amino-6-(4-fluorophenoxy)-3-[(4-hydroxypiperidin-4-yl)meth yl] pyrimidin-4-one (166 mg, 0.50 mmol) and (lR,2R)-4-[2-(6-aminopyridin-2-yl)ethynyl]-4- fluoro-2-phenylcyclo hexane- 1 -carboxylic acid (175 mg) following procedure described in Step 3 of EXAMPLE 94, the obtained residue was purified via flash chromatography using DCM-9 % MeOH (gradient) as eluent to give the still impure product as colourless oil. Final purification was performed via prep HPLC Prep (HPLC Column: Gemini pH9 Dimensions: 21.1 mm x 150 mm 5 pm) to afford EXAMPLE 161 as a white solid.

LC/MS (Method B): RT = 1.15; m/z = 655 [M+H] ⁺

1H NMR (399 MHz, DMSO- ) d 7.54-7.49 (m, 1H), 7.34 (ddd, J = 8.5, 7.2, 1.6 Hz, 1H), 7.28-7.07 (m, 7H), 7.03-6.99 (m, 2H), 6.67 (dd, J= 7.0, 2.5 Hz, 1H), 6.43 (dt, J= 8.5, 1.2 Hz, 1H), 6.18 (s, 2H), 4.76 (s, 1H), 4.61 (m, 2H), 3.88-3.53 (m, 4H), 3.18-2.77 (m, 3H), 2.57 (m, 1H), 2.26-1.94 (m, 4H), 1.75 (m, 2H), 1.36-0.93 (m, 3H), 0.71-0.45 (m, 1H). HRMS (TOF, ESI) m/z: Calculated for CseHseFzNeCE 654.2766, Found: 655.281 [M+H] ⁺

^■ 5-amino-3-{[(4S)-3,3-difluoro-l-[(lR,2R,4R)-4-fluoro-4-[2-(6 -methylpyridazin-3- yl)ethynyl]-2-phenylcyclohexanecarbonyl]-4-hydroxypiperidin- 4-yl]methyl}-6-(4- fluorophenoxy)-3,4-dihydropyrimidin-4-one (EXAMPLE 162)

Step 1: tert-butyl (lR,2R) -4-hydroxy-4-[2-(6-methylpyridazin-3-yl)ethynylJ -2- ph enyl eye I o h ex a n e - / -carboxylate

Starting from tert-butyl (lR,2R)-4-oxo-2-phenylcyclohexane-l -carboxylate (400 mg, 1.46 mmol) and 3-ethynyl-6-methylpyridazine (224 mg, 1.90 mmol) following procedure described in Step 2 of EXAMPLES 122 and 123, the obtained residue was purified via flash chromatography using Heptane- 100 % EtO Ac/Heptane (gradient) as eluent to afford tert- butyl ( 1 R,2R)-4-hydroxy-4- [2-(6-methylpyridazin-3 -yl)ethynyl] -2-phenylcyclo hexane- 1 - carboxylate as a yellow solid.

FC/MS (Method B): RT = 1.206; m/z = 393 [M+H] ⁺

Step 2: tert-butyl (lR,2R) -4-fluoro-4-[2-(6-methylpyridazin-3-yl)ethynyl] -2- ph enyl eye l o h ex a n e - / -carboxylate

Starting from tert-butyl (lR,2R)-4-hydroxy-4-[2-(6-methylpyridazin-3-yl)ethynyl]-2- phenylcyclo hexane- 1 -carboxylate (293 mg, 0.75 mmol) following procedure described in Step 4 of EXAMPLES 122 and 123, the obtained residue was purified via flash chromatography using Heptane-30 % EtO Ac/Heptane (gradient) as eluent to afford tert- butyl (lR,2R)-4-fluoro-4-[2-(6-methylpyridazin-3-yl)ethynyl]-2-phe nylcyclohexane- 1 - carboxylate as an off- white solid.

FC/MS (Method B): RT = 1.19; m/z = 395 [M+H] ⁺ Step 3: ( I R,2R) -4 -fluoro -4 -[2 -( 6 -methylpyridazin -3 -yl) ethynyl ] -2 -pheny /cyclohexane -/ - carboxylic acid

Starting from tert-butyl (lR,2R)-4-fluoro-4-[2-(6-methylpyridazin-3-yl)ethynyl]-2- phenylcyclo hexane- 1 -carboxylate (98 mg, 0.25 mmol) following procedure described in Step 5 of EXAMPLE 133, (lR,2R)-4-fluoro-4-[2-(6-methylpyridazin-3-yl)ethynyl]-2- phenylcyclo hexane- 1 -carboxylic acid was obtained as a red oil. The compound was used without further purification.

LC/MS (Method B): RT = 1.032; m/z = 339 [M-H]- Step 4: EXAMPLE 162

Starting from ((lR,2R)-4-fluoro-4-[2-(6-methylpyridazin-3-yl)ethynyl]-2- phenylcyclo hexane- 1 -carboxylic acid (150 mg) and 5-amino-3-{[(4S)-3,3-difluoro-4- hydroxypiperidin-4-yl]methyl}-6-(4-fluorophenoxy)-3,4-dihydr opyrimidin-4-one

(98.5 mg, 0.27 mmol) following procedure described in Step 3 of EXAMPLE 94, the obtained residue was purified via prep HPLC Prep (HPLC Column: Gemini pH4 Dimensions: 21.1 mm x 150 mm 5 pm) to afford EXAMPLE 162 as a white solid.

LC/MS (Method B): RT = 1.225; m/z = 691 [M+H] ⁺

1H NMR (399 MHz, DMSO- ) 7.87 (dd, J = 8.6, 3.1 Hz, 1H), 7.70-7.62 (m, 2H), 7.32- 7.17 (m, 7H), 7.13-7.07 (m, 2H), 6.05 (s, 1H), 4.77-4.72 (m, 2H), 4.47-4.20 (m, 2H), 4.02- 3.74 (m, 2H), 3.45-3.08 (m, 4H), 2.69 (s, 3H), 2.45-2.12 (m, 4H), 1.96-1.75 (m, 2H), 1.51-

1.20 (m, 2H)

HRMS (TOF, ESI) m/z: Calculated for C ₃₆ H ₃₄ F ₄ N ₆ O ₄ 690.2578, Found: 691.2685 [M+H] ⁺ 5- amino-3- { [(4S)- 1- [(lR,2R,4R)-4- [2-(6-aminopyridin-2-yl)ethynyl] -4-fluoro-2- phenylcyclohexanecarbonyl]-3,3-difluoro-4-hydroxypiperidin-4 -yl]methyl}-6-(4- fluorophenoxy)-3,4-dihydropyrimidin-4-one (EXAMPLE 163)

Starting from 5-amino-3- {[(4S)-3,3-difluoro-4-hydroxypiperidin-4-yl]methyl} -6-(4- fluorophenoxy)-3,4-dihydropyrimidin-4-one (100 mg, 0.13 mmol) and (lR,2R)-4-[2-(6- aminopyridin-2-yl)ethynyl]-4-fluoro-2-phenylcyclohexane-l -carboxylic acid (91 mg) following procedure described in Step 3 of EXAMPLE 94, the obtained residue was purified via flash chromatography using Heptane- 100 % EtOAc (gradient) as eluent to give the still impure product as colourless oil. Final purification was performed via prep HPFC Prep (HPFC Column: Gemini pH4 Dimensions: 30 mm x 250 mm 5 pm) to afford EXAMPLE 163 as a white solid.

FC/MS (Method B): RT = 1.210; m/z = 691 [M+H] ⁺ 1H NMR (399 MHz, DMSO-d6) d 7.67-7.62 (m, 1H), 7.41 (dd, J = 8.4, 7.2 Hz, 1H), 7.31- 7.17 (m, 7H), 7.13-7.07 (m, 2H), 6.75 (dd, J = 7.2, 2.6 Hz, 1H), 6.50 (d, J = 8.4, 1H), 6.25 (s, 2H), 6.07 (s, 1H), 4.76-4.72 (m, 2H), 4.47-4.20 (m, 2H), 4.01-3.74 (m, 2H), 3.20-3.07 (m, 4H), 2.43-2.07 (m, 4H), 1.91-1.67 (m, 2H), 1.48-1.21 (m, 2H).

HRMS (TOF, ESI) m/z: Calculated for C ₃₆ H ₃₄ F ₄ N ₆ O ₄ 690.2578, Found: 691.2663 [M+H] ⁺ 5-amino-3-{[(4S)-l-[(lR,2R,4R)-4-[2-(6-aminopyridin-2-yl)eth ynyl]-4-methoxy-2- phenylcyclohexanecarbonyl]-3,3-difluoro-4-hydroxypiperidin-4 -yl]methyl}-6-(4- fluorophenoxy)-3,4-dihydropyrimidin-4-one (EXAMPLE 164)

Step 1: tert-butyl ( lR,2R)-4-(2-{6-[bis(tert-butoxycarbonyl)amino]pyridin-2-yl}e thynyl)-4 - hydroxy-2-phenylcyclohexane-l-carboxylate

Starting from tert-butyl (lR,2R)-4-[2-(6- (bis [(tert-butoxy)carbonyl] amino }pyridin-2- yl)ethynyl]-4-hydroxy-2-phenylcyclohexane-l-carboxylate (90 mg, 0.15 mmol) following procedure described in Step 1 of EXAMPLES 146 and 147, tert-butyl (lR,2R)-4-(2-{6- [bis(tert-butoxycarbonyl)amino]pyridin-2-yl} ethynyl)-4-hydroxy-2-phenylcyclo hexane- 1 - carboxylate was obtained as a colourless oil

FC/MS (Method B): RT = 1.61; m/z = 507 [M-BOC+H] ⁺

Step 2: ( JR , 2R)-4-[ 2-(6-aminopyridin-2-yl)ethynyl]-4-methoxy-2-phenylcyclohexan e-l- carboxylic acid

Starting from tert-butyl (lR,2R)-4-(2-{6-[bis(tert-butoxycarbonyl)amino]pyridin-2- yl}ethynyl)-4-hydroxy-2-phenylcyclo hexane- 1 -carboxylate (50 mg, 0.08 mmol) following procedure described in Step 5 of EXAMPLE 133, (lR,2R)-4-[2-(6-aminopyridin-2- yl)ethynyl]-4-methoxy-2-phenylcyclo hexane- 1 -carboxylic acid was obtained as a yellow solid. The compound was used without further purification.

FC/MS (Method B): RT = 0.98; m/z = 351 [M+H] ⁺ Step 3: EXAMPLE 164

Starting from 5-amino-3- {[(4S)-3,3-difluoro-4-hydroxypiperidin-4-yl]methyl} -6-(4- fluorophenoxy)-3,4-dihydropyrimidin-4-one (48 mg, 0.13 mmol) and (lR,2R)-4-[2-(6- aminopyridin-2-yl)ethynyl]-4-methoxy-2-phenylcyclo hexane- 1 -carboxylic acid (45 mg) following procedure described in Step 3 of EXAMPLE 94, the obtained residue was purified via flash chromatography using Heptane- 100 % EtOAc (gradient) as eluent to give the still impure product as colourless oil. Final purification was performed via prep HPLC Prep (HPLC Column: Gemini pH7 Dimensions: 30 mm x 250 mm 5 pm) to afford EXAMPLE 164 as a white solid.

LC/MS (Method B): RT = 1.16; m/z = 703 [M+H] ⁺

1H NMR (399 MHz, DMSO-d6) d 7.60-7.55 (m, 1H), 7.32 (dd, J = 8.4, 7.2 Hz, 1H), 7.24- 7.09 (m, 7H), 7.04-6.99 (m, 2H), 6.65 (ddd, J = 7.2, 2.9, 0.9 Hz, 1H), 6.39 (dd, J = 8.4, 0.9 Hz, 1H), 6.13 (s, 2H), 5.97 (m, 1H), 4.66 (m, 2H), 4.40-4.12 (m, 2H), 3.99-3.67 (m, 2H), 3.27-3.00 (m, 7H), 2.35-2.01 (m, 2H), 1.81-1.58 (m, 4H), 1.41-1.15 (m, 2H).

HRMS (TOF, ESI) m/z: Calculated for C ₃₇ H ₃₇ F ₃ N ₆ O ₅ 702.2778, Found: 703.288 [M+H] ⁺ 5-amino-3-{[(4S)-3,3-difluoro-4-hydroxy-l-{[(lR,2R,4R)-4-met hoxy-2-phenyl-4-[2- (pyridazin-3-yl)ethynyl] cyclohexyl] carbonyl}piperidin-4-yl] methyl}-6-(4- fluorophenoxy)pyrimidin-4-one (EXAMPLE 165) Starting from 5-amino-3-{[(4S)-3,3-difluoro-4-hydroxypiperidin-4-yl]methyl }-6-(4- fluorophenoxy)-3,4-dihydropyrimidin-4-one (83 mg, 0.22 mmol) and (lR,2R)-4-methoxy- 2 -phenyl-4-[2-(pyridazin-3-yl)ethynyl]cyclo hexane- 1 -carboxylic acid (75 mg, 0.22 mmol) following procedure described in Step 3 of EXAMPLE 94, the obtained residue was purified via flash chromatography using Heptane- 100 % EtO Ac/Heptane (gradient) as eluent to give the still impure product as colourless oil. Final purification was performed via prep HPFC Prep (HPFC Column: Gemini pH4 Dimensions: 21.1 mm x 150 mm 5 pm) to afford EXAMPLE 165 as a white foam.

FC/MS (Method B): RT = 1.18; m/z = 689 [M+H] ⁺

1H NMR (399 MHz, DMSO- ) d 9.20 (dd, J = 5.0, 1.7 Hz, 1H), 7.86 (ddd, J = 8.5, 3.4, 1.7 Hz, 1H), 7.72 (dd, J = 8.5, 5.0 Hz, 1H), 7.60-7.55 (m, 1H), 7.22-6.99 (m, 9H), 6.03-

5.97 (m, 1H), 4.67 (m, 2H), 4.40-4.13 (m, 2H), 3.95-3.67 (m, 2H), 3.33 (s, 3H), 3.25-3.00 (m, 4H), 2.37-2.05 (m, 2H), 1.85-1.66 (m, 4H), 1.44-1.16 (m, 2H).

HRMS (TOF, ESI) m/z: Calculated for C ₃₆ H ₃₅ F ₃ N ₆ O ₅ 688.2621, Found: 689.2724 [M+H] ⁺ 5-amino-3-{[(4S)-3,3-difluoro-4-hydroxy-l-[(lR,2R,4R)-4-meth oxy-2-phenyl-4-[2- (pyridin-2-yl)ethynyl]cyclohexanecarbonyl]piperidin-4-yl]met hyl}-6-(4- fluorophenoxy)-3,4-dihydropyrimidin-4-one (EXAMPLE 166)

Step 1: tert-butyl ( I R,2R) -4 -hydroxy -2 -phenyl -4 -[2 -(pyridin -2 -yl) ethynyl ] cyclohexane -/ - carboxylate

Starting from tert-butyl (lR,2R)-4-oxo-2-phenylcyclohexane-l -carboxylate (300 mg, 1.09 mmol) and 2-ethynylpyridine (150 mg, 1.42 mmol) following procedure described in Step 2 of EXAMPLES 122 and 123, the obtained residue was purified via flash chromatography using Heptane- 100 % EtO Ac/Heptane (gradient) as eluent to afford tert- butyl ( 1 R,2R)-4-hydroxy-2-phenyl-4- [2-(pyridin-2-yl)ethynyl]cyclo hexane- 1 -carboxylate as a white solid.

LC/MS (Method B): RT = 1.267; m/z = 378 [M+H] ⁺

Step 2: tert-butyl (1R,2R) -4 -methoxy -2 -phenyl -4 -[2 -(pyridin -2 -yl) ethynyl] cyclohexane -1 - carboxylate

Starting from tert-butyl (lR,2R)-4-hydroxy-2-phenyl-4-[2-(pyridin-2-yl)ethynyl] cyclohexane- 1 -carboxylate (47 mg, 0.12 mmol) following procedure described in Step 1 of EXAMPLES 146 and 147, the obtained residue was purified via flash chromatography using Heptane-88 % EtO Ac/Heptane (gradient) as eluent to afford tert-butyl (lR,2R)-4-methoxy- 2-phenyl-4- [2-(pyridin-2-yl)ethynyl]cyclo hexane- 1 -carboxylate as an yellow solid.

LC/MS (Method B): RT = 1.424; m/z = 392 [M+H] ⁺

Step 3: (lR,2R)-4 -methoxy -2 -phenyl -4 -[ 2 -(pyridin -2 -yl) ethynyl] cyclohexane -/ -carboxylic acid

Starting from tert-butyl (lR,2R)-4-methoxy-2-phenyl-4-[2-(pyridin-2-yl)ethynyl] cyclohexane- 1 -carboxylate (41 mg, 0.1 mmol) following procedure described in Step 5 of EXAMPLE 133, (lR,2R)-4-methoxy-2-phenyl-4-[2-(pyridin-2-yl)ethynyl]cyclo hexane- 1- carboxylic acid was obtained as a red oil. The compound was used without further purification.

LC/MS (Method B): RT = 1.098; m/z = 336 [M-H] ⁺ Step 4: EXAMPLE 166

Starting from (lR,2R)-4-methoxy-2-phenyl-4-[2-(pyridin-2-yl)ethynyl]cyclo hexane- 1- carboxylic acid (35 mg) and 5-amino-3-{[(4S)-3,3-difluoro-4-hydroxypiperidin-4- yl]methyl}-6-(4-fluorophenoxy)-3,4-dihydropyrimidin-4-one (39 mg, 0.1 mmol) following procedure described in Step 3 of EXAMPLE 94, the obtained residue was purified via prep HPFC Prep (HPFC Column: Gemini pH4 Dimensions: 21.1 mm x 150 mm 5 pm) to afford EXAMPLE 166 as a white solid.

FC/MS (Method B): RT = 1.256; m/z = 688 [M+H] ⁺

1H NMR (399 MHz, DMSO-d ₆ ) 8.62 (ddt, J = 4.8, 1.8, 0.9 Hz, 1H), 7.87 (td, J = 7.7, 1.8 Hz, 1H), 7.67-7.61 (m, 2H), 7.45 (ddd, J = 7.7, 4.9, 1.2 Hz, 1H), 7.30-7.07 (m, 9H), 6.06- 6.01 (m, 1H), 4.77-4.72 (m, 2H), 4.48-4.21 (m, 2H), 4.03-3.74 (m, 2H), 3.38 (s, 3H), 3.22- 3.08 (m, 3H), 2.44 -2.14 (m, 4H), 1.89-1.73 (m, 3H), 1.51-1.26 (m, 2H)

HRMS (TOF, ESI) m/z: Calculated for C ₃₇ H ₃₆ F ₃ N ₅ O ₅ 687.2669, Found: 688.2769 [M+H] ⁺ 5-amino-3-{[(4S)-3,3-difluoro-l-[(lR,2R,4R)-4-fluoro-2-pheny l-4-[2-(pyrimidin-2- yl)ethynyl]cyclohexanecarbonyl]-4-hydroxypiperidin-4-yl]meth yl}-6-(4- fluorophenoxy)-3,4-dihydropyrimidin-4-one (EXAMPLE 167)

Starting from (lR,2R)-4-fluoro-2-phenyl-4-[2-(pyrimidin-2-yl)ethynyl]cyclo hexane- 1 - carboxylic acid (87 mg) and 5-amino-3-{[(4S)-3,3-difluoro-4-hydroxypiperidin-4- yl]methyl}-6-(4-fluorophenoxy)-3,4-dihydropyrimidin-4-one (99 mg, 0.27 mmol) following procedure described in Step 3 of EXAMPLE 94, the obtained residue was purified via prep HPFC Prep (HPFC Column: Gemini pH4 Dimensions: 21.1 mm x 150 mm 5 pm) to afford EXAMPLE 167 as a white solid.

FC/MS (Method B): RT = 1.23; m/z = 677 [M+H] ⁺

1H NMR (399 MHz, DMSO- ) 8.89 (dd, J = 5.0, 0.8 Hz, 2H), 7.67-7.59 (m, 2H), 7.32- 7.17 (m, 7H), 7.13-7.07 (m, 2H), 6.08-6.02 (m, 1H), 4.77-4.72 (m, 2H), 4.47-4.20 (m, 2H),

4.02-3.74 (m, 2H), 3.44-3.08 (m, 4H), 2.45-2.12 (m, 4H), 1.96-1.72 (m, 2H), 1.50-1.20 (m, 2H).

HRMS (TOF, ESI) m/z: Calculated for C ₃₅ H ₃₂ F ₄ N ₆ O ₄ 676.2421, Found: 677.2498 [M+H] ^{+ ■} 5-amino-3-{[(4S)-3,3-difluoro-l-{[(lR,2R,4R)-4-fluoro-2-phen yl-4-[2-(pyridazin-3- yl)ethynyl] cyclohexyl] carbonyl}-4-hydroxypiperidin-4-yl]methyl}-6-(4- fluorophenoxy)pyrimidin-4-one (EXAMPLE 168)

Starting from 5-amino-3-{[(4S)-3,3-difluoro-4-hydroxypiperidin-4-yl]methyl }-6-(4- fluorophenoxy)-3,4-dihydropyrimidin-4-one (80 mg, 0.12 mmol, 1 eq.) and (lR,2R)-4- fluoro-2-phenyl-4-[2-(pyridazin-3-yl)ethynyl]cyclohexane-l -carboxylic acid (70 mg, 0.22 mmol, 1 eq.) following procedure described in Step 3 of EXAMPLE 94, the obtained residue was purified via flash chromatography using DCM-4 % MeOH/DCM (gradient) as eluent to give the still impure product as colourless oil. Final purification was performed via prep HPLC Prep (HPLC Column: Gemini pH4 Dimensions: 21.1 mm x 150 mm 5 pm) to afford EXAMPLE 168 as a pale yellow solid.

LC/MS (Method B): RT = 1.20; m/z = 677 [M+H] ⁺

1H NMR (399 MHz, DMSO- ) d 9.31 (dd, J = 5.1, 1.7 Hz, 1H), 7.99 (ddd, J = 8.5, 3.2, 1.7 Hz, 1H), 7.82 (dd, J = 8.5, 5.1 Hz, 1H), 7.68-7.63 (m, 1H), 7.32-7.07 (m, 9H), 6.09- 6.03 (m, 1H), 4.76-4.71 (m 2H), 4.48-4.21 (m, 2H), 4.02-3.74 (m, 2H), 3.43-3.08 (m, 4H), 2.44-2.12 (m, 4H), 1.97-1.73 (m, 2H), 1.53-1.19 (m, 2H).

HRMS (TOF, ESI) m/z: Calculated for C35H32F4N6O4 676.2421, Found: 677.2533 [M+H] ⁺

^■ 5-amino-3-{[(4S)-3,3-difluoro-4-hydroxy-l-[(lR,2R,4R)-4-meth oxy-4-[2-(5- methylpyridazin-3-yl)ethynyl]-2-phenylcyclohexanecarbonyl]pi peridin-4-yl]methyl}- 6-(4-fluorophenoxy)-3,4-dihydropyrimidin-4-one (EXAMPLE 169)

Step 1: 5 -methyl -3 -[2 -(trimethylsilyl)ethynyl] pyridazine

Starting from 3-chloro-5-methyl-pyridazine (1 g, 7.78 mmol) and ethynyltrimethylsilane (0.97 g, 9.33 mmol, 1.2 eq.) following procedure described in Step 1 of EXAMPLES 135 and 136, the obtained residue was purified via flash chromatography using Heptane- 100 % EtO Ac/Heptane (gradient) as eluent to afford 5 -methyl-3 -[2-(trimethylsilyl)ethynyl] pyridazine as a brown solid.

LC/MS (Method B): RT = 0.97; m/z = 191 [M+H] ⁺

Step 2: 3-ethynyl-5-methylpyridazine To a solution of 5 -methyl-3 -[2-(trimethylsilyl)ethynyl]pyridazine (0.93 g, 4.89 mmol) in THF/MeOH (1 :1, 20 mL) was added potassium carbonate (68 mg, 0.49 mmol, 0.1 eq.). The reaction mixture was stirred at r.t. for 1 hour and evaporated in vacuo. The residue was purified via flash chromatography using Heptane- 100 % EtO Ac/Heptane (gradient) as eluent to afford 3-ethynyl-5-methylpyridazine as an off- white solid.

LC/MS (Method B): RT = 0.426; m/z = 119 [M+H] ⁺

Step 3: tert-butyl (1R,2R) -4 -hydroxy -4 -[2 -(5 -methylpyridazin-3 -yl)ethynyl] -2 - ph enyl eye I o h ex a n e - / -carboxylate

Starting from tert-butyl (lR,2R)-4-oxo-2-phenylcyclohexane-l -carboxylate (400 mg, 1.46 mmol) and 3-ethynyl-5-methylpyridazine (241 mg, 2.04 mmol) following procedure described in Step 2 of EXAMPLES 122 and 123, the obtained residue was purified via flash chromatography using Heptane- 100 % EtO Ac/Heptane (gradient) as eluent to afford tert- butyl ( 1 R,2R)-4-hydroxy-4- [2-(5 -methylpyridazin-3 -yl)ethynyl] -2-phenylcyclo hexane- 1 - carboxylate as a white solid.

LC/MS (Method B): RT = 1.028; m/z = 393 [M+H] ⁺

Step 4: tert-butyl (1R,2R) -4-methoxy-4-[2 -(5 -methylpyridazin-3 -yl)ethynyl] -2- ph enyl eye I h ex a n e - / -carboxylate

Starting from tert-butyl (lR,2R)-4-hydroxy-4-[2-(5 -methylpyridazin-3 -yl)ethynyl] -2- phenylcyclo hexane- 1 -carboxylate (142 mg, 0.36 mmol) following procedure described in Step 1 of EXAMPLES 146 and 147, the obtained residue was purified via flash chromatography using Heptane- 100 % EtO Ac/Heptane (gradient) as eluent to afford tert- butyl ( 1 R,2R)-4-methoxy-4- [2-(5 -methylpyridazin-3 -yl)ethynyl] -2-phenylcyclo hexane- 1 - carboxylate as an oil.

LC/MS (Method B): RT = 1.172; m/z = 407 [M+H] ⁺ Step 5: (1R,2R) -4 -methoxy -4 -[2 -(5 -methylpyridazin-3 -yl)ethynyl] -2 -phenylcyclohexane-1 - carboxylic acid

Starting from tert-butyl (lR,2R)-4-methoxy-4-[2-(5 -methylpyridazin-3 -yl)ethynyl] -2- phenylcyclo hexane- 1 -carboxylate (76 mg, 0.19 mmol) following procedure described in Step 5 of EXAMPLE 133, (lR,2R)-4-methoxy-4-[2-(5-methylpyridazin-3-yl)ethynyl]-2- phenylcyclo hexane- 1 -carboxylic acid was obtained as a yellow oil. The compound was used without further purification.

LC/MS (Method B): RT = 0.858; m/z = 351 [M-H] ⁺

Step 6: EXAMPLE 169

Starting from (lR,2R)-4-methoxy-4-[2-(5-methylpyridazin-3-yl)ethynyl]-2- phenylcyclo hexane- 1 -carboxylic acid (73 mg) and 5-amino-3-{[(4S)-3,3-difluoro-4- hydroxypiperidin-4-yl]methyl} -6-(4-fluorophenoxy)-3,4-dihydropyrimidin-4-one (77 mg, 0.21 mmol) following procedure described in Step 3 of EXAMPLE 94, the obtained residue was purified via flash chromatography using Heptane- 100 % EtO Ac/Heptane (gradient) as eluent to afford EXAMPLE 169 as a white solid.

LC/MS (Method B): RT = 1.025; m/z = 703 [M+H] ⁺

1H NMR (399 MHz, DMSO- ) 9.15 (d, J = 2.1 Hz, 1H), 7.79 (m, 1H), 7.67-7.63 (m, 1H), 7.30-7.17 (m, 7H), 7.13-7.07 (m, 2H), 6.07-6.02 (m, 1H), 4.77-4.72 (m, 2H), 4.47-4.21 (m, 2H), 4.03-3.74 (m, 2H), 3.39 (s, 3H), 3.28-3.08 (m, 4H), 2.37 (s, 3H), 2.26 -2.17 (m, 2H), 1.91-1.77 (m, 4H), 1.51-1.23 (m, 2H).

HRMS (TOF, ESI) m/z: Calculated for C37H37F3N6O5 702.2778, Found: 703.2877 [M+H] ⁺ 5-amino-3-{[(4S)-3,3-difluoro-4-hydroxy-l-[(lR,2R,4R)-4-meth oxy-4-[2-(4- methylpyridazin-3-yl)ethynyl]-2-phenylcyclohexanecarbonyl]pi peridin-4-yl]methyl}- 6-(4-fluorophenoxy)-3,4-dihydropyrimidin-4-one (EXAMPLE 170) Step 1: 4-methyl-3-[2-(trimethylsilyl)ethynyl]pyridazine

Starting from 3-chloro-4-methyl-pyridazine (525 mg, 4.08 mmol) and ethynyltrimethylsilane (481 mg, 4.90 mmol, 1.2 eq.) following procedure described in Step 1 of EXAMPLES 135 and 136, the obtained residue was purified via flash chromatography using Heptane- 100 % EtO Ac/Heptane (gradient) as eluent to afford 4- methyl-3 -[2-(trimethylsilyl)ethynyl]pyridazine as a yellow solid.

LC/MS (Method B): RT = 0.963; m/z = 191 [M+H] ⁺

Step 2: 3-ethynyl-4-methylpyridazine To a solution of 4-methyl-3-[2-(trimethylsilyl)ethynyl]pyridazine (0.723 g, 3.80 mmol) in THF/MeOH (1 :1, 20 mL) was added potassium carbonate (52 mg, 0.38 mmol, 0.1 eq.). The reaction mixture was stirred at r.t. for 1 hour and evaporated in vacuo. The residue was purified via flash chromatography using Heptane- 100 % EtO Ac/Heptane (gradient) as eluent to afford 3-ethynyl-4-methylpyridazine as an off- white solid.

LC/MS (Method B): RT = 0.419; m/z = 119 [M+H] ⁺

Step 3: tert-butyl (lR,2R) -4-hydroxy-4-[2-(4-methylpyridazin-3-yl)ethynylJ -2- ph enyl eye I o h ex a n e - / -carboxylate

Starting from tert-butyl (lR,2R)-4-oxo-2-phenylcyclohexane-l -carboxylate (400 mg, 1.46 mmol) and 3-ethynyl-4-methylpyridazine (241 mg, 2.04 mmol) following procedure described in Step 2 of EXAMPLES 122 and 123, the obtained residue was purified via flash chromatography using Heptane- 100 % EtO Ac/Heptane (gradient) as eluent to afford tert- butyl ( 1 R,2R)-4-hydroxy-4- [2-(4-methylpyridazin-3 -yl)ethynyl] -2-phenylcyclo hexane- 1 - carboxylate as a off- white solid.

LC/MS (Method B): RT = 1.017; m/z = 393 [M+H] ⁺

Step 4: tert-butyl (lR,2R) -4-methoxy-4-[2-(4-methylpyridazin-3-yl)ethynyl] -2- ph enyl eye l o h ex a n e - / -carboxylate

Starting from tert-butyl (lR,2R)-4-hydroxy-4-[2-(4-methylpyridazin-3-yl)ethynyl]-2- phenylcyclo hexane- 1 -carboxylate (100 mg, 0.25 mmol) following procedure described in Step 1 of EXAMPLES 146 and 147, the obtained residue was purified via flash chromatography using Heptane- 100 % EtO Ac/Heptane (gradient) as eluent to afford tert- butyl ( 1 R,2R)-4-methoxy-4- [2-(4-methylpyridazin-3 -yl)ethynyl] -2-phenylcyclo hexane- 1 - carboxylate as an yellow oil.

LC/MS (Method B): RT = 1.152; m/z = 407 [M+H] ⁺ Step 5: ( I R,2R) -4 -methoxy -4 -[2 -( 4 -methylpyridazin -3 -yl) ethynyl ] -2 -pheny /cyclohexane -/ - carboxylic acid

Starting from tert-butyl (lR,2R)-4-methoxy-4-[2-(4-methylpyridazin-3-yl)ethynyl]-2- phenylcyclo hexane- 1 -carboxylate (73 mg, 0.18 mmol) following procedure described in Step 5 of EXAMPLE 133, (lR,2R)-4-methoxy-4-[2-(5-methylpyridazin-3-yl)ethynyl]-2- phenylcyclo hexane- 1 -carboxylic acid was obtained as a yellow oil. The compound was used without further purification.

LC/MS (Method B): RT = 0.841; m/z = 351 [M-H] ⁺

Step 6: EXAMPLE 170

Starting from (lR,2R)-4-methoxy-4-[2-(4-methylpyridazin-3-yl)ethynyl]-2- phenylcyclo hexane- 1 -carboxylic acid (56 mg) and 5-amino-3-{[(4S)-3,3-difluoro-4- hydroxypiperidin-4-yl]methyl} -6-(4-fluorophenoxy)-3,4-dihydropyrimidin-4-one (59 mg, 0.16 mmol) following procedure described in Step 3 of EXAMPLE 94, the obtained residue was purified via flash chromatography using Heptane- 100 % EtO Ac/Heptane (gradient) as eluent to afford EXAMPLE 170 as a white solid.

LC/MS (Method B): RT = 1.015; m/z = 703 [M+H] ⁺

1H NMR (399 MHz, DMSO- ) 9.10 (d, J = 2.1 Hz, 1H), 7.72-7.62 (m, 2H), 7.30-7.07 (m, 9H), 6.07-6.01 (m, 1H), 4.77-4.71 (m, 2H), 4.47-4.20 (m, 2H), 4.06-3.74 (m, 2H), 3.43 (s, 3H), 3.30-3.07 (m, 4H), 2.53 (s, 3H), 2.29 -2.20 (m, 2H), 1.92-1.77 (m, 4H), 1.51-1.23 (m, 2H).

HRMS (TOF, ESI) m/z: Calculated for C37H37FN6O5 702.2778, Found: 703.288 [M+H] ⁺

^■ 5-amino-3-{[(4S)-3,3-difluoro-l-[(lR,2R,4R)-4-fluoro-4-[2-(4 -methylpyridazin-3- yl)ethynyl]-2-phenylcyclohexanecarbonyl]-4-hydroxypiperidin- 4-yl]methyl}-6-(4- fluorophenoxy)-3,4-dihydropyrimidin-4-one (EXAMPLE 171)

Step 1: tert-butyl (lR,2R) -4-fluoro-4-[2-(4-methylpyridazin-3-yl)ethynyl] -2- ph enyl eye I o h ex a n e - / -carboxylate

Starting from tert-butyl (lR,2R)-4-hydroxy-4-[2-(4-methylpyridazin-3-yl)ethynyl]-2- phenylcyclo hexane- 1 -carboxylate (334 mg, 0.85 mmol) following procedure described in Step 4 of EXAMPLES 122 and 123, the obtained residue was purified via flash chromatography using Heptane- 100 % EtO Ac/Heptane (gradient) as eluent to afford tert- butyl (lR,2R)-4-fluoro-4-[2-(4-methylpyridazin-3-yl)ethynyl]-2-phe nylcyclohexane- 1 - carboxylate as an brown oil.

LC/MS (Method B): RT = 1.16; m/z = 395 [M+H] ⁺ Step 2: (lR,2R)-4 -fluoro -4 -[2 -(4 -methylpyridazin -3 -yl)ethynyl] -2 -phenylcyclohexane -1 - carboxylic acid

Starting from tert-butyl (lR,2R)-4-fluoro-4-[2-(4-methylpyridazin-3-yl)ethynyl]-2- phenylcyclohexane-l-carboxylate (176 mg, 0.45 mmol) following procedure described in Step 5 of EXAMPLE 133, (lR,2R)-4-fluoro-4-[2-(4-methylpyridazin-3-yl)ethynyl]-2- phenylcyclo hexane- 1 -carboxylic acid was obtained as a brown oil. The compound was used without further purification.

LC/MS (Method B): RT = 0.866; m/z = 339 [M-H] ⁺

Step 3: EXAMPLE 171

Starting from ((lR,2R)-4-fluoro-4-[2-(4-methylpyridazin-3-yl)ethynyl]-2- phenylcyclo hexane- 1 -carboxylic acid (151 mg) and 5-amino-3-{[(4S)-3,3-difluoro-4- hydroxypiperidin-4-yl]methyl} -6-(4-fluorophenoxy)-3 ,4-dihydropyrimidin-4-one (165 mg, 0.45 mmol) following procedure described in Step 3 of EXAMPLE 94, the obtained residue was purified via prep HPLC Prep (HPLC Column: Gemini pH4 Dimensions: 21.1 mm x 150 mm 5 pm) to afford EXAMPLE 171 as a white solid.

LC/MS (Method B): RT = 1.044; m/z = 691 [M+H] ⁺

1H NMR (399 MHz, DMSO- ) 9.07 (d, J = 5.2 Hz, 1H), 7.65 (d, J = 5.2 Hz, 1H), 7.60- 7.55 (m, 1H), 7.25-6.99 (m, 9H), 6.07-5.99 (m, 1H), 4.69-4.64 (m, 2H), 4.39-4.15 (m, 2H), 3.94-3.66 (m, 2H), 3.36-2.99 (m, 4H), 2.43 (s, 3H), 2.33-2.06 (m, 4H), 1.92-1.67 (m, 2H), 1.44-1.15 (m, 2H)

HRMS (TOF, ESI) m/z: Calculated for C36H34F4N6O4 690.2578, Found: 691.2689 [M+H] ⁺

^■ 5-amino-3-{[(4S)-3,3-difluoro-l-[(lR,2R,4R)-4-fluoro-4-[2-(5 -methylpyridazin-3- yl)ethynyl]-2-phenylcyclohexanecarbonyl]-4-hydroxypiperidin- 4-yl]methyl}-6-(4- fluorophenoxy)-3,4-dihydropyrimidin-4-one (EXAMPLE 172) Step 1: tert-butyl (1R,2R) -4-fluoro -4 -[2 -(5 -methylpyridazin -3 -yl)ethynyl] -2 - phenylcyclohexane J -carboxylate

Starting from tert-butyl (lR,2R)-4-hydroxy-4-[2-(5-methylpyridazin-3-yl)ethynyl]-2- phenylcyclo hexane- 1 -carboxylate (246 mg, 0.63 mmol) following procedure described in Step 4 of EXAMPLES 122 and 123, the obtained residue was purified via flash chromatography using Heptane- 100 % EtO Ac/Heptane (gradient) as eluent to afford tert- butyl (lR,2R)-4-fluoro-4-[2-(4-methylpyridazin-3-yl)ethynyl]-2-phe nylcyclohexane- 1 - carboxylate as a yellow oil.

LC/MS (Method B): RT = 1.2; m/z = 395 [M+H] ⁺ Step 2: ( / R,2R) -4 -fluoro -4 -[2 -(5 -methylpyridazin -3 -ylj ethynyl ] -2 -pheny /cyclohexane -/ - carboxylic acid

Starting from tert-butyl (lR,2R)-4-fluoro-4-[2-(5-methylpyridazin-3-yl)ethynyl]-2- phenylcyclo hexane- 1 -carboxylate (207 mg, 0.52 mmol) following procedure described in Step 5 of EXAMPLE 133, (lR,2R)-4-fluoro-4-[2-(5-methylpyridazin-3-yl)ethynyl]-2- phenylcyclo hexane- 1 -carboxylic acid was obtained as a brown oil. The compound was used without further purification.

LC/MS (Method B): RT = 0.898; m/z = 339 [M-H] ⁺

Step 3: EXAMPLE 172

Starting from ((1 R,2R)-4-fluoro-4- [2-(5 -methylpyridazin- 3 -yl)ethynyl] -2- phenylcyclo hexane- 1 -carboxylic acid (177 mg) and 5-amino-3-{[(4S)-3,3-difluoro-4- hydroxypiperidin-4-yl]methyl} -6-(4-fluorophenoxy)-3 ,4-dihydropyrimidin-4-one (194 mg, 0.52 mmol) following procedure described in Step 3 of EXAMPLE 94, the obtained residue was purified via prep HPLC Prep (HPLC Column: Gemini pH4 Dimensions: 21.1 mm x 150 mm 5 pm) to afford EXAMPLE 172 as a white solid.

LC/MS (Method B): RT = 1.053; m/z = 691 [M+H] ⁺

1H NMR (399 MHz, DMSO- ) 9.11 (s, 1H), 7.77 (m, 1H), 7.60-7.55 (m, 1H), 7.24-7.10 (m, 7H), 7.03-6.99 (m, 2H), 5.99 (s, 1H), 4.69-4.64 (m, 2H), 4.40-4.11 (m, 2H), 3.94-3.67 (m, 2H), 3.15-3.00 (m, 4H), 2.30 (s, 3H), 2.25-2.06 (m, 4H), 1.91-1.67 (m, 2H), 1.44-1.15 (m, 2H)

HRMS (TOL, ESI) m/z: Calculated for C36H34L4N6O4 690.2578, Lound: 691.2686 [M+H] ⁺

^■ 5-amino-3-{[(4S)-3,3-difluoro-4-hydroxy-l-[(lR,2R,4R)-4-meth oxy-4-[2-(5- methoxypyridazin-3-yl)ethynyl]-2-phenylcyclohexanecarbonyl]p iperidin-4- yl]methyl}-6-(4-fluorophenoxy)-3,4-dihydropyrimidin-4-one (EXAMPLE 173) Step 1: 5 -methoxy-3 -[2 -(trimethylsilyl)ethynyljpyridazine

Starting from 3-chloro-5-methoxypyridazine (1 g, 6.92 mmol) and ethynyltrimethylsilane (0.82 mg, 8.30 mmol, 1.2 eq.) following procedure described in Step 1 of EXAMPLES 135 and 136, the obtained residue was purified via flash chromatography using Heptane- 100 % EtO Ac/Heptane (gradient) as eluent to afford 5 -methoxy-3 -[2-

(trimethylsilyl)ethynyl]pyridazine as a brown solid.

LC/MS (Method B): RT = 0.950; m/z = 207 [M+H] ⁺

Step 2: 3-ethynyl-5-methoxypyridazine

To a solution of 5 -methoxy-3 -[2-(trimethylsilyl)ethynyl]pyridazine (0.651 g, 3.16 mmol) in THF/MeOH (1 :1, 20 mL), was added potassium carbonate (44 mg, 0.32 mmol, 0.1 eq.). The reaction mixture was stirred at r.t. for 1 hour and evaporated in vacuo. The obtained residue was purified via flash chromatography using Heptane- 100 % EtO Ac/Heptane (gradient) as eluent to afford 3-ethynyl-5-methoxypyridazine as an off- white solid

LC/MS (Method B): RT = 0.373; m/z = 135 [M+H] ⁺ Step 3: tert-butyl (1R,2R) -4 -hydroxy -4 -[2 -(5 -methoxypyridazin-3 -yl)ethynyl] -2 - ph enyl eye I o h ex a n e - / -carboxylate

Starting from tert-butyl (lR,2R)-4-oxo-2-phenylcyclohexane-l -carboxylate (400 mg, 1.46 mmol) and 3-ethynyl-5-methoxypyridazine (254 mg, 1.90 mmol) following procedure described in Step 2 of EXAMPLES 122 and 123, the obtained residue was purified via flash chromatography using Heptane-85 % EtOAc/Heptane (gradient) as eluent to afford tert- butyl ( 1 R,2R)-4-hydroxy-4- [2-(5 -methoxypyridazin-3 -yl)ethynyl] -2-phenylcyclo hexane- 1 - carboxylate as an off- white solid.

LC/MS (Method B): RT = 1.208; m/z = 409 [M+H] ⁺

Step 4: tert-butyl (1R,2R) -4-methoxy-4-[2 -(5 -methoxypyridazin-3 -yl)ethynyl] -2 - ph enyl eye l h ex a n e - / -carboxylate

Starting from ( 1 R,2R)-4-hydroxy-4- [2 -(5 -methoxypyridazin-3 -yl)ethynyl] -2- phenylcyclo hexane- 1 -carboxylate (109 mg, 0.27 mmol) following procedure described in Step 1 of EXAMPLES 146 and 147, the obtained residue was purified via flash chromatography using Heptane-70 % EtOAc/Heptane (gradient) as eluent to afford tert- butyl ( 1 R,2R)-4-methoxy-4- [2-(5 -methoxypyridazin-3 -yl)ethynyl] -2-phenylcyclohexane- l-carboxylate as a yellow oil.

LC/MS (Method B): RT = 1.346; m/z = 423 [M+H] ⁺

Step 5: (lR,2R)-4 -methoxy -4 -[2 -(5 -methoxypyridazin -3 -yl)ethynyl] -2 -phenylcyclohexane - 1 -carboxylic acid

Starting from tert-butyl (lR,2R)-4-methoxy-4-[2-(5-methoxypyridazin-3-yl)ethynyl]-2- phenylcyclohexane-l-carboxylate (95 mg, 0.22 mmol) following procedure described in Step 5 of EXAMPLE 133, (lR,2R)-4-methoxy-4-[2-(5-methoxypyridazin-3-yl)ethynyl]-2- phenylcyclo hexane- 1 -carboxylic acid was obtained as a yellow oil. The compound was used without further purification.

LC/MS (Method B): RT = 1.037; m/z = 367 [M-H] ⁺

Step 6: EXAMPLE 173

Starting from ( 1 R,2R)-4-methoxy-4- [2 -(5 -methoxypyridazin- 3 -yl)ethynyl] -2- phenylcyclo hexane- 1 -carboxylic acid (110 mg) and 5-amino-3-{[(4S)-3,3-difluoro-4- hydroxypiperidin-4-yl]methyl}-6-(4-fluorophenoxy)-3,4-dihydr opyrimidin-4-one (83 mg, 0.23 mmol) following procedure described in Step 3 of EXAMPLE 94, the obtained residue was purified via prep HPLC Prep (HPLC Column: Gemini pH4 Dimensions: 21.1 mm x 150 mm 5 pm) to afford EXAMPLE 173 as a white solid.

LC/MS (Method B): RT = 1.203; m/z = 719 [M+H] ⁺

1H NMR (399 MHz, DMSO- ) 9.02 (d, J = 2.1 Hz, 1H), 7.64 (m, 1H), 7.51 (m, 1H), 7.30-

7.17 (m, 7H), 7.13-7.07 (m, 2H), 6.07-6.02 (m, 1H), 4.76-4.71 (m, 2H), 4.47-4.21 (m, 2H), 4.04-3.74 (m, 5H), 3.41 (s, 3H), 3.28-3.09 (m, 4H), 2.27-2.19 (m, 2H), 1.90-1.77 (m, 4H), 1.55-1.24 (m, 2H).

HRMS (TOF, ESI) m/z: Calculated for CsyHsyFsNeOe 718.2727, Found: 719.2832 [M+H] ^{+ ■} 5-amino-3-{[(4S)-3,3-difluoro-4-hydroxy-l-[(lR,2R,4R)-4-meth oxy-4-[2-(5- methylpyrimidin-2-yl)ethynyl]-2-phenylcyclohexanecarbonyl]pi peridin-4-yl]methyl}- 6-(4-fluorophenoxy)-3,4-dihydropyrimidin-4-one (EXAMPLE 174) Step 1: tert-butyl (lR,2R) -4-hydroxy-4-[2-(5-methylpyrimidin-2-yl)ethynyl] -2- ph enyl eye I o h ex a n e - / -carboxylate

Starting from tert-butyl (lR,2R)-4-oxo-2-phenylcyclohexane-l -carboxylate (400 mg, 1.46 mmol) and 2-ethynyl-5-methylpyrimidine (224 mg, 1.90 mmol) following procedure described in Step 2 of EXAMPLES 122 and 123, the obtained residue was purified via flash chromatography using Heptane- 100 % EtO Ac/Heptane (gradient) as eluent to afford tert- butyl ( 1 R,2R)-4-hydroxy-4- [2-(5 -methylpyrimidin-2-yl)ethynyl] -2-phenylcyclo hexane- 1 - carboxylate as an off- white solid.

LC/MS (Method B): RT = 1.248; m/z = 393 [M+H] ⁺ Step 2: tert-butyl (1R,2R) -4-methoxy-4-[2 -(5 -methylpyrimidin-2 -yl)ethynyl] -2 - ph enyl eye l o h ex a n e - / -carboxylate

Starting from tert-butyl (lR,2R)-4-hydroxy-4-[2-(5-methylpyrimidin-2-yl)ethynyl]-2- phenylcyclo hexane- 1 -carboxylate (100 mg, 0.25 mmol) following procedure described in Step 1 of EXAMPLES 146 and 147, the obtained residue was purified via flash chromatography using Heptane- 100 % EtO Ac/Heptane (gradient) as eluent to afford tert- butyl ( 1 R,2R)-4-methoxy-4- [2-(5 -methylpyrimidin-2-yl)ethynyl] -2-phenylcyclo hexane- 1 - carboxylate as a white solid.

LC/MS (Method B): RT = 1.406; m/z = 407 [M+H] ⁺

Step 3: (lR,2R)-4 -methoxy -4 -[2 -(5 -methylpyrimidin -2 -yl)ethynyl] -2 -phenylcyclohexane -/ - carboxylic acid

Starting from tert-butyl (lR,2R)-4-methoxy-4-[2-(5-methylpyrimidin-2-yl)ethynyl]-2- phenylcyclo hexane- 1 -carboxylate (100 mg, 0.25 mmol) following procedure described in Step 5 of EXAMPLE 133, (lR,2R)-4-methoxy-4-[2-(5-methylpyrimidin-2-yl)ethynyl]-2- phenylcyclo hexane- 1 -carboxylic acid was obtained as a yellow oil.

LC/MS (Method B): RT = 1.075; m/z = 351 [M-H] ⁺

Step 4: EXAMPLE 174

Starting from ( 1 R,2R)-4-methoxy-4- [2-(5 -methylpyrimidin-2-yl)ethynyl] -2- phenylcyclo hexane- 1 -carboxylic acid (43 mg, 0.12 mmol) and 5-amino-3-{[(4S)-3,3- difluoro-4-hydroxypiperidin-4-yl]methyl}-6-(4-fluorophenoxy) -3,4-dihydropyrimidin-4- one (45 mg, 0.12 mmol) following procedure described in Step 3 of EXAMPLE 94, the obtained residue was purified via prep HPLC Prep (HPLC Column: Gemini pH7 Dimensions: 21.1 mm x 150 mm 5 pm) to afford EXAMPLE 174 as a white solid.

LC/MS (Method B): RT = 1.24; m/z = 703 [M+H] ⁺

1H NMR (399 MHz, DMSO- ) 8.70 (s, 2H), 7.67-7.63 (m, 1H), 7.30-7.15 (m, 7H), 7.13- 7.07 (m, 2H), 6.06-6.01 (m, 1H), 4.76-4.71 (m, 2H), 4.47-4.20 (m, 2H), 4.02-3.74 (m, 2H), 3.39 (s, 3H), 3.27-3.09 (m, 4H), 2.43-2.15 (m, 5H), 1.88-1.74 (m, 4H), 1.53-1.26 (m, 2H). HRMS (TOF, ESI) m/z: Calculated for C ₃₇ H ₃₇ F ₃ N ₆ O ₅ 702.2778, Found: 703.291 [M+H] ⁺ 5-amino-3-{[(4S)-3,3-difluoro-4-hydroxy-l-[(lR,2R,4R)-4-meth oxy-2-phenyl-4-[2- (pyrimidin-5-yl)ethynyl]cyclohexanecarbonyl]piperidin-4-yl]m ethyl}-6-(4- fluorophenoxy)-3,4-dihydropyrimidin-4-one (EXAMPLE 175)

Starting from (lR,2R)-4-methoxy-2-phenyl-4-[2-(pyrimidin-5-yl)ethynyl]cycl ohexane- 1 - carboxylic acid (80 mg, 0.24 mmol) and 5-amino-3-{[(4S)-3,3-difluoro-4- hydroxypiperidin-4-yl]methyl} -6-(4-fluorophenoxy)-3,4-dihydropyrimidin-4-one (88 mg, 0.24 mmol) following procedure described in Step 3 of EXAMPLE 94, the obtained residue was purified via prep HPFC Prep (HPFC Column: Gemini pH7 Dimensions: 21.1 mm x 150 mm 5 pm) to afford EXAMPLE 175 as a white solid.

FC/MS (Method B): RT = 1.229; m/z = 689 [M+H] ⁺

1H NMR (399 MHz, DMSO- ) 9.05 (d, J = 2.1 Hz, 1H), 7.67 - 7.58 (m, 2H), 7.30-7.17 (m, 8H), 7.12-7.07 (m, 2H), 6.08-6.02 (m, 1H), 4.76-4.71 (m, 2H), 4.47-4.21 (m, 2H), 4.02-3.75 (m, 5H), 3.22-3.08 (m, 4H), 2.45-2.11 (m, 4H), 1.96-1.74 (m, 2H), 1.55-1.24 (m, 2H).

HRMS (TOF, ESI) m/z: Calculated for C ₃₆ H ₃₅ F ₃ N ₆ O ₅ 688.2621, Found: 689.2763 [M+H] ⁺ 5-amino-3-{[(4S)-3,3-difluoro-4-hydroxy-l-[(lR,2R,4R)-4-meth oxy-4-[2-(4- methylpyrimidin-2-yl)ethynyl]-2-phenylcyclohexanecarbonyl]pi peridin-4-yl]methyl}- 6-(4-fluorophenoxy)-3,4-dihydropyrimidin-4-one (EXAMPLE 176)

Step 1: tert-butyl (lR,2R) -4-hydroxy-4-[2-(4-methylpyrimidin-2-yl)ethynyl] -2- ph enyl eye I o h ex a n e - / -carboxylate Starting from tert-butyl (lR,2R)-4-oxo-2-phenylcyclohexane-l-carboxylate (600 mg, 2.19 mmol) and 2-ethynyl-4-methylpyrimidine (336 mg, 2.84 mmol) following procedure described in Step 2 of EXAMPLES 122 and 123, the obtained residue was purified via flash chromatography using Heptane- 100 % EtO Ac/Heptane (gradient) as eluent to afford tert- butyl ( 1 R,2R)-4-hydroxy-4- [2-(4-methylpyrimidin-2-yl)ethynyl] -2-phenylcyclo hexane- 1 - carboxylate as an off- white solid.

LC/MS (Method B): RT = 1.243; m/z = 393 [M+H] ⁺

Step 2: tert-butyl (lR,2R) -4-methoxy-4-[2-(4-methylpyrimidin-2-yl)ethynylJ -2- ph enyl eye l o h ex a n e - / -carboxylate

Starting from tert-butyl (lR,2R)-4-hydroxy-4-[2-(4-methylpyrimidin-2-yl)ethynyl]-2- phenylcyclo hexane- 1 -carboxylate (214 mg, 0.55 mmol) following procedure described in Step 1 of EXAMPLES 146 and 147, the obtained residue was purified via flash chromatography using Heptane- 100 % EtO Ac/Heptane (gradient) as eluent to afford tert- butyl ( 1 R,2R)-4-methoxy-4- [2-(4-methylpyrimidin-2-yl)ethynyl] -2-phenylcyclo hexane- 1 - carboxylate as an oil.

LC/MS (Method B): RT = 1.207; m/z = 407 [M+H] ⁺

Step 3: (lR,2R)-4 -methoxy-4 -[2 -(4 -methylpyrimidin -2 -yl)ethynyl] -2 -phenylcyclohexane -7 - carboxylic acid

Starting from tert-butyl (lR,2R)-4-methoxy-4-[2-(4-methylpyrimidin-2-yl)ethynyl]-2- phenylcyclohexane- 1 -carboxylate (121 mg, 0.30 mmol) following procedure described in Step 5 of EXAMPLE 133, (lR,2R)-4-methoxy-4-[2-(4-methylpyrimidin-2-yl)ethynyl]-2- phenylcyclo hexane- 1 -carboxylic acid was obtained as a yellow oil.

LC/MS (Method B): RT = 1.060; m/z = 351 [M-H] ⁺

Step 4: EXAMPLE 176

Starting from (lR,2R)-4-methoxy-4-[2-(4-methylpyrimidin-2-yl)ethynyl]-2- phenylcyclo hexane- 1 -carboxylic acid (52 mg, 0.15 mmol) and 5-amino-3-{[(4S)-3,3- difluoro-4-hydroxypiperidin-4-yl]methyl}-6-(4-fluorophenoxy) -3,4-dihydropyrimidin-4- one (55 mg, 0.15 mmol) following procedure described in Step 3 of EXAMPLE 94, the obtained residue was purified via prep HPLC Prep (HPLC Column: Gemini pH7 Dimensions: 21.1 mm x 150 mm 5 pm) to afford EXAMPLE 176 as a white solid.

LC/MS (Method B): RT = 1.038; m/z = 703 [M+H] ⁺

1H NMR (399 MHz, DMSO- ) 8.68 (d, J = 5.2 Hz, 1H), 7.67-7.63 (m, 1H), 7.43 (d, J = 5.2 Hz, 1H), 7.30-7.15 (m, 7H), 7.12-7.07 (m, 2H), 6.06-6.01 (m, 1H), 4.75-4.71 (m, 2H), 4.47-4.20 (m, 2H), 4.02-3.74 (m, 2H), 3.38 (s, 3H), 3.30-3.09 (m, 4H), 2.50-2.15 (m, 5H), 1.88-1.74 (m, 4H), 1.52-1.24 (m, 2H).

HRMS (TOF, ESI) m/z: Calculated for C ₃₇ H ₃₇ F ₃ N ₆ O ₅ 702.2778, Found: 703.2915 [M+H] ⁺ 5-amino-3-{[(4S)-3,3-difluoro-4-hydroxy-l-[(lR,2R,4R)-4-meth oxy-4-[2-(2- methylpyrimidin-5-yl)ethynyl]-2-phenylcyclohexanecarbonyl]pi peridin-4-yl]methyl}- 6-(4-fluorophenoxy)-3,4-dihydropyrimidin-4-one (EXAMPLE 177)

Step 1: tert-butyl (1R,2R) -4-hydroxy-4-[2 -(2 -methylpyrimidin-5 -yl)ethynyl] -2- ph enyl eye I o h ex a n e - / -carboxylate

Starting from tert-butyl (lR,2R)-4-oxo-2-phenylcyclohexane-l -carboxylate (600 mg, 2.19 mmol) and 5-ethynyl-2-methylpyrimidine (362 mg, 3.06 mmol) following procedure described in Step 2 of EXAMPLES 122 and 123, the obtained residue was purified via flash chromatography using Heptane-65 % EtO Ac/Heptane (gradient) as eluent to afford tert- butyl ( 1 R,2R)-4-hydroxy-4- [2-(2-methylpyrimi din-5 -yl)ethynyl] -2-phenylcyclo hexane- 1 - carboxylate as an oil.

FC/MS (Method B): RT = 1.032; m/z = 393 [M+H] ⁺

Step 2: tert-butyl (1R,2R) -4-methoxy-4 -[2 -(2 -methylpyrimidin-5 -yl)ethynyl] -2 - ph enyl eye I o h ex a n e - / -carboxylate

Starting from tert-butyl (lR,2R)-4-hydroxy-4-[2-(2-methylpyrimidin-5-yl)ethynyl]-2- phenylcyclo hexane- 1 -carboxylate (326 mg, 0.83 mmol) following procedure described in Step 1 of EXAMPLES 146 and 147, the obtained residue was purified via flash chromatography using Heptane-70 % EtO Ac/Heptane (gradient) as eluent to afford tert- butyl ( 1 R,2R)-4-methoxy-4- [2-(2-methylpyrimi din-5 -yl)ethynyl] -2-phenylcyclo hexane- 1 - carboxylate as an off- white solid.

FC/MS (Method B): RT = 1.217; m/z = 407 [M+H] ⁺ Step 3: (lR,2R)-4 -methoxy -4 -[2 -(2 -methylpyrimidin -5 -yl)ethynyl] -2 -phenylcyclohexane -1 - carboxylic acid

Starting from tert-butyl (lR,2R)-4-methoxy-4-[2-(2-methylpyrimidin-5-yl)ethynyl]-2- phenylcyclohexane-l-carboxylate (170 mg, 0.42 mmol) following procedure described in Step 5 of EXAMPLE 133, (lR,2R)-4-methoxy-4-[2-(2-methylpyrimidin-5-yl)ethynyl]-2- phenylcyclo hexane- 1 -carboxylic acid was obtained as a yellow oil. The compound was used without further purification.

LC/MS (Method B): RT = 0.898; m/z = 351 [M-H] ⁺

Step 4: EXAMPLE 177

Starting from (lR,2R)-4-methoxy-4-[2-(2-methylpyrimidin-5-yl)ethynyl]-2- phenylcyclo hexane- 1 -carboxylic acid (78 mg) and 5-amino-3-{[(4S)-3,3-difluoro-4- hydroxypiperidin-4-yl]methyl} -6-(4-fluorophenoxy)-3,4-dihydropyrimidin-4-one (82 mg, 0.22 mmol) following procedure described in Step 3 of EXAMPLE 94, the obtained residue was purified via prep HPLC Prep (HPLC Column: Gemini pH7 Dimensions: 21.1 mm x 150 mm 5 pm) to afford EXAMPLE 177 as a white solid.

LC/MS (Method B): RT = 1.054; m/z = 703 [M+H] ⁺

1H NMR (399 MHz, DMSO- ) 8.88 (m, 2H), 7.67-7.63 (m, 1H), 7.29-7.15 (m, 7H), 7.13- 7.07 (m, 2H), 6.08-6.02 (m, 1H), 4.77-4.72 (m, 2H), 4.47-4.21 (m, 2H), 4.02-3.74 (m, 2H), 3.38 (s, 3H), 3.27-3.07 (m, 4H), 2.67 (s, 3H), 2.43-2.14 (m, 2H), 1.87-1.74 (m, 4H), 1.53- 1.26 (m, 2H).

HRMS (TOF, ESI) m/z: Calculated for C ₃₇ H ₃₇ F ₃ N ₆ O ₅ 702.2778, Found: 703.2907 [M+H] ⁺

PHARMACOLOGICAL STLDY

EXAMPLE A: Evaluation of the inhibition of USP7 by the Fluorescence Intensity

(FLINT) readings

USP7 activity was measured using Rhodamine-l 10 c-terminal labelled Ubiquitin as a substrate ( UbiQ Bio). Incubation with USP7 results in the release of Rhodamine-l 10 leading to an increase in fluorescence which can be used in the continuous measurement of USP7 activity.

The USP7 reactions were performed in a 50 pL volume, in 384 well black solid low binding plates (Coming #3575). The reaction buffer consisted of 100 mM Bicine pH 8.0, 0.01 % TritonXlOO, 1 mM TCEP, and 10 % DMSO.

0.25 nM His-His-USP7 (aa208-560, [C315A]) was incubated with compound (final concentration 10 % DMSO) for 60 minutes at 30 °C. The reaction was then initiated by the addition of 500 nM Ubiquitin- Rhodamine-l 10 substrate and the plate read every 3 minutes for 21 minutes to measure the release of Rhodamine-l 10. Fluorescence Intensity (FLINT) readings were measured using a Biomek Neo plate reader (Ex.485 nm, Em.535 nm).

The inhibition of increasing doses of compound was expressed as a percentage reduction in kinetic rate compared to the kinetic rates established between‘DMSO only’ and‘total inhibition’ controls (no USP7). The inhibitory concentrations that gave a 50 % reduction in kinetic rate (IC50) were determined, from 11 -point dose response curves, in XL-Fit using a 4-Parameter Logistic Model 205 (Sigmoidal Dose-Response Model).

The results presented in Table 1 below show that compounds of the invention inhibit interaction between USP7 protein and the fluorescent peptide described hereinbefore. EXAMPLE B: In vitro cytotoxicity

The cytotoxicity studies were evaluated by MTT [3-(4,5-dimethylthiazol-2-yl)-2,5- diphenyltetrazolium bromide] assay and carried out on Z 138 mantle cell lymphoma tumour cell lines. The cells are distributed onto microplates and exposed to the test compounds for 96 hours. MTT is then added for 4 hours and converted by NAD(P)H-dependent cellular oxidoreductase enzymes in formazan, which has a purple color. The viable cell number is proportional to the production of formazan salts and cell viability can be quantified by the absorbance of the solution at 540nm with a spectrophotometer.(Carmichael et al, Cancer Res. 1987, 47, 936-942). The results are expressed in IC ₅₀ (the concentration of compound that inhibits cell viability by 50 % compared to DMSO treated cells only) and are presented in Table 1 below.

The results show that the compounds of the invention are cytotoxic.

Table 1: ICsn of USP7 inhibition and of cytotoxicity for Z138 cells

NT: not tested

EXAMPLE C: Pharmaceutical composition: Tablets

1000 tablets containing a dose of 5 mg of a compound selected from Examples 1 to 177. 5 g

Wheat starch . 20 g Maize starch . 20 g

Lactose . 30 g

Magnesium stearate . 2 g

Silica . 1 g

Hydroxypropylcellulose . 2 g