IL326602A - Tertiary pyridyl amine modulators of cholesterol biosynthesis and their uses for promoting remyelination - Google Patents

Description

WO 2025/049495 PCT / US2024 / 0440 TERTIARY PYRIDYL AMINE MODULATORS OF CHOLESTEROL BIOSYNTHESIS AND THEIR USE FOR PROMOTING REMYLINATION [ 1 ] CROSS REFERENCE TO RELATED APPLICATIONS This application claims the benefit of priority to United States Provisional Patent Application No. 63 / 579,221 , filed August 28 , 2023 , the contents of which is incorporated by reference in its entirety for all purposes . [ 2 ] FIELD The subject matter described herein is directed to myelin - promoting compounds of Formula I , methods of making the compounds , their pharmaceutical compositions , and their use in the treatment of myelin - related disorders . [ 3 ] BACKGROUND Myelin - related disorders are disorders that result in abnormalities of the myelin sheath ( e.g. , dysmyelination , demyelination and hypomyelination ) in a subject's neural cells , e.g. , CNS neurons including their axons . Loss or degradation of the myelin sheath in such disorders produces a slowing or cessation of nerve cell conduction . The resulting myelin related disorders are characterized by deficits in sensation , motor function , cognition , or other physiological functions . Myelin related disorders include , but are not limited to , multiple sclerosis ( MS ) , neuromyelitis optica ( NMO ) , optic neuritis , pediatric leukodystrophies , neonatal white matter injury , age - related dementia , schizophrenia , progressive multifocal leukoencephalopathy ( PML ) , encephalomyelitis ( EPL ) , central pontine myelolysis ( CPM ) , adrenoleukodystrophy , Alexander's disease , Pelizaeus Merzbacher disease ( PMD ) , Vanishing White Matter Disease , Wallerian Degeneration , transverse myelitis , amylotrophic lateral sclerosis ( ALS ) , Huntington's disease , Alzheimer's disease , Parkinson's disease , spinal cord injury , traumatic brain injury , post radiation injury , neurologic complications of chemotherapy , stroke , acute ischemic optic neuropathy , vitamin E deficiency , isolated vitamin E deficiency syndrome , Bassen - Kornzweig syndrome , Marchiafava - Bignami syndrome , metachromatic leukodystrophy , trigeminal neuralgia , acute disseminated encephalitis , Guillian- Barre syndrome , Charcot - Marie - Tooth disease , Bell's palsy and radiation - induced demyelination . [ 4 ] MS is the most common myelin - related disorder affecting several million people globally and is estimated to result in about 18,000 deaths per year . MS is a complex neurological disease characterized by deterioration of central nervous system ( CNS ) myelin . Myelin , composed in its majority by lipids ( 70 % lipids , 30 % protein ) , protects axons and makes saltatory conduction possible , which speeds axonal electric impulse . Demyelination of axons in chronic MS can result in axon degeneration and neuronal cell death . Additionally , MS destroys oligodendrocytes , the highly specialized CNS cells that generate and maintain myelin . A repair process , called remyelination , takes place in early phases of the disease , but over time , the 1 WO 2025/049495 PCT / US2024 / 0440 oligodendrocytes are unable to completely rebuild and restore the myelin sheath . Repeated attacks lead to successively less effective remyelination , until a scar - like plaque is built up around the damaged axons . [ 5 ] At present , there is no cure for myelin - related disorders , and no current therapy prevents progression in MS . Accordingly , there is a need for new therapeutic approaches to the treatment of myelin- related disorders , including the promotion of remyelination . The subject matter described herein addresses this unmet need . [ 6 ] Formula A : BRIEF SUMMARY In certain embodiments , the subject matter described herein is directed to a compound of R1a · N · R1 R2a ³R ( EA ﻭ A wherein , A is selected from the group consisting of ₁C - C6 alkyl , C3 - C8 cycloalkyl , phenyl , 5- to 6- membered heteroaryl and 5- to 6 - membered heterocyclyl , each of which is optionally substituted with one or more of RAI , RA2 and RA3 . " wherein , RA1 , RA2 and RA3 are each independently selected from the group consisting of C1 - C6 alkyl , halo - ₁C - C6 alkyl , ₁C - C6 alkoxy , halo , cyano , halo , cyano , oxo , -C ( O ) -RA4 , oxo , -C ( O ) -RA4 , -S ( O ) -RAand -S ( O ) 2 - RA + wherein , R + is ₁C - C6 alkyl or C3 - C8 cycloalkyl , and Awherein the oxo , if present , is formed by two of RAI , RA2 and ³AR together with a carbon to which each is attached ; G is -CH , C - OH , or N ; E , if present , is -C ( O ) - or -0- ; Y is -CH or N ; p is 1 , 2 or 3 ; 2 WO 2025/049495 PCT / US2024 / 0440 q is 1 or 0 ; r is 1 or 0 ; wherein , when r is 0 , A is other than ₁C - C6 alkyl ; ¹R is selected from the group consisting of C1 - C6 alkyl , C3 - C8 cycloalkyl and halo - ₁C - C6 alkyl ; or ¹R is halo and q is 0 ; la a₁R is selected from the group consisting of hydrogen , halo , C1 - C6 alkyl ; ²R is selected from the group consisting of halo , halo - ₁C - C6 alkyl , halo - C1 - C6 alkoxy and -S ( O ) 2- ( C1 - C6 alkyl ) ; and . R2a is selected from the group consisting of hydrogen and halo ; ³R is hydrogen , halo , or ₁C - C6 alkyl , or a pharmaceutically acceptable salt or solvate thereof . [ 7 ] Formula I : In certain embodiments , the subject matter described herein is directed to a compound of R1a N R1 R2a ³R A , I wherein , A is selected from the group consisting of C1 - C6 alkyl , C3 - C8 cycloalkyl , phenyl , 5- to 6- membered heteroaryl and 5- to 6 - membered heterocyclyl , each of which is optionally substituted with one or more of ¹AR , RA2 and ³AR , wherein , RA , RA2 and RA3 are each independently selected from the group consisting of C1 - C6 alkyl , halo - ₁C - C6 alkyl , halo , cyano , oxo , -C ( O ) -RA4 , -S ( O ) -RA4 and -S ( O ) 2 - RA4 , wherein , R4 is ₁C - C6 alkyl or C3 - C8 cycloalkyl , and Awherein the oxo , if present , is formed by two of RA1 , RA2 and ³AR together with a carbon to which each is attached : 3 WO 2025/049495 PCT / US2024 / 0440 Gis -CH or N ; Y is -CH or N ; p is 1 , 2 or 3 ; q is 1 or 0 ; r is 1 or 0 : wherein , when r is 0 , A is other than ₁C - C6 alkyl ; R ' is selected from the group consisting of C1 - C6 alkyl , C3 - Cs cycloalkyl and halo - C1 - C6 alkyl ; la a¹R is selected from the group consisting of hydrogen , halo , and C1 - C6 alkyl ; ²R is selected from the group consisting of halo , halo - C1 - C6 alkyl , halo - ₁C - C6 alkoxy and -S ( O ) 2- ( C1 - C6 alkyl ) ; and , 2a R2 is selected from the group consisting of hydrogen and halo ; ³R is hydrogen , halo , or C1 - C6 alkyl , or a pharmaceutically acceptable salt or solvate thereof . [ 8 ] In certain embodiments , the subject matter described herein is directed to a pharmaceutical composition comprising a compound of Formula A or Formula I , or a pharmaceutically acceptable salt or solvate thereof , and a pharmaceutically acceptable excipient . [ 9 ] In certain embodiments , the subject matter described herein is directed to methods of promoting myelination in a subject in need thereof , comprising administering to the subject an effective amount of a compound of Formula A or Formula I , or a pharmaceutically acceptable salt or solvate thereof , or a pharmaceutical composition comprising a compound of Formula A or Formula I , or a pharmaceutically acceptable salt or solvate thereof , and a pharmaceutically acceptable excipient . In certain embodiments , the subject has a myelin - related disorder . [ 10 ] In certain embodiments , the subject matter described herein is directed to a compound of Formula A or Formula I , or a pharmaceutically acceptable salt or solvate thereof , or a pharmaceutical composition comprising a compound of Formula A or Formula I , or a pharmaceutically acceptable salt or solvate thereof , and a pharmaceutically acceptable excipient , for use in treating a myelin - related disorder . [ 11 ] In certain embodiments , the subject matter described herein is directed to the use of a compound of Formula A or Formula I , or a pharmaceutically acceptable salt or solvate thereof , or a pharmaceutical composition comprising a compound of Formula A or Formula I , or a pharmaceutically acceptable salt or solvate thereof , and a pharmaceutically acceptable excipient , in the manufacture of a medicament for treating a myelin - related disorder . [ 12 ] In certain embodiments , the subject matter described herein is directed to methods of preparing compounds of Formula A or Formula I , or a pharmaceutically acceptable salt or solvate thereof . 4 WO 2025/049495 PCT / US2024 / 0440 [ 13 ] In certain embodiments , the subject matter described herein is directed to methods of inhibiting CYP51 ( lanosterol demethylase ) comprising , contacting CYP51 with a compound of Formula A or Formula I , or a pharmaceutically acceptable salt or solvate thereof , or a pharmaceutical composition comprising a compound of Formula A or Formula I , or a pharmaceutically acceptable salt or solvate thereof , and a pharmaceutically acceptable excipient . [ 14 ] Other embodiments are also described . [ 15 ] DETAILED DESCRIPTION Described herein are myelin - promoting compounds of Formula A and Formula I , methods of making the compounds , their pharmaceutical compositions , and their use in the treatment of myelin - related disorders . [ 16 ] The enhancement and / or inducement of the accumulation of A8,9 - unsaturated sterol intermediates of the cholesterol biosynthesis pathway in oligodendrocyte progenitor cells ( OPCs ) can induce oligodendrocyte generation . Enhancement and / or inducement of the accumulation of A8,9- unsaturated sterol intermediates can be provided by modulating and / or inhibiting enzymes within the cholesterol biosynthesis pathway in OPCs that enhance and / or induce A8,9 - unsaturated sterol intermediate accumulation and / or for which the A8,9 - unsaturated sterol intermediates are substrates as well as directly and / or indirectly administering A8,9 - unsaturated sterol intermediates to the OPCs . Enhancement and / or inducement of the accumulation of A8,9 - unsaturated sterol intermediates can promote OPC differentiation , survival , proliferation and / or maturation and treat disease and / or disorders in subjects where myelination is beneficial to the subject . [ 17 ] As such , in some embodiments an agent , such as a compound of Formula A or Formula I , or a pharmaceutically acceptable salt or solvate thereof , that can enhance and / or induce accumulation of A8,9- unsaturated sterol intermediates of the cholesterol biosynthesis pathway in the OPCs can be administered to a subject and / or the OPCs at an amount effective to promote and / or induce OPC differentiation , proliferation and / or maturation as well as oligodendrocyte generation . In certain embodiments , the agent , for example a compound of Formula A or Formula I , or a pharmaceutically acceptable salt or solvate thereof , is a compound that inhibits enzyme mediated synthesis of one or more sterol intermediates in the cholesterol biosynthesis pathway of the OPCs and / or promotes accumulation of A8,9 - unsaturated sterol intermediates . [ 18 ] In certain embodiments , the compound of Formula A or Formula I , or a pharmaceutically acceptable salt or solvate thereof , can modulate and / or inhibit one or more enzyme - mediated conversion steps of the cholesterol biosynthesis pathway , such as in the pathway from lanosterol to cholesterol , for example , between lanosterol and / or lathosterol ; modulating and / or inhibiting one or more of these steps in WO 2025/049495 PCT / US2024 / 0440 OPCs may promote and / or induce oligodendrocyte generation . For example , the compound of Formula A or Formula I can inhibit CYP51 , sterol 14 - reductase ( TM7SF2 and / or LBR ) , SC4MOL , NSDHL , and / or EBP enzyme mediated synthesis of sterol intermediates in the cholesterol biosynthesis pathway . In certain embodiments , the compound of Formula A or Formula I can inhibit CYP51 , sterol 14 - reductase and / or EBP . In certain embodiments , the compound of Formula A or Formula I can inhibit CYP51 . [ 19 ] For example , in certain embodiments , the compound of Formula A or Formula I used in the methods described herein can inhibit CYP51 enzyme activity in the cholesterol biosynthetic pathway . Alternatively , in certain embodiments , the compound of Formula I used in the methods described herein can inhibit sterol C14 reductase enzyme activity in the cholesterol biosynthesis pathway or can inhibit enzyme mediated conversion of zymostenol to lathosterol through the inhibition of emopamil binding protein ( EBP ) isomerase enzyme activity . [ 20 ] CYP51 belongs to the cytochrome P450 ( CYP ) monooxygenase superfamily and mediates an essential step in the sterol biosynthesis pathway . CYP51 proteins are the most conserved protein in the CYP superfamily . Unlike other CYP enzymes , CYP51 has a strong substrate specificity . It catalyzes the demethylation of a narrow range of substrates , including lanosterol , and 24,25 - dihydrolanosterol . CYPproteins are also referred to as sterol α41 - demethylases and are the only invariant P450 present in all sterol biosynthetic pathways . [ 21 ] Without being bound by a particular theory , it is believed that compounds of Formula A and Formula I , or a pharmaceutically acceptable salt or solvate thereof , can inhibit CYP51 mediated conversion of lanosterol to 14 - demethyl - 14 - dehydrolanosterol ( FF - MAS ) and 24,25 - dihydrolanosterol to MAS - 412 in the cholesterol biosynthesis pathway of OPCs resulting in enhancement and / or inducement of the accumulation of A8.9 - unsaturated sterol intermediates . In some embodiments , enhancement and / or inducement of the accumulation of A8,9 - unsaturated sterol intermediates can promote OPC differentiation , survival , proliferation and / or maturation and treat disease and / or disorders in subjects where myelination or myelinization is beneficial to the subject . This mechanism of promoting myelination is distinct from the primary action of immunomodulatory agents that are often used to treat myelin - related disorders . [ 22 ] The presently disclosed subject matter will now be described more fully hereinafter . However , many modifications and other embodiments of the presently disclosed subject matter set forth herein will come to mind to one skilled in the art to which the presently disclosed subject matter pertains having the benefit of the teachings presented in the foregoing descriptions . Therefore , it is to be understood that the presently disclosed subject matter is not to be limited to the specific embodiments disclosed and that modifications and other embodiments are intended to be included within the scope of the appended claims . In other words , the subject matter described herein covers all alternatives , modifications , and equivalents . Unless otherwise defined , all technical and scientific terms used herein have the same meaning as 6 WO 2025/049495 PCT / US2024 / 0440 commonly understood by one of ordinary skill in this field . All publications , patent applications , patents , and other references mentioned herein are incorporated by reference in their entirety . In the event that one or more of the incorporated literature , patents , and similar materials differs from or contradicts this application , including but not limited to defined terms , term usage , described techniques , or the like , this application controls .

I. [ 23 ] Definitions As used in the present specification , the following words , phrases and symbols are generally intended to have the meanings as set forth below , except to the extent that the context in which they are used indicates otherwise . [ 24 ] A dash ( " - " ) that is not between two letters or symbols is used to indicate a point of attachment for a substituent . For example , -C ( O ) NH2 is attached through the carbon atom . A dash at the front or end of a chemical group is a matter of convenience ; chemical groups may be depicted with or without one or more dashes without losing their ordinary meaning . A wavy line or a dashed line drawn through or perpendicular across the end of a line in a structure indicates a specified point of attachment of a group . Unless chemically or structurally required , no directionality or stereochemistry is indicated or implied by the order in which a chemical group is written or named . [ 25 ] The prefix " Cu - ₁C " indicates that the following group has from u to v carbon atoms . For example , " ₁C - C6 alkyl " indicates that the alkyl group has from 1 to 6 carbon atoms . [ 26 ] Reference to " about " a value or parameter herein includes ( and describes ) embodiments that are directed to that value or parameter per se . In certain embodiments , the term " about " includes the indicated amount ± 50 % . In certain other embodiments , the term " about " includes the indicated amount ± % . In certain other embodiments , the term " about " includes the indicated amount ± 10 % . In other embodiments , the term " about " includes the indicated amount ± 5 % . In certain other embodiments , the term " about " includes the indicated amount ± 1 % . In certain other embodiments , the term " about " includes the indicated amount ± 0.5 % and in certain other embodiments , 0.1 % . Such variations are appropriate to perform the disclosed methods or employ the disclosed compositions . Also , to the term " about x " includes description of " x " . Also , the singular forms " a " and " the " include plural references unless the context clearly dictates otherwise . Thus , e.g. , reference to " the compound " includes a plurality of such compounds and reference to " the assay " includes reference to one or more assays and equivalents thereof known to those skilled in the art . [ 27 ] " Alkyl " refers to an unbranched or branched saturated hydrocarbon chain . As used herein , alkyl has 1 to 20 carbon atoms ( i.e. , C1 - C20 alkyl ) , 1 to 12 carbon atoms ( i.e. , ₁C - C12 alkyl ) , 1 to 8 carbon atoms ( i.e. , C1 - Cs alkyl ) , 1 to 6 carbon atoms ( i.e. , ₁C - C6 alkyl ) , 1 to 4 carbon atoms ( i.e. , C1 - C4 alkyl ) , or 1 to 7 WO 2025/049495 PCT / US2024 / 0440 carbon atoms ( i.e. , ₁C - C3 alkyl ) . Examples of alkyl groups include , e.g. , methyl , ethyl , propyl , isopropyl , n - butyl , sec - butyl , iso - butyl , tert - butyl , pentyl , 2 - pentyl , isopentyl , neopentyl , hexyl , 2 - hexyl , 3 - hexyl and - methylpentyl . When an alkyl residue having a specific number of carbons is named by chemical name or identified by molecular formula , all positional isomers having that number of carbons may be encompassed ; thus , for example , " butyl " includes n - butyl ( i.e. , - ( CH2 ) 3CH3 ) , sec - butyl ( i.e. , -CH ( CH3 ) CH2CH3 ) , isobutyl ( i.e. , -CH2CH ( CH3 ) 2 ) and tert - butyl ( i.e. , -C ( CH3 ) 3 ) ; and " propyl " includes n - propyl ( i.e. , - ( CH2 ) 2CH3 ) and isopropyl ( i.e. , -CH ( CH3 ) 2 ) . [ 28 ] Certain commonly used alternative chemical names may be used . For example , a divalent group such as a divalent " alkyl " group , a divalent " aryl " group , etc. , may also be referred to as an " alkylene " group or an " alkylenyl " group , an " arylene " group or an " arylenyl " group , respectively . Also , unless indicated explicitly otherwise , where combinations of groups are referred to herein as one moiety , e.g. , arylalkyl or aralkyl , the last - mentioned group contains the atom by which the moiety is attached to the rest of the molecule . [ 29 ] " Alkenyl " refers to an alkyl group containing at least one carbon - carbon double bond and having from 2 to 20 carbon atoms ( i.e. , C2 - C20 alkenyl ) , 2 to 8 carbon atoms ( i.e. , C2 - C8 alkenyl ) , 2 to carbon atoms ( i.e. , C2 - C6 alkenyl ) or 2 to 4 carbon atoms ( i.e. , C2 - C4 alkenyl ) . Examples of alkenyl groups include , e.g. , ethenyl , propenyl , butadienyl ( including 1,2 - butadienyl and 1,3 - butadienyl ) . [ 30 ] " Alkynyl " refers to an alkyl group containing at least one carbon - carbon triple bond and having from 2 to 20 carbon atoms ( i.e. , C2 - C20 alkynyl ) , 2 to 8 carbon atoms ( i.e. , C2 - C8 alkynyl ) , 2 to 6 carbon atoms ( i.e. , C2 - C6 alkynyl ) or 2 to 4 carbon atoms ( i.e. , C2 - C4 alkynyl ) . The term " alkynyl " also includes those groups having one triple bond and one double bond . [ 31 ] " Alkoxy " refers to the group " alkyl - O- " ( e.g. , ₁C - C3 alkoxy or ₁C - C6 alkoxy ) . Examples of alkoxy groups include , e.g. , methoxy , ethoxy , n - propoxy , iso - propoxy , n - butoxy , tert - butoxy , sec - butoxy , n - pentoxy , n - hexoxy and 1,2 - dimethylbutoxy . [ 32 ] " Alkylthio " refers to the group " alkyl - S- " . [ 33 ] " Acyl " refers to a group -C ( O ) RY , wherein Ry is hydrogen , alkyl , alkenyl , alkynyl , cycloalkyl , heterocyclyl , aryl , heteroalkyl or heteroaryl ; each of which may be optionally substituted , as defined herein . Examples of acyl include , e.g. , formyl , acetyl , cyclohexylcarbonyl , cyclohexylmethyl - carbonyl and benzoyl . [ 34 ] " Amido " refers to both a " C - amido " group which refers to the group -C ( O ) ²R³RN and an ‘ N- amido " group which refers to the group C³RN- ( O ) ²R , wherein Ry and ²R are independently hydrogen , alkyl , alkenyl , alkynyl , cycloalkyl , heterocyclyl , aryl , heteroalkyl or heteroaryl ; each of which may be optionally substituted , as defined herein , or Ry and ²R are taken together to form a heterocyclyl ; which may be optionally substituted , as defined herein . 8 WO 2025/049495 PCT / US2024 / 0440 [ 35 ] " Amino " refers to the group ²RYRN- wherein Ry and ²R are independently hydrogen , alkyl , alkenyl , alkynyl , cycloalkyl , heterocyclyl , aryl , heteroalkyl or heteroaryl ; each of which may be optionally substituted , as defined herein . [ 36 ] " Amidino " refers to -C ( NR ) ( ²RN ) , wherein Ry and ²R are independently hydrogen , alkyl , alkenyl , alkynyl , cycloalkyl , heterocyclyl , aryl , heteroalkyl or heteroaryl ; each of which may be optionally substituted , as defined herein . [ 37 ] " Aryl " refers to an aromatic carbocyclic group having a single ring ( e.g. , monocyclic ) or multiple rings ( e.g. , bicyclic or tricyclic ) including fused systems . As used herein , aryl has 6 to 20 ring carbon atoms ( i.e. , C6 - C20 aryl ) , 6 to 12 carbon ring atoms ( i.e. , C6 - C12 aryl ) , or 6 to 10 carbon ring atoms ( i.e. , C6 - C10 aryl ) . Examples of aryl groups include , e.g. , phenyl , naphthyl , fluorenyl and anthryl . Aryl , however , does not encompass or overlap in any way with heteroaryl defined below . If one or more aryl groups are fused with a heteroaryl , the resulting ring system is heteroaryl regardless of the point of attachment . If one or more aryl groups are fused with a heterocyclyl , the resulting ring system is heterocyclyl regardless of the point of attachment . [ 38 ] " Arylalkyl " or " Aralkyl " refers to the group " aryl - alkyl- " , such as ( C6 - C10 aryl ) -C1 - C3 alkyl . A non - limiting example of arylalkyl is benzyl . [ 39 ] " Carbamoyl " refers to both an " O - carbamoyl " group which refers to the group -O - C ( O ) ²RYRN and an " N - carbamoyl " group which refers to the group -NRYC ( O ) ²RO , wherein Ry and ²R are independently hydrogen , alkyl , alkenyl , alkynyl , cycloalkyl , heterocyclyl , aryl , heteroalkyl or heteroaryl ; each of which may be optionally substituted , as defined herein . [ 40 ] " Carboxyl ester " or " ester " refer to both -OC ( O ) R * and -C ( O ) OR * , wherein Rx is alkyl , alkenyl , alkynyl , cycloalkyl , heterocyclyl , aryl , heteroalkyl or heteroaryl ; each of which may be optionally substituted , as defined herein . [ 41 ] " Cycloalkyl " refers to a saturated or partially unsaturated cyclic alkyl group having a single ring or multiple rings including fused , bridged and spiro ring systems . The term " cycloalkyl " includes cycloalkenyl groups ( i.e. , the cyclic group having at least one double bond ) and carbocyclic fused ring systems having at least one ³ps carbon atom ( i.e. , at least one non - aromatic ring ) . As used herein , cycloalkyl has from 3 to 20 ring carbon atoms ( i.e. , C3 - C20 cycloalkyl ) , 3 to 12 ring carbon atoms ( i.e. , C3 - Ccycloalkyl ) , 3 to 10 ring carbon atoms ( i.e. , C3 - C10 cycloalkyl ) , 3 to 8 ring carbon atoms ( i.e. , C3 - Ccycloalkyl ) , 3 to 7 ring carbon atoms ( i.e. , C3 - C7 cycloalkyl ) , or 3 to 6 ring carbon atoms ( i.e. , C3 - Ccycloalkyl ) . Monocyclic groups include , for example , cyclopropyl , cyclobutyl , cyclopentyl , cyclohexyl , cycloheptyl and cyclooctyl . Polycyclic groups include , for example , bicyclo [ 2.2.1 ] heptanyl , bicyclo [ 2.2.2 ] octanyl , adamantyl , norbornyl , decalinyl , 7,7 - dimethyl - bicyclo [ 2.2.1 ] heptanyl and the like . Further , the term cycloalkyl is intended to encompass any moiety comprising a non - aromatic alkyl ring 9 WO 2025/049495 PCT / US2024 / 0440 which may be fused to an aryl ring , regardless of the attachment to the remainder of the molecule . Still further , cycloalkyl also includes " spirocycloalkyl " when there are two positions for substitution on the same carbon atom , for example spiro [ 2.5 ] octanyl , spiro [ 4.5 ] decanyl , or spiro [ 5.5 ] undecanyl . As used herein , " halocycloalkyl , " such as C3 - C7 halocycloalkyl , refers to a C3 - C7 cycloalkyl group that is substituted with one or more halogens . [ 42 ] alkyl . [ 43 ] " Cycloalkylalkyl " refers to the group " cycloalkyl - alkyl- " , such as ( C3 - C6 cycloalkyl ) -C1 - C " Guanidino " refers to -NRYC ( = ²RN ) ( ²RRN ) , wherein each R and ²R are independently hydrogen , alkyl , alkenyl , alkynyl , cycloalkyl , heterocyclyl , aryl , heteroalkyl or heteroaryl ; each of which may be optionally substituted , as defined herein . [ 44 ] [ 45 ] " Hydrazino " refers to -NHNH2 . " Imino " refers to a group -C ( ³RN ) ²R , wherein Ry and ²R are each independently hydrogen , alkyl , alkenyl , alkynyl , cycloalkyl , heterocyclyl , aryl , heteroalkyl or heteroaryl ; each of which may be optionally substituted , as defined herein . [ 46 ] " Imido " refers to a group -C ( O ) NR ¥ C ( O ) ²R , wherein Ry and ²R are each independently hydrogen , alkyl , alkenyl , alkynyl , cycloalkyl , heterocyclyl , aryl , heteroalkyl or heteroaryl ; each of which may be optionally substituted , as defined herein . [ 47 ] " Halogen " or " halo " refers to atoms occupying group VIIA of the periodic table , such as fluoro ( fluorine ) , chloro ( chlorine ) , bromo ( bromine ) or iodo ( iodine ) . [ 48 ] " Haloalkyl " refers to an unbranched or branched alkyl group as defined above , wherein one or more ( e.g. , 1 to 6 , or 1 to 3 ) hydrogen atoms are replaced by a halogen . For example , halo - C1 - C3 alkyl refers to an alkyl group of 1 to 3 carbons wherein at least one hydrogen atom is replaced by a halogen . Halo - -₁C C6 alkyl refers to an alkyl group of 1 to 6 carbons wherein at least one hydrogen atom is replaced by a halogen . Where a residue is substituted with more than one halogen , it may be referred to by using a prefix corresponding to the number of halogen moieties attached . Dihaloalkyl and trihaloalkyl refer to alkyl substituted with two ( " di " ) or three ( " tri " ) halo groups , which may be , but are not necessarily , the same halogen . Examples of haloalkyl include , e.g. , trifluoromethyl , difluoromethyl , fluoromethyl , trichloromethyl , 2,2,2 - trifluoroethyl , 1,2 - difluoroethyl , 3 - bromo - 2 - fluoropropyl , 1,2 - dibromoethyl and the like . [ 49 ] " Haloalkoxy " refers to an alkoxy group as defined above , wherein one or more ( e.g. , 1 to 6 , or to 3 ) hydrogen atoms are replaced by a halogen . For example , halo - ₁C - C3 alkoxy refers to an alkoxy group of 1 to 3 carbons wherein at least one hydrogen atom is replaced by a halogen . Halo - ₁C - C6 alkoxy refers to an alkoxy group of 1 to 6 carbons wherein at least one hydrogen atom is replaced by a halogen . Non - limiting examples of haloalkoxy are -OCH2CF3 , -OCF2H , and -OCF3 .

WO 2025/049495 PCT / US2024 / 0440 [ 50 ] " Hydroxyalkyl " refers to an alkyl group as defined above , wherein one or more ( e.g. , 1 to 6 , or to 3 ) hydrogen atoms are replaced by a hydroxy group ( e.g. , hydroxy - ₁C - C3 - alkyl , hydroxy - ₁C - C6 - alkyl ) . The term " hydroxy - ₁C - C3 alkyl " refers to a one to three carbon alkyl chain where one or more hydrogens on any carbon is replaced by a hydroxy group , in particular , one hydrogen on one carbon of the chain is replaced by a hydroxy group . The term " hydroxy - C1 - C6 alkyl " refers to a one to six carbon alkyl chain where one or more hydrogens on any carbon is replaced by a hydroxy group , in particular , one hydrogen on one carbon of the chain is replaced by a hydroxy group . Non - limiting examples of hydroxyalkyl include HO₂HC- , HO₂HC₂HC- , and -C ( CH3 ) 2CH2OH . [ 51 ] " Heteroalkyl " refers to an alkyl group in which one or more of the carbon atoms ( and any associated hydrogen atoms ) are each independently replaced with the same or different heteroatomic group , provided the point of attachment to the remainder of the molecule is through a carbon atom . In certain embodiments , the heteroalkyl can have 1 to 3 carbon atoms ( e.g. , ₁C - C3 heteroalkyl ) or 1 to 6 carbon atoms ( e.g. , ₁C - C6 heteroalkyl ) , and one or more ( e.g. , 1 , 2 , or 3 ) heteroatoms or heteroatomic groups . The term " ❞lyklaoreteh includes unbranched or branched saturated chain having carbon and heteroatoms . By way of example , 1 , 2 , or 3 carbon atoms of the alkyl group in the " heteroalkyl " may be independently replaced with the same or different heteroatomic group . Heteroatomic groups include , but are not limited to , -NRY- , -O- , -S- , -S ( O ) - , -S ( O ) 2- , and the like , wherein R is hydrogen , alkyl , alkenyl , alkynyl , cycloalkyl , heterocyclyl , aryl , heteroalkyl or heteroaryl ; each of which may be optionally substituted , as defined herein . Examples of heteroalkyl groups include , e.g. , ethers ( e.g. , HCO₂HC- 3 , CH ( CH3 ) OCH3 , ³HCO₂HC₂HC- , 3HCO₂HC2HCO₂HC₂HC- , etc. ) , thioethers ( e.g. , ³HCS₂HC- , CH ( CH3 ) SCH 3 , HCS₂HC₂HC- 3 , HCS2HC2HCS₂HC₂HC- 3 , etc. ) , sulfoxides ( e.g. , S₂HC- ( O ) CH3 , CH ( CH3 ) S ( O ) CH3 , S₂HC₂HC- ( O ) CH3 , S₂HC₂HC- ( O ) 3HCO₂HC2HC , etc. ) , sulfones ( e.g. , S₂HC- ( O ) 2CH3 , -CH ( CH3 ) S ( O ) 2CH3 , -CH2CH2S ( O ) 2CH3 , -CH2CH2S ( O ) 3HCO₂HC2HC2 , etc. ) , and ( e.g. , 3HCYRN₂HC- , -CH ( CH3 ) NRYCH3 , ³HCÝRN₂HC₂HC- , 3HCYRN₂HC₂HCYRN2HC2HC- , etc. , where RY is hydrogen , alkyl , alkenyl , alkynyl , cycloalkyl , heterocyclyl , aryl , heteroalkyl , or heteroaryl ; each of which may be optionally substituted , as defined herein ) . In certain embodiments , heteroalkyl can have 1 to carbon atoms , 1 to 15 carbon atoms , 1 to 12 carbon atoms , 1 to 10 carbon atoms , 1 to 8 carbon atoms , or to 4 carbon atoms ; and 1 to 3 heteroatoms , 1 to 2 heteroatoms , or 1 heteroatom . amines [ 52 ] " Heteroaryl " refers to an aromatic group having a single ring , multiple rings or multiple fused rings , with one or more ring heteroatoms independently selected from nitrogen , oxygen , and sulfur . As used herein , heteroaryl includes 1 to 20 ring carbon atoms ( i.e. , C1 - C20 heteroaryl ) , 3 to 12 ring carbon atoms ( i.e. , C3 - C12 heteroaryl ) , or 3 to 8 carbon ring atoms ( i.e. , C3 - Cs heteroaryl ) , and 1 to 5 ring heteroatoms , to 4 ring heteroatoms , 1 to 3 ring heteroatoms , 1 to 2 ring heteroatoms , or 1 ring heteroatom independently selected from nitrogen , oxygen and sulfur . In certain instances , heteroaryl includes 9-10 membered ring 11 WO 2025/049495 PCT / US2024 / 0440 systems ( i.e. , 9-10 membered heteroaryl ) , 5-10 membered ring systems ( i.e. , 5-10 membered heteroaryl ) , 5-7 membered ring systems ( i.e. , 5-7 membered heteroaryl ) , 5-6 membered ring systems ( i.e. , 5-membered heteroaryl ) , or 4-6 membered ring systems ( i.e. , 4-6 membered heteroaryl ) , each independently having 1 to 4 ring heteroatoms , 1 to 3 ring heteroatoms , 1 to 2 ring heteroatoms , or 1 ring heteroatom independently selected from nitrogen , oxygen and sulfur . Examples of heteroaryl groups include , e.g. , acridinyl , benzimidazolyl , benzothiazolyl , benzindolyl , benzofuranyl , benzothiazolyl , benzothiadiazolyl , benzonaphthofuranyl , benzoxazolyl , benzothienyl ( benzothiophenyl ) , benzotriazolyl , benzo [ 4,6 ] imidazo [ 1,2 - a ] pyridyl , carbazolyl , cinnolinyl , dibenzofuranyl , dibenzothiophenyl , furanyl , isothiazolyl , imidazolyl , indazolyl , indolyl , indazolyl , isoindolyl , isoquinolyl , isoxazolyl , naphthyridinyl , oxadiazolyl , oxazolyl , 1 - oxidopyridinyl , 1 - oxidopyrimidinyl , 1 - oxidopyrazinyl , 1 - oxidopyridazinyl , phenazinyl , phthalazinyl , pteridinyl , purinyl , pyrrolyl , pyrazolyl , pyridinyl , pyrazinyl , pyrimidinyl , pyridazinyl , quinazolinyl , quinoxalinyl , quinolinyl , quinuclidinyl , isoquinolinyl , thiazolyl , thiadiazolyl , triazolyl , tetrazolyl and triazinyl . Examples of the fused - heteroaryl rings include , but are not limited to , benzo [ d ] thiazolyl , quinolinyl , isoquinolinyl , benzo [ b ] thiophenyl , indazolyl , benzo [ d ] imidazolyl , pyrazolo [ 1,5 - a ] pyridinyl and imidazo [ 1,5 - a ] pyridinyl , where the heteroaryl can be bound via either ring of the fused system . Any aromatic group , having a single or multiple fused rings , containing at least one heteroatom , is considered a heteroaryl regardless of the attachment to the remainder of the molecule ( i.e. , through any one of the fused rings ) . Heteroaryl does not encompass or overlap with aryl as defined above . [ 53 ] " Heteroarylalkyl " refers to the group " heteroaryl - alkyl- " , such as ( 5- to 10 - membered monocyclic heteroaryl ) -C1 - C3 alkyl . [ 54 ] " Heterocyclyl " refers to a saturated or partially unsaturated cyclic alkyl group , with one or more ring heteroatoms independently selected from nitrogen , oxygen and sulfur . The term " heterocyclyl " includes heterocycloalkenyl groups ( i.e. , the heterocyclyl group having at least one double bond ) , bridged- heterocyclyl groups , fused - heterocyclyl groups and spiro - heterocyclyl groups . A heterocyclyl may be a single ring or multiple rings wherein the multiple rings may be fused , bridged or spiro . Any non - aromatic ring containing at least one heteroatom is considered a heterocyclyl , regardless of the attachment ( i.e. , can be bound through a carbon atom or a heteroatom ) . Further , the term heterocyclyl is intended to encompass a moiety comprising any non - aromatic ring containing at least one heteroatom , which ring may be fused to an aryl or heteroaryl ring , regardless of the attachment to the remainder of the molecule . The term heterocyclyl is also intended to encompass a moiety comprising a cycloalkyl ring which is fused to a heteroaryl ring , regardless of the attachment to the remainder of the molecule . Additionally , the term heterocyclyl is intended to encompass a moiety comprising a cycloalkyl ring which is fused to a heterocyclyl ring , regardless of the attachment to the remainder of the molecule . As used herein , heterocyclyl has 2 to 20 ring carbon atoms ( i.e. , C2 - C20 heterocyclyl ) . 2 to 12 ring carbon atoms ( i.e. , C2- 12 WO 2025/049495 PCT / US2024 / 0440 C12 heterocyclyl ) , 2 to 10 ring carbon atoms ( i.e. , C2 - C10 heterocyclyl ) , 2 to 8 ring carbon atoms ( i.e. , C2- Cs heterocyclyl ) , 3 to 12 ring carbon atoms ( i.e. , C3 - C12 heterocyclyl ) , 3 to 8 ring carbon atoms ( i.e. , C3 - Cheterocyclyl ) , or 3 to 6 ring carbon atoms ( i.e. , C3 - C6 heterocyclyl ) ; having 1 to 5 ring heteroatoms , 1 to ring heteroatoms , 1 to 3 ring heteroatoms , 1 to 2 ring heteroatoms , or 1 ring heteroatom independently selected from nitrogen , sulfur or oxygen . When the heterocyclyl ring contains 4- to 6- ring atoms , it is also referred to herein as a 4- to 6 - membered heterocyclyl . Also disclosed herein are 5- or 6 - membered heterocyclyls , having 5 or 6 ring atoms , respectively , and 5- to 10 - membered heterocyclyls , having 5 to ring atoms . Examples of heterocyclyl groups include , e.g. , azetidinyl , azepinyl , benzodioxolyl , benzo [ b ] [ 1,4 ] dioxepinyl , 1,4 - benzodioxanyl , benzopyranyl , benzodioxinyl , benzopyranonyl , benzofuranonyl , dioxolanyl , dihydropyranyl , hydropyranyl , thienyl [ 1,3 ] dithianyl , decahydroisoquinolyl , furanonyl , imidazolinyl , imidazolidinyl , indolinyl , indolizinyl , isoindolinyl , isothiazolidinyl , isoxazolidinyl , morpholinyl , octahydroindolyl , octahydroisoindolyl , 2 - oxopiperazinyl , 2 - oxopiperidinyl , - oxopyrrolidinyl , oxazolidinyl , oxiranyl , oxetanyl , phenothiazinyl , phenoxazinyl , piperidinyl , piperazinyl , - piperidonyl , pyrrolidinyl , pyrazolidinyl , quinuclidinyl , thiazolidinyl , tetrahydrofuryl , tetrahydropyranyl , trithianyl , tetrahydroquinolinyl , thiophenyl ( i.e. , thienyl ) , tetrahydropyranyl , thiomorpholinyl , thiamorpholinyl , 1 - oxo - thiomorpholinyl and 1,1 - dioxo - thiomorpholinyl . In certain embodiments , the term " heterocyclyl " can include " spiroheterocyclyl " when there are two positions for substitution on the same carbon atom , wherein at least one ring of the spiro system comprises at least one heteroatom . Examples of the spiro - heterocyclyl rings include , e.g. , bicyclic and tricyclic ring systems , such as 2 - oxa - 7- azaspiro [ 3.5 ] nonanyl , 2 - oxa - 6 - azaspiro [ 3.4 ] octanyl and 6 - oxa - 1 - azaspiro [ 3.3 ] heptanyl . Examples of the fused - heterocyclyl rings include , but are not limited to , 1,2,3,4 - tetrahydroisoquinolinyl , 4,5,6,7- tetrahydrothieno [ 2,3 - c ] pyridinyl , indolinyl and isoindolinyl , where the heterocyclyl can be bound via either ring of the fused system . [ 55 ] [ 56 ] " Heterocyclylalkyl " refers to the group " heterocyclyl - alkyl- . ﻭﻭ " Oxime " refers to the group -CRY ( = NOH ) wherein R is hydrogen , alkyl , alkenyl , alkynyl , cycloalkyl , heterocyclyl , aryl , heteroalkyl or heteroaryl ; each of which may be optionally substituted , as defined herein .

" N - oxide " refers to the group ( -NO ) . [ 57 ] " Oxo " refers to the group ( = 0 ) . [ 58 ] " Cyano " refers to the group ( -CN ) . [ 59 ] [ 60 ] [ 61 ] " Thiol " refers to the group ( -SH ) . " Sulfonyl " refers to the group -S ( O ) YR₂ , where R is hydrogen , alkyl , alkenyl , alkynyl , cycloalkyl , heterocyclyl , aryl , heteroalkyl or heteroaryl ; cach of which may be optionally substituted , as defined herein . A non - limiting example of a sulfonyl group is ₂OS- ( C1 - C6 alkyl ) , which is herein referred 13 WO 2025/049495 PCT / US2024 / 0440 to as alkylsulfonyl . Examples of sulfonyl are methylsulfonyl , ethylsulfonyl , phenylsulfonyl and toluenesulfonyl . [ 62 ] " Sulfinyl " refers to the group -S ( O ) RY , where RY is hydrogen , alkyl , alkenyl , alkynyl , cycloalkyl , heterocyclyl , aryl , heteroalkyl or heteroaryl ; each of which may be optionally substituted , as defined herein . Examples of sulfinyl are methylsulfinyl , ethylsulfinyl , phenylsulfinyl and toluenesulfinyl . [ 63 ] " Sulfonamido " refers to the groups -SO ²RRN and ²R₂OSYRN- , where R and ²R are each independently hydrogen , alkyl , alkenyl , alkynyl , cycloalkyl , heterocyclyl , aryl , heteroalkyl or heteroaryl ; each of which may be optionally substituted , as defined herein . [ 64 ] The terms " optional " or " optionally " means that the subsequently described event or circumstance may or may not occur and that the description includes instances where said event or circumstance occurs and instances in which it does not . Also , the term " optionally substituted " refers to any one or more ( e.g. , 1 to 5 , 1 to 4 , or 1 to 3 ) hydrogen atoms on the designated atom or group may or may not be replaced by a moiety other than hydrogen . [ 65 ] The term " substituted " used herein means any of the above groups ( i.e. , alkyl , alkenyl , alkynyl , alkylene , alkoxy , haloalkyl , haloalkoxy , cycloalkyl , aryl , heterocyclyl , heteroaryl , and / or heteroalkyl ) wherein at least one ( e.g. , 1 to 5 , 1 to 4 , or 1 to 3 ) hydrogen atom is replaced by a bond to a non - hydrogen atom such as , but not limited to alkyl , alkenyl , alkynyl , alkoxy , alkylthio , acyl , amido , amino , amidino , aryl , aralkyl , azido , carbamoyl , carboxyl , carboxyl ester , cyano , cycloalkyl , cycloalkylalkyl , guanidino , halo , haloalkyl , haloalkoxy , hydroxyalkyl , heteroalkyl , heteroaryl , heteroarylalkyl , heterocyclyl , heterocyclylalkyl , ₂HNHN- , = NNH2 , imino , imido , hydroxy , oxo , oxime , nitro , sulfonyl , sulfinyl , alkylsulfonyl , alkylsulfinyl , thiocyanate , -S ( O ) OH , -S ( O ) HO₂ , sulfonamido , thiol , thioxo , N - oxide or Si ( R ) , wherein each R is independently hydrogen , alkyl , alkenyl , alkynyl , heteroalkyl , cycloalkyl , aryl , heteroaryl or heterocyclyl . - [ 66 ] In certain embodiments , " substituted " includes any of the above alkyl , alkenyl , alkynyl , cycloalkyl , heterocyclyl , aryl or heteroaryl groups in which one or more ( e.g. , 1 to 5 , 1 to 4 , or 1 to 3 ) hydrogen atoms are independently replaced with deuterium , halo , cyano , nitro , azido , oxo , alkyl , alkenyl , alkynyl , haloalkyl , cycloalkyl , heterocyclyl , aryl , heteroaryl , -NR & R , -NRC ( = O ) ³R , C³RN- ( = O ) ³R³RN , - NRC ( = O ) ³RO , -NRS ( = O ) ³R2-1 , -C ( = O ) ³R , -C ( = O ) ³RO , -OC ( = O ) ³RO , -OC ( = O ) ¸³R -C ( = O ) ³R³RN , OC ( = O ) ¸³R³RN ³RO- , ³RS- , -S ( = O ) ³R , -S ( = O ) ³R₂ , -OS ( = O ) ³R2-1 , -S ( = O ) ¸³RO2-1 S³RN- ( = O ) ³R³RN2-1 , = ¸³R₂OSN = ªRON , -S ( = O ) 1-2NRER , -SF5 , -SCF3 or -OCF3 . In certain embodiments , " substituted " also means any of the above groups in which one or more ( e.g. , 1 to 5 , 1 to 4 , or 1 to 3 ) hydrogen atoms are replaced with -C ( = O ) ³R , -C ( = O ) OR , -C ( = O ) NR & ³R , R₂OS₂HC- , or RN₂OS₂HC- & R . In the foregoing , R and Rh are the same or different and independently hydrogen , alkyl , alkenyl , alkynyl , alkoxy , thioalkyl , aryl , aralkyl , cycloalkyl , cycloalkylalkyl , haloalkyl , heterocyclyl , heterocyclylalkyl , heteroaryl , and / or 14 WO 2025/049495 PCT / US2024 / 0440 heteroarylalkyl . In certain embodiments , " substituted " also means any of the above groups in which one or more ( e.g. , 1 to 5 , 1 to 4 , or 1 to 3 ) hydrogen atoms are replaced by a bond to an amino , cyano , hydroxyl , imino , nitro , oxo , thioxo , halo , alkyl , alkoxy , alkylamino , thioalkyl , aryl , aralkyl , cycloalkyl , cycloalkylalkyl , haloalkyl , heterocyclyl , N - heterocyclyl , heterocyclylalkyl , heteroaryl , and / or heteroarylalkyl , or two of R5 and R and ₁R are taken together with the atoms to which they are attached to form a heterocyclyl ring optionally substituted with oxo , halo or alkyl optionally substituted with oxo , halo , amino , hydroxyl , or alkoxy . [ 67 ] Polymers or similar indefinite structures arrived at by defining substituents with further substituents appended ad infinitum ( e.g. , a substituted aryl having a substituted alkyl which is itself substituted with a substituted aryl group , which is further substituted by a substituted heteroalkyl group , etc. ) are not intended for inclusion herein . Unless otherwise noted , the maximum number of serial substitutions in compounds described herein is three . For example , serial substitutions of substituted aryl groups with two other substituted aryl groups are limited to ( ( substituted aryl ) substituted aryl ) substituted aryl . Similarly , the above definitions are not intended to include impermissible substitution patterns ( e.g. , methyl substituted with 5 fluorines or heteroaryl groups having two adjacent oxygen ring atoms ) . Such impermissible substitution patterns are well known to the skilled artisan . When used to modify a chemical group , the term " substituted " may describe other chemical groups defined herein . [ 68 ] In certain embodiments , as used herein , the phrase " one or more " refers to one to five . In certain embodiments , as used herein , the phrase " one or more " refers to one to four . In certain embodiments , as used herein , the phrase " one or more " refers to one to three . [ 69 ] Any compound or structure given herein , is intended to represent unlabeled forms as well as isotopically labeled forms ( isotopologues ) of the compounds . These forms of compounds may also be referred to as and include " isotopically enriched analogs . " Isotopically labeled compounds have structures depicted herein , except that one or more atoms are replaced by an atom having a selected atomic mass or mass number . Examples of isotopes that can be incorporated into the disclosed compounds include isotopes of hydrogen , carbon , nitrogen , oxygen , phosphorous , fluorine , chlorine and iodine , such as 2H , 3H , 11C , 13C , 14C , 13N , 15N , 150 , 170 , 180 , 31P , 32P , 35S , 18F , 36C1 , 123I , and 125I , respectively . Various isotopically labeled compounds of the present disclosure , for example those into which radioactive isotopes such as H³ , 13C and 14C are incorporated . Such isotopically labelled compounds may be useful in metabolic studies , reaction kinetic studies , detection or imaging techniques , such as positron emission tomography ( PET ) or single- photon emission computed tomography ( SPECT ) including drug or substrate tissue distribution assays or in radioactive treatment of patients . [ 70 ] The term " isotopically enriched analogs " includes " deuterated analogs " of compounds described herein in which one or more hydrogens is / are replaced by deuterium , such as a hydrogen on a WO 2025/049495 PCT / US2024 / 0440 carbon atom . Such compounds exhibit increased resistance to metabolism and are thus useful for increasing the half - life of any compound when administered to a mammal , particularly a human . See , for example , Foster , " Deuterium Isotope Effects in Studies of Drug Metabolism , " Trends Pharmacol . Sci . 5 ( 12 ) : 524-5( 1984 ) . Such compounds are synthesized by means well known in the art , for example by employing starting materials in which one or more hydrogens have been replaced by deuterium . [ 71 ] Deuterium labelled or substituted therapeutic compounds of the disclosure may have improved DMPK ( drug metabolism and pharmacokinetics ) properties , relating to adsorption , distribution , metabolism , and excretion ( ADME ) . Substitution with heavier isotopes such as deuterium may afford certain therapeutic advantages resulting from greater metabolic stability , for example increased in vivo half- life , reduced dosage requirements and / or an improvement in therapeutic index . An 18F , 3H , 11C labeled compound may be useful for PET or SPECT or other imaging studies . Isotopically labeled compounds of this disclosure can generally be prepared by carrying out the procedures disclosed in the schemes or in the examples and preparations described below by substituting a readily available isotopically labeled reagent for a non - isotopically labeled reagent . It is understood that deuterium in this context is regarded as a substituent in a compound described herein . [ 72 ] The concentration of such a heavier isotope , specifically deuterium , may be defined by an isotopic enrichment factor . In the compounds of this disclosure any atom not specifically designated as a particular isotope is meant to represent any stable isotope of that atom . Unless otherwise stated , when a position is designated specifically as " H " or " hydrogen " , the position is understood to have hydrogen at its natural abundance isotopic composition . Accordingly , in the compounds of this disclosure any atom specifically designated as a deuterium ( D ) is meant to represent deuterium . Further , in some embodiments , the corresponding deuterated analog is provided . [ 73 ] In many cases , the compounds of this disclosure are capable of forming acid and / or base salts by virtue of the presence of amino and / or carboxyl groups or groups similar thereto . [ 74 ] Provided also are a pharmaceutically acceptable salt , isotopically enriched analog , deuterated analog , isomer ( such as a stereoisomer ) , and mixture of isomers ( such as a mixture of stereoisomers ) , of the compounds described herein . [ 75 ] " Pharmaceutically acceptable " or " physiologically acceptable " refer to compounds , salts , compositions , dosage forms and other materials which are useful in preparing a pharmaceutical composition that is suitable for veterinary or human pharmaceutical use . [ 76 ] The term " pharmaceutically acceptable salt " of a given compound refers to salts that retain the biological effectiveness and properties of the given compound and which are not biologically or otherwise undesirable . " Pharmaceutically acceptable salts " or " physiologically acceptable salts " include , for example , salts with inorganic acids and salts with an organic acid . In addition , if the compounds described herein are 16 WO 2025/049495 PCT / US2024 / 0440 obtained as an acid addition salt , the free base can be obtained by basifying a solution of the acid salt . Conversely , if the product is a free base , an addition salt , particularly a pharmaceutically acceptable addition salt , may be produced by dissolving the free base in a suitable organic solvent and treating the solution with an acid , in accordance with conventional procedures for preparing acid addition salts from base compounds . Those skilled in the art will recognize various synthetic methodologies that may be used to prepare nontoxic pharmaceutically acceptable addition salts . Pharmaceutically acceptable acid addition salts may be prepared from inorganic and organic acids . Salts derived from inorganic acids include , e.g. , hydrochloric acid , hydrobromic acid , sulfuric acid , nitric acid , phosphoric acid and the like . Salts derived from organic acids include , e.g. , acetic acid , propionic acid , gluconic acid , glycolic acid , pyruvic acid , oxalic acid , malic acid , malonic acid , succinic acid , maleic acid , fumaric acid , tartaric acid , citric acid , benzoic acid , cinnamic acid , mandelic acid , methanesulfonic acid , ethanesulfonic acid , p - toluene - sulfonic acid , salicylic acid and the like . Likewise , pharmaceutically acceptable base addition salts can be prepared from inorganic and organic bases . Salts derived from inorganic bases include , by way of example only , sodium , potassium , lithium , aluminum , ammonium , calcium and magnesium salts . Salts derived from organic bases include , but are not limited to , salts of primary , secondary and tertiary amines , such as alkyl amines ( i.e. , ₂HN ( alkyl ) ) , dialkyl amines ( i.e. , HN ( alkyl ) 2 ) , trialkyl amines ( i.e. , N ( alkyl ) 3 ) , substituted alkyl amines ( i.e. , NH2 ( substituted alkyl ) ) , di ( substituted alkyl ) amines ( i.e. , HN ( substituted alkyl ) 2 ) , tri ( substituted alkyl ) amines ( i.e. , N ( substituted alkyl ) 3 ) , alkenyl amines ( i.e. , ₂HN ( alkenyl ) ) , dialkenyl amines ( i.e. , HN ( alkenyl ) 2 ) , trialkenyl amines ( i.e. , N ( alkenyl ) 3 ) , substituted alkenyl amines ( i.e. , NH2 ( substituted alkenyl ) ) , di ( substituted alkenyl ) amines ( i.e. , HN ( substituted alkenyl ) 2 ) , tri ( substituted alkenyl ) amines ( i.e. , N ( substituted alkenyl ) , mono- , di- or tri- cycloalkyl amines ( i.e. , NH2 ( cycloalkyl ) , HN ( cycloalkyl ) 2 , N ( cycloalkyl ) 3 ) , mono- , di- or tri- arylamines ( i.e. , ₂HN ( aryl ) , HN ( aryl ) 2 , N ( aryl ) 3 ) or mixed amines , etc. Specific examples of suitable amines include , by way of example only , isopropylamine , trimethyl amine , diethyl amine , tri ( iso- propyl ) amine , tri ( n - propyl ) amine , ethanolamine , 2 - dimethylaminoethanol , piperazine , piperidine , morpholine , N - ethylpiperidine and the like . [ 77 ] The term " hydrate " refers to the complex formed by the combining of a compound described herein and water . [ 78 ] A " solvate " refers to an association or complex of one or more solvent molecules and a compound of the disclosure . Examples of solvents that form solvates include , but are not limited to , water , isopropanol , ethanol , methanol , dimethylsulfoxide , ethylacetate , acetic acid and ethanolamine . Solvates include hydrates . [ 79 ] Some of the compounds described herein may exist as tautomers . Tautomers are in equilibrium with one another . For example , amide containing compounds may exist in equilibrium with imidic acid tautomers . Regardless of which tautomer is shown and regardless of the nature of the equilibrium among 17 WO 2025/049495 PCT / US2024 / 0440 tautomers , the compounds are understood by one of ordinary skill in the art to comprise both amide and imidic acid tautomers . Thus , the amide containing compounds are understood to include their imidic acid tautomers . Likewise , the imidic acid containing compounds are understood to include their amide tautomers . [ 80 ] The compounds described herein , or their pharmaceutically acceptable salts , may include an asymmetric center and may thus give rise to enantiomers , diastereomers , and other stereoisomeric forms that may be defined , in terms of absolute stereochemistry , as ( R ) - or ( S ) - or , as ( D ) - or ( L ) - for amino acids . The present disclosure is meant to include all such possible isomers , as well as their racemic and optically pure forms . Optically active ( + ) and ( - ) , ( R ) - and ( S ) - , or ( D ) - and ( L ) - isomers may be prepared using chiral synthons or chiral reagents , or resolved using conventional techniques , for example , chromatography and fractional crystallization . Conventional techniques for the preparation / isolation of individual enantiomers include chiral synthesis from a suitable optically pure precursor or resolution of the racemate ( or the racemate of a salt or derivative ) using , for example , chiral high performance liquid chromatography ( HPLC ) . When the compounds described herein contain olefinic double bonds or other centers of geometric asymmetry , and unless specified otherwise , it is intended that the compounds include both E and Z geometric isomers . [ 81 ] A " stereoisomer " refers to a compound made up of the same atoms bonded by the same bonds but having different three - dimensional structures , which are not interchangeable . The present disclosure contemplates various stereoisomers and mixtures thereof and includes " enantiomers , " which refers to two stereoisomers whose molecules are non - superimposable mirror images of one another . [ 82 ] " Diastereomers " are stereoisomers that have at least two asymmetric atoms , but which are not mirror - images of each other . [ 83 ] Relative centers of the compounds as depicted herein are indicated graphically using the " thick bond " style ( bold or parallel lines ) and absolute stereochemistry is depicted using wedge bonds ( bold or parallel lines ) . [ 84 ] " Treatment " or " treating " is an approach for obtaining beneficial or desired results including clinical results . Beneficial or desired clinical results may include one or more of the following : a ) inhibiting the disease or condition ( e.g. , decreasing one or more symptoms resulting from the disease or condition , and / or diminishing the extent of the disease or condition ) ; b ) slowing or arresting the development of one or more clinical symptoms associated with the disease or condition ( e.g. , stabilizing the disease or condition , preventing or delaying the worsening or progression of the disease or condition , and / or preventing or delaying the spread ( e.g. , metastasis ) of the disease or condition ) ; and / or c ) relieving the disease or condition , that is , causing the regression of clinical symptoms ( e.g. , ameliorating the disease state , providing partial or total remission of the disease or condition , enhancing effect of another medication , delaying the 18 WO 2025/049495 PCT / US2024 / 0440 progression of the disease , increasing the quality of life , and / or prolonging survival ) . [ 85 ] " Prevention " or " preventing " means any treatment of a disease or condition that causes the clinical symptoms of the disease or condition not to develop . Compounds may , in some embodiments , be administered to a subject ( including a human ) who is at risk or has a family history of the disease or condition . [ 86 ] " Subject " refers to an animal , such as a mammal ( including a human ) , that has been or will be the object of treatment , observation or experiment . The methods described herein may be useful in human therapy and / or veterinary applications . In some embodiments , the subject is a mammal . In one embodiment , the subject is a human . [ 87 ] The term " therapeutically effective amount " or " effective amount " of a compound described herein or a pharmaceutically acceptable salt , tautomer , stereoisomer , mixture of stereoisomers , or deuterated analog thereof means an amount sufficient to effect treatment when administered to a subject , to provide a therapeutic benefit such as amelioration of symptoms or slowing of disease progression . The therapeutically effective amount may vary depending on the subject , and disease or condition being treated , the weight and age of the subject , the severity of the disease or condition , and the manner of administering , which can readily be determined by one of ordinary skill in the art . The effective amount of a compound of the disclosure in such a therapeutic method is , for example , from about 0.01 mg / kg / day to about 10mg / kg / day , or from about 0.1 mg / kg / day to about 100 mg / kg / day . [ 88 ] The term " excipient " as used herein refers to an inert or inactive substance that may be used in the production of a drug or pharmaceutical composition , such as a tablet containing a compound as described herein ( or pharmaceutically acceptable salt ) as an active ingredient . Various substances may be embraced by the term excipient , including without limitation any substance used as a diluent , filler or extender , binder , disintegrant , humectant , coating , emulsifier or dispersing agent , compression / encapsulation aid , cream or lotion , lubricant , solution for parenteral administration , material for chewable tablets , sweetener or flavoring , suspending / gelling agent , or wet granulation agent . Binders may include , e.g. , carbomers , povidone , xanthan gum , etc .; coatings may include , e.g. , cellulose acetate phthalate , ethylcellulose , gellan gum , maltodextrin , enteric coatings , etc .; compression / encapsulation aids include e.g. calcium carbonate , dextrose , fructose dc ( dc - " directly compressible " ) , honey dc , lactose ( anhydrate or monohydrate ; optionally in combination with aspartame , cellulose , or microcrystalline cellulose ) , starch dc , sucrose , etc .; disintegrants include , e.g. , croscarmellose sodium , gellan gum , sodium starch glycolate , etc .; creams or lotions include , e.g. , maltodextrin , carrageenans , etc .; lubricants include , e.g. , magnesium stearate , stearic acid , sodium stearyl fumarate , etc .; materials for chewable tablets include , e.g. dextrose , fructose dc , lactose ( monohydrate , optionally in combination with aspartame or cellulose ) , etc .; suspending / gelling agents include , e.g. , carrageenan , sodium starch glycolate , xanthan gum , etc .; 19 WO 2025/049495 PCT / US2024 / 0440 sweeteners include , e.g. , aspartame , dextrose , fructose dc , sorbitol , sucrose dc , etc .; and wet granulation agents include , e.g. , calcium carbonate , maltodextrin , microcrystalline cellulose , etc. In some cases , the term " excipient " encompasses pharmaceutically acceptable carriers . [ 89 ] II . [ 90 ] Formula A : Additional definitions may also be provided below as appropriate .

Compounds In certain embodiments , the subject matter described herein is directed to a compound of R1a N R • N • A R1 R2a ²R wherein , A is selected from the group consisting of ₁C - C6 alkyl , C3 - C8 cycloalkyl , phenyl , 5- to 6- membered heteroaryl and 5- to 6 - membered heterocyclyl , each of which is optionally substituted with one or more of RA1 , RA2 and ³AR , A wherein , RA , RA2 and RA3 are each independently selected from the group consisting of ₁C - C6 alkyl , halo - ₁C - C6 alkyl , ₁C - C6 alkoxy , halo , cyano , 1- and -S ( O ) 2 - RAAwherein , RA is ₁C - C6 alkyl or C3 - C8 cycloalkyl , and oxo , -C ( O ) -RA4 -S ( O ) -RA wherein the oxo , if present , is formed by two of RA1 , RA2 and ³AR together with a carbon to which each is attached : G is -CH , C - OH , or N ; E , if present , is -C ( O ) - or -O- ; Y is -CH or N ; p is 1 , 2 or 3 ; q is 1 or 0 ; r is 1 or 0 ; WO 2025/049495 PCT / US2024 / 0440 wherein , when r is 0 , A is other than ₁C - C6 alkyl ; 1- ¹R is selected from the group consisting of ₁C - C6 alkyl , C3 - C8 cycloalkyl and halo - ₁C - C6 alkyl ; or ¹R is halo and q is 0 ; la a¹R is selected from the group consisting of hydrogen , halo , ₁C - C6 alkyl ; ²R is selected from the group consisting of halo , halo - ₁C - C6 alkyl , halo - ₁C - C6 alkoxy and -S ( O ) 2- ( C1 - C6 alkyl ) ; and , 2a Rza is selected from the group consisting of hydrogen and halo ; ³R is hydrogen , halo , or ₁C - C6 alkyl , or a pharmaceutically acceptable salt or solvate thereof . [ 91 ] In certain embodiments , compounds include those of Formula A , or pharmaceutically acceptable salts or solvates thereof , wherein G is CH , r is 1 , and E is -O- , having a structure of Formula A- i : R1a R N · N · R1 R2a R A A - i [ 92 ] la 2a In certain embodiments , compounds include those of Formula A - i , or pharmaceutically acceptable salts or solvates thereof , wherein p is 2 ; a¹R , ª2R , and ³R are each hydrogen , and having a structure of Formula A - i ' : 21 R A PCT / US2024 / 0440 A - i ' [ 93 ] ²R In certain embodiments , compounds include those of Formula A , or pharmaceutically acceptable salts or solvates thereof , wherein G is C - OH and r is 0 , having a structure of Formula A - ii : N ROH -A R1a- ₁N- RR2a ²R A - ii [ 94 ] In certain embodiments , compounds include those of Formula A , or pharmaceutically acceptable salts or solvates thereof , wherein p is 2 and Rla , R2a , and ³R are each hydrogen , having a structure of Formula A - ii * : 22 N OH -A ( ° ) a R PCT / US2024 / 0440 A - ii * [ 95 ] ²R In certain embodiments , compounds include those of Formula A - i , Formula A - i ' , Formula A- ii , or Formula A - ii ' or pharmaceutically acceptable salts or solvates thereof , wherein q is 1 and ¹R is CH3 . In certain embodiments , compounds include those of Formula A - i , Formula A - i ' , Formula A - ii , or Formula A - ii ' , or pharmaceutically acceptable salts or solvates thereof , wherein ²R is CF3 or OCHF2 . In certain embodiments , compounds include those of Formula A - i , Formula A - i ' , Formula A - ii , or Formula A - ii ' , or pharmaceutically acceptable salts or solvates thereof , wherein Y is CH . [ 96 ] In certain embodiments , compounds include those of Formula A , or pharmaceutically acceptable salts or solvates thereof , wherein E is -C ( O ) - , having a structure of Formula I. [ 97 ] Formula I : In certain embodiments , the subject matter described herein is directed to a compound of R1a ³R N R2a ²R , I wherein , A is selected from the group consisting of C1 - C6 alkyl , C3 - C8 cycloalkyl , phenyl , 5- to 6 - membered heteroaryl and 5- to 6 - membered heterocyclyl , each of which is optionally substituted with one or more of RAI RA2 and RAﻭ 23 WO 2025/049495 PCT / US2024 / 0440 Al Awherein , RAI , RA2 and ³AR are each independently selected from the group consisting of ₁C - C6 alkyl , halo - ₁C - C6 alkyl , halo , cyano , oxo , -C ( O ) 4ªR- , -S ( O ) -R + and -S ( O ) 2 - 4ªR , Awherein , RA is C1 - C6 alkyl or C3 - C8 cycloalkyl , and wherein the oxo , if present , is formed by two of RA1 , RA2 and ³AR together with a carbon to which each is attached : G is -CH or N : Y is -CH or N ; p is 1 , 2 or 3 ; q is 1 or 0 ; r is 1 or 0 ; ﻭ wherein , when r is 0 , A is other than ₁C - C6 alkyl ; R ' is selected from the group consisting of ₁C - C6 alkyl , C3 - C8 cycloalkyl and halo - ₁C - C6 alkyl ; a¹R is selected from the group consisting of hydrogen , halo , and C1 - C6 alkyl ; ²R is selected from the group consisting of halo , halo - ₁C - C6 alkyl , halo - ₁C - C6 alkoxy and -S ( O ) 2- ( C1 - C6 alkyl ) ; and . R2a is selected from the group consisting of hydrogen and halo ; ³R is hydrogen , halo , or C1 - C6 alkyl , or a pharmaceutically acceptable salt or solvate thereof . [ 98 ] In certain embodiments , compounds include those of Formulae A and I , or pharmaceutically acceptable salts or solvates thereof , wherein G is CH . [ 99 ] In certain embodiments , compounds include those of Formula I , or pharmaceutically acceptable salts or solvates thereof , wherein G is N and include compounds having a structure of Formula I ' : R [ 100 ] R ' N · A I ' ²R In certain embodiments , compounds include those of Formula I or I ' , or pharmaceutically 224 WO 2025/049495 PCT / US2024 / 0440 acceptable salts or solvates thereof , where q is 1. In certain embodiments , compounds include those of Formula I or I ' , or pharmaceutically acceptable salts or solvates thereof , where q is 0 . [ 101 ] In certain embodiments , compounds include those of Formula I or I ' , or pharmaceutically acceptable salts or solvates thereof , where ¹R is C1 - C6 alkyl or C3 - C8 cycloalkyl . In certain embodiments , compounds include those of Formula I or I ' , or pharmaceutically acceptable salts or solvates thereof , where R ' is methyl , ethyl or cyclopropyl . [ 102 ] In certain embodiments , compounds of Formula I or I ' , or pharmaceutically acceptable salts or solvates thereof , include compounds , or pharmaceutically acceptable salts or solvates thereof , having a structure of Formulae Ia , Ib , or Ic : ³R N R R H ²R A A la ☑ Ib H Ic Rﻭ WO 2025/049495 PCT / US2024 / 0440 [ 103 ] In certain embodiments , compounds include those of Formula A , or pharmaceutically acceptable salts or solvates thereof , wherein q is 0 and ¹R is halogen . In certain embodiments , compounds include those of Formula A , or pharmaceutically acceptable salts or solvates thereof , wherein q is 0 and ¹R is -Cl . In certain embodiments , compounds include those of Formula A , or pharmaceutically acceptable salts or solvates thereof , wherein r and q are each 0 , ª¹R and b¹R are each hydrogen , and R ' is halogen , having a structure of Formula Id : R R ²R G- A Id [ 104 ] In certain embodiments , compounds include those of Formula Id , where ¹R is -Cl . In certain embodiments , compounds include those of Formula Id , where ²R is CF3 . In certain embodiments , compounds include those of Formula Id , where ³R is hydrogen . In certain embodiments , compounds include those of Formula Id , where Y is N. In certain embodiments , compounds include those of Formula Id , where G is N and p is 2 . [ 105 ] In certain embodiments , compounds include those of Formulae A , A - i , A - i ' , A - ii , A - ii ' , I , I ' , Ia , Ib , Ic or Id , where one or more hydrogen atoms is replaced with deuterium . [ 106 ] A - iii : In certain embodiments , compounds include those of Formula A , having a structure of Formula 26 D D R1 R2a ³R ( E ) A PCT / US2024 / 0440 A - iii [ 107 ] In certain embodiments , compounds include those of Formulae A , A - i , A - ³i , A - ii , A - ii " , A - iii , I , I ' , Ia , Ib , Ic or Id , wherein ¹R is -CD3 . [ 108 ] In certain embodiments , compounds include those of Formulae A , A - i , A - i ' , A - ii , A - ii " , A - iii , I , I , Ia , Ib , Ic , or Id , wherein Y is N. In certain embodiments , compounds include those of Formulae A , A- i , A - i ' , A - ii , A - ii ' , A - iii , I , I ' , Ia , Ib , Ic , or Id where Y is -CH . [ 109 ] In certain embodiments , compounds include those of Formulae A , A - i , A - i ' , A - ii , A - ii ' , A - iii , I , I ' , Ia , Ib , Ic , or Id where ²R is halo - ₁C - C6 alkyl or halo - ₁C - C6 alkoxy . In certain embodiments , compounds include those of Formulac A , A - i , A - i ' , A - ii , A - ii ' , A - iii , I , I ' , Ia , Ib , Ic , or Id where ²R is halo - C1 - C6 alkyl . In certain embodiments , compounds include those of Formulae I , I ' , Ia , Ib , or Ic , where ²R is -CF3 . In certain embodiments , compounds include those of Formulae A , A - i , A - i ' , A - ii , A - ii * , A - iii , I , ˚I , Ia , Ib , Ic , or Id , where ²R is halo - ₁C - C6 alkyloxy . In certain embodiments , compounds include those of Formulae A , A - i , A - i ' , A - ii , A - ii ' , A - iii , I , I ' , Ia , Ib , Ic , or Id , where ²R is -O - CHF2 . [ 110 ] , In certain embodiments , compounds include those of Formulae A , A - i , A - i ' , A - ii , A - ii ' , A - iii , I , I ' , Ia , Ib , Ic , or Id , where p is 1 or 2. In certain embodiments , compounds include those of Formulac A , A - i , A - ii , A - iii , I , ˆI , Ia , Ib , Ic , or Id , where p is 1. In certain embodiments , compounds include those of Formulae A. A - i , A - i ' , A - ii , A - ii ' , A - iii , I , I , Ia , Ib , Ic , or Id , where p is 2 . [ 111 ] In certain embodiments , compounds include those of Formulae A , A - i , A - i ' , A - ii , A - ii ' , A - iii , I , I ' , Ia , Ib , Ic , or Id , where ³R is ₁C - C6 alkyl . In certain embodiments , compounds include those of Formulae A , A - i , A - i ' , A - ii , A - ii ' , A - iii , I , I ' , Ia , Ib , Ic , or Id , where ³R is methyl . In certain embodiments , compounds include those of Formulae A , A - i , A - i ' , A - ii , A - ii ' , A - iii , I , I ' , Ia , Ib , Ic , or Id , where ³R is hydrogen . [ 112 ] In certain embodiments , compounds include those of Formulae A , A - i , A - i * , A - iii , I , I ' , Ia , Ib , or Ic , where r is 1. In certain embodiments , compounds include those of Formulae A , A - i , A - i ' , A - iii , I , I ' , Ia , Ib , or Ic , where r is 1 and A is ₁C - C6 alkyl . In certain embodiments , compounds include those of Formulae A , A - i , A - i ' , A - iii , I , I ' , Ia , Ib , or Ic , where r is 1 and A is -CH3 or -CH2CH3 . In certain 27 WO 2025/049495 PCT / US2024 / 0440 embodiments , compounds include those of Formulae A , A - ii , A - ii * , A - iii , I , I ' , Ia , Ib , Ic , or Id , where r is 0 . In certain embodiments , compounds include those of Formulae A , A - ii , A - ³ii , A - iii , I , I ' , Ia , Ib , Ic , or Id , where r is 0 and A is C3 - Cs cycloalkyl , optionally substituted with one or more of RAI , RA2 , and ³AR [ 113 ] A In certain embodiments , compounds include those of Formulae A , A - i , A - i * , A - ii , A - ii ' , A - iii , I , I ' , Ia , Ib , Ic , or Id , where r is 0 or 1 and A is C3 - C5 cycloalkyl , optionally substituted with one or more of A2 ARAI RAZ , and ³AR . In certain embodiments , compounds include those of Formulae A , A - i , A - i ' , A - ii , A - ii ' , A - iii , I , I , Ia , Ib , Ic , or Id , where A is ﻭ or RA. In instances of the above embodiments , compounds include those of Formulae A , A - i , A - i ' , A - ii , A - ii ' , A - iii , I , I ' , Ia , Ib , Ic , or Id , where RA1 is cyano or halo ₁C - C6 alkyl . In instances of the above embodiments , compounds include those of Formulae A , A - i , A - i ' , A - ii , A - ii ' , A - iii , I , I ' , Ia , Ib , or Ic , where RA1 is -CF3 . In instances of the above embodiments , compounds include those of Formulae A , A - i , A - i ' , A - iii , I , I ' , Ia , Ib , or Ic , where r is 1 . [ 114 ] AIn certain embodiments , compounds include those of Formulae A , A - ii , A - ii ' , I , I ' , Ia , Ib , Ic , or Id , where r is 0 and A is phenyl , optionally substituted with one or more of RAI , RA2 , and ³AR . In certain embodiments , compounds include those of Formulae A , A - ii , A - ii ' , A - iii , I , I ' , Ia , Ib , Ic , or Id , where r is and A is phenyl , optionally substituted with one or more of RA1 and RA2 . In certain embodiments , compounds include those of Formulac A , A - ii , A - ³ii , A - iii , I , I ' , Ia , Ib , Ic , or Id , where r is 0 and A has the RA structure : RAAl . In instances of the above embodiments , compounds include those of Formulae A , A - ii , A - ii ' , A - iii , I , I , Ia , Ib , Ic , or Id , where ¹AR is -S ( O ) 2 - RA4 and RA2 is halo . In certain embodiments , compounds include those of Formulae A , A - ii , A - ii ' , A - iii , I , I ' , Ia , Ib , Ic , or Id , where r is -RAand A has the structure : . In instances of the above embodiment , compounds include those of Formulae A , A - ii , A - ii ' , A - iii , I , I ' , Ia , Ib , Ic , or Id , where RA1 is selected from the group consisting of halo , cyano , -S ( O ) 2 - R * 4 and -C ( O ) -R * 4 . [ 115 ] In certain embodiments , compounds include those of Formulae A , A - i , A - i * , A - ii , A - ii ' , A - iii , I , I ' , Ia , Ib , Ic , or Id , where r is 0 or 1 and A is 5- to 6 - membered heterocyclyl , optionally substituted with 28 WO 2025/049495 PCT / US2024 / 0440 Aone or more of RAI , RAZ , and RA3 . In instances of the above embodiment , compounds include those of Formulae A , A - i , A - i ' , A - ii , A - ii ' , A - iii , I , I ' , Ia , Ib , Ic , or Id , where A is heterocyclyl comprising 1 or heteroatoms selected from the group consisting of N , S , and O. In instances of the above embodiments , compounds include those of Formulae A , A - i , A - i ' , A - ii , A - ii ' , A - iii , I , I ' , Ia , Ib , Ic , or Id , where A is 5 - to - membered heterocyclyl . In instances of the above embodiment , compounds include those of Formulae A , A - i , A - i ' , A - ii , A - ii " , A - iii , I , I ' , Ia , Ib , Ic , or Id , where A is 5- to 6 - membered heterocyclyl comprising or 2 heteroatoms selected from the group consisting of N , S , and O. In instances of the above embodiments , compounds include those of Formulae A , A - i , A - i ' , A - ii , A - ³ii , A - iii , I , I ' , Ia , Ib , Ic , or Id , where A is [ 116 ] or In certain embodiments , compounds include those of Formulae A , A - i , A - i ' , A - ii , A - ii ' , A - iii , I , I ' , Ia , Ib , Ic , or Id , where r is 0 or 1 and A is 5- to 6 - membered heterocyclyl , substituted with RA1 , RA2 , and ³AR . In instances of the above embodiment , compounds include those of Formulae A , A - i , A - i ' , A - ii , A - iii , A - ii " , I , I ' , Ia , Ib , Ic or Id , where RA2 and ³AR together with a carbon to which each is attached form A an oxo , A is RA' N · or RA· N ' ﻭ and RA is C1 - C6 alkyl . In instances of the above embodiment , compounds include those of Formulae A , A - i , A - i ' , A - ii , A - ii ' , A - iii , I , I ' , Ia , Ib , Ic , or Id , where R ^ 2 is ethyl . [ 117 ] A A A In certain embodiments , compounds include those of Formulae A , A - i , A - i ' , A - ii , A - ii ' , A - iii , I , I ' , Ia , Ib , or Ic , where r is 0 or 1 and A is 5- to 6 - membered heteroaryl , optionally substituted with one or more of RAI , RA2 , and ³AR . In instances of the above embodiment , compounds include those of Formulae A , A - i , A - i ' , A - ii , A - ³ii , A - iii , I , I ' , Ia , Ib , Ic , or Id , where A is selected from the group consisting of pyridinyl , pyridazinyl , pyrimidinyl , pyrazinyl , triazinyl , oxadiazolyl , pyrrolyl , imidazolyl , pyrazolyl , and thiazolyl , optionally substituted with one or more of RA1 , RA2 and ³AR . In instances of the above embodiments , compounds include those of Formulae A , A - i , A - i ' , A - ii , A - ii ' , A - iii , I , I ' , la , Ib , Ic . or Id , where A is selected from the group consisting of pyridinyl , pyrimidinyl , pyrazinyl , oxadiazolyl , and pyrrolyl , optionally substituted with one or more of RA1 , RA2 and ³AR . In instances of the above embodiments , compounds include those of Formulae A , A - i , A - i ' , A - ii , A - ii ' , A - iii , I , I ' , Ia , Ib , Ic , or Id , where A is pyridinyl , optionally substituted with one or more of ¹AR , RA2 , and RA3 . In instances of the above Al ﻭ A 29 WO 2025/049495 PCT / US2024 / 0440 embodiments , compounds include those of Formulae A , A - i , A - i ' , A - ii , A - ii ' , A - iii , I , I ' , Ia , Ib , Ic , or Id , where A pyridinyl , optionally substituted with RA1 . In instances of the above embodiments , compounds include those of Formulae A , A - i , A - i * , A - ii , A - ³ii , A - iii , I , I ' , Ia , Ib , Ic , or Id , where A is -RAARAor RAIn instances of the above embodiments , compounds include those of Formulae I , I ' , Ia , Ib , or Ic , where RA1 is selected from the group consisting of ₁C - C6 alkyl , halo - ₁C - C6 alkyl , halo , cyano and -S ( O ) 2 - 4ªR . In instances of the above embodiments , compounds include those of Formulae A , A - i , A - i ' , A - ii , A - ii ' , A - iii , I. I ' , Ia , -N -CN Ib . Ic or Id , where A is , In instances of the above embodiments , compounds include those of Formulae A , A - i , A - i ' , A - ii , A - ii ' , A - iii , I , I ' , Ia , Ib , Ic , or Id , where A is pyrimidinyl or pyrazinyl , optionally substituted with one or more of RAI , RA2 and RA3 . In instances of the above embodiments , compounds include those of Formulae A , A - i , A - i ' , A - ii , A - ii " , A - iii , I , I ' , Ia , Ib , Ic . or Id , where A is pyrimidinyl or pyrazinyl , optionally substituted with RA1 In instances of the above embodiments , compounds include those of Formulae A , A - i , A - i ' , A - ii , A - ii ' , A - iii , I , I ' , la , Ib , Ic . or Id , N where A is N N.

RA N RA N RA or In instances of the above embodiments , compounds include those of Formulae I , I ' , Ia , Ib , Ic , or Id , where RA is selected from the group consisting of ₁C - C6 alkyl , halo - ₁C - C alkyl , halo , cyano and -S ( O ) 2 - RA4 . In instances of the above embodiments , compounds include those of Formulae A , A - i , A - i ' , A - ii , A - ii ' , A - iii , I , I ^ , Ia , Ib , Ic or Id , where RA is 3HCO₂HC . In instances of the above embodiments , compounds include those of Formulae A , N.

PCT / US2024 / 0440 A - i , A - i , A - ii , A - ii ' , A - iii , I , I ' , Ia , Ib , Ic or Id , where A is CN AIn instances of the above embodiments , compounds include those of Formulae I , I ' , Ia , Ib , or Ic , where A is oxadiazolyl and pyrrolyl , optionally substituted with one or more of RAI , RA2 and ³AR . In instances of the above embodiments , compounds include those of Formulae A , A - i , A - i ' , A - ii , A - ii ' , A - iii , I , I ' , Ia , Ib , Ic , or Id , where oxadiazolyl and pyrrolyl , optionally substituted with ¹AR . In instances of the above embodiments , compounds include those of Formulae A , A - i , A - i ' , A - ii , A - ii ' , A - iii , I , I ' , Ia , Ib , Ic , Id , where N A is [ 118 ] or RA The subject matter described herein includes the following compounds in Table 1 , or pharmaceutically acceptable salts thereof . Individual enantiomers and diastereomers are included in the table below by compound name , and their corresponding structures can be readily determined therefrom . In some instances , the enantiomers or diastereomers of the present disclosure may be identified by their respective properties , for example , retention times by chiral HPLC , NMR peaks , and / or biological activities ( e.g. , as described further in the Examples ) , whereas the absolute stereo configurations of one or more chiral centers has not been assigned . Table 1. Compounds [ 119 ] Cpd . No. N Structure Compound Name N CF LCF( S ) -4 - cyclopropyl - N- ( 4- ( trifluoromethyl ) phenyl ) -N- ( 1- ( 5- ( trifluoromethyl ) pyridin - 2 - yl ) pyrrolidin - 3 - yl ) pyridin - 3 - amine 2- ( 4 - ( ( 4 - cyclopropylpyridin - 3- yl ) ( 6- ( trifluoromethyl ) pyridin - 3- yl ) amino ) piperidin - 1- yl ) pyrimidine - 5 - carbonitrile 31 Cpd . No. Structure b N PCT / US2024 / 0440 Compound Name 4 - cyclopropyl - N- ( 1- ( 4- ( methylsulfonyl ) phenyl ) piperidin- - yl ) -N- ( 6- ( trifluoromethyl ) pyridin - 3 - yl ) pyridin - 3 - amine 2- ( 4 - ( ( 4 - ethylpyridin - 3 - yl ) ( 6- ( trifluoromethyl ) pyridin - 3 - yl ) amino ) piperidin - 1 - yl ) pyrimidine- - carbonitrile 2- ( 4 - ( ( 4 - methoxypyridin - 3 - yl ) ( 6- ( trifluoromethyl ) pyridin - 3 - yl ) amino ) piperidin - 1 - yl ) pyrimidine- - carbonitrile ﻊﻣﺭﻭ 1- ( 4 - ( ( 4 - cyclopropylpyridin - 3- yl ) ( 4- ( trifluoromethyl ) phenyl ) amino ) pip eridin - 1 - yl ) ethan - 1 - one 1- ( 4 - ( ( 4 - cyclopropylpyridin - 3- yl ) ( 4- ( trifluoromethyl ) phenyl ) amino ) pip eridin - 1 - yl ) propan - 1 - one Cpd . No. Structure N PCT / US2024 / 0440 Compound Name 2- ( 4 - ( ( 4 - cyclopropoxypyridin - 3- yl ) ( 6- ( trifluoromethyl ) pyridin - 3- yl ) amino ) piperidin - 1- yl ) pyrimidine - 5 - carbonitrile 4- ( 4 - ( ( 4 - methoxypyridin - 3 - yl ) ( 4- ( methylsulfonyl ) phenyl ) amino ) pip eridin - 1 - yl ) benzonitrile good - cyclopropyl - N- ( 1- ( 4- ( cyclopropylsulfonyl ) phenyl ) piper idin - 4 - yl ) -N- ( 6- ( trifluoromethyl ) pyridin - 3 - yl ) pyridin - 3 - amine N N 6- ( 4 - ( ( 4 - methoxypyridin - 3 - yl ) ( 6- ( trifluoromethyl ) pyridin - 3 - yl ) amino ) piperidin - 1 - yl ) nicotinonitrile ' N ' 4 - methoxy - N- ( 1- ( 5- ( methylsulfonyl ) pyrimidin - 2 - yl ) piperidin - 4 - yl ) -N- ( 4- ( trifluoromethyl ) phenyl ) pyridin - 3- amine Cpd . No. Structure F PCT / US2024 / 0440 good Compound Name 4 - methoxy - N- ( 4- ( trifluoromethyl ) phenyl ) -N- ( 1- ( 5- ( trifluoromethyl ) pyridin - 2- yl ) piperidin - 4 - yl ) pyridin - 3 - amine N N 6- ( 4 - ( ( 4 - methoxypyridin - 3 - yl ) ( 4- ( trifluoromethyl ) phenyl ) amino ) pip eridin - 1 - yl ) nicotinonitrile 2- ( 4 - ( ( 4 - methoxypyridin - 3 - yl ) ( 4- ( trifluoromethyl ) phenyl ) amino ) pip eridin - 1 - yl ) pyrimidine - 5- carbonitrile foot - methoxy - N- ( 1- ( 4- ( methylsulfonyl ) phenyl ) piperidin- - yl ) -N- ( 4- ( trifluoromethyl ) phenyl ) pyridin - 3- amine ' N ' N - methoxy - N- ( 1- ( 5- ( methylsulfonyl ) pyrimidin - 2- yl ) piperidin - 4 - yl ) -N- ( 6- ( trifluoromethyl ) pyridin - 3- yl ) pyridin - 3 - amine 34 Cpd . No. Structure N PCT / US2024 / 0440 Compound Name 2- ( 4 - ( ( 4- ( difluoromethoxy ) phenyl ) ( 4- methoxypyridin - 3- yl ) amino ) piperidin - 1- yl ) pyrimidine - 5 - carbonitrile N gob 2- ( 4 - ( ( 4- ( difluoromethoxy ) phenyl ) ( 4- methylpyridin - 3- yl ) amino ) piperidin - 1- yl ) pyrimidine - 5 - carbonitrile 4 - methoxy - N- ( 1- ( 1 - methyl - 1H- pyrazol - 5 - yl ) piperidin - 4 - yl ) -N- ( 4- ( trifluoromethyl ) phenyl ) pyridin - 3- amine ( R ) - ( 4 - ( ( 4 - methoxypyridin - 3- yl ) ( 4- ( trifluoromethyl ) phenyl ) amino ) pip eridin - 1 - yl ) ( tetrahydrofuran - 3- yl ) methanone N ' N ' 1- ( 4 - ( ( 4 - ethoxypyridin - 3 - yl ) ( 4- ( trifluoromethyl ) phenyl ) amino ) -2- methylpiperidin - 1 - yl ) propan - 1- one WO 2025/049495 PCT / US2024 / 0440 Cpd . No. Structure Compound Name F N N N N 1- ( 4 - ( ( 4- ( difluoromethoxy ) phenyl ) ( 4- methoxypyridin - 3- yl ) amino ) piperidin - 1 - yl ) propan - 1- one N- ( 4- ( difluoromethoxy ) phenyl ) -4- methoxy - N- ( 1- ( 5- ( methylsulfonyl ) pyrimidin - 2- yl ) piperidin - 4 - yl ) pyridin - 3 - amine 2- ( 4 - ( ( 6- ( difluoromethoxy ) pyridin - 3 - yl ) ( 4- methoxypyridin - 3- yl ) amino ) piperidin - 1- yl ) pyrimidine - 5 - carbonitrile 6- ( difluoromethoxy ) -N- ( 4- methoxypyridin - 3 - yl ) -N- ( 1- ( 5- ( methylsulfonyl ) pyrimidin - 2- yl ) piperidin - 4 - yl ) pyridin - 3 - amine N- ( 4- ( difluoromethoxy ) phenyl ) -4- methoxy - N- ( 1- ( 1 - methyl - 1H- pyrazol - 5 - yl ) piperidin - 4- yl ) pyridin - 3 - amine WO 2025/049495 PCT / US2024 / 0440 Cpd . No. Structure Compound Name N ( 4 - ( ( 4- ( difluoromethoxy ) phenyl ) ( 4- methoxypyridin - 3- yl ) amino ) piperidin - 1 - yl ) ( pyridin- - yl ) methanone 8 ( 4 - ( ( 4 - methoxypyridin - 3 - yl ) ( 4- ( trifluoromethyl ) phenyl ) amino ) pip eridin - 1 - yl ) ( pyridin - 4- yl ) methanone 6- ( difluoromethoxy ) -N- ( 4- methoxypyridin - 3 - yl ) -N- ( 1- ( 1- methyl - 1H - pyrazol - 5 - yl ) piperidin- - yl ) pyridin - 3 - amine F ( 4 - chlorophenyl ) ( 4 - ( ( 4- ( difluoromethoxy ) phenyl ) ( 4- methoxypyridin - 3- yl ) amino ) piperidin - 1- yl ) methanone ﻱﺓ ' N ' gola 4- ( 4 - ( ( 4- ( difluoromethoxy ) phenyl ) ( 4- methoxypyridin - 3- yl ) amino ) piperidine - 1- carbonyl ) benzonitrile 37 Cpd . No.

PCT / US2024 / 0440 Structure Compound Name N gola F ( 4 - ( ( 4- ( difluoromethoxy ) phenyl ) ( 4- methoxypyridin - 3- yl ) amino ) piperidin - 1 - yl ) ( 4- ( methylsulfonyl ) phenyl ) methanon 6- ( 4 - ( ( 4- ( difluoromethoxy ) phenyl ) ( 4- methoxypyridin - 3- yl ) amino ) piperidin - 1- yl ) nicotinonitrile F cyclobutyl ( 4 - ( ( 4- ( difluoromethoxy ) phenyl ) ( 4- methoxypyridin - 3- yl ) amino ) piperidin - 1- yl ) methanone Bob N ' N ' F 3HC₂OS 20F cyclobutyl ( 4 - ( ( 4 - methoxypyridin- - yl ) ( 4- ( trifluoromethyl ) phenyl ) amino ) pip eridin - 1 - yl ) methanone ( 4 - Fluoro - 2- ( methylsulfonyl ) phenyl ) ( 4 - ( ( 4- methoxypyridin - 3 - yl ) ( 4- ( trifluoromethyl ) phenyl ) amino ) pip eridin - 1 - yl ) methanone 38 Cpd . No.

N N Structure OCHF ` N ' N · SO2CH PCT / US2024 / 0440 Compound Name N- ( 4- ( Difluoromethoxy ) phenyl ) -4- methoxy - N- ( 1- ( 4- ( methylsulfonyl ) phenyl ) piperidin- - yl ) pyridin - 3 - amine H₂FC N- ( 1- ( 5- ( Difluoromethyl ) pyridin- - yl ) piperidin - 4 - yl ) -4 - methoxy - N- ( 4- ( trifluoromethyl ) phenyl ) pyridin - 3- amine N 6- ( 4 - ( ( 4 - Methoxypyridin - 3 - yl ) ( 4- ( trifluoromethyl ) phenyl ) amino ) pip eridin - 1 - yl ) -1 - methylpyridin- ( 1H ) -one F F N F bicyclo [ 1.1.1 ] pentan - 1 - yl ( 4 - ( ( 4- ( difluoromethoxy ) phenyl ) ( 4- methoxypyridin - 3- yl ) amino ) piperidin - 1- vl ) methanone ( 4 - ( ( 4- ( difluoromethoxy ) phenyl ) ( 4- methoxypyridin - 3- yl ) amino ) piperidin - 1 - yl ) ( 3- fluorobicyclo [ 1.1.1 ] pentan - 1- yl ) methanone Cpd . No. Structure PCT / US2024 / 0440 Compound Name 3- ( 4 - ( ( 4- ( difluoromethoxy ) phenyl ) ( 4- methoxypyridin - 3- yl ) amino ) piperidine - 1- carbonyl ) bicyclo [ 1.1.1 ] pentane - 1- carbonitrile 4 - methoxy - N- ( 1- ( pyrazin - 2- yl ) piperidin - 4 - yl ) -N- ( 4- ( trifluoromethyl ) phenyl ) pyridin - 3- amine H N · F CN F L bicyclo [ 1.1.1 ] pentan - 1 - yl ( 4 - ( ( 4- methoxypyridin - 3 - yl ) ( 4- ( trifluoromethyl ) phenyl ) amino ) pip eridin - 1 - yl ) methanone ( 3 - fluorobicyclo [ 1.1.1 ] pentan - 1- yl ) ( 4 - ( ( 4 - methoxypyridin - 3 - yl ) ( 4- ( trifluoromethyl ) phenyl ) amino ) pip eridin - 1 - yl ) methanone 3- ( 4 - ( ( 4 - methoxypyridin - 3 - yl ) ( 4- ( trifluoromethyl ) phenyl ) amino ) pip eridine - 1- carbonyl ) bicyclo [ 1.1.1 ] pentane - 1- carbonitrile ( 4 - ( ( 4 - methoxypyridin - 3 - yl ) ( 4- ( trifluoromethyl ) phenyl ) amino ) pip eridin - 1 - yl ) ( 3- ( trifluoromethyl ) bicyclo [ 1.1.1 ] pen tan - 1 - yl ) methanone Cpd . No.

N F.

Structure N N CF PCT / US2024 / 0440 Compound Name ( 4 - ( ( 4- ( difluoromethoxy ) phenyl ) ( 4- methoxypyridin - 3- yl ) amino ) piperidin - 1 - yl ) ( 3- ( trifluoromethyl ) bicyclo [ 1.1.1 ] pen tan - 1 - yl ) methanone F 4 - methoxy - N- ( 1- ( 5- methylpyrazin - 2 - yl ) piperidin - 4- yl ) -N- ( 4- ( trifluoromethyl ) phenyl ) pyridin - 3- amine 4 - methoxy - N- ( 1- ( pyrimidin - 5- yl ) piperidin - 4 - yl ) -N- ( 4- ( trifluoromethyl ) phenyl ) pyridin - 3- amine 4 - methoxy - N- ( 1- ( 2- methylpyrimidin - 5 - yl ) piperidin - 4- yl ) -N- ( 4- ( trifluoromethyl ) phenyl ) pyridin - 3- amine LL F - ( 4 - ( ( 4 - methoxypyridin - 3 - yl ) ( 4- ( trifluoromethyl ) phenyl ) amino ) pip cridin - 1 - yl ) pyrimidine - 2- carbonitrile WO 2025/049495 PCT / US2024 / 0440 Cpd . No. Structure Compound Name F ..... good 4 - methoxy - N- ( 4- ( trifluoromethyl ) phenyl ) -N- ( 1- ( 2- ( trifluoromethyl ) pyrimidin - 5- yl ) piperidin - 4 - yl ) pyridin - 3 - amine N- ( 4- ( difluoromethoxy ) phenyl ) -4- methoxy - N- ( 1- ( pyrazin - 2- yl ) piperidin - 4 - yl ) pyridin - 3 - amine N OCHF OCHF N- ( 4- ( difluoromethoxy ) phenyl ) -4- methoxy - N- ( 1- ( 5 - methylpyrazin- - yl ) piperidin - 4 - yl ) pyridin - 3- amine N- ( 4- ( difluoromethoxy ) phenyl ) -4- methoxy - N- ( 1- ( pyrimidin - 5- yl ) piperidin - 4 - yl ) pyridin - 3 - amine OCHFIN F - ( 4 - ( ( 4- ( difluoromethoxy ) phenyl ) ( 4- methoxypyridin - 3- yl ) amino ) piperidin - 1- yl ) pyrimidine - 2 - carbonitrile 42 WO 2025/049495 PCT / US2024 / 0440 Cpd . No. Structure N. F good gob gob N gola N OCHF CF Compound Name N- ( 4- ( difluoromethoxy ) phenyl ) -4- methoxy - N- ( 1- ( 2- ( trifluoromethyl ) pyrimidin - 5- yl ) piperidin - 4 - yl ) pyridin - 3 - amine ( ( 4 - Methoxypyridin - 3 - yl ) ( 4- ( trifluoromethyl ) phenyl ) amino ) pip eridin - 1 - yl ) ( 2 - methylpyridin - 4- yl ) methanone 4 - ( ( 4 - Methoxypyridin - 3 - yl ) ( 4- ( trifluoromethyl ) phenyl ) amino ) pip eridin - 1 - yl ) ( 2- ( trifluoromethyl ) pyridin - 4- yl ) methanone 4 - ( ( 4- ( Difluoromethoxy ) phenyl ) ( 4- methoxypyridin - 3- yl ) amino ) piperidin - 1 - yl ) ( 2- methylpyridin - 4 - yl ) methanone N ﻻﻯ -CH4 - Methoxy - N- ( 1- ( 4- ( methylsulfinyl ) phenyl ) piperidin- - yl ) -N- ( 4- ( trifluoromethyl ) phenyl ) pyridin - 3- amine Cpd . No. Structure S - CH N Book · N · N ' N ' F N CN PCT / US2024 / 0440 Compound Name N- ( 1- ( 2 - Fluoro - 4- ( methylsulfonyl ) phenyl ) piperidin- - yl ) -4 - methoxy - N- ( 4- ( trifluoromethyl ) phenyl ) pyridin - 3- amine 2- ( 4 - ( ( 4 - Fluorophenyl ) ( 4- methoxypyridin - 3- yl ) amino ) piperidin - 1- yl ) pyrimidine - 5 - carbonitrile 4 - cyclopropoxy - N- ( 4- ( difluoromethoxy ) phenyl ) -N- ( 1- ( 1 - methyl - 1H - pyrazol - 5- yl ) piperidin - 4 - yl ) pyridin - 3 - amine N 4 - cyclopropoxy - N- ( 1- ( 1 - methyl- 1H - pyrazol - 5 - yl ) piperidin - 4 - yl ) - N- ( 4- ( trifluoromethyl ) phenyl ) pyridin - 3- amine 6- ( 4 - ( ( 4 - cyclopropoxypyridin - 3- yl ) ( 4- ( difluoromethoxy ) phenyl ) amino ) p iperidin - 1 - yl ) nicotinonitrile WO 2025/049495 PCT / US2024 / 0440 Cpd . No. Structure Compound Name F - N 2- ( 4 - ( ( 4 - cyclopropoxypyridin - 3- yl ) ( 4- ( difluoromethoxy ) phenyl ) amino ) p iperidin - 1 - yl ) pyrimidine - 5- carbonitrile N- ( 1- ( 1,2,4 - oxadiazol - 3- yl ) piperidin - 4 - yl ) -4 - cyclopropoxy- N- ( 4- ( trifluoromethyl ) phenyl ) pyridin - 3- amine CF F 6- ( 4 - ( ( 4 - cyclopropoxypyridin - 3- yl ) ( 4- ( trifluoromethyl ) phenyl ) amino ) pip eridin - 1 - yl ) nicotinonitrile 2- ( 4 - ( ( 4 - cyclopropoxypyridin - 3- yl ) ( 4- ( trifluoromethyl ) phenyl ) amino ) pip eridin - 1 - yl ) pyrimidine - 5- carbonitrile -N- N- ( 1- ( 1,2,4 - oxadiazol - 3- yl ) piperidin - 4 - yl ) -4 - cyclopropoxy- N- ( 4- ( difluoromethoxy ) phenyl ) pyridin- - amine WO 2025/049495 PCT / US2024 / 0440 Cpd . No. Structure Compound Name N = 5 = O = G = O , 2- ( 4 - ( ( 4- ( difluoromethoxy ) -3- fluorophenyl ) ( 4 - methoxypyridin- - yl ) amino ) piperidin - 1- yl ) pyrimidine - 5 - carbonitrile N- ( 4- ( difluoromethoxy ) phenyl ) -4- methoxy - N- ( 1- ( 5- ( methylsulfonyl ) pyridin - 2- yl ) piperidin - 4 - yl ) pyridin - 3 - amine 4 - methoxy - N- ( 1- ( 5- ( methylsulfonyl ) pyridin - 2- yl ) piperidin - 4 - yl ) -N- ( 4- ( trifluoromethyl ) phenyl ) pyridin - 3- amine ' N ' ' • N • ( ( trans ) -4 - ( ( 4- ( difluoromethoxy ) phenyl ) ( 4- methoxypyridin - 3 - yl ) amino ) cyclohexyl ) ( morpholino ) methanone 46 Cpd . No.

N ' N " ' PCT / US2024 / 0440 Structure Compound Name ( ( cis ) -4 - ( ( 4 - methoxypyridin - 3 - yl ) ( 4- ( trifluoromethyl ) phenyl ) amino ) cy clohexyl ) ( morpholino ) methanone · F O == O , Book F N- ( 4- ( difluoromethoxy ) phenyl ) -5- fluoro - 4 - methoxy - N- ( 1- ( 5- ( methylsulfonyl ) pyrimidin - 2- yl ) piperidin - 4 - yl ) pyridin - 3 - amine [ 120 ] The subject matter described herein includes the following compounds in Table A , or pharmaceutically acceptable salts thereof . Table A. Compounds [ 121 ] Cpd . No.

N 1 Structure Compound Name F ELE F F F ( 4 - methyl - 3 - pyridyl ) [ p- ( trifluoromethyl ) phenyl ] { 1- [ 5- ( trifluoromethyl ) -2 - pyridyl ] -4- piperidyl } amine Cpd . No. Structure N ' N ' 1 L • N • ﻪﻣ 1' N ' N F F N PCT / US2024 / 0440 Compound Name 2-4 - [ ( 4 - methyl - 3 - pyridyl ) [ 6- ( trifluoromethyl ) -3- pyridyl ] amino ] -1 - piperidyl } -5- pyrimidinecarbonitrile 2- { 4 - [ ( 4 - chloro - 3 - pyridyl ) [ 6- ( trifluoromethyl ) -3- pyridyl ] amino ] -1 - piperidyl } -5- pyrimidinecarbonitrile ( p - difluoromethoxyphenyl ) ( 4- methoxy - 3 - pyridyl ) [ 1- ( 2 - methyl- - pyrimidinyl ) -4 - piperidyl ] amine 104 - a N OCHFN goa N OCHF trans - 5- { 4 - [ ( p- difluoromethoxyphenyl ) ( 4- methoxy - 3- pyridyl ) amino ] cyclohexyloxy } -2- pyridinecarbonitrile N ` N 104 - b OCHF N = cis - 5- [ 4 - [ ( p- difluoromethoxyphenyl ) ( 4- methoxy - 3- pyridyl ) amino ] cyclohexyloxy } -2- pyridinecarbonitril Cpd . No. 105 - a Structure goa ' N ' N = 105 - b N F CF ' N ' CF ` N N 1 108 - a PCT / US2024 / 0440 Compound Name trans- 5- { 4 - [ ( 4 - methoxy - 3- pyridyl ) [ p- ( trifluoromethyl ) phenyl ] amino ] cy clohexyloxy } -2- pyridinecarbonitrile cis - 5- { 4 - [ ( 4 - methoxy - 3- pyridyl ) [ p- ( trifluoromethyl ) phenyl ] amino ] cy clohexyloxy } -2- pyridinecarbonitrile ( p - difluoromethoxyphenyl ) ( 4- methoxy - 3 - pyridyl ) { 1- [ p- ( methylsulfinyl ) phenyl ] -4- piperidyl } amine ( p - difluoromethoxyphenyl ) [ 1- ( 2- fluoro - 4 - mesylphenyl ) -4- piperidyl ] ( 4 - methoxy - 3- pyridyl ) amine F. trans- 5- { 4 - [ ( p- difluoromethoxyphenyl ) ( 4- methoxy - 3- pyridyl ) amino ] cyclohexyl } -2- pyridinecarbonitrile 49 Cpd . No. 108 - b PCT / US2024 / 0440 N Structure N goo N ' N ' OCHFN 8' N ' N N Compound Name cis - 5- { 4 - [ ( p- difluoromethoxyphenyl ) ( 4- methoxy - 3- pyridyl ) amino ] cyclohexyl } -2- pyridinecarbonitrile OCHF N N ( p - difluoromethoxyphenyl ) ( 4- methoxy - 3 - pyridyl ) [ 1- ( 4- pyridyl ) -4 - piperidyl ] amine OCHF 8( 4 - methoxy - 3 - pyridyl ) [ 1- ( 4- pyridyl ) -4 - piperidyl ] [ p- ( trifluoromethyl ) phenyl ] amine CF 50 Cpd . No. 111 - a 111 - b N Structure N N goo CF N ' N ' N N CF N N 114 - a N ' N ' N CFCN CF OCHF N N = PCT / US2024 / 0440 Compound Name trans - 5- [ 4 - [ ( 4 - methoxy - 3- pyridyl ) [ p- ( trifluoromethyl ) phenyl ] amino ] cy clohexyl - 2 - pyridinecarbonitrile cis - 5- [ 4 - [ ( 4 - methoxy - 3- pyridyl ) [ p- ( trifluoromethyl ) phenyl ] amino ] cy clohexyl - 2 - pyridinecarbonitrile ( 4 - cyclopropoxy - 3 - pyridyl ) [ 1- ( 2- methyl - 5 - pyrimidinyl ) -4- piperidyl ] [ p- ( trifluoromethyl ) phenyl ] amine 3- { 4 - [ ( 4 - methoxy - 3 - pyridyl ) [ p- ( trifluoromethyl ) phenyl ] amino ] - 1- piperidyl } bicyclo [ 1.1.1 ] pentane- - carbonitrile trans - 2- { 4 - [ ( p- difluoromethoxyphenyl ) ( 4- methoxy - 3- pyridyl ) amino ] cyclohexyloxy } -5- pyrimidinecarbonitrile Cpd . No. 114 - b ' N ' Structure N N = PCT / US2024 / 0440 Compound Name cis - 2- { 4 - [ ( p- difluoromethoxyphenyl ) ( 4- methoxy - 3- pyridyl ) amino ] cyclohexyloxy } -5- pyrimidinecarbonitrile OCHF 8( 4 - methyl - 3 - pyridyl ) [ 1- ( 2- methyl - 5 - pyrimidinyl ) -4- piperidyl ] [ p- ( trifluoromethyl ) phenyl ] amine N N N • N • CFN N OCHFN CF ⋅N OCHF ( p - difluoromethoxyphenyl ) ( 4- methyl - 3 - pyridyl ) [ 1- ( 2 - methyl - 5- pyrimidinyl ) -4 - piperidyl ] amine { 1- [ 2- ( methoxymethyl ) -5- pyrimidinyl ] -4 - piperidyl } ( 4- methoxy - 3 - pyridyl ) [ p- ( trifluoromethyl ) phenyl ] amine ( 4 - cyclopropyl - 3 - pyridyl ) ( p- difluoromethoxyphenyl ) [ 1- ( 2- methyl - 5 - pyrimidinyl ) -4- piperidyl ] amine WO 2025/049495 PCT / US2024 / 0440 Cpd . No. Structure Compound Name 18( 4 - cyclopropyl - 3 - pyridyl ) [ 1- ( 2- methyl - 5 - pyrimidinyl ) -4- piperidyl ] [ p- ( trifluoromethyl ) phenyl ] amine 120 - a ' N ' 120 - b CF ' N ' CF N N N = N = CF CF N = N F F trans - 2- [ 4 - [ ( 4 - methoxy - 3- pyridyl ) [ p- ( trifluoromethyl ) phenyl ] amino ] cy clohexyloxy } -5- pyrimidinecarbonitrile cis - 2- [ 4 - [ ( 4 - methoxy - 3- pyridyl ) [ p- ( trifluoromethyl ) phenyl ] amino ] cy clohexyloxy } -5- pyrimidinecarbonitrile ( 4 - ethyl - 3 - pyridyl ) [ 1- ( 2 - methyl- - pyrimidinyl ) -4 - piperidyl ] [ p- ( trifluoromethyl ) phenyl ] amine 2- { 4 - [ ( 4 - cyclopropyl - 3- pyridyl ) [ 6- ( difluoromethyl ) -3- pyridyl ] amino ] -1 - piperidyl } -5- pyrimidinecarbonitrile WO 2025/049495 PCT / US2024 / 0440 Cpd . No. Structure Compound Name 18 OCHF 1N CN ( p - difluoromethoxyphenyl ) ( 4- ethyl - 3 - pyridyl ) [ 1- ( 2 - methyl - 5- pyrimidinyl ) -4 - piperidyl ] amine 2- ( 4 - { [ 6- ( difluoromethyl ) -3- pyridyl ] ( 4 - ethyl - 3- pyridyl ) amino } -1 - piperidyl ) -5- pyrimidinecarbonitrile CHF 8( R ) -4- { 4 - [ ( p- difluoromethoxyphenyl ) ( 4- methoxy - 3 - pyridyl ) amino ] -1- piperidyl ) -1 - ethyl - 2- pyrrolidinone N N OCHF SO2CH CFN CN 1` N CF [ 1- ( 5 - mesyl - 2 - pyrimidinyl ) -4- piperidyl ] ( 4 - methyl - 3 - pyridyl ) [ p- ( trifluoromethyl ) phenyl ] amine - { 4 - [ ( 4 - methyl - 3 - pyridyl ) [ p- ( trifluoromethyl ) phenyl ] amino ] - - piperidyl } -2- pyrimidinecarbonitrile WO 2025/049495 PCT / US2024 / 0440 Cpd . No. Structure Compound Name 80N 1( S ) -1 ' - ethyl - 4 - [ ( 4 - methoxy - 3- pyridyl ) [ p- ( trifluoromethyl ) phenyl ] amino ] [ , 3 ' - bipiperidyl ] -6 ' - one CFN D N D 1N C₂D - C D N 1D -C³D N CF N = SO2CH 1D3C- OCHF ` N · N 1' N ' CFHC₂OS OCHF [ 4- ( H ) methoxy ( 2,5,6-2H3 ) -3- pyridyl ] [ 1- ( 2 - methyl - 5- pyrimidinyl ) -4 - piperidyl ] [ p- ( trifluoromethyl ) phenyl ] amine ( p - difluoromethoxyphenyl ) [ 1- ( 5- mesyl - 2 - pyrimidinyl ) -4- piperidyl ] [ 4- ( ³H² ) methoxy ( 2,5,6- 2H3 ) -3 - pyridyl ] amine [ 4- ( H3 ) methoxy - 3 - pyridyl ] [ 1- ( 2- methyl - 5 - pyrimidinyl ) -4- piperidyl ] [ p- ( trifluoromethyl ) phenyl ] amine ( p - difluoromethoxyphenyl ) [ 1- ( 5- mesyl - 2 - pyrimidinyl ) -4- piperidyl ] [ 4- ( H3 ) methoxy - 3- pyridyl ] amine Cpd . No. Structure ' N ' 134 - a 134 - b 135 - a N OHI CN CFCN N = OH ' N ' N CF OH 8' N ' CN OCHF OH ' N ' 135 - b CN PCT / US2024 / 0440 Compound Name 2 - { ( 1S , 4S ) -1 - hydroxy - 4 - [ ( 4- methoxy - 3 - pyridyl ) [ p- ( trifluoromethyl ) phenyl ] amino ] cy clohexyl } -5- pyrimidinecarbonitrile 2 - { ( 1R , 4R ) -1 - hydroxy - 4 - [ ( 4- methoxy - 3 - pyridyl ) [ p- ( trifluoromethyl ) phenyl ] amino ] cy clohexyl ) -5- pyrimidinecarbonitrile 2 - { ( 1S , 4S ) -4 - [ ( 4- difluoromethoxyphenyl ) ( 4- methoxy - 3 - pyridyl ) amino ] -1- hydroxycyclohexyl } -5- pyrimidinecarbonitrile 2 - { ( 1R , 4R ) -4 - [ ( 4- difluoromethoxyphenyl ) ( 4- methoxy - 3 - pyridyl ) amino ] -1- hydroxycyclohexyl } -5- pyrimidinecarbonitrile [ 122 ] OCHFIn certain embodiments , the subject matter described herein is directed to a compound selected from Table 1. In certain embodiments , the subject matter described herein is directed to a compound selected from Table A. In certain embodiments , the subject matter described herein is directed to a compound selected from Table 1 and Table A.

III . [ 123 ] Pharmaceutical Compositions and Modes of Administration Compounds provided herein are usually administered in the form of pharmaceutical 56 WO 2025/049495 PCT / US2024 / 0440 compositions . Thus , provided herein are also pharmaceutical compositions that comprise one or more of the compounds described herein or a pharmaceutically acceptable salt , a stereoisomer , or a mixture of stereoisomers thereof and one or more pharmaceutically acceptable excipients . Suitable pharmaceutically acceptable excipients may include , for example , inert solid diluents and fillers , liquid diluents , including sterile aqueous solution and various organic solvents , permeation enhancers , solubilizers and adjuvants . Such compositions are prepared in a manner well known in the pharmaceutical art . See , e.g. , Remington's Pharmaceutical Sciences , Mace Publishing Co. , Philadelphia , Pa . 17th Ed . ( 1985 ) ; and Modern Pharmaceutics , Marcel Dekker , Inc. 3rd Ed . ( G.S. Banker & C.T. Rhodes , Eds . ) . [ 124 ] In some embodiments , the pharmaceutical composition comprises a compound of Formula A , or a pharmaceutically acceptable salt or solvate thereof , and a pharmaceutically acceptable excipient . In some embodiments , the pharmaceutical composition comprises a compound of Formula A - i , or a pharmaceutically acceptable salt or solvate thereof , and a pharmaceutically acceptable excipient . In some embodiments , the pharmaceutical composition comprises a compound of Formula A - i ' , or a pharmaceutically acceptable salt or solvate thereof , and a pharmaceutically acceptable excipient . In some embodiments , the pharmaceutical composition comprises a compound of Formula A - ii , or a pharmaceutically acceptable salt or solvate thereof , and a pharmaceutically acceptable excipient . In some embodiments , the pharmaceutical composition comprises a compound of Formula A - ii ' , or a pharmaceutically acceptable salt or solvate thereof , and a pharmaceutically acceptable excipient . In some embodiments , the pharmaceutical composition comprises a compound of Formula A - iii , or a pharmaceutically acceptable salt or solvate thereof , and a pharmaceutically acceptable excipient . In some embodiments , the pharmaceutical composition comprises a compound of Formula I , or a pharmaceutically acceptable salt or solvate thereof , and a pharmaceutically acceptable excipient . In some embodiments , the pharmaceutical composition comprises a compound of Formula I , or a pharmaceutically acceptable salt or solvate thereof , and a pharmaceutically acceptable excipient . In some embodiments , the pharmaceutical composition comprises a compound of Formula la , or a pharmaceutically acceptable salt or solvate thereof , and a pharmaceutically acceptable excipient . In some embodiments , the pharmaceutical composition comprises a compound of Formula Ib , or a pharmaceutically acceptable salt or solvate thereof , and a pharmaceutically acceptable excipient . In some embodiments , the pharmaceutical composition comprises a compound of Formula Ic , or a pharmaceutically acceptable salt or solvate thereof , and a pharmaceutically acceptable excipient . In some embodiments , the pharmaceutical composition comprises a compound of Formula Id , or a pharmaceutically acceptable salt or solvate thereof , and a pharmaceutically acceptable excipient . In some embodiments , the pharmaceutical composition comprises a compound of Table 1 , or a pharmaceutically acceptable salt or solvate thereof , and a pharmaceutically acceptable excipient . In some embodiments , the pharmaceutical composition comprises a compound of Table A , or a pharmaceutically 57 WO 2025/049495 PCT / US2024 / 0440 acceptable salt or solvate thereof , and a pharmaceutically acceptable excipient . In some embodiments , the pharmaceutical composition comprises a compound of Table 1 and Table A , or a pharmaceutically acceptable salt or solvate thereof , and a pharmaceutically acceptable excipient . [ 125 ] The pharmaceutical compositions may be administered in either single or multiple doses . The pharmaceutical composition may be administered by various methods including , for example , rectal , buccal , intranasal , and transdermal routes . In certain embodiments , the pharmaceutical composition may be administered by intra - arterial injection , intravenously , intraperitoneally , parenterally , intramuscularly , subcutaneously , orally , topically , or as an inhalant . [ 126 ] One mode for administration is parenteral , for example , by injection . The forms in which the pharmaceutical compositions described herein may be incorporated for administration by injection include , for example , aqueous or oil suspensions , or emulsions , with sesame oil , corn oil , cottonseed oil , or peanut oil , as well as elixirs , mannitol , dextrose , or a sterile aqueous solution , and similar pharmaceutical vehicles . [ 127 ] Oral administration may be another route for administration of the compounds described herein . Administration may be via , for example , capsule or tablet , such as enteric coated tablets . In making the pharmaceutical compositions that include at least one compound described herein or a pharmaceutically acceptable salt , a stereoisomer , or a mixture of stereoisomers thereof , the active ingredient is usually diluted by an excipient and / or enclosed within such a carrier that can be in the form of a capsule , sachet , paper or other container . When the excipient serves as a diluent , it can be in the form of a solid , semi - solid , or liquid material , which acts as a vehicle , carrier or medium for the active ingredient . Thus , the compositions can be in the form of tablets , pills , powders , lozenges , sachets , cachets , elixirs , suspensions , emulsions , solutions , syrups , aerosols ( as a solid or in a liquid medium ) , ointments containing , for example , up to 10 % by weight of the active compound , soft and hard gelatin capsules , sterile injectable solutions , and sterile packaged powders . [ 128 ] Some examples of suitable excipients include lactose , dextrose , sucrose , sorbitol , mannitol , starches , gum acacia , calcium phosphate , alginates , tragacanth , gelatin , calcium silicate , microcrystalline cellulose , polyvinylpyrrolidone , cellulose , sterile water , syrup , and methyl cellulose . The formulations can additionally include lubricating agents such as talc , magnesium stearate , and mineral oil ; wetting agents ; emulsifying and suspending agents ; preserving agents such as methyl and propylhydroxy - benzoates ; sweetening agents ; and flavoring agents . [ 129 ] The compositions that include at least one compound described herein or a pharmaceutically acceptable salt , a stereoisomer , or a mixture of stereoisomers thereof can be formulated so as to provide quick , sustained , or delayed release of the active ingredient after administration to the subject by employing procedures known in the art . Controlled release drug delivery systems for oral administration include osmotic pump systems and dissolutional systems containing polymer - coated reservoirs or drug - polymer 58 WO 2025/049495 PCT / US2024 / 0440 matrix formulations . Examples of controlled release systems are given in U.S. Patent Nos . 3,845,770 ; 4,326,525 ; 4,902,514 ; and 5,616,345 . Another formulation for use in the methods disclosed herein employ transdermal delivery devices ( " patches " ) . Such transdermal patches may be used to provide continuous or discontinuous infusion of the compounds described herein in controlled amounts . The construction and use of transdermal patches for the delivery of pharmaceutical agents is well known in the art . See , e.g. , U.S. Patent Nos . 5,023,252 , 4,992,445 and 5,001,139 . Such patches may be constructed for continuous , pulsatile , or on demand delivery of pharmaceutical agents . [ 130 ] For preparing solid compositions such as tablets , the principal active ingredient may be mixed with a pharmaceutical excipient to form a solid preformulation composition containing a homogeneous mixture of a compound described herein or a pharmaceutically acceptable salt , a stereoisomer , or a mixture of stereoisomers thereof . When referring to these preformulation compositions as homogeneous , the active ingredient may be dispersed evenly throughout the composition so that the composition may be readily subdivided into equally effective unit dosage forms such as tablets , pills and capsules . [ 131 ] The tablets or pills of the compounds described herein may be coated or otherwise compounded to provide a dosage form affording the advantage of prolonged action , or to protect from the acid conditions of the stomach . For example , the tablet or pill can include an inner dosage and an outer dosage component , the latter being in the form of an envelope over the former . The two components can be separated by an enteric layer that serves to resist disintegration in the stomach and permit the inner component to pass intact into the duodenum or to be delayed in release . A variety of materials can be used for such enteric layers or coatings , such materials including a number of polymeric acids and mixtures of polymeric acids with such materials as shellac , cetyl alcohol , and cellulose acetate . [ 132 ] Compositions for inhalation or insufflation may include solutions and suspensions in pharmaceutically acceptable , aqueous or organic solvents , or mixtures thereof , and powders . The liquid or solid compositions may contain suitable pharmaceutically acceptable excipients as described herein . In some embodiments , the compositions are administered by the oral or nasal respiratory route for local or systemic effect . In other embodiments , compositions in pharmaceutically acceptable solvents may be nebulized by use of inert gases . Nebulized solutions may be inhaled directly from the nebulizing device or the nebulizing device may be attached to a facemask tent , or intermittent positive pressure breathing machine . Solution , suspension , or powder compositions may be administered , preferably orally or nasally , from devices that deliver the formulation in an appropriate manner . [ 133 ] The specific dose level of a compound of the present application for any particular subject will depend upon a variety of factors including the activity of the specific compound employed , the age , body weight , general health , sex , diet , time of administration , route of administration , and rate of excretion , drug combination and the severity of the particular disease in the subject undergoing therapy . For example , a 59 WO 2025/049495 PCT / US2024 / 0440 dosage may be expressed as a number of milligrams of a compound described herein per kilogram of the subject's body weight ( mg / kg ) . Dosages of between about 0.1 and 150 mg / kg may be appropriate . In some embodiments , about 0.1 and 100 mg / kg may be appropriate . In other embodiments a dosage of between 0.and 60 mg / kg may be appropriate . Normalizing according to the subject's body weight is particularly useful when adjusting dosages between subjects of widely disparate size , such as occurs when using the drug in both children and adult humans or when converting an effective dosage in a non - human subject such as dog to a dosage suitable for a human subject . A dose may be administered once a day ( QID ) , twice per day ( BID ) , or more frequently , depending on the pharmacokinetic and pharmacodynamic properties , including absorption , distribution , metabolism , and excretion of the particular compound . In addition , toxicity factors may influence the dosage and administration regimen . When administered orally , the pill , capsule , or tablet may be ingested daily or less frequently for a specified period of time . The regimen may be repeated for a number of cycles of therapy .

IV . [ 134 ] Methods of Treatment Described herein are methods for promoting myelination of central nervous system neurons in a subject suffering from a myelin - related disorder , the method comprising administering to the subject a therapeutically effective amount of a compound of Formulae A , A - i , A - i ' , A - ii , A - ii ' , A - iii , I , I , Ia , Ib , Ic , and Id , or a pharmaceutical composition comprising the same . In certain embodiments , the subject matter disclosed herein is directed to a compound of Formulae A , A - i , A - i ' , A - ii , A - ²ii , A - iii , I , I ' , Ia , Ib , Ic , and Id , or a pharmaceutically acceptable salt or solvate thereof , for promoting myelination of central nervous system neurons in a subject suffering from a myelin - related disorder . In another embodiment , the subject matter described herein is directed to the use of a compound of Formulae A , A - i , A - i ' , A - ii , A - ii ' , A - iii , I , I ' , Ia , Ib , Ic , and Id , or a pharmaceutically acceptable salt or solvate thereof , for the manufacture of a medicament for promoting myelination of central nervous system neurons in a subject suffering from a myelin - related disorder . [ 135 ] In certain embodiments , in the methods for promoting myelination of central nervous system neurons in a subject suffering from a myelin - related disorder , the compound of Formulae A , A - i , A - i ' , A- ii , A - ii ' , A - iii , I , I , Ia , Ib , Ic , and Id , or a pharmaceutically acceptable salt or solvate thereof , or a pharmaceutical composition comprising the same , inhibits enzyme mediated synthesis of one or more sterol intermediates in the cholesterol biosynthesis pathway . [ 136 ] In certain embodiments , in the methods for promoting myelination of central nervous system neurons in a subject suffering from a myelin - related disorder , the compound of Formulae A , A - i , A - i ' , A- ii , A - ³ii , A - iii , I , I ' , Ia , Ib , Ic , and Id , or a pharmaceutically acceptable salt or solvate thereof , or a pharmaceutical composition comprising the same , promotes accumulation of A8,9 - unsaturated sterol 60 WO 2025/049495 PCT / US2024 / 0440 intermediates in the cholesterol biosynthesis pathway . [ 137 ] In certain embodiments , in the methods for promoting myelination of central nervous system neurons in a subject suffering from a myelin - related disorder , the compound of Formulae A , A - i , A - i ' , A- ii , A - ii ' , A - iii , I , I ' , Ia , Ib , Ic , and Id , or a pharmaceutically acceptable salt or solvate thereof , or a pharmaceutical composition comprising the same , inhibits one or more of CYP51 , sterol - 14 - reductase , or EBP enzyme mediated synthesis of sterol intermediates in the cholesterol biosynthesis pathway . In certain embodiments , the compound of Formulae A , A - i , A - i ' , A - ii , A - ii ' , A - iii , I , I ^ , Ia , Ib , and Ic , and Id , or a pharmaceutically acceptable salt or solvate thereof , or a pharmaceutical composition comprising the same , inhibits CYP51 . [ 138 ] In certain embodiments , in the methods for promoting myelination of central nervous system neurons in a subject suffering from a myelin - related disorder , the compound of Formulae A , A - i , A - i ' , A- ii , A - ii ' , A - iii , I , I ' , Ia , Ib , Ic , and Id , or a pharmaceutically acceptable salt or solvate thereof , or a pharmaceutical composition comprising the same , induces , promotes , and / or modulates oligodendrocyte precursor cell ( OPC ) differentiation , proliferation and / or maturation . In certain embodiments , the induction of OPC differentiation is characterized by an increase in myelin basic protein ( MBP ) expression . [ 139 ] In certain embodiments , the subject matter described herein is directed to a method of treating a disorder in a subject in need thereof , the method comprising administering to the subject in need thereof a therapeutically effective amount of a compound of Formulae A , A - i , A - i ' , A - ii , A - ii ' , A - iii , I , I ' , Ia , Ib , Ic , and Id , or a pharmaceutically acceptable salt or solvate thereof . In certain embodiments , the subject has a myelin - related disorder . In some embodiments , the compound of Formula A is a compound of Formula I , or a pharmaceutically acceptable salt or solvate thereof . In some embodiments , the compound of Formula A is a compound of Formula A - i , or a pharmaceutically acceptable salt or solvate thereof . In some embodiments , the compound of Formula A is a compound of Formula A - i ' , or a pharmaceutically acceptable salt or solvate thereof . In some embodiments , the compound of Formula A is a compound of Formula A - ii , or a pharmaceutically acceptable salt or solvate thereof . In some embodiments , the compound of Formula A is a compound of Formula A - ii ' , or a pharmaceutically acceptable salt or solvate thereof . In some embodiments , the compound of Formula A is a compound of Formula A - iii , or a pharmaceutically acceptable salt or solvate thereof . In some embodiments , the compound of Formula A is a compound of Formula Id , or a pharmaceutically acceptable salt or solvate thereof . In some embodiments , the compound of Formula I is a compound of Formula I ' , or a pharmaceutically acceptable salt or solvate thereof . In some embodiments , the compound of Formula I is a compound of Formula la , or a pharmaceutically acceptable salt or solvate thereof . In other embodiments , the compound of Formula I is a compound of Formula Ib , or a pharmaceutically acceptable salt or solvate thereof . In other embodiments , the compound of Formula I is a compound of Formula Ic , or a pharmaceutically acceptable salt or solvate thereof . In some embodiments , 61 WO 2025/049495 PCT / US2024 / 0440 the compound of Formula I is a compound of Table 1 , or a pharmaceutically acceptable salt or solvate thereof . In some embodiments , the compound of Formula A is a compound of Table A , or a pharmaceutically acceptable salt or solvate thereof . [ 140 ] In certain embodiments , the subject matter disclosed herein is directed to a compound of Formulae A , A - i , A - ˆi , A - ii , A - ii ^ , A - iii , I , I ^ , Ia , Ib , Ic , and Id , or a pharmaceutically acceptable salt or solvate thereof , for use in treating a disorder in a subject in need thereof . In certain embodiments , the subject has a myelin - related disorder . In some embodiments , the compound of Formula A is a compound of Formula I , or a pharmaceutically acceptable salt or solvate thereof . In some embodiments , the compound of Formula A is a compound of Formula A - i , or a pharmaceutically acceptable salt or solvate thereof . In some embodiments , the compound of Formula A is a compound of Formula A - i ' , or a pharmaceutically acceptable salt or solvate thereof . In some embodiments , the compound of Formula A is a compound of Formula A - ii , or a pharmaceutically acceptable salt or solvate thereof . In some embodiments , the compound of Formula A is a compound of Formula A - ii ' , or a pharmaceutically acceptable salt or solvate thereof . In some embodiments , the compound of Formula A is a compound of Formula A - iii , or a pharmaceutically acceptable salt or solvate thereof . In some embodiments , the compound of Formula A is a compound of Formula Id , or a pharmaceutically acceptable salt or solvate thereof . In some embodiments , the compound of Formula I is a compound of Formula I ' , or a pharmaceutically acceptable salt or solvate thereof . In some embodiments , the compound of Formula I is a compound of Formula la , or a pharmaceutically acceptable salt or solvate thereof . In other embodiments , the compound of Formula I is a compound of Formula Ib , or a pharmaceutically acceptable salt or solvate thereof . In other embodiments , the compound of Formula I is a compound of Formula Ic , or a pharmaceutically acceptable salt or solvate thereof . In some embodiments , the compound of Formula I is a compound of Table 1 , or a pharmaceutically acceptable salt or solvate thereof . In some embodiments , the compound of Formula A is a compound of Table A , or a pharmaceutically acceptable salt or solvate thereof . [ 141 ] In certain embodiments , the subject matter disclosed herein is directed to the use of a compound of Formulae A , A - i , A - i ' , A - ii , A - ii ' , A - iii , I , I ' , Ia , Ib , Ic , and Id , or a pharmaceutically acceptable salt or solvate thereof , in the manufacture of a medicament for treating a disorder in a subject in need thereof . In certain embodiments , the subject has a myelin - related disorder . In some embodiments , the compound of Formula A is a compound of Formula I , or a pharmaceutically acceptable salt or solvate thereof . In some embodiments , the compound of Formula A is a compound of Formula A - i , or a pharmaceutically acceptable salt or solvate thereof . In some embodiments , the compound of Formula A is a compound of Formula A - i ' , or a pharmaceutically acceptable salt or solvate thereof . In some embodiments , the compound of Formula A is a compound of Formula A - ii , or a pharmaceutically acceptable salt or solvate thereof . In some embodiments , the compound of Formula A is a compound of Formula A - ii ' , or a pharmaceutically 62 WO 2025/049495 PCT / US2024 / 0440 acceptable salt or solvate thereof . In some embodiments , the compound of Formula A is a compound of Formula A - iii , or a pharmaceutically acceptable salt or solvate thereof . In some embodiments , the compound of Formula A is a compound of Formula Id , or a pharmaceutically acceptable salt or solvate thereof . In some embodiments , the compound of Formula I is a compound of Formula I ' , or a pharmaceutically acceptable salt or solvate thereof . In some embodiments , the compound of Formula I is a compound of Formula la , or a pharmaceutically acceptable salt or solvate thereof . In other embodiments , the compound of Formula I is a compound of Formula Ib , or a pharmaceutically acceptable salt or solvate thereof . In other embodiments , the compound of Formula I is a compound of Formula Ic , or a pharmaceutically acceptable salt or solvate thereof . In some embodiments , the compound of Formula I is a compound of Table 1 , or a pharmaceutically acceptable salt or solvate thereof . In some embodiments , the compound of Formula A is a compound of Table A , or a pharmaceutically acceptable salt or solvate thereof . [ 142 ] In certain embodiments , the subject matter disclosed herein is directed to a method of promoting myelination in a subject in need thereof , comprising administering to the subject a therapeutically effective amount of a compound of Formulae A , A - i , A - i ' , A - ii , A - ii ' , A - iii , I , I ' , Ia , Ib , Ic , and Id , or a pharmaceutically acceptable salt or solvate thereof . In certain embodiments , the subject has a myelin - related disorder . In some embodiments , the compound of Formula A is a compound of Formula I , or a pharmaceutically acceptable salt or solvate thereof . In some embodiments , the compound of Formula A is a compound of Formula A - i , or a pharmaceutically acceptable salt or solvate thereof . In some embodiments , the compound of Formula A is a compound of Formula A - i ' , or a pharmaceutically acceptable salt or solvate thereof . In some embodiments , the compound of Formula A is a compound of Formula A - ii , or a pharmaceutically acceptable salt or solvate thereof . In some embodiments , the compound of Formula A is a compound of Formula A - ii ' , or a pharmaceutically acceptable salt or solvate thereof . In some embodiments , the compound of Formula A is a compound of Formula A - iii , or a pharmaceutically acceptable salt or solvate thereof . In some embodiments , the compound of Formula A is a compound of Formula Id , or a pharmaceutically acceptable salt or solvate thereof . In some embodiments , the compound of Formula I is a compound of Formula I ' , or a pharmaceutically acceptable salt or solvate thereof . In certain embodiments , the subject has a myelin - related disorder . In some embodiments , the compound of Formula I is a compound of Formula la , or a pharmaceutically acceptable salt or solvate thereof . In other embodiments , the compound of Formula I is a compound of Formula Ib , or a pharmaceutically acceptable salt or solvate thereof . In other embodiments , the compound of Formula I is a compound of Formula lc , or a pharmaceutically acceptable salt or solvate thereof . In some embodiments , the compound of Formula I is a compound of Table 1 , or a pharmaceutically acceptable salt or solvate thereof . In some embodiments , the compound of Formula A is a compound of Table A , or a pharmaceutically acceptable salt or solvate thereof . [ 143 ] In certain embodiments , the subject matter disclosed herein is directed to a compound of 63 WO 2025/049495 PCT / US2024 / 0440 Formulae A , A - i , A - i ' , A - ii , A - ii ' , A - iii , I , I ' , Ia , Ib , Ic , and Id , or a pharmaceutically acceptable salt or solvate thereof , or a pharmaceutical composition comprising the compound , for use in promoting myelination in a subject in need thereof . In certain embodiments , the subject has a myelin - related disorder . In some embodiments , the compound of Formula A is a compound of Formula I , or a pharmaceutically acceptable salt or solvate thereof . In some embodiments , the compound of Formula A is a compound of Formula A - i , or a pharmaceutically acceptable salt or solvate thereof . In some embodiments , the compound of Formula A is a compound of Formula A - i ' , or a pharmaceutically acceptable salt or solvate thereof . In some embodiments , the compound of Formula A is a compound of Formula A - ii , or a pharmaceutically acceptable salt or solvate thereof . In some embodiments , the compound of Formula A is a compound of Formula A - ii , or a pharmaceutically acceptable salt or solvate thereof . In some embodiments , the compound of Formula A is a compound of Formula A - iii , or a pharmaceutically acceptable salt or solvate thereof . In some embodiments , the compound of Formula A is a compound of Formula Id , or a pharmaceutically acceptable salt or solvate thereof . In some embodiments , the compound of Formula I is a compound of Formula I ' , or a pharmaceutically acceptable salt or solvate thereof . In some embodiments , the compound of Formula I is a compound of Formula la , or a pharmaceutically acceptable salt or solvate thereof . In other embodiments , the compound of Formula I is a compound of Formula Ib , or a pharmaceutically acceptable salt or solvate thereof . In other embodiments , the compound of Formula I is a compound of Formula Ic , or a pharmaceutically acceptable salt or solvate thereof . In some embodiments , the compound of Formula I is a compound of Table 1 , or a pharmaceutically acceptable salt or solvate thereof . In some embodiments , the compound of Formula A is a compound of Table A , or a pharmaceutically acceptable salt or solvate thereof . [ 144 ] In certain embodiments , the subject matter disclosed herein is directed to use of a compound of Formulae A , A - i , A - i ' , A - ii , A - ii ' , A - iii , I , I ' , Ia , Ib , Ic , and Id , or a pharmaceutically acceptable salt or solvate thereof , or a pharmaceutical composition comprising the compound , in the manufacture of a medicament for promoting myelination in a subject in need thereof . In certain embodiments , the subject has a myelin - related disorder . In some embodiments , the compound of Formula A is a compound of Formula I , or a pharmaceutically acceptable salt or solvate thereof . In some embodiments , the compound of Formula A is a compound of Formula A - i , or a pharmaceutically acceptable salt or solvate thereof . In some embodiments , the compound of Formula A is a compound of Formula A - i ' , or a pharmaceutically acceptable salt or solvate thereof . In some embodiments , the compound of Formula A is a compound of Formula A - ii , or a pharmaceutically acceptable salt or solvate thereof . In some embodiments , the compound of Formula A is a compound of Formula A - ii ' , or a pharmaceutically acceptable salt or solvate thereof . In some embodiments , the compound of Formula A is a compound of Formula A - iii , or a pharmaceutically acceptable salt or solvate thereof . In some embodiments , the compound of Formula A is a compound of 64 WO 2025/049495 PCT / US2024 / 0440 Formula Id , or a pharmaceutically acceptable salt or solvate thereof . In some embodiments , the compound of Formula I is a compound of Formula I ' , or a pharmaceutically acceptable salt or solvate thereof . In some embodiments , the compound of Formula I is a compound of Formula la , or a pharmaceutically acceptable salt or solvate thereof . In other embodiments , the compound of Formula I is a compound of Formula Ib , or a pharmaceutically acceptable salt or solvate thereof . In other embodiments , the compound of Formula I is a compound of Formula Ic , or a pharmaceutically acceptable salt or solvate thereof . In some embodiments , the compound of Formula I is a compound of Table 1 , or a pharmaceutically acceptable salt or solvate thereof . In some embodiments , the compound of Formula A is a compound of Table A , or a pharmaceutically acceptable salt or solvate thereof . [ 145 ] In certain embodiments , the subject matter disclosed herein is directed to a method of inducing endogenous oligodendrocyte precursor cell ( OPC ) differentiation in a subject in need thereof , the method comprising administering to the subject a therapeutically effective amount of a compound of Formulae A , A - i , A - i ' , A - ii , A - ii ' , A - iii , I , I ' , Ia , Ib , Ic , and Id , or a pharmaceutically acceptable salt or solvate thereof , or a pharmaceutical composition comprising the same . In certain embodiments , the subject is suffering from a myelin - related disorder . In certain embodiments , the myelin - related disorder is multiple sclerosis . [ 146 ] Such myelin - related disorders include , but are not limited to , multiple sclerosis ( MS ) , neuromyelitis optica ( NMO ) , optic neuritis , pediatric leukodystrophies , neonatal white matter injury , age- related dementia , schizophrenia , progressive multifocal leukoencephalopathy ( PML ) , encephalomyelitis ( EPL ) , central pontine myelolysis ( CPM ) , adrenoleukodystrophy , Alexander's disease , Pelizaeus Merzbacher disease ( PMD ) , Vanishing White Matter Disease , Wallerian Degeneration , transverse myelitis , amylotrophic lateral sclerosis ( ALS ) , Huntington's disease , Alzheimer's disease , Parkinson's disease , spinal cord injury , traumatic brain injury , post radiation injury , neurologic complications of chemotherapy , stroke , acute ischemic optic neuropathy , vitamin E deficiency , isolated vitamin E deficiency syndrome , Bassen- Kornzweig syndrome , Marchiafava - Bignami syndrome , metachromatic leukodystrophy , trigeminal neuralgia , acute disseminated encephalitis , Guillian - Barre syndrome , Charcot - Marie - Tooth disease , Bell's palsy , and radiation - induced demyelination . [ 147 ] The compound of Formulae A , A - i , A - i ' , A - ii , A - ii ' , A - iii , I , I ' , Ia , Ib , Ic , and Id , or a pharmaceutically acceptable salt or solvate thereof can be administered alone or in combination with another agent to a subject suffering from a myelin - related disorder to promote myelination of neurons ( e.g. , neuronal axons ) . A myelin - related disorder can include any disease , condition ( e.g. , those occurring from traumatic spinal cord injury and cerebral infarction ) , or disorder resulting in abnormalities of the myelin sheath . Abnormalities can be caused by loss of myelin referred to as demyelination , dysfunctional myelin referred to as dysmyelination , or failure to form enough myelin referred to as hypomyelination . A myelin related disorder as described herein can arise from a genetic disorder or from one or more of a variety of 65 WO 2025/049495 PCT / US2024 / 0440 neurotoxic insults . In some embodiments , the compound of Formula A is a compound of Formula I , or a pharmaceutically acceptable salt or solvate thereof . In some embodiments , the compound of Formula A is a compound of Formula A - i , or a pharmaceutically acceptable salt or solvate thereof . In some embodiments , the compound of Formula A is a compound of Formula A - i ' , or a pharmaceutically acceptable salt or solvate thereof . In some embodiments , the compound of Formula A is a compound of Formula A - ii , or a pharmaceutically acceptable salt or solvate thereof . In some embodiments , the compound of Formula A is a compound of Formula A - ii ' , or a pharmaceutically acceptable salt or solvate thereof . In some embodiments , the compound of Formula A is a compound of Formula A - iii , or a pharmaceutically acceptable salt or solvate thereof . In some embodiments , the compound of Formula A is a compound of Formula Id , or a pharmaceutically acceptable salt or solvate thereof . In some embodiments , the compound of Formula I is a compound of Formula I ' , or a pharmaceutically acceptable salt or solvate thereof . In some embodiments , the compound of Formula I is a compound of Formula Ia , or a pharmaceutically acceptable salt or solvate thereof . In other embodiments , the compound of Formula I is a compound of Formula Ib , or a pharmaceutically acceptable salt or solvate thereof . In other embodiments , the compound of Formula I is a compound of Formula Ic , or a pharmaceutically acceptable salt or solvate thereof . In some embodiments , the compound of Formula I is a compound of Table 1 , or a pharmaceutically acceptable salt or solvate thereof . In some embodiments , the compound of Formula A is a compound of Table A , or a pharmaceutically acceptable salt or solvate thereof . [ 148 ] " Demyelination " as used herein , refers to the act of demyelinating , or the damage or loss of part or all of the myelin sheath insulating the nerves , and is the hallmark of myelin - related disorders . In certain embodiments , demyelination refers to the damage or loss of part or all of the myelin sheath insulating a subset of nerves in an individual , such as , for example , one or more nerves localized in a particular area of the body ( e.g. , neurons in the brain or spinal cord , or both brain and spinal cord ; or the optic nerve ) . [ 149 ] Myelination of neurons requires oligodendrocytes . The term " myelination " , as used herein , refers to the generation of the nerve's myelin sheath by replacing myelin producing cells or restoring their function . The neurons that undergo remyelination may be in the brain , spinal cord , or both the brain and spinal cord . Restoring the function of a myelin producing cell may include , for example , increasing the rate of myelin production in a cell ( or cells ) with a less - than - average production level . Such increase may encompass raising the rate of myelin production up to or exceeding average production level ; but also may encompass raising the rate of myelin production to a level that is still less than average , but higher than the previous level . [ 150 ] " Promoting Myelination " as used herein refers to increasing the rate of myelin production rather than a mere net increase in the amount of myelin as compared to a baseline level of myelin production 66 WO 2025/049495 PCT / US2024 / 0440 rate in a subject . An increase in the rate of myelin production can be determined using imaging techniques or functional measurements . In some embodiments , myelination is promoted by increasing the differentiation of OPCs , increasing the accumulation of 8,9 - unsaturated sterol intermediates in the biosynthetic pathway , increasing the formation of OPCs , or any combinations thereof . Such activities may be evaluated , for example , using one or more in vitro assays , such as those described herein or known to one of skill in the art . [ 151 ] A " baseline level of myelin production rate " as used herein , refers to the rate of myelin production in subject being treated before the onset of treatment .

V. Methods of Preparing Compounds of Formula A and Formula I and Pharmaceutically Acceptable Salts Thereof [ 152 ] Compounds can be synthesized by synthetic routes that include processes analogous to those well - known in the chemical arts , particularly in light of the description contained herein , and those for other heterocycles described in : Comprehensive Heterocyclic Chemistry II , Editors Katritzky and Rees , Elsevier , 1997 , e.g. , Volume 3 ; Liebigs Annalen der Chemie , ( 9 ) : 1910-16 , ( 1985 ) ; Helvetica Chimica Acta , 41 : 1052- , ( 1958 ) ; Arzneimittel - Forschung , 40 ( 12 ) : 1328-31 , ( 1990 ) , each of which are expressly incorporated by reference . Starting materials are generally available from commercial sources such as Aldrich Chemicals ( Milwaukee , WI ) or are readily prepared using methods well known to those skilled in the art ( e.g. , prepared by methods generally described in Louis F. Fieser and Mary Fieser , Reagents for Organic Synthesis , v . 1- , Wiley , N.Y. ( 1967-2006 ed . ) , or Beilsteins Handbuch der organischen Chemie , 4 , Aufl . ed . Springer- Verlag , Berlin , including supplements ( also available via the Beilstein online database ) . [ 153 ] Synthetic chemistry transformations and protecting group methodologies ( protection and deprotection ) useful in synthesizing compounds and necessary reagents and intermediates are known in the art and include , for example , those described in R. Larock , Comprehensive Organic Transformations , VCH Publishers ( 1989 ) ; T. W. Greene and P. G .M . Wuts , Protective Groups in Organic Synthesis , 3rd Ed . , John Wiley and Sons ( 1999 ) ; and L. Paquette , ed . , Encyclopedia of Reagents for Organic Synthesis , John Wiley and Sons ( 1995 ) and subsequent editions thereof . [ 154 ] Compounds may be prepared singly or as compound libraries comprising at least 2 , for example to 1,000 compounds , or 10 to 100 compounds . Libraries of compounds of Formula A and Formula I , or pharmaceutically acceptable salts thereof , may be prepared by a combinatorial ‘ split and mix ' approach or by multiple parallel syntheses using either solution phase or solid phase chemistry , by procedures known to those skilled in the art . Thus , according to a further aspect , there is provided a compound library comprising at least 2 compounds , or pharmaceutically acceptable salts thereof . 67 WO 2025/049495 PCT / US2024 / 0440 VI . Further Embodiments [ 155 ] . The subject matter described herein includes the following embodiments : A compound of Formula I : R1a ( ۵ ) R1 R2a R R A I wherein , A is selected from the group consisting of ₁C - C6 alkyl , C3 - C8 cycloalkyl , phenyl , 5- to 6- membered heteroaryl and 5- to 6 - membered heterocyclyl , each of which is optionally substituted with one or more of ¹AR , RA2 and RA3 , " Awherein , RA1 , RA2 and RA3 are each independently selected from the group consisting of ₁C - C6 alkyl , halo - ₁C - C6 alkyl , halo , cyano , oxo , -C ( O ) ªªR- , -S ( O ) ªªR- and -S ( O ) 2 - 4ªR , wherein , R4 is C1 - C6 alkyl or C3 - Cs cycloalkyl , and Awherein the oxo , if present , is formed by two of RAI , RA and ³AR together with a carbon to which each is attached : Gis -CH or N ; Y is -CH or N : p is 1 , 2 or 3 ; , q is 1 or 0 : r is 1 or 0 ; wherein , when r is 0 , A is other than ₁C - C6 alkyl ; R ' is selected from the group consisting of ₁C - C6 alkyl , C3 - C8 cycloalkyl and halo - ₁C - C6 alkyl ; la a¹R is selected from the group consisting of hydrogen , halo , and C1 - C6 alkyl ; ²R is selected from the group consisting of halo , halo - ₁C - C6 alkyl , halo - ₁C - C6 alkoxy and -S ( O ) 2- ( C1 - C6 alkyl ) ; R2a is selected from the group consisting of hydrogen and halo ; 68 and .

WO 2025/049495 PCT / US2024 / 0440 R3 is hydrogen , halo , or ₁C - C6 alkyl , or a pharmaceutically acceptable salt or solvate thereof . 2 . The compound of embodiment 1 , or a pharmaceutically acceptable salt or solvate thereof , wherein G is N and having a structure of Formula I ' : N ( 0 ) R -N R R ' N A I ' 3 . The compound of embodiment 1 or 2 , or a pharmaceutically acceptable salt or solvate thereof , wherein q is 1 . 4 . The compound of embodiment 1 or 2 , or a pharmaceutically acceptable salt or solvate thereof , wherein q is 0 .

. The compound of any one of embodiments 1-4 , or a pharmaceutically acceptable salt or solvate thereof , wherein ¹R is C1 - C6 alkyl or C3 - C8 cycloalkyl . 6 . The compound of embodiment 5 , or a pharmaceutically acceptable salt or solvate thereof , wherein R ' is methyl , ethyl or cyclopropyl . 7 . The compound of any one of embodiments 1-6 , or a pharmaceutically acceptable salt or solvate thereof , having a structure of Formula la , Ib or Ic : 69 R H A R ²R -N Ho A N R R ²R A ﻭ Ic Ib PCT / US2024 / 0440 la WO 2025/049495 PCT / US2024 / 0440 8 . The compound of any one of embodiments 1-7 , or a pharmaceutically acceptable salt or solvate thereof , wherein Y is N. 9 The compound of any one of embodiments 1-7 , or a pharmaceutically acceptable salt or solvate thereof , wherein Y is -CH .

. The compound of any one of embodiments 1-9 , or a pharmaceutically acceptable salt or solvate thereof , wherein ²R is halo - ₁C - C6 alkyl or halo - ₁C - C6 alkoxy . 11. The compound of embodiment 10 , or a pharmaceutically acceptable salt or solvate thereof , wherein ²R is halo - C1 - C6 alkyl . 12. The compound of embodiment 11 , or a pharmaceutically acceptable salt or solvate thereof , wherein ²R is -CF3 . 13. The compound of embodiment 10 , or a pharmaceutically acceptable salt or solvate thereof , wherein ²R is halo - ₁C - C6 alkoxy . 14 . The compound of embodiment 11 , or a pharmaceutically acceptable salt or solvate thereof , wherein ²R is -O - CHF2 .

. The compound of any one of embodiments 1-14 , or a pharmaceutically acceptable salt or solvate thereof , wherein p is 1 or 2 . 16. The compound of any one of embodiments 1-15 , or a pharmaceutically acceptable salt or solvate thereof , wherein p is 1 . 17. The compound of any one of embodiments 1-15 , or a pharmaceutically acceptable salt or solvate thereof , wherein p is 2 . 18. The compound of any one of embodiments 1-17 , or a pharmaceutically acceptable salt or solvate thereof , wherein ³R is ₁C - C6 alkyl . 71 WO 2025/049495 PCT / US2024 / 0440 19. The compound of embodiment 18 , or a pharmaceutically acceptable salt or solvate thereof , wherein ³R is methyl .

. The compound of any one of embodiments 1-17 , or a pharmaceutically acceptable salt or solvate thereof , wherein ³R is hydrogen . 21. The compound of any one of embodiments 1-20 , or a pharmaceutically acceptable salt or solvate thereof , wherein r is 1 . 22. The compound of embodiment 21 , or a pharmaceutically acceptable salt or solvate thereof , wherein A is ₁C - C6 alkyl . 23 . The compound of embodiment 22 , or a pharmaceutically acceptable salt or solvate thereof , wherein A is -CH3 or -CH2CH3 . 24. The compound of any one of embodiments 1-20 , or a pharmaceutically acceptable salt or solvate thereof , wherein r is 0 .

. The compound of embodiment 21 or 24 , or a pharmaceutically acceptable salt or solvate thereof , wherein A is C3 - C8 cycloalkyl , optionally substituted with one or more of RAI , RA2 and ³AR . 26 . The compound of embodiment 25 , or a pharmaceutically acceptable salt or solvate thereof , wherein A is C3 - Cs cycloalkyl , optionally substituted with one or more of RAI , RA2 and ³AR . A 27. The compound of embodiment 26 , or a pharmaceutically acceptable salt or solvate thereof , wherein A is or , RA 28 . The compound of embodiment 27 , or a pharmaceutically acceptable salt or solvate thereof , wherein RA is cyano or halo - ₁C - C6 alkyl . 72 WO 2025/049495 PCT / US2024 / 0440 29 . The compound of embodiment 28 , or a pharmaceutically acceptable salt or solvate thereof , wherein ¹ªR is -CF3 .

. The compound of embodiment 21 or 24 , or a pharmaceutically acceptable salt or solvate thereof , wherein A is phenyl , optionally substituted with one or more of RAI , ²AR and ³ªR . 31 . The compound of embodiment 30 , or a pharmaceutically acceptable salt or solvate thereof , wherein A is phenyl , optionally substituted with one or more of RA1 and ²AR . A 32 . The compound of embodiment 31 , or a pharmaceutically acceptable salt or solvate thereof , wherein A is RA RA 33 . The compound of embodiment 32 , or a pharmaceutically acceptable salt or solvate thereof , wherein RA is -S ( O ) 2 - RA4 ; and , ²AR is halo . 34. The compound of embodiment 31 , or a pharmaceutically acceptable salt or solvate thereof , wherein A is RA The compound of embodiment 34 , or a pharmaceutically acceptable salt or solvate thereof , wherein ¹AR is selected from the group consisting of halo , cyano , -S ( O ) 2 - RA4 and -C ( O ) 4ªR- . . 36. The compound of embodiment 21 or 24 , or a pharmaceutically acceptable salt or solvate thereof , wherein A is 5- to 6 - membered heterocyclyl , optionally substituted with one or more of RAI , RA2 and ³ªR .

The compound of embodiment 36 , or a pharmaceutically acceptable salt or solvate thereof , wherein the heterocyclyl comprises 1 or 2 heteroatoms selected from the group consisting of N , S , and O. . 73 WO 2025/049495 PCT / US2024 / 0440 38 . The compound of embodiment 36 , or a pharmaceutically acceptable salt or solvate thereof , wherein A is 5- to 6 - membered heterocyclyl . 39. The compound of embodiment 38 , or a pharmaceutically acceptable salt or solvate thereof , wherein A is 5- to 6 - membered heterocyclyl comprising 1 or 2 heteroatoms selected from the group consisting of N , S and O. 40 . The compound of embodiment 39 , or a pharmaceutically acceptable salt or solvate thereof , wherein A is FOTO · N ' or viv 41. The compound of embodiment 21 or 24 , or a pharmaceutically acceptable salt or solvate thereof , wherein A is 5- to 6 - membered heteroaryl , optionally substituted with one or more of RAI , RA2 and ³AR . 42. The compound of embodiment 41 , or a pharmaceutically acceptable salt or solvate thereof , wherein A is selected from the group consisting of pyridinyl , pyrazinyl , pyrimidinyl , A pyrazinyl , triazinyl , oxadiazolyl , pyrrolyl , imidazolyl , pyrazolyl , and thiazolyl , optionally substituted with one or more of RAI , RA2 and RA3 . 43. The compound of embodiment 42 , or a pharmaceutically acceptable salt or solvate thereof , wherein A is selected from the group consisting of pyridinyl , pyrimidinyl , pyrazinyl , oxadiazolyl and pyrrolyl , optionally substituted with one or more of RA1 , RA2 and ³AR . A 44. The compound of embodiment 43 , or a pharmaceutically acceptable salt or solvate thereof , wherein A is pyridinyl , optionally substituted with one or more of RAI , RA2 and ³AR . A 45. The compound of embodiment 44 , or a pharmaceutically acceptable salt or solvate thereof , wherein A is pyridinyl substituted with ¹AR . 46 . The compound of embodiment 45 , or a pharmaceutically acceptable salt or solvate thereof , wherein A is 74 RA PCT / US2024 / 0440 , RARAor RA 47. The compound of embodiment 46 , or a pharmaceutically acceptable salt or solvate thereof , wherein ¹AR is selected from the group consisting of ₁C - C6 alkyl , halo - ₁C - C6 alkyl , halo , cyano and -S ( O ) ₂ - RA + 48. The compound of embodiment 43 , or a pharmaceutically acceptable salt or solvate thereof , wherein A is pyrimidinyl or pyrazinyl , optionally substituted with one or more of RAI , ²AR and ³AR . A1 A2 A 49. The compound of embodiment 48 , or a pharmaceutically acceptable salt or solvate thereof , wherein A is pyrimidinyl or pyrazinyl , optionally substituted with ¹AR 50 . The compound of embodiment 49 , or a pharmaceutically acceptable salt or solvate thereof , wherein A is aaa N N. -N RA or 75 WO 2025/049495 PCT / US2024 / 0440 51. The compound of embodiment 50 , or a pharmaceutically acceptable salt or solvate thereof , wherein RA is selected from the group consisting of C1 - C6 alkyl , halo - C1 - C6 alkyl , halo , cyano and -S ( O ) 2 - RA 52. The compound of embodiment 43 , or a pharmaceutically acceptable salt or solvate thereof , wherein A is oxadiazolyl and pyrrolyl , optionally substituted with one or more of ¹AR . RA2 and ³AR . A 53. The compound of embodiment 52 , wherein or a pharmaceutically acceptable salt or solvate thereof , A is oxadiazolyl and pyrrolyl , optionally substituted with ¹AR 54 . The compound of embodiment 53 , or a pharmaceutically acceptable salt or solvate thereof , wherein A is N or RA 55 . The compound of embodiment 54 , or a pharmaceutically acceptable salt or solvate thereof , wherein ¹AR ₁C - C6 alkyl . 56 .

Al The compound of embodiment 1 , or a pharmaceutically acceptable salt or solvate thereof selected from Table 1 . 57. A pharmaceutical composition comprising a compound of any one of embodiments 1-56 , or a pharmaceutically acceptable salt or solvate thereof , and a pharmaceutically acceptable excipient . 58 . A method of promoting myelination in a subject in need thereof , the method comprising administering to the subject in need thereof a therapeutically effective amount of a compound according 76 WO 2025/049495 PCT / US2024 / 0440 to any one of embodiments 1-56 , or a pharmaceutically acceptable salt or solvate thereof , or the pharmaceutical composition of embodiment 57 . 59. A compound of any one of embodiments 1-56 , or a pharmaceutically acceptable salt or solvate thereof , or the pharmaceutical composition of embodiment 57 , for use in treating a disorder in a subject in need thereof . 60. A compound of any one of embodiments 1-56 , or a pharmaceutically acceptable salt or solvate thereof , or the pharmaceutical composition of embodiment 57 , for use in promoting myelination in a subject in need thereof . 61 . Use of a compound of any one of embodiments 1-56 , or a pharmaceutically acceptable salt or solvate thereof , or the pharmaceutical composition of embodiment 57 , in the manufacture of a medicament for treating a disorder in a subject in need thereof . 62. Use of a compound of any one of embodiments 1-56 , or a pharmaceutically acceptable salt or solvate thereof , or the pharmaceutical composition of embodiment 57 , in the manufacture of a medicament for promoting myelination in a subject in need thereof . 63 . The method of embodiment 58 , wherein the subject has a myelin - related disorder . 64 . disorder . The compound for use of embodiment 59 or 60 , wherein the subject has a myelin - related 65 . The use of embodiment 61 or 62 , wherein the subject has a myelin - related disorder . 66. The method of embodiment 63 , compound for use of embodiment 64 , or use of embodiment 65 , wherein the myelin - related disorder is multiple sclerosis ( MS ) , neuromyelitis optica ( NMO ) , optic neuritis , pediatric leukodystrophy , neonatal white matter injury , age - related dementia , schizophrenia , progressive multifocal leukoencephalopathy ( PML ) , encephalomyelitis ( EPL ) , central pontine myelolysis ( CPM ) , adrenoleukodystrophy , Alexander's disease , Pelizaeus Merzbacher disease ( PMD ) , Vanishing White Matter Disease , Wallerian Degeneration , transverse myelitis , amylotrophic lateral sclerosis ( ALS ) , Huntington's discase , Alzheimer's discase , Parkinson's discasc , spinal cord injury , traumatic brain injury , post radiation injury , neurologic complications of chemotherapy , stroke , acute ischemic optic neuropathy , 77 WO 2025/049495 PCT / US2024 / 0440 vitamin E deficiency , isolated vitamin E deficiency syndrome , Bassen - Kornzweig syndrome , Marchiafava - Bignami syndrome , metachromatic leukodystrophy , trigeminal neuralgia , acute disseminated encephalitis , Guillian - Barre syndrome , Charcot - Marie - Tooth disease , Bell's palsy , or radiation - induced demyelination . 67. The method of embodiment 63 , the compound of embodiment 64 , or the use of embodiment 65 , wherein the disorder is multiple sclerosis . 68. A method of inhibiting CYP51 ( lanosterol demethylase ) comprising , contacting CYP51 with a compound according to any one of embodiments 1-56 , or a pharmaceutically acceptable salt or solvate thereof , or the pharmaceutical composition of embodiment 57 .

EXAMPLES [ 156 ] The Examples provide exemplary methods for preparing compounds . Those skilled in the art will appreciate that other synthetic routes may be used to synthesize the compounds . Although specific starting materials and reagents are depicted and discussed in the Schemes , General Procedures , and Examples , other starting materials and reagents can be easily substituted to provide a variety of derivatives and / or reaction conditions . In addition , many of the exemplary compounds prepared by the described methods can be further modified in light of this disclosure using conventional chemistry well known to those skilled in the art . [ 157 ] Example A : S ) -4 - Cyclopropyl - N- ( 4- ( trifluoromethyl ) phenyl ) -N- ( 1- ( 5- ( trifluoromethyl ) pyridine - 2 - yl ) pyrrolidin - 3 - yl ) pyridin - 3 - amine ( Compound 1 ) : [ 158 ] [ 159 ] IN N. -CF CFStep 1 : Tert - Butyl ( S ) -3 - ( ( 4 - chloropyridin - 3 - yl ) amino ) pyrrolidine - 1 - carboxylate N - Boc ﺲﻤﻳﺓ To a mixture of tert - butyl ( 3S ) -3 - aminopyrrolidine - 1 - carboxylate ( 1.16 g . 6.24 mmol , 1. 78 WO 2025/049495 PCT / US2024 / 0440 mL ) , 3 - bromo - 4 - chloro - pyridine ( 1 g , 5.20 mmol ) , and t - BuONa ( 1.50 g , 15.59 mmol ) in toluene ( 15 mL ) was added Pd ( OAc ) 2 ( 233.33 mg , 1.04 mmol ) and t - Bu3P ( 2.08 mmol , 487.85 Lµ , 10wt % in toluene ) , the mixture was degassed and purged with N2 for 3 times , and then the mixture was stirred at 100 ° C for hrs under N2 atmosphere . The reaction mixture was filtered and concentrated in vacuo . The residue was purified by silica flash chromatography ( Eluent of 0 ~ 25 % Ethyl acetate in Petroleum ether ) to afford the title compound ( 633 mg , 2.13 mmol , 41 % yield ) . LCMS [ M + H ] + = 298.2 . [ 160 ] Step 2 : Tert - butyl ( S ) -3 - ( ( 4 - chloropyridin - 3 - yl ) ( 4- ( trifluoromethyl ) phenyl ) amino ) pyrrolidine- - carboxylate N - Boc [ 161 ] CFTo a mixture of tert - butyl ( 3S ) -3 - [ ( 4 - chloro - 3 - pyridyl ) amino ] pyrrolidine - 1 - carboxylate ( 4mg , 1.34 mmol ) , 1 - bromo - 4- ( trifluoromethyl ) benzene ( 604 mg , 2.69 mmol ) and tBuONa ( 516 mg , 5.mmol ) in toluene ( 5 mL ) were added Pd ( OAc ) 2 ( 60.32 mg , 268.65 lomµ ) and t - P³uB ( 537.31 lomµ , 1.mL , 10 wt % in toluene ) , the mixture was degassed and purged with N2 for 3 times , and then the mixture was stirred at 120 ° C for 16 hrs under N2 atmosphere . The reaction mixture was filtered and concentrated in vacuo . The residue was purified by silica flash chromatography ( Eluent of 0 ~ 25 % Ethyl acetate in Petroleum ether ) to provide title compound ( 409 mg , 925.60 lomµ , 69 % yield ) . LCMS ( ESI ) [ M + H ] + = 386.[ 162 ] Step 3 : Tert - butyl ( S ) -3 - ( ( 4 - cyclopropylpyridin - 3 - yl ) ( 4- ( trifluoromethyl ) phenyl ) amino ) pyrrolidine - 1 - carboxylate NN N - Boc CF[ 163 ] A mixture of tert - butyl ( 3S ) -3- [ N- ( 4 - chloro - 3 - pyridyl ) -4- ( trifluoromethyl ) anilino ] pyrrolidine- - carboxylate ( 200 mg , 0.452 mmol ) , cyclopropylboronic acid ( 117 mg , 1.36 mmol ) , Pd ( OAc ) 2 ( 10.16 mg , 0.0452 mmol ) , Cs2CO3 ( 442.4 mg , 1.36 mmol ) and bis ( 1 - adamantyl ) -butyl - phosphane ( 32 mg , 0.0mmol ) in toluene ( 1 mL ) and O₂H ( 0.1 mL ) was degassed and purged with N2 for 3 times , and then the mixture was stirred at 120 ° C for 1 hr under N2 atmosphere in microwave reactor . The reaction mixture was 79 WO 2025/049495 PCT / US2024 / 0440 filtered and concentrated in vacuo . The residue was purified by prep - TLC ( SiO2 , 50 % Ethyl acetate in Petroleum ether ) to provide title compound ( 100.4 mg , 224 lomμ , 50 % yield ) . LCMS ( ESI ) [ M + H ] + = 448.3 . Step 4 : ( S ) -4 - Cyclopropyl - N- ( pyrrolidin - 3 - yl ) -N- ( 4- ( trifluoromethyl ) phenyl ) pyridin - 3 - amine [ 164 ] hydrochloride NH HCI CF[ 165 ] To a mixture of tert - butyl ( 3S ) -3- [ N- ( 4 - cyclopropyl - 3 - pyridyl ) -4- ( trifluoromethyl ) anilino ] pyrrolidine - 1 - carboxylate ( 180 mg , 402.24 lomμ ) was added HCl / dioxane ( 4 M , 3.00 mL ) in one portion at 25 ° C and stirred for 1 hours . The reaction mixture was concentrated under reduced pressure to give the title compound ( 130 mg , 374.23 lomμ , 93.04 % yield ) , which was used into the next step without further purification . LCMS ( ESI ) [ M + H ] + = 348.[ 166 ] Step 5 : ( S ) -4 - Cyclopropyl - N- ( 4- ( trifluoromethyl ) phenyl ) -N- ( 1- ( 5- ( trifluoromethyl ) pyri - din - 2- yl ) pyrrolidin - 3 - yl ) pyridin - 3 - amine ( Compound 1 ) N N N. .CF [ 167 ] CF To a mixture of 4 - cyclopropyl - N - [ ( 3S ) -pyrrolidin - 3 - yl ] -N- [ 4- ( trifluoromethyl ) phenyl ] pyridin - 3 - amine ( 130 mg , 338.68 lomμ , HCl ) and 2 - fluoro - 5- ( trifluoromethyl ) pyridine ( 83.87 mg , 508.lomμ ) in DMF ( 1 mL ) was added DIEA ( 131.31 mg , 1.02 mmol ) in one portion at 25 ° C . The mixture was stirred at 80 ° C for 4 hours . The reaction was diluted with water ( 10 mL ) and extracted with ethyl acetate ( mL x 3 ) . The combined organics were washed with brine ( 10 mL x 3 ) , dried with anhydrous Na2SO4 , filtered and concentrated in vacuum . The residue was purified by silica gel chromatography ( 10 % -50 % Ethyl acetate in Petroleum ether ) to provide the title compound 140 mg , 284.29 lomμ , 83.94 % yield ) as yellow solid . ( SFC : 30:70 ) . The mixture of enantiomers ( 130 mg , 263.98 lomμ ) was purified by SFC ( SFC- ; DAICEL CHIRALCEL OD ( 250 mm * 30 mm , 10 um ) , 0.1 % O₂H3HN ETOH ; 30 % ~ 30 % , 60 mL / min ) to afford the title compound - 1 ( the first peak on SFC , Compound 1 , 50.7 mg , 101.92 lomµ , 38.61 % yield ) . 80 WO 2025/049495 PCT / US2024 / 0440 LCMS ( ESI ) [ M + H ] * = 493.1 . Only the above enantiomer of Compound 1 displayed activity . [ 168 ] - Compound 1 : HNMR : ( 400 MHz , CDCl3 ) 8 8.50 - 8.20 ( m , 3H ) , 7.63 - 7.57 ( m , 1H ) , 7.49 - 7.41 ( m , 2H ) , 6.82 - 6.72 ( m , 1H ) , 6.65 - 6.58 ( m , 2H ) , 6.35 - 6.27 ( m , 1H ) , 4.85-4.81 ( m , 1H ) , 4.07 - 4.( m , 1H ) , 3.66 - 3.63 ( m , 1H ) , 3.48 - 3.45 ( m , 2H ) , 2.44 - 2.42 ( m , 1H ) , 2.15 - 2.03 ( m , 1H ) , 1.90 - 1.80 ( m , IH ) , 1.10 0.95 ( m , 2H ) , 0.86 - 0.76 ( m , 2H ) . [ 169 ] Example B : 2- ( 4 - ( ( 4 - Cyclopropylpyridin - 3 - yl ) ( 6- ( trifluoromethyl ) pyridin - 3- yl ) amino ) piper - idin - 1 - yl ) pyrimidine - 5 - carbonitrile ( Compound 2 ) : N [ 170 ] N F F Step 1 : Tert - butyl 4 - ( ( 4 - chloropyridin - 3 - yl ) amino ) piperidine - 1 - carboxylate N ' N- ﻢﻣ ' N ' Boc [ 171 ] A mixture of tert - butyl 4 - amino - 1 - piperidinecarboxylate ( 3747 mg , 18.71mmol ) , tBuONa ( 4494 mg , 46.77 mmol ) , 3 - bromo - 4 - chloro - pyridine ( 3000.0 mg , 15.59 mmol ) , Bu3P ( 7.33 mL , 3.12 mmol , 10wt % in toluene ) and Pd ( OAc ) 2 ( 350 mg , 1.56 mmol ) in toluene ( 50 mL ) was degassed and purged with N2 for 3 times , and then the mixture was stirred at 80 ° C for 19 hours under N2 . [ 172 ] The mixture was concentrated under reduced pressure to dryness and the residue was purified by silica flash chromatography ( silica gel , 100 - 200 mesh , 50 % ethyl acetate in petroleum ether ) to give the title compound ( 2200 mg , 7.056 mmol , 45 % yield ) . LCMS ( ESI ) [ M + H ] + = 312.1 . ' H NMR ( 400 MHz , CDC13 ) 8 ppm 8.07 ( s , 1H ) , 7.89 ( s , 1H ) , 7.23 ( d , J = 5.2 Hz , 1H ) , 4.15 ( d , J = 6.8 Hz , 1H ) , 4.00 -4.12 ( m , 2H ) , 3.51 3.65 ( m , 1H ) , 2.98 ( t , J = 11.6 Hz , 2H ) , 2.05 - 2.10 ( m , 2H ) , 1.50 ( d , J = 1.6 Hz , 2H ) , 1.48 ( s , - 9H ) . [ 173 ] = Step 2 : Tert - butyl 4 - ( ( 4 - chloropyridin - 3 - yl ) ( 6- ( trifluoromethyl ) pyridin - 3 - yl ) amino ) piper- idine - 1 - carboxylate 81 CI ` N · N- Boc PCT / US2024 / 0440 [ 174 ] F F A mixture of 5 - bromo - 2- ( trifluoromethyl ) pyridine ( 870 mg , 3.85 mmol ) , tBuONa ( 555 mg , 5.77 mmol ) , tert - butyl 4 - [ ( 4 - chloro - 3 - pyridyl ) amino ] piperidine - 1 - carboxylate ( 600.0 mg , 1.92 mmol ) , PзuBt ( 1.81 mL , 0.77 mmol , 10wt % in toluene ) and Pd ( OAc ) 2 ( 86.4 mg , 0.38 mmol ) in toluene ( 10 mL ) was stirred at 120 ° C for 12 hours under N2 . The mixture was concentrated under reduced pressure to dryness and the residue was purified by silica flash chromatography ( 0 to 50 % ethyl acetate in petroleum ether ) to give the title compound ( 600 mg , 1.31 mmol , 68 % yield ) . LCMS ( ESI ) [ M + H ] + = 401.2 . [ 175 ] Step 3 : Tert - butyl 4 - ( ( 4 - cyclopropylpyridin - 3 - yl ) ( 6- ( trifluoromethyl ) pyridin - 3 - yl ) amino ) piperidine - 1 - carboxylate Boc ` N ` ´N F_F [ 176 ] A mixture of cyclopropylboronic acid ( 594 mg , 2.5 mmol ) , tert - butyl 4 - ( ( 4 - chloropyridin - 3- yl ) ( 6- ( trifluoromethyl ) pyridin - 3 - yl ) amino ) piperidine - 1 - carboxylate ( 1000.0 mg . 2.28 mmol ) , CS2CO( 2.224 g , 6.83 mmol ) , di ( adamantan - 1 - yl ) ( butyl ) phosphane ( 331 mg , 0.46 mmol ) and Pd ( OAc ) 2 ( 51.1 mg , 0.23 mmol ) in water ( 1 mL ) and toluene ( 10 mL ) was purged with N2 for 3 min . The mixture was heated to 120 ° C for 1 hr under N2 in microwave reactor . The mixture was added water ( 20 mL ) and extracted with ethyl acetate ( 50 mL x 3 ) . The organic layers were dried over anhydrous sodium sulfate , filtered and concentrated under reduced pressure . The residue was purified by silica flash chromatography ( 0-50 % ethyl acetate in petroleum ether ) to afford the title compound ( 600 mg , 1.30 mmol , 57 % yield ) . LCMS ( ESI ) [ M + H ] + = 463.2 . [ 177 ] Step 4 : 4 - Cyclopropyl - N- ( piperidin - 4 - yl ) -N- ( 6- ( trifluoromethyl ) pyridin - 3 - yl ) pyridin - 3 - amine hydrochloride 82 N NH HCI PCT / US2024 / 0440 F F [ 178 ] To a solution of tert - butyl 4 - [ ( 4 - cyclopropyl - 3 - pyridyl ) - [ 6- ( trifluoromethyl ) -3 - pyridyl ] amino ] piperidine - 1 - carboxylate ( 600.0 mg , 1.3 mmol ) in dioxane ( 5 mL ) was added HCl / dioxane ( 5.0 mL , 20.0 mmol , 4M ) and stirred at 25 ° C for 2 hrs . The reaction mixture was concentrated under vacuum to give the title compound ( 517 mg , 1.3 mmol , 100 % yield ) as a white solid . LCMS ( ESI ) [ M + H ] + = 363.2 . [ 179 ] Step 5 : 2- ( 4 - ( ( 4 - Cyclopropylpyridin - 3 - yl ) ( 6- ( trifluoromethyl ) pyridin - 3 - yl ) amino ) piperi - din- - yl ) pyrimidine - 5 - carbonitrile ( Compound 2 ) : ` N N [ 180 ] F F To a solution of N- ( 4 - cyclopropyl - 3 - pyridyl ) -N- ( 4 - piperidyl ) -6- ( trifluoromethyl ) pyridin - 3- amine ( 50.0 mg , 0.14 mmol ) and 2 - chloropyrimidine - 5 - carbonitrile ( 23.1 mg , 0.17 mmol ) in N , N- dimethylformamide ( 1 mL ) at 0 ° C was added N , N - diisopropylethylamine ( 0.07 mL , 0.41 mmol ) and stirred for 1 hr . The reaction mixture was diluted with water ( 10 mL ) and extracted with ethyl acetate ( 20 mL x 3 ) . The combined organics were washed with brine ( 10 mL x 3 ) , dried over sodium sulfate , filtered and concentrated . The residue was purified by prep - TLC ( 50 % ethyl acetate in petroleum ether ) to provide the title compound ( 10.5 mg , 0.0205 mmol , 15 % yield ) . LCMS ( ESI ) [ M + H ] + = 466.3 . [ 181 ] == Compound 2 : ' H NMR ( 400 MHz , CDC13 ) 8 ppm 8.49 ( s , 3H ) , 8.28 ( s , 1H ) , 8.11 ( s , 1H ) , 7.( d , J 9.2 Hz , 1H ) , 6.83 ( d , J = 6.4 Hz , 2H ) , 5.06 ( d , J = 14.0 Hz , 2H ) , 4.35 ( s , 1H ) , 3.09 ( t , J = 12.8 Hz , = 2H ) , 2.23 ( d , J = 12.0 Hz , 2H ) , 1.91 ( s , 1H ) , 1.48 ( d , J = 13.6 Hz , 2H ) , 1.15 ( d , J = 6.4 Hz , 2H ) , 0.89 ( d , J = 6.4 Hz , 2H ) . = [ 182 ] Example C : 4 - cyclopropyl - N- ( 1- ( 4- ( methylsulfonyl ) phenyl ) piperidin - 4 - yl ) -N- ( 6- ( trifluoromethyl ) pyridin - 3 - yl ) pyridin - 3 - amine ( Compound 3 ) : 83 [ 183 ] ﻡﻭاﺩ b PCT / US2024 / 0440 Step 1 : 4 - Cyclopropyl - N- ( piperidin - 4 - yl ) -N- ( 6- ( trifluoromethyl ) pyridin - 3 - yl ) pyridin - 3 - amine N N F F NH [ 184 ] To a solution of N- ( 4 - cyclopropyl - 3 - pyridyl ) -N- ( 4 - piperidyl ) -6- ( trifluoromethyl ) pyridin - 3- amine hydrochloride ( 500.0 mg , 1.25 mmol ) in methanol ( 10 mL ) was added basic resin ( 1.0 g ) and stirred at 25 ° C for 2 hr . The reaction mixture was filtered and the methanol was concentrated under vacuum to give the title compound ( 420 mg , 1.16 mmol , 93 % yield ) . [ 185 ] Step 2 : 4 - Cyclopropyl - N- ( 1- ( 4- ( methylsulfonyl ) phenyl ) piperidin - 4 - yl ) -N- ( 6- ( trifluoro- methyl ) pyridin - 3 - yl ) pyridin - 3 - amine ( Compound 3 ) : ﻡﻮﻟﻭﺩ [ 186 ] To a solution of N- ( 4 - cyclopropyl - 3 - pyridyl ) -N- ( 4 - piperidyl ) -6- ( trifluoromethyl ) pyridin - 3- amine ( 50.0 mg , 0.14 mmol ) , RuPhos Pd G3 ( 12 mg , 0.01 mmol ) , 1 - bromo - 4- ( methylsulfonyl ) benzene ( mg , 0.17 mmol ) and BuONa ( 40 mg , 0.41 mmol ) in 1,4 - dioxane ( 3 mL ) was purged with N2 for 3 times . And the reaction mixture was stirred at 110 ° C for 16 hrs . The resulting residue was concentrated under reduced pressure and the residue was purified by prep - TLC ( 50 % ethyl acetate in petroleum ether ) to afford 84 WO 2025/049495 PCT / US2024 / 0440 the title compound ( 53 mg , 0.0995 mmol , 72 % yield ) . LCMS ( ESI ) [ M + H ] + = 517.3 . [ 187 ] Compound 3 : ' H NMR ( 400 MHz , CDC13 ) 8 ppm 8.53 ( d , J = 5.6 Hz , 1H ) , 8.30 ( s , 1H ) , 8.( d , J = 2.4 Hz , 1H ) , 7.77 ( d , J = 8.8 Hz , 2H ) , 7.49 ( d , J = 8.8 Hz , 1H ) , 7.28 ( s , 1H ) , 6.93 ( d , J = 9.2 Hz , 2H ) , 6.78 -6.86 ( m , 1H ) , 4.24 ( t , J = 11.6 Hz , 1H ) , 4.00 ( d , J = 12.8 Hz , 2H ) , 3.04 -3.13 ( m , 2H ) , 3.03 ( s , 3H ) , 2.25 -2.21 ( m , 2H ) , 1.86 -1.92 ( m , 1H ) , 1.66 -1.63 ( m , 2H ) , 1.12 ( d , J = 6.4 Hz , 2H ) , 0.88 ( d , J = 6.0 Hz , 2H ) . [ 188 ] Example D : 2- ( 4 - ( ( 4 - Ethylpyridin - 3 - yl ) ( 6- ( trifluoromethyl ) pyridin - 3 - yl ) amino ) piperidin - 1 - yl ) pyrimidine - 5 - carbonitrile ( Compound 4 ) : ` N [ 189 ] F F Step 1 : Tert - butyl 4 - ( ( 6- ( trifluoromethyl ) pyridin - 3 - yl ) ( 4 - vinylpyridin - 3 - yl ) amino ) piper - idine- - carboxylate Boc ` N N F F [ 190 ] A mixture of tert - butyl 4 - [ ( 4 - chloro - 3 - pyridyl ) - [ 6- ( trifluoromethyl ) -3 - pyridyl ] amino ] piperidine - 1 - carboxylate ( 300.0 mg , 0.66 mmol ) , Cs2CO3 ( 642 mg , 1.97 mmol ) , Pd ( OAc ) 2 ( 7.4 mg , 0.0mmol ) , bis ( 1 - adamantyl ) -butyl - phosphane ( 23.5 mg , 0.066 mmol ) and 4,4,5,5 - tetramethyl - 2 - vinyl - 1,3,2- dioxaborolane ( 303.0 mg , 1.97 mmol ) in water ( 1 mL ) and toluene ( 9 mL ) was purged with N2 for 3 times . The mixture was heated to 120 ° C for 1 hr under microwave reactor . [ 191 ] The reaction was diluted with water ( 20 mL ) and extracted with ethyl acetate ( 20 mL x 3 ) . The organics were washed with brine ( 20 mL x 2 ) , dried over sodium sulfate , filtered and concentrated under reduced pressure and the residue was purified by silica flash chromatography ( 0-50 % ethyl acetate in petroleum ether ) to provide the title compound ( 200 mg , 0.646 mmol , 68 % ) . LCMS ( ESI ) [ M + H ] + = 449.2 . 85 WO 2025/049495 PCT / US2024 / 0440 [ 192 ] Step 2 : Tert - butyl 4 - ( ( 4 - ethylpyridin - 3 - yl ) ( 6- ( trifluoromethyl ) pyridin - 3 - yl ) amino ) piperidine- - carboxylate N N Boc [ 193 ] F F A mixture of Pd / C ( 40 mg , 10wt % on carbon ) and tert - butyl 4 - [ [ 6- ( trifluoromethyl ) -3 - pyridyl ] - ( 4 - vinyl - 3 - pyridyl ) amino ] piperidine - 1 - carboxylate ( 200.0 mg , 0.45 mmol ) in Ethanol ( 10 mL ) was stirred at 25 ° C for 1 hr . The reaction mixture was filtered and the filtrate was concentrated under reduced pressure to give the title compound ( 180 mg , 0.40 mmol , 90 % yield ) . LCMS ( ESI ) [ M - 56 + H ] + = 395.1 . Step 3 : 4 - Ethyl - N- ( piperidin - 4 - yl ) -N- ( 6- ( trifluoromethyl ) pyridin - 3 - yl ) pyridin - 3 - amine [ 194 ] hydrochloride N ' N ' NH HCI [ 195 ] F F Tert - butyl - 4 - [ ( 4 - ethyl - 3 - pyridyl ) - [ 6- ( trifluoromethyl ) -3 - pyridyl ] amino ] piperidine - 1- carboxylate ( 180.0 mg , 0.40 mmol ) was dissolved in HCl / dioxane ( 4 mL , 4 M ) and stirred at 25 ° C for 3 hrs . The reaction mixture was concentrated under reduced pressure to give the title compound ( 200 mg , 0.00mmol , 0.90 % yield ) . LCMS ( ESI ) [ M + H ] + = 350.2 . [ 196 ] Step 4 : 2- ( 4 - ( ( 4 - Ethylpyridin - 3 - yl ) ( 6- ( trifluoromethyl ) pyridin - 3 - yl ) amino ) piperidin - 1 - yl ) pyrimidine - 5 - carbonitrile ( Compound 4 ) : ` ´N F F 86 WO 2025/049495 PCT / US2024 / 0440 [ 197 ] To a solution of N- ( 4 - ethyl - 3 - pyridyl ) -N- ( 4 - piperidyl ) -6- ( trifluoromethyl ) pyridin - 3 - amine ( 80.0 mg , 0.23 mmol ) in N , N - dimethylformamide ( 2 mL ) was added N , N - diisopropylethylamine ( 0.12 mL , 0.68 mol ) at 0 ° C , and the mixture was stirred at 0 ° C for 5 min , then 2 - chloropyrimidine - 5 - carbonitrile ( mg , 0.23 mmol ) was added . Then the reaction mixture was stirred at 25 ° C for 1 hr . The solvent was removed under reduced pressure and the residue was purified by silica flash chromatography ( 0-30 % ethyl acetate in petroleum ether ) to afford the title compound ( 11.6 mg . 0.0026 mmol , 12 % yield ) . LCMS ( ESI ) [ M + H ] + = 454.2 . [ 198 ] Compound 4 : ' H NMR ( 400 MHz , CD3OD ) 8 8.57 - 8.52 ( m , 3H ) , 8.32 - 8.28 ( m , 1H ) , 7.- 7.84 ( m , 1H ) , 7.63 - 7.57 ( m , 2H ) , 7.16 - 7.11 ( m , 1H ) , 4.99 ( d , J = 13.6 Hz , 2H ) , 4.64 - 4.48 ( m , 1H ) , 3.22 3.11 ( m , 2H ) , 2.65 ( s , 2H ) , 2.22 - 2.02 ( m , 2H ) , 1.39 -1.28 ( m , 2H ) , 1.18 ( t , J = 7.6 Hz , 3H ) . - [ 199 ] Example E : 2- ( 4 - ( ( 4 - Methoxypyridin - 3 - yl ) ( 6- ( trifluoromethyl ) pyridin - 3 - yl ) amino ) piperidin - 1 - yl ) pyrimidine - 5 - carbonitrile ( Compound 5 ) : N [ 200 ] F Step 1 : Tert - butyl 4 - [ ( 4 - methoxy - 3 - pyridyl ) amino ] piperidine - 1 - carboxylate N Boc ' N ' [ 201 ] To a solution of 4 - methoxypyridin - 3 - amine ( 10 g , 80.55 mmol ) and tert - butyl 4 - oxopiperidine- - carboxylate ( 19.26 g , 96.66 mmol ) in isopropyl acetate ( 100 mL ) was added NaBH ( OAc ) 3 ( 20.49 g , 96.66 mmol ) and stirred at 0 ° C for 0.1 hr .Then 2,2,2 - trifluoroacetic acid ( 27.56 g , 241.66 mmol , 17.mL ) was added to the mixture and stirred at ice bath for 2 hr , and then stirred at 30 ° C for 24 hr . The reaction mixture was adjusted with saturated NaHCO3 aq . ( 200 mL ) and stirred for 30 min . The resulting mixture was extracted with ethyl acetate ( 150 mLx3 ) and the combined organic layer was washed with brine ( mLx3 ) . The organic phase was dried over Na2SO4 , filtered and concentrated under reduced pressure to give a residue . The residue was purified by column chromatography ( Petroleum ether / Ethyl acetate 5/1 to 1/1 then turn to use 3 % -10 % methanol in DCM ) to give the title compound ( 21 g , 68.32 mmol , % yield , 100 % purity ) . LCMS ( ESI ) [ M + H ] + = 308.2 . ' HNMR ( 400 MHz , DMSO - ²d ) : 8.10 ( d , J – 6. 87 WO 2025/049495 PCT / US2024 / 0440 Hz , 1H ) , 8.05 ( s , 1H ) , 7.32 ( d , J = 6.0 Hz , 1H ) , 5.84 ( d , J = 8.4 Hz , 1H ) , 4.04 ( s , 3H ) , 3.96-3.93 ( m , 2H ) , 3.57-3.54 ( m , 2H ) , 2.84 ( brs , 2H ) , 1.86-1.82 ( m , 2H ) , 1.40 ( s , 9H ) . [ 202 ] Step 2 : Tert - butyl piperidine - 1 - carboxylate - ( ( 4 - methoxypyridin - 3 - yl ) ( 5- ( trifluoromethyl ) pyridin - 2 - yl ) amino ) N Boc N- ` N F F [ 203 ] A mixture of tert - butyl 4 - [ ( 4 - methoxy - 3 - pyridyl ) amino ] piperidine - 1 - carboxylate ( 3 g , 9.mmol ) , 5 - bromo - 2- ( trifluoromethyl ) pyridine ( 4.41 g . 19.52 mmol ) , Bu3P Pd G2 ( 1.00 g , 1.mmol ) , † BuONa ( 2.81 g , 29.28 mmol ) in toluene ( 20 mL ) was degassed and purged with N2 for 3 times , and then the mixture was stirred at 120 ° C for 12 hr under N2 atmosphere . The reaction mixture was filtered and concentrated under reduced pressure and the residue was purified by silica flash chromatography ( 0-60 % Ethyl acetate in Petroleum ether ) to provide the title compounds ( 2.78 g , 6.14 mmol , 63 % yield ) . LCMS ( ESI ) [ M + H ] + = 453.[ 204 ] Step 3 : 4 - Methoxy - N- ( piperidin - 4 - yl ) -N- ( 6- ( trifluoromethyl ) pyridin - 3 - yl ) pyridin - 3 - amine N NH F F [ 205 ] To a solution of tert - butyl 4 - [ ( 4 - methoxy - 3 - pyridyl ) - [ 6- ( trifluoromethyl ) -3 - pyridyl ] amino ] piperidine - 1 - carboxylate ( 600 mg , 1.33 mmol ) in dioxane ( 2 mL ) was added HCl / dioxane ( 4 M , 3 mL ) . The mixture was stirred at 25 ° C for 1 hr . The reaction mixture was concentrated under reduced pressure to provide the title compound ( 510 mg , 1.31 mmol , 99 % yield ) . LCMS ( ESI ) [ M + H ] + = 353.2 . [ 206 ] Step 4 : 2- ( 4 - ( ( 4 - Methoxypyridin - 3 - yl ) ( 6- ( trifluoromethyl ) pyridin - 3 - yl ) amino ) piperidin - 1- yl ) pyrimidine - 5 - carbonitrile ( Compound 5 ) : 88 WO 2025/049495 PCT / US2024 / 0440 [ 207 ] N To a solution of N- ( 4 - methoxy - 3 - pyridyl ) -N- ( 4 - piperidyl ) -6- ( trifluoromethyl ) pyridin - 3 - amine ( 50.0 mg , 0.13 mmol ) and N , N - Diisopropylethylamine ( 0.07 mL , 0.39 mmol ) in N , N - dimethylformamide ( 1 mL ) at 0 ° C was added 2 - chloropyrimidine - 5 - carbonitrile ( 22 mg , 0.15 mmol ) and stirred for 1 hr . The reaction was diluted with water ( 10 mL ) and extracted with ethyl acetate ( 20 mL x 3 ) . The combined organics were washed with brine ( 10 mL x 3 ) , dried over sodium sulfate , filtered and concentrated . The residue was purified by prep - TLC ( 50 % ethyl acetate in petroleum ether ) to provide the title compound ( 27.8 mg , 0.0574 mmol , 45 % yield ) . LCMS ( ESI ) [ M + H ] + = 456.[ 208 ] Compound 5 : ' H NMR ( 400 MHz , CDCl3 ) 8 ppm 8.58 ( d , J = 5.2 Hz , 1H ) , 8.47 ( s , 2H ) , 8.( s , 1H ) , 8.01 ( s , 1H ) , 7.45 ( d , J = 8.8 Hz , 1H ) , 7.00 ( d , J = 5.2Hz , 1H ) , 6.84 ( d , J = 7.2 Hz , 1H ) , 5.01 ( d , J = 13.2 Hz , 2H ) , 4.23 ( t , J = 11.6 Hz , 1H ) , 3.82 ( s , 3H ) , 3.01 - 3.10 ( m , 1H ) , 2.15 ( d , J = 13.2 Hz , 2H ) , 1.( d , J = 9.2 Hz , 2H ) . [ 209 ] Example F : 1- ( 4 - ( ( 4 - Cyclopropylpyridin - 3 - yl ) ( 4- ( trifluoromethyl ) phenyl ) amino ) piperidin - 1 - yl ) ethan - 1 - one ( Compound 6 ) : [ 210 ] carboxylate Step 1 : Tert - butyl 4- [ N- ( 4 - chloro - 3 - pyridyl ) -4- ( trifluoromethyl ) anilino ] piperidine - 1- 89 N N BOC PCT / US2024 / 0440 [ 211 ] A mixture of tert - butyl 4 - [ ( 4 - chloro - 3 - pyridyl ) amino ] piperidine - 1 - carboxylate ( 600 mg , 1.mmol ) , 1 - bromo - 4- ( trifluoromethyl ) benzene ( 866 mg , 3.85 mmol ) , Pd ( OAc ) 2 ( 87 mg , 384.85 lomμ ) , t- P³uB ( 1.56 g , 769.71 lomµ , 1.81 mL , 10 % purity ) and BuONa ( 740 mg , 7.70 mmol ) in toluene ( mL ) was degassed and purged with N2 for 3 times , and then the mixture was stirred at 120 ° C for hr under N2 atmosphere . The reaction mixture was filtered and concentrated under reduced pressure . The residue was purified by flash silica gel chromatography ( 0 ~ 40 % Ethyl acetate in Petroleum ether ) to provide the title compound ( 420 mg , 921.25 lomμ , 47.88 % yield ) . LCMS ( ESI ) [ M - 56 + H ] + = 400.Step 2 : Tert - butyl 4 - ( ( 4 - cyclopropylpyridin - 3 - yl ) ( 4- ( trifluoromethyl ) phenyl ) amino ) [ 212 ] piperidine - 1 - carboxylate BOC [ 213 ] A mixture of tert - butyl 4- [ N- ( 4 - chloro - 3 - pyridyl ) -4- ( trifluoromethyl ) anilino ] piperidine - 1- carboxylate ( 250 mg , 548 lomµ ) , cyclopropylboronic acid ( 94.21 mg , 1.10 mmol ) , Pd ( OAc ) 2 ( 12.31 mg , lomµ ) , bis ( 1 - adamantyl ) -butyl - phosphane ( 39 mg , 110 lomµ ) and Cs2CO3 ( 536.00 mg , 1.65 mmol ) in O₂H ( 0.4 mL ) and toluene ( 4 mL ) was degassed and purged with N2 for 3 times , and then the mixture was stirred at 120 ° C for 1 hr under microwave reactor . The reaction mixture was filtered and concentrated under reduced pressure . The residue was purified by flash silica gel chromatography ( Eluent of 0-45 % Ethyl acetate in Petroleum ether ) to provide the title compound ( 240 mg ) . LCMS ( ESI ) [ M + H ] + = 462.3 . [ 214 ] Step 3 : 4 - Cyclopropyl - N- ( piperidin - 4 - yl ) -N- ( 4- ( trifluoromethyl ) phenyl ) pyridin - 3 - amine 90 NH N PCT / US2024 / 0440 [ 215 ] To a solution of tert - butyl 4- [ N- ( 4 - cyclopropyl - 3 - pyridyl ) -4- ( trifluoromethyl ) anilino ] piperidine - 1 - carboxylate ( 240 mg , 520.02 lomµ ) in dioxane ( 2 mL ) was added HCl / dioxane ( 4 M , 1.30 mL ) and the mixture was stirred at 25 ° C for 1 hr . The mixture was concentrated under reduced pressure to provide the title compound ( 200 mg , crude ) as HCl salt . LCMS ( ESI ) : [ M + H ] + = 362.2 . [ 216 ] Step 4 : 1- ( 4 - ( ( 4 - Cyclopropylpyridin - 3 - yl ) ( 4- ( trifluoromethyl ) phenyl ) amino ) piperidin - 1- yl ) ethan - 1 - one ( Compound 6 ) : [ 217 ] To a solution of 4 - cyclopropyl - N- ( 4 - piperidyl ) -N- [ 4- ( trifluoromethyl ) phenyl ] pyridin - 3 - amine ( 100 mg , 277 lomμ ) and acetyl chloride ( 43.44 mg , 553.40 lomμ ) in dichloromethane ( 2 mL ) was added triethylamine ( 84 mg , 830 lomµ ) at 0 ° C and the mixture was stirred for 1 hr . The reaction mixture was concentrated in vacuo and the residue was purified by reversed - phase HPLC ( Welch Xtimate C150 * 30 mm * 5 um ; mobile phase : [ water ( FA ) -ACN ] ; B % : 29 % -59 % , 7 min ) to provide the title compound ( 33.3 mg , 82.54 lomμ , 30 % yield ) . LCMS ( ESI ) [ M + H ] + = 403.9 . [ 218 ] Compound 6 : ' H NMR ( 400 MHz , CDCl3 ) 8 8.57 - 8.41 ( m , 1H ) , 8.29 - 8.14 ( m , 1H ) , 7.46 - 7.39 ( m , 2H ) , 6.80 - 6.68 ( m , 1H ) , 6.54 ( d , J = 8.8 Hz , 2H ) , 4.79 -4.75 ( m , 1H ) , 4.26 - 4.16 ( m , 1H ) , 3.96 - 3.88 ( m , 1H ) , 3.28 -3.17 ( m , 1H ) , 2.71 - 2. 61 ( m , 1H ) , 2.19 - 2.09 ( m , 2H ) , 2.08 ( s , 3H ) , 1.92 1.84 ( m , 1H ) , 1.48 - 1.35 ( m , 2H ) , 1.08 - 1.01 ( m , 2H ) , 0.82 - 0.81 ( m , 2H ) . [ 219 ] Example G : 1- ( 4 - ( ( 4 - Cyclopropylpyridin - 3 - yl ) ( 4- ( trifluoromethyl ) phenyl ) amino ) piperidin - 1 - yl ) propan - 1 - one ( Compound 7 ) 91 WO 2025/049495 PCT / US2024 / 0440 [ 220 ] To a solution of 4 - cyclopropyl - N- ( 4 - piperidyl ) -N- [ 4- ( trifluoromethyl ) phenyl ] pyridin - 3 - amine ( 50 mg , 125.67 lomμ ) and propanoyl chloride ( 23.26 mg , 251.34 lomµ ) in dichloromethane ( 2 mL ) was added triethylamine ( 38 mg , 377.01 lomμ ) and the mixture was stirred at 0 ° C for 1 hr . The reaction mixture was concentrated under reduced pressure and the residue was purified by reversed - phase HPLC ( Welch Xtimate C18 150 * 30 mm * 5 um ; mobile phase : [ water ( FA ) -ACN ] ; B % : 29 % - 59 % , 7 min ) to provide title compound ( Compound 7 , 33.3 mg , 79.77 lomμ , 63 % yield ) . LCMS ( ESI ) [ M + H ] + 418.[ 221 ] = Compound 7 : ' H NMR ( 400 MHz , CDCl3 ) 8 8.54 - 8.41 ( m , 1H ) , 8.27 - 8.17 ( m , 1H ) , 7.45 - 7.39 ( m , 2H ) , 6.80 - 6.72 ( m , 1H ) , 6.57 - 6.51 ( m , 2H ) , 4.80 -4.77 ( m , 1H ) , 4.29 - 4.14 ( m , 1H ) , 4.04 -3.( m , 1H ) , 3.26-3.10 ( m , 1H ) , 2.67 - 2.65 ( m , 1H ) , 2.32 ( q , J = 7.2 Hz , 2H ) , 2.16 - 2.08 ( m , 2H ) , 1.92 -1.( m , 1H ) , 1.41 - 1.30 ( m , 2H ) , 1.12 ( t , J = 7.6 Hz , 3H ) , 1.08 - 1.03 ( m , 2H ) , 0.82 - 0.81 ( m , 2H ) . [ 222 ] = Example H : 2- ( 4 - ( ( 4 - Cyclopropoxypyridin - 3 - yl ) ( 6- ( trifluoromethyl ) pyridin - 3 - yl ) amino ) piperidin - 1 - yl ) pyrimidine - 5 - carbonitrile ( Compound 8 ) : N N N [ 223 ] Step 1 : 4 - Cyclopropoxy - 3 - nitropyridine [ 224 ] NOﻢﻌﻜﻣ To a solution of cyclopropanol ( 1.21 g , 20.81 mmol ) and NaH ( 832.51 mg , 20.81 mmol , 60 % 92 WO 2025/049495 PCT / US2024 / 0440 purity ) in DMF ( 20 mL ) was added 4 - Chloro - 3 - nitro - pyridine ( 2.2 g . 13.88 mmol ) at 0 ° C and stirred at that temperature for 2 hr under N2 atmosphere . The reaction mixture was quenched with NH4Cl ( 70 mL ) and extracted with ethyl acetate ( 100 mL x 2 ) . The combined organic layer was washed with brine ( 50 mL x 3 ) , dried over anhydrous Na2SO4 , filtered and concentrated under reduced pressure . The residue was purified by flash silica gel chromatography ( Eluent of 0 ~ 30 % Ethyl acetate in Petroleum ether ) to provide the title compound ( 1.93 g , 10.50 mmol , 76 % yield ) . LCMS ( ESI ) [ M + H ] + = 181.0 . Step 2 : 4 - Cyclopropoxypyridin - 3 - amine [ 225 ] NH [ 226 ] A mixture of 4- ( cyclopropoxy ) -3 - nitro - pyridine ( 2.13 g , 11.82 mmol ) and Pd / C ( 0.5 g , 10 % purity ) in EtOH ( 20 mL ) was degassed and purged with ₂H for 3 times , and then the mixture was stirred at 25 ° C for 1 hr under ₂H ( 15 psi ) atmosphere . The reaction mixture was filtered and concentrated in vacuo to provide the title compound ( 1.73 g , 11.52 mmol , 97 % yield ) . LCMS ( ESI ) [ M + H ] + = 151.2 . [ 227 ] Step 3 : Tert - butyl 4 - ( ( 4 - cyclopropoxypyridin - 3 - yl ) amino ) piperidine - 1 - carboxylate N N Boc H [ 228 ] To a solution of 4- ( cyclopropoxy ) pyridin - 3 - amine ( 1.73 g , 11.52 mmol ) and tert - butyl 4- oxopiperidine - 1 - carboxylate ( 3.44 g , 17.28 mmol ) in isopropyl acetate ( 30 mL ) was added NaBH ( OAc ) ( 2.93 g , 13.82 mmol ) at 0 ° C , and then TFA ( 3.94 g , 34.56 mmol , 2.56 mL ) was added to above mixture in dropwise at 0 ° C . The mixture was stirred at 25 ° C for 12 hrs . The reaction mixture was adjusted with saturated NaOH aq . ( 50 mL ) and stirred for 10 min . The resulting mixture was extracted with ethyl acetate ( 100 mL * 3 ) . The combined organic layers were washed with brine ( 50 mL ) , dried over Na2SO4 , filtered and concentrated under reduced pressure . The residue was purified by flash silica gel chromatography ( Eluent of 0-3 % Methanol in Dichloromethane ) to provide the title compound ( 1.65 g , 4.95 mmol , 43 % yield ) . LCMS ( ESI ) [ M + H ] + = 334.3 . [ 229 ] Step 4 : Tert - butyl 4 - ( ( 4 - cyclopropoxypyridin - 3 - yl ) ( 6- ( trifluoromethyl ) pyridin - 3 - yl ) amino Opiperidine - 1 - carboxylate 93 ' N ' F F Boc ` N PCT / US2024 / 0440 [ 230 ] A mixture of tert - butyl 4 - [ [ 4- ( cyclopropoxy ) -3 - pyridyl ] amino ] piperidine - 1 - carboxylate ( 5mg , 1.50 mmol ) , 5 - bromo - 2- ( trifluoromethyl ) pyridine ( 677.80 mg , 3.00 mmol ) , tBuONa ( 576.46 mg , 6.mmol ) , Pd ( OAc ) 2 ( 67.33 mg , 299.92 lomμ ) and t - PзuB ( 599.84 lomμ , 1.41 mL , 10 % purity ) in toluene ( mL ) was degassed and purged with N2 for 3 times , and then the mixture was stirred at 120 ° C for hr under N2 atmosphere . The reaction mixture was filtered and concentrated under reduced pressure and the residue was purified by flash silica gel chromatography ( Eluent of 0-60 % Ethyl acetate in Petroleum ether ) to provide the title compound ( 319 mg , 667 lomµ , 44 % yield ) . LCMS ( ESI ) [ M + H ] + = 479.3 . [ 231 ] Step 5 4 - Cyclopropoxy - N- ( piperidin - 4 - yl ) -N- ( 6- ( trifluoromethyl ) pyridin - 3 - yl ) pyridin - 3- amine NH ' N ' [ 232 ] To a solution of tert - butyl - 4 - [ [ 4- ( cyclopropoxy ) -3 - pyridyl ] - [ 6- ( trifluoromethyl ) -3- pyridyl ] amino ] piperidine - 1 - carboxylate ( 100 mg , 208.98 lomμ ) in dioxane ( 2 mL ) was added HCl / dioxane ( 4 M , 5 mL ) and the mixture was stirred at 25 ° C for 1 hr . The reaction mixture was concentrated under reduced pressure to provide the title compound ( 78 mg , 206.14 lomµ crude ) as yellow solid . LCMS ( ESI ) [ M + H ] + = 379.2 . [ 233 ] Step 6 : 2- ( 4 - ( ( 4 - Cyclopropoxypyridin - 3 - yl ) ( 6- ( trifluoromethyl ) pyridin - 3 - yl ) amino ) piper - idin- - yl ) pyrimidine - 5 - carbonitrile ( Compound 8 ) : 94 N N PCT / US2024 / 0440 [ 234 ] To a solution of N- [ 4- ( cyclopropoxy ) -3 - pyridyl ] -N- ( 4 - piperidyl ) -6- ( trifluoromethyl ) pyrid - in- - amine ( 78 mg , 206.14 lomμ ) and DIEA ( 79.92 mg , 618.41 lomμ , 107.72 Lµ ) in DMF ( 2 mL ) was added 2 - chloropyrimidine - 5 - carbonitrile ( 28.76 mg , 206.14 lomμ ) at 0 ° C and the mixture was stirred at 0 ° C for 0.5 hr . The reaction mixture was diluted with water ( 10 mL ) and extracted with ethyl acetate ( mL x 3 ) . The combined organic layers were washed with brine ( 20 mL x 3 ) , dried over Na2SO4 , filtered and concentrated under reduced pressure to give crude residue . The residue was purified by reversed - phase HPLC ( Welch Xtimate C18 150 * 30mm * 5um ; mobile phase : [ water ( FA ) -ACN ] ; B % : 39 % -69 % , 7 min ) to provide the title compound ( 55.1 mg , 114.44 lomμ , 56 % yield ) . LCMS ( ESI ) [ M + H ] + = 482.[ 235 ] Compound 8 : ' H NMR ( 400 MHz , CDCl3 ) 8 8.55 ( d , J = 5.6 Hz , 1H ) , 8.47 ( s , 2H ) , 8.24 ( s , 1H ) , 7.98 ( d , J = 2.8 Hz , 1H ) , 7.46 - 7.41 ( m , 1H ) , 7.31 ( d , J = 5.6 Hz , 1H ) , 6.80 ( dd , J = 2.8 , 8.8 Hz , 1H ) , 5.04 4.96 ( m , 2H ) , 4.25 -4.16 ( m , 1H ) , 3.80 -3.74 ( m , 1H ) , 3.09 - 3.00 ( m , 2H ) , 2.15 -2.10 ( m , 2H ) , 1.- 1.36 ( m , 2H ) , 0.85 -0.77 ( m , 2H ) , 0.60 -0.53 ( m , 2H ) . [ 236 ] Example I : 4- ( 4 - ( ( 4 - Methoxypyridin - 3 - yl ) ( 4- ( methylsulfonyl ) phenyl ) amino ) piperidin - 1- yl ) benzonitrile : ( Compound 9 ) [ 237 ] carboxylate : N O = $ = Step 1 : Tert - butyl 4 - ( ( 4 - methoxypyridin - 3 - yl ) ( 4- ( methylsulfonyl ) phenyl ) amino ) piper - idine - 1- 95 ' N ' Boc N · PCT / US2024 / 0440 [ 238 ] A mixture of tert - butyl 4 - [ ( 4 - methoxy - 3 - pyridyl ) amino ] piperidine - 1 - carboxylate ( 1 g , 3.mmol ) , 1 - bromo - 4 - methylsulfonyl - benzene ( 1.53 g , 6.51 mmol ) , PзuB Pd G2 ( 333.39 mg , 650.65 lomμ ) and tBuONa ( 1.25 g , 13.01 mmol ) in toluene ( 20 mL ) and stirred at 125 ° C for 12 hr under N2 atmosphere . The reaction mixture was concentrated under reduced pressure and the residue was purified by flash silica gel chromatography ( 0-5 % MeOH in DCM ) to provide the title compound ( 430 mg , 931.60 lomμ , 29 % yield ) . LCMS ( ESI ) , [ M + H ] + = 462.3 . [ 239 ] Step 2 : 4 - Methoxy - N- ( 4- ( methylsulfonyl ) phenyl ) -N- ( piperidin - 4 - yl ) pyridin - 3 - amine : N N O = $ = NH [ 240 ] Tert - butyl - 4- ( N- ( 4 - methoxy - 3 - pyridyl ) -4 - methylsulfonyl - anilino ) piperidine - 1 - carboxylate ( 430 mg , 931.60 lomμ ) dissolved in HCl / dioxane ( 4 M , 4 mL ) and the mixture was stirred at 25 ° C for hr . The mixture was concentrated under reduced pressure to give the title compound ( 336 mg , 929.57 lomµ , 99.78 % yield ) . [ 241 ] Step 3 : 4- ( 4 - ( ( 4 - Methoxypyridin - 3 - yl ) ( 4- ( methylsulfonyl ) phenyl ) amino ) piperidin - 1 - yl ) benzonitrile ( Compound 9 ) : [ 242 ] N N A mixture of 4 - methoxy - N- ( 4 - methylsulfonylphenyl ) -N- ( 4 - piperidyl ) pyridin - 3 - amine ( 50 mg , 96 WO 2025/049495 PCT / US2024 / 0440 138.33 lomμ ) , 4 - fluorobenzonitrile ( 25.13 mg , 207.49 lomμ ) and K2CO3 ( 95.59 mg , 691.64 lomμ ) in DMSO ( 3 mL ) and then the mixture was stirred at 120 ° C for 12 hr . The reaction mixture was purified by pre- HPLC ( column : Welch Xtimate C18 150 * 30mm * 5um ; mobile phase : [ water ( FA ) -ACN ] ; B % : 22 % -52 % , min ) to provide the title compound ( 25 mg , 54.05 lomμ , 39 % yield ) . LCMS ( ESI ) , [ M + H ] + = 463.3 . [ 243 ] Compound 9 : ' H NMR ( 400 MHz , CD3OD ) 8.51 ( s , 1H ) , 8.19 ( s , 1H ) , 7.68 ( d , J = 8.8 Hz , 3H ) , 7.48 ( d , J = 8.4 Hz , 2H ) , 7.27 ( d , J = 5.6 Hz , 1H ) , 6.97 ( d , J = 8.4 Hz , 2H ) , 6.70 ( d , J = 8.0 Hz , 2H ) , 4.35 4.33 ( m , 1H ) , 4.02 - 3.99 ( m , 2H ) , 3.85 ( s , 3H ) , 3.04 ( s , 3H ) , 2.14 - 2.11 ( m , 2H ) , 1.46 - 1.43 ( m , 2H ) , 1.31 - 1.29 ( m , 2H ) . [ 244 ] Example J : 4 - Cyclopropyl - N- ( 1- ( 4- ( cyclopropylsulfonyl ) phenyl ) piperidin - 4 - yl ) -N- ( 6- ( tri- fluoromethyl ) pyridin - 3 - yl ) pyridin - 3 - amine ( Compound 10 ) : ` N [ 245 ] ) . [ 246 ] F F The title compound was synthesized following a procedure similar to Example C ( Compound * mm * The compound was purified by reversed - phase HPLC ( Welch Xtimate C18 1um ; mobile phase : [ water ( FA ) -ACN ] ; B % : 37 % -67 % , 7 min ) to provide the title compound ( 1 mg , 1.lomμ , 2.23 % yield ) . LCMS ( ESI ) , [ M + H ] + = 543.0 . [ 247 ] Compound 10 : ' H NMR ( 400 MHz , CDC13 ) 8 8.54 - 8.48 ( m , 1H ) , 8.30 -8.25 ( m , 1H ) , 8.09 - 8.07 ( m , 1H ) , 7.74 - 7.70 ( m , 2H ) , 7.49 - 7.45 ( m , 1H ) , 6.91 ( d , J = 9.2 Hz , 2H ) , 6.82 - 6.76 ( m , 2H ) , 4.- . - - 4.17 ( m , 1H ) , 4.02 - 3.95 ( m , 2H ) , 3.09 - 2.99 ( m , 2H ) , 2.46 ( s , 1H ) , 2.26 - 2.18 ( m , 2H ) , 1.90 - 1.84 ( m , 1H ) , 1.26 ( s , 2H ) , 1.10 - 1.06 ( m , 2H ) , 1.01 - 0.97 ( m , 2H ) , 0.89 - 0.80 ( m , 4H ) . [ 248 ] Example K : 6- ( 4 - ( ( 4 - Methoxypyridin - 3 - yl ) ( 6- ( trifluoromethyl ) pyridin - 3 - yl ) amino ) piperidin - 1 - yl ) nicotinonitrile ( Compound 11 ) : 97 N 8 N PCT / US2024 / 0440 [ 249 ] ) . [ 250 ] F The title compound was synthesized following a procedure similar to Example E ( Compound The title compound was purified by flash silica gel chromatography ( Eluent of 0 ~ 30 % Ethyl acetate in Petroleum ether ) to provide the title compound ( 30 mg , 66.01 lomμ , 32 % yield ) . LCMS ( ESI ) , [ M + H ] + = 455.3 . [ 251 ] Compound 11 : ' H NMR ( 400 MHz , CDC13 ) 8 8.58 - 8.54 ( m , 1H ) , 8.39 - 8.36 ( m , 1H ) , 8.26 - 8.24 ( m , 1H ) , 8.01 ( d , J = 2.8 Hz , 1H ) , 7.62-7.57 ( m , 1H ) , 7.47 - 7.43 ( m , 1H ) , 6.98 - 6.95 ( m , 1H ) , 6.- 6.80 ( m , 1H ) , 6.61 - 6.58 ( m , 1H ) , 4.60 - 4.53 ( m , 2H ) , 4.25 - 4.16 ( m , 1H ) , 3.81 ( s , 3H ) , 3.09 - 3.01 ( m , 2H ) , 2.18 - 2.11 ( m , 2H ) , 1.47 - 1.37 ( m , 2H ) . [ 252 ] Example L : 4 - Methoxy - N- ( 1- ( 5- ( methylsulfonyl ) pyrimidin - 2 - yl ) piperidin - 4 - yl ) -N- ( 4- ( trifluoromethyl ) phenyl ) pyridin - 3 - amine ( Compound 12 ) : [ 253 ] carboxylate N N S Step 1 : Tert - butyl 4- [ N- ( 4 - methoxy - 3 - pyridyl ) -4- ( trifluoromethyl ) anilino ] piperidine - 1- 98 N BOC ` N PCT / US2024 / 0440 [ 254 ] CFTo a mixture of tert - butyl 4 - [ ( 4 - methoxy - 3 - pyridyl ) amino ] piperidine - 1 - carboxylate ( 2 g , 6.mmol ) and 1 - bromo - 4- ( trifluoromethyl ) benzene ( 2.93 g , 13.01 mmol ) in toluene ( 20 mL ) was added tBu3P Pd G2 ( 333.39 mg , 650.65 lomµ ) and tBuONa ( 1.88 g , 19.52 mmol ) in one portion under N2 and the reaction was stirred at 120 ° C for 24 hr . The mixture was concentrated under reduced pressure and the residue was purified by silica flash chromatography ( 0 ~ 40 % Ethyl acetate in Petroleum ether ) to provide the title compound ( 2.9 g , 6.42 mmol , 99 % yield ) . LCMS ( ESI ) , [ M + H ] + = 452.2 . Step 2 : 4 - Methoxy - N- ( piperidin - 4 - yl ) -N- ( 4- ( trifluoromethyl ) phenyl ) pyridin - 3 - amine [ 255 ] hydrochloride NH -N- HCI [ 256 ] Tert - butyl - 4- [ N- ( 4 - methoxy - 3 - pyridyl ) -4- ( trifluoromethyl ) anilino ] piperidine - 1 - carboxylate ( 2.9 g , 6.42 mmol ) was dissolved in dioxane ( 3.0 mL ) , HCl / dioxane ( 4 M , 10 mL ) was added and the mixture was stirred at 25 ° C for 1 hr . The mixture was concentrated under reduced pressure to provide the title compound ( 2.4 g , 6.19 mmol , 96 % yield ) as a yellow solid . LCMS ( ESI ) , [ M + H ] + = 352.1 . [ 257 ] Step : - Methoxy - N- ( 1- ( 5- ( methylsulfonyl ) pyrimidin - 2 - yl ) piperidin - 4 - yl ) -N- ( 4- ( trifluoromethyl ) phenyl ) pyridin - 3 - amine ( Compound 12 ) : N b 99 WO 2025/049495 PCT / US2024 / 0440 [ 258 ] To a solution of 4 - methoxy - N- ( 4 - piperidyl ) -N- [ 4- ( trifluoromethyl ) phenyl ] pyridin - 3 - amine ( mg , 128.92 lomμ ) and 2 - chloro - 5 - methylsulfonyl - pyrimidine ( 24.83 mg , 128.92 lomμ ) in DMF ( 1 mL ) was added DIEA ( 49.99 mg , 386.77 lomμ ) in one portion at 0 ° C and the mixture was stirred at 0 ° C for 0.5 hr . The reaction was diluted with water ( 10 mL ) and extracted with ethyl acetate ( 20 mL x 3 ) . The combined organic phase was washed with brine ( 20 mL x 3 ) , dried over anhydrous Na2SO4 , filtered and concentrated under reduced pressure . The resulting residue was purified by prep - HPLC ( water ( NH3H2O + NH4HCO3 ) - ACN ] ; B % : 45 % -75 % , 7 min ) to provide the title compound ( 36.2 mg , 71.33 lomμ , 55.32 % yield ) . LCMS ( ESI ) , [ M + H ] + = 508.1 . [ 259 ] Compound 12 : ' H NMR ( 400 MHz , CDC13 ) 8 8.66 ( s , 2H ) , 8.53 ( d , J = 5.6 Hz , 1H ) , 8.22 ( s , 1H ) , 7.40 ( d , J = 8.8 Hz , 2H ) , 7.00 -6.98 ( m , 1H ) , 7.00 -6.93 ( m , 1H ) , 6.55 ( d , J = 8.8 Hz , 2H ) , 5.04 ( d , J = 13.6 Hz , 2H ) , 4.32 -4.19 ( m , 1H ) , 3.81 ( s , 3H ) , 3.17 - 3.07 ( m , 2H ) , 3.06 ( s , 3H ) , 2.18 - 2.15 ( m , 2H ) , 1.46 - 1.24 ( m , 2H ) . [ 260 ] Example M : 4 - Methoxy - N- ( 4- ( trifluoromethyl ) phenyl ) -N- ( 1- ( 5- ( trifluoromethyl ) pyridin- - yl ) piperidin - 4 - yl ) pyridin - 3 - amine ( Compound 13 ) : N F F [ 261 ] ) . [ 262 ] F The title compound was synthesized following a procedure similar to Example L ( Compound = The title compound was purified by prep - HPLC ( acetonitrile 50 % / 0.2 % formic acid in water ) to provide the title compound ( 120 mg , 241.72 lomµ , 42.58 % yield ) . LCMS ( ESI ) , [ M + H ] + = 497.2 . Compound 13 : ' H NMR ( 400 MHz , CD3OD ) 8.46 ( d , J = 5.6 Hz , 1H ) , 8.28 ( s , 1H ) , 8.16 ( s , [ 263 ] 1H ) , 7.69-7.60 ( m , 1H ) , 7.39 ( d , J = 8.8 Hz , 2H ) , 7.23 ( d , J = 5.6 Hz , 1H ) , 6.85 ( d , J = 9.2 Hz , 1H ) , 6.( d , J = 8.8 Hz , 2H ) , 4.55 -4.52 ( m , 2H ) , 4.39 - 4.28 ( m , 1H ) , 3.83 ( s , 3H ) , 3.11 - 3.08 ( m , 2H ) , 2.14 - 2.( m , 2H ) ,, 1.47 -1.28 ( m , 2H ) . [ 264 ] Example N : 6- ( 4 - ( ( 4 - Methoxypyridin - 3 - yl ) ( 4- ( trifluoromethyl ) phenyl ) amino ) piperidin- - yl ) nicotinonitrile ( Compound 14 ) : 100 N F F PCT / US2024 / 0440 [ 265 ] ) . [ 266 ] The title compound was synthesized following a procedure similar to Example L ( Compound The title compound was purified by prep - HPLC ( acetonitrile 50 % / 0.2 % formic acid in water ) to provide the title compound ( 120 mg , 264.63 lomµ , 46.49 % yield ) . LCMS ( ESI ) , [ M + H ] + = 454.2 . [ 267 ] Compound 14 : ' H NMR ( 400 MHz , CD3OD ) 8.46 ( d , J = 5.6 Hz , 1H ) , 8.34 ( d , J = 1.6 Hz , 1H ) , 8.16 ( s , 1H ) , 7.69 - 7.6 ( m , 1H ) , 7.39 ( d , J = 8.8 Hz , 2H ) , 7.22 ( d , J = 5.6 Hz , 1H ) , 6.82 ( d , J = 8.Hz , 1H ) , 6.65 ( d , J = 8.8 Hz , 2H ) , 4.59 - 4.56 ( m , 2H ) , 4.44 - 4.34 ( m , 1H ) , 3.83 ( s , 3H ) , 3.18 - 3.05 ( m , 2H ) , 2.14 - 2.12 ( m , 2H ) , 1.36 - 1.28 ( m , 2H ) . – [ 268 ] Example O : 2- ( 4 - ( ( 4 - Methoxypyridin - 3 - yl ) ( 4- ( trifluoromethyl ) phenyl ) amino ) piperidin- - yl ) pyrimidine - 5 - carbonitrile ( Compound 15 ) : N ` N F F ' N [ 269 ] ) . [ 270 ] The title compound was synthesized following a procedure similar to Example L ( Compound The title compound was purified by prep - HPLC ( acetonitrile 35-50 % / 0.2 % formic acid in water ) to provide the title compound ( 120 mg , 264.06 lomµ , 46.39 % yield ) . LCMS ( ESI ) , [ M + H ] + = 455.2 . [ 271 ] Compound 15 : ' H NMR ( 400 MHz , CD3OD ) 8.54 ( s , 2H ) , 8.46 ( d , J – 6.4 Hz , 1H ) , 8.16 ( s , 1H ) , 7.39 ( d , J = 8.4 Hz , 2H ) , 7.22 ( d , J = 2.0 Hz , 1H ) , 6.65 ( d , J = 8.4 Hz , 2H ) , 4.97 - 4.94 ( m , 2H ) , 4.- 4.36 ( m , 1H ) , 3.83 ( s , 3H ) , 3.17 3.11 ( m , 2H ) , 2.16 -2.13 ( m , 2H ) , 1.33 - 1.26 ( m , 1H ) , 1.40 1.21 ( m , - 101 1H ) .

WO 2025/049495 PCT / US2024 / 0440 [ 272 ] Example P : 4 - Methoxy - N- ( 1- ( 4- ( methylsulfonyl ) phenyl ) piperidin - 4 - yl ) -N- ( 4- ( trifluoromethyl ) phenyl ) pyridin - 3 - amine ( Compound 16 ) : • N • F F [ 273 ] The title compound was synthesized following a procedure similar to Example C ( Compound ) . [ 274 ] The title compound was purified by prep - HPLC ( Welch Xtimate C18 150 * 30mm * 5um ; mobile phase : [ water ( NH3H2O + NH4HCO3 ) -ACN ] ; B % : 50 % -80 % , 8min ) to provide the title compound ( 82.5 mg , 163.19 lomµ , 48.53 % yield ) . LCMS ( ESI ) , [ M + H ] + = 506.1 . [ 275 ] Compound 16 : ' H NMR ( 400 MHz , CD3OD ) 8.47 ( d , J = 6.0 Hz , 1H ) , 8.18 ( s , 1H ) , 7.69 ( d , J = 8.8 Hz , 2H ) , 7.39 ( d , J = 8.8 Hz , 2H ) , 7.24 ( d , J = 6.4 Hz , 1H ) , 7.03 ( d , J = 8.8 Hz , 2H ) , 6.64 ( d , J = 8.Hz , 2H ) , 4.34 - 4.22 ( m , 1H ) , 4.07 - 4.03 ( m , 2H ) , 3.83 ( s , 3H ) , 3.10 - 3.07 ( m , 2H ) , 3.02 ( s , 3H ) , 2.16 - 2.12 ( m , 2H ) , 1.52 - 1.39 ( m , 2H ) . [ 276 ] Example Q : 4 - Methoxy - N- ( 1- ( 5- ( methylsulfonyl ) pyrimidin - 2 - yl ) piperidin - 4 - yl ) -N- ( 6- ( trifluoromethyl ) pyridin - 3 - yl ) pyridin - 3 - amine ( Compound 17 ) : F ` N · [ 277 ] ) . The title compound was synthesized following a procedure similar to Example E ( Compound [ 278 ] The title compound was purified by pre - HPLC ( column : Welch Xtimate C18 150 * 30 mm * 102 WO 2025/049495 PCT / US2024 / 0440 5um ; mobile phase : [ water ( O₂H3HN + NH4HCO3 ) -ACN ] ; B % : 37 % -67 % , 8 min ) to provide the title compound ( 180 mg , 353.97 lomµ , 44.40 % yield ) . LCMS ( ESI ) , [ M + H ] + = 509.1 . [ 279 ] = = Compound 17 : ' H NMR ( 400 MHz , CD3OD ) 8.65 ( s , 2H ) , 8.51 ( d , J = 5.6 Hz , 1H ) , 8.24 ( s , 1H ) , 7.87 ( d , J = 2.8 Hz , 1H ) , 7.58 ( d , J = 8.8 Hz , 1H ) , 7.27 ( d , J = 5.6 Hz , 1H ) , 7.18 ( dd , J = 2.8 , 8.8 Hz , IH ) , 5.04 5.01 ( m , 2H ) , 4.48 - 4.39 ( m , 1H ) , 3.86 ( s , 3H ) , 3.21 3.16 ( m , 2H ) , 3.11 ( s , 3H ) , 2.17 -2.( m , 2H ) , 1.38 -1.30 ( m , 2H ) . [ 280 ] - Example R : 2- ( 4 - ( ( 4- ( Difluoromethoxy ) phenyl ) ( 4 - methoxypyridin - 3 - yl ) amino ) piperidin- - yl ) pyrimidine - 5 - carbonitrile ( Compound 18 ) : F. [ 281 ] Step 1 : Tert - butyl 4 - ( ( 4- ( difluoromethoxy ) phenyl ) ( 4 - methoxypyridin - 3 - yl ) amino ) piper - idine- - carboxylate N Boc ~ N ~ F [ 282 ] A mixture of tert - butyl 4 - [ ( 4 - methoxy - 3 - pyridyl ) amino ] piperidine - 1 - carboxylate ( 2.0 g , 6.mmol ) , 1 - bromo - 4- ( difluoromethoxy ) benzene ( 2.32 g , 10.41 mmol ) , P³uBt Pd G2 ( 666.78 mg , 1.30 mmol ) , and tBuONa ( 1.88 g , 19.52 mmol ) in dioxane ( 50 mL ) was degassed and purged with N2 for 3 times . and then the mixture was stirred at 120 ° C for 24 hr under N2 atmosphere . The mixture was concentrated under reduced pressure and the residue was purified by silica flash chromatography ( 0 ~ 40 % Ethyl acetate in Petroleum ether ) to provide the title compound ( 1600 mg , 3.45 mmol , 52.98 % yield ) . LCMS ( ESI ) , [ M + H ] + = 450.1 . [ 283 ] Step 2 : N- ( 4- ( Difluoromethoxy ) phenyl ) -4 - methoxy - N- ( piperidin - 4 - yl ) pyridin - 3 - amine hydrochloride 103 HCI F NH PCT / US2024 / 0440 [ 284 ] Tert - butyl - 4 - ( ( 4- ( difluoromethoxy ) phenyl ) ( 4 - methoxypyridin - 3 - yl ) amino ) piperidine - 1- carboxylate ( 1.6 g , 3.56 mmol ) was dissolved in dioxane ( 3.0 mL ) , HCl / dioxane ( 4 M , 6 mL ) was added and the mixture was stirred at 25 ° C for 1 hr . The mixture was concentrated under reduced pressure to provide the title compound ( 1.37 g , 3.56 mmol , 100 % yield ) . LCMS ( ESI ) , [ M + H ] + = 350.1 . [ 285 ] Step 3 : 2- ( 4 - ( ( 4- ( Difluoromethoxy ) phenyl ) ( 4 - methoxypyridin - 3 - yl ) amino ) piperidin - 1 - yl ) - pyrimidine - 5 - carbonitrile ( Compound 18 ) : N F. [ 286 ] To a mixture of N- [ 4- ( difluoromethoxy ) phenyl ] -4 - methoxy - N- ( 4 - piperidyl ) pyridin - 3 - amine ( 260 mg , 744.19 lomμ ) and triethylamine ( 301.22 mg , 2.98 mmol ) in DMF ( 5 mL ) was added 2- chloropyrimidine - 5 - carbonitrile ( 103.85 mg , 744.19 lomμ ) at 0 ° C under ₁N . The mixture was stirred at ° C for 30 min . The reaction was diluted with water ( 10 mL ) and extracted with ethyl acetate ( 20 mL x 3 ) . The combined organic phase was washed with brine ( 20 mL x 3 ) , dried over anhydrous Na2SO4 , filtered and concentrated under reduced pressure . The resulting residue was purified by prep - HPLC ( water ( NH3H2O + NH4HCO3 ) -ACN ] ; B % : 45 % -75 % , 7 min ) to provide the title compound ( 153.4 mg , 339.lomμ , 45.56 % yield ) . LCMS ( ESI ) , [ M + H ] + = 453.2 . [ 287 ] Compound 18 : ' H NMR ( 400 MHz , CD3OD ) 8 8.53 ( s , 2H ) , 8.41 ( d , J = 5.6 Hz , 1H ) , 8.14 ( s , 1H ) , 7.18 ( d , J = 5.6 Hz , 1H ) , 6.94 ( d , J = 9.2 Hz , 2H ) , 6.84 - 6.36 ( m , 3H ) , 4.94 - 4.92 ( m , 2H ) , 4.32 - 4.26 ( m , 1H ) , 3.81 ( s , 3H ) , 3.20 - 3.04 ( m , 2H ) , 2.13 - 2.10 ( m , 2H ) , 1.32 - 1.23 ( m , 2H ) . [ 288 ] Example S : 2- ( 4 - ( ( 4- ( Difluoromethoxy ) phenyl ) ( 4 - methylpyridin - 3 - yl ) amino ) piperidin - 1- yl ) pyrimidine - 5 - carbonitrile ( Compound 19 ) : 104 [ 289 ] carboxylate N F PCT / US2024 / 0440 Step 1 : Tert - butyl - 4 - ( ( 4- ( difluoromethoxy ) phenyl ) ( 4 - methylpyridin - 3 - yl ) amino ) piperid - ine - 1- BOC N N F [ 290 ] A mixture of tert - butyl 4 - [ ( 4 - methyl - 3 - pyridyl ) amino ] piperidine - 1 - carboxylate ( 1 g , 3.mmol ) , 1 - bromo - 4- ( difluoromethoxy ) benzene ( 1.53 g . 6.86 mmol ) , Buz ₂GdPP ( 351.70 mg , 686.37 lomµ ) , tBuONa ( 989.44 mg , 10.30 mmol ) in toluene ( 20 mL ) was degassed and purged with N2 for 3 times , and then the mixture was stirred at 120 ° C for 12 hr under ₂N atmosphere . The reaction mixture was filtered and concentrated under reduced pressure and the residue was purified by flash silica gel chromatography ( Eluent of 0-35 % Ethyl acetate in Petroleum ether ) to provide the title compound ( 0.99 g , 2.28 mmol , 66.55 % yield ) . LCMS ( ESI ) , [ M + H ] + = 434.2 . [ 291 ] Step 2 : N- ( 4- ( Difluoromethoxy ) phenyl ) -4 - methyl - N- ( piperidin - 4 - yl ) pyridin - 3 - aminc F NH [ 292 ] To a solution of tert - butyl - 4- [ 4- ( difluoromethoxy ) -N- ( 4 - methyl - 3 - pyridyl ) anilino ] piper - idine- - carboxylate ( 0.99 g , 2.28 mmol ) in dioxane ( 5 mL ) was added HCl / dioxane ( 4 M , 5 mL ) . The mixture was stirred at 25 ° C for 1 hr . The reaction mixture was concentrated under reduced pressure to provide the 105 WO 2025/049495 PCT / US2024 / 0440 title compound ( 0.9 g , crude , HCl salt ) . [ 293 ] Step 3 : 2- ( 4 - ( ( 4- ( Difluoromethoxy ) phenyl ) ( 4 - methylpyridin - 3 - yl ) amino ) piperidin - 1- yl ) pyrimidine - 5 - carbonitrile ( Compound 19 ) : F .N [ 294 ] To a solution of N- [ 4- ( difluoromethoxy ) phenyl ] -4 - methyl - N- ( 4 - piperidyl ) pyridin - 3 - amine ( 300 mg , 811.17 lomμ ) and 2 - chloropyrimidine - 5 - carbonitrile ( 135.83 mg , 973.40 lomμ ) in acetonitrile ( mL ) was added DIEA ( 524.19 mg , 4.06 mmol ) . The mixture was stirred at 0 ° C for 0.5 hr . The reaction mixture was filtered and concentrated under reduced pressure and the residue was purified by reversed- phase HPLC ( Boston Prime C18 150 * 30 mm * 5 um ; mobile phase : [ water ( NH3H2O + NH4HCO3 ) -ACN ] ; B % : 60 % -90 % , 7min ] ) to provide the title compound ( 100.8 mg , 230.95 lomμ , 28.47 % yield ) . LCMS ( ESI ) , [ M + H ] = 437.[ 295 ] Compound 19 : ' H NMR ( 400 MHz , CD3OD ) 8 8.59 - 8.46 ( m , 2H ) , 8.41 - 8.33 ( m , 1H ) , 8.- 8.20 ( m , 1H ) , 7.46 7.36 ( m , 1H ) , 7.03 - 6.93 ( m , 2H ) , 6.84 - 6.41 ( m , 3H ) , 5.01 - 4.92 ( m , 2H ) , 4.45 - 4.33 ( m , 1H ) , 3.20 - 3.09 ( m , 2H ) , 2.16 ( s , 3H ) , 2.13 - 2.10 ( m , 2H ) , 1.35 - 1.31 ( m , 2H ) . [ 296 ] Example T : 4 - Methoxy - N- ( 1- ( 1 - methyl - 1H - pyrazol - 5 - yl ) piperidin - 4 - yl ) -N- ( 4- ( trifluoro- methyl ) phenyl ) pyridin - 3 - amine ( Compound 20 ) : [ 297 ] ) .

FIF The title compound was synthesized following a procedure similar to Example C ( Compound [ 298 ] The title compound was purified by prep - HPLC ( Welch Xtimate C18 150 * 30mm * 5um ; mobile phase : [ water ( O₂H3HN + NH4HCO3 ) -ACN ] ; B % : 25 % -40 % , 8 min ) to provide the title compound ( 75 mg , 106 WO 2025/049495 PCT / US2024 / 0440 == 173.83 lomμ , 20.36 % yield ) . LCMS ( ESI ) , [ M + H ] + = 432.2 . [ 299 ] == Compound 20 : ' H NMR ( 400 MHz , CD3OD ) 8.51 ( d , J = 6.0 Hz , 1H ) , 8.23 ( s , 1H ) , 7.39 ( d , J 8.8 Hz , 2H ) , 7.30 - 7.27 ( m , 2H ) , 6.63 ( d , J = 8.8 Hz , 2H ) , 5.90 ( d , J = 2.0 Hz , 1H ) , 4.20 - 4.14 ( m , 1H ) , 3.86 ( s , 3H ) , 3.61 ( s , 3H ) , 3.22 - 3.19 ( m , 2H ) , 2.91 - 2.85 ( m , 2H ) , 2.14 - 2.10 ( m , 2H ) , 1.67 - 1.57 ( m , 2H ) . [ 300 ] Example U : ( R ) - ( 4 - ( ( 4 - Methoxypyridin - 3 - yl ) ( 4- ( trifluoromethyl ) phenyl ) amino ) piper- idin - 1 - yl ) ( tetrahydrofuran - 3 - yl ) methanone ( Compound 21 ) : ' N ' [ 301 ] F To a mixture of 4 - methoxy - N- ( 4 - piperidyl ) -N- [ 4- ( trifluoromethyl ) phenyl ] pyridin - 3 - amine ( 200 mg , 569.21 lomμ ) and ( 3R ) -tetrahydrofuran - 3 - carboxylic acid ( 66.09 mg , 569.21 lomμ ) in DMF ( mL ) was added DIEA ( 220.70 mg , 1.71 mmol ) and HATU ( 324.65 mg , 853.82 lomμ ) in one portion at 20 ° C . The mixture was stirred at 20 ° C for 1 hr . The reaction mixture was purified by pre - HPLC ( water ( NH3H2O + NH4HCO3 ) -ACN ] ; B % : 45 % -75 % , 7min ) to provide the title compound ( 45.9 mg , 102.12 lomµ , 17.94 % yield , 100 % purity ) . LCMS ( ESI ) , [ M + H ] + = 450.2 . [ 302 ] Compound 21 : ' H NMR ( 400 MHz , CDC13 ) 8 8.55 ( d , J = 5.6 Hz , 1H ) , 8.22 ( s , 1H ) , 7.39 ( d , J = 8.8 Hz , 2H ) , 6.99 ( d , J = 5.6 Hz , 1H ) , 6.52 ( d , J = 8.8 Hz , 2H ) , 4.77 - 4.73 ( m , 1H ) , 4.15 - 4.08 ( m , 1H ) , 4.04 - 3.97 ( m , 2H ) , 3.87 - 3.83 ( m , 3H ) , 3.81 ( s , 3H ) , 3.26 - 3.15 ( m , 2H ) , 2.69 - 2.64 ( m , 1H ) , 2.18 - 2.04 ( m , 4H ) , 1.78 - 1.73 ( m , 1H ) , 1.35 - 1.18 ( m , 2H ) . [ 303 ] Example V : 1- ( 4 - ( ( 4 - Ethoxypyridin - 3 - yl ) ( 4- ( trifluoromethyl ) phenyl ) amino ) -2 - methyl- piperidin - 1 - yl ) propan - 1 - one ( Compound 22 ) : N N CF[ 304 ] Step 1 : Tert - butyl - 4- [ N- ( 4 - ethoxy - 3 - pyridyl ) -4- ( trifluoromethyl ) anilino ] -2 - methyl - piper- 107 idine - 1 - carboxylate N N CF N Boc PCT / US2024 / 0440 [ 305 ] To a mixture of tert - butyl 4 - [ ( 4 - ethoxy - 3 - pyridyl ) amino ] -2 - methyl - piperidine - 1 - carboxylate ( 500 mg , 1.49 mmol ) and 1 - bromo - 4- ( trifluoromethyl ) benzene ( 670.78 mg , 2.98 mmol ) in toluene ( mL ) was added tBu3P Pd G2 ( 76.38 mg , 149.06 lomμ ) and tBuONa ( 429.73 mg , 4.47 mmol ) in one portion and the mixture was stirred at 120 ° C for 19 hr under N2 . The mixture was concentrated in vacuum and the residue was purified by silica flash chromatography ( 0 ~ 30 % Ethyl acetate in Petroleum ether ) to provide the title compound ( 600 mg , 1.25 mmol , 83.94 % yield ) . LCMS ( ESI ) , [ M + H ] + = 480.2 . [ 306 ] ' H NMR ( 400MHz , CD3CN ) 88.50 -8.45 ( m , 1H ) , 8.19 ( s , 1H ) , 7.40 ( d , J – 8.8 Hz , 2H ) , 7.- 7.04 ( m , 1H ) , 6.60 ( d , J = 8.8 Hz , 2H ) , 4.11 - 4.05 ( m , 2H ) , 3.83-3.84 ( m , 1H ) , 3.57- 3.54 ( m , 1H ) , 3.- 3.20 ( m , 1H ) , 2.90 - 2.78 ( m , 2H ) , 1.43 ( s . 9H ) , 1.23 - 1.16 ( m , 6H ) . [ 307 ] Step 2 : 4 - Ethoxy - N- ( 2 - methyl - 4 - piperidyl ) -N- [ 4- ( trifluoromethyl ) phenyl ] pyridin - 3 - amine N • N • CF NH [ 308 ] To a solution of tert - butyl 4- [ N- ( 4 - ethoxy - 3 - pyridyl ) -4- ( trifluoromethyl ) anilino ] -2 - methyl- piperidine - 1 - carboxylate ( 600 mg , 1.25 mmol ) in dioxane ( 2.0 mL ) was added HCl / dioxane ( 4 M , 1.61 mL ) and the mixture was stirred at 25 ° C for 1 hr . The reaction mixture was concentrated under reduced pressure to provide the title compound ( 520 mg , 1.25 mmol , 99.93 % yield , HCl salt ) as a yellow solid . LCMS ( ESI ) , [ M + H ] + = 380.1 . [ 309 ] Step 3 : 1- ( 4 - ( ( 4 - Ethoxypyridin - 3 - yl ) ( 4- ( trifluoromethyl ) phenyl ) amino ) -2 - methylpiper - idin - 1- yl ) propan - 1 - one ( Compound 22 ) : 108 N CF PCT / US2024 / 0440 [ 310 ] To a solution of 4 - ethoxy - N- ( 2 - methyl - 4 - piperidyl ) -N- [ 4- ( trifluoromethyl ) phenyl ] pyridin - 3- amine ( 500 mg , 1.32 mmol ) and Et3N ( 400.05 mg , 3.95 mmol ) in dichloromethane ( 3.0 mL ) at 0 ° C was added propanoyl chloride ( 182.89 mg , 1.98 mmol ) in dropwise . The mixture was stirred at 0 ° C for 1 hr . The mixture was concentrated in was concentrated in vacuum and the resulting residue was purified by pre- HPLC ( water ( 0.05 % FA ) -ACN , 35 % ~ 65 % ) to provide the title compound ( 280 mg , 623.68 lomµ , 47.33 % yield ) . LCMS ( ESI ) . [ M + H ] + = - 436.2 . [ 311 ] . Compound 22 : ' H NMR ( 400 MHz , CDCl3 ) 8 8.55 ( d , J = 5.6 Hz , 1H ) , 8.29 ( s , 1H ) , 8.15 ( s , 1H ) , 7.38 ( d , J = 8.8 Hz , 2H ) , 7.00 ( d , J = 5.6 Hz , 1H ) , 6.53 ( d , J = 8.8 Hz , 2H ) , 4.32 ( s , 1H ) , 4.16 - 4.( m , 3H ) , 3.86 ( s , 1H ) , 3.41 - 3.21 ( m , 1H ) , 2.47 -2.26 ( m , 3H ) , 2.14 - 2.10 ( m , 1H ) , 1.59 1.53 ( m , 1H ) , 1.51 1.39 ( m , 1H ) , 1.26 ( t , J = 7.2 Hz , 3H ) , 1.22 - 1.16 ( m , 6H ) . - - [ 312 ] Example W : 1- ( 4 - ( ( 4- ( Difluoromethoxy ) phenyl ) ( 4 - methoxypyridin - 3yl ) amino ) piperidin- - yl ) propan - 1 - one ( Compound 23 ) : ` N ° [ 313 ] ) . [ 314 ] The title compound was synthesized following a procedure similar to Example V ( Compound * The title compound was purified by pre - HPLC ( column : Welch Xtimate C18 150 * 30 mm 5um ; mobile phase : ( water ( 0.05 % FA ) -ACN , 20 % ~ 50 % , 8 min ) to provide the title compound ( 87.1 mg , 214.83 lomμ , 41.44 % yield , 100 % purity ) . LCMS ( ESI ) , [ M + H ] + = 406.1 . [ 315 ] – Compound 23 : ' H NMR ( 400 MHz , CDCl3 ) 8.50 ( d , J = 5.6 Hz , 1H ) , 8.25 -8.15 ( m , 1H ) , 6.98 6.91 ( m , 3H ) , 6.64 - 6.60 ( m , 1H ) , 6.57 ( s , 1H ) , 6.48 ( d , J = 8.8 Hz , 2H ) , 6.38 ( s , 1H ) , 4.74 - 4.- - ( m , 1H ) , 4.08 - 4.02 ( m , 1H ) , 3.98 - 3.86 ( m , 1H ) , 3.79 ( s , 3H ) , 3.16 - 3.09 ( m , 1H ) , 2.64 - 2.61 ( m , 1H ) , 109 WO 2025/049495 PCT / US2024 / 0440 2.38 2.25 ( m , 2H ) , 2.07 - 2.02 ( m , 2H ) , 1.38 - 1.19 ( m , 2H ) , 1.10 ( t , J = 7.6 Hz , 3H ) . [ 316 ] Example X : N- ( 4- ( Difluoromethoxy ) phenyl ) -4 - methoxy - N- ( 1- ( 5- ( methylsulfonyl ) pyr- imidin - 2 - yl ) piperidin - 4 - yl ) pyridin - 3 - amine ( Compound 24 ) : F [ 317 ] ) . [ 318 ] The title compound was synthesized following a procedure similar to Example L ( Compound The title compound was purified by prep - HPLC ( acetonitrile 26 - 35 % / 0.2 % formic acid in water ) to provide the title compound ( 172.4 mg , 334.20 lomμ , 42.98 % yield , 98 % purity ) . LCMS ( ESI ) , [ M + H ] + = 506.0 . [ 319 ] Compound 24 : ' H NMR ( 400 MHz , CDCl3 ) 8.66 ( s , 2H ) , 8.49 ( d , J = 5.6 Hz , 1H ) , 8.23 ( s , 1H ) , 7.00 -6.93 ( m , 3H ) , 6.58 ( s , 1H ) , 6.54 - 6.49 ( m , 2H ) , 6.41 - 6.18 ( m , 1H ) , 5.03 -4.99 ( m , 2H ) , 4.25 - 4.15 ( m , 1H ) , 3.80 ( s , 3H ) , 3.12 - 3.02 ( m , 5H ) , 2.16 - 2.13 ( m , 2H ) , 1.42 - 1.31 ( m , 2H ) . [ 320 ] Example Y : 2- ( 4 - ( ( 6- ( Difluoromethoxy ) pyridin - 3 - yl ) ( 4 - methoxypyridin - 3 - yl ) amino ) piperidin - 1 - yl ) pyrimidine - 5 - carbonitrile ( Compound 25 ) : F [ 321 ] Step 1 : Tert - butyl 4 - ( ( 6 - chloropyridin - 3 - yl ) ( 4 - methoxypyridin - 3 - yl ) amino ) piperidine - 1- carboxylate 110 ' N ' ` N- Boc PCT / US2024 / 0440 [ 322 ] A mixture of tert - butyl 4 - [ ( 4 - methoxy - 3 - pyridyl ) amino ] piperidine - 1 - carboxylate ( 4.0 g , 13.mmol ) , 5 - bromo - 2 - chloro - pyridine ( 5.01 g , 26.02 mmol ) , ( tBu ) P³ Pd G2 ( 666.78 mg , 1.30 mmol ) , and tBuONa ( 5.00 g , 52.04 mmol in toluene ( 20 mL ) was degassed and purged with N2 for 3 times , and then the mixture was stirred at 120 ° C for 12 hrs under N2 atmosphere . The reaction mixture was filtered and concentrated in vacuo . The residue was purified by silica flash chromatography ( 20 ~ 70 % Ethyl acetate in Petroleum ether ) to provide the title compound ( 4.0 g . 9.55 mmol , 73.39 % yield ) . LCMS ( ESI ) [ M + H ] + = 419.2 . = [ 323 ] carboxylate Step 2 : Tert - butyl 4 - ( ( 6 - hydroxypyridin - 3 - yl ) ( 4 - methoxypyridin - 3 - yl ) amino ) piperidine - 1- N.

N BOC ` N [ 324 ] OH To a solution of tert - butyl - 4 - [ ( 6 - chloro - 3 - pyridyl ) - ( 4 - methoxy - 3 - pyridyl ) amino ] piperi - dine - 1- carboxylate ( 2000 mg , 4.77 mmol ) in dioxane ( 20 mL ) and O₂H ( 4 mL ) was added ditert - butyl- [ 2,3,4,5- tetramethyl - 6- ( 2,4,6 - triisopropylphenyl ) phenyl ] phosphane ( 183.45 mg , 381.60 lomμ ) , ₂dP ( dba ) 3 ( 174.mg , 190.80 lomμ ) and KOH ( 1.07 g , 19.08 mmol ) . The reaction mixture was concentrated under reduced pressure to give the title compound ( 1.91 g , 3.86 mmol , 80.99 % yield , 81 % purity ) , crude used directly for next step . LCMS ( ESI ) [ M + H ] + = 401.2 . [ 325 ] .

Step 3 : Tert - butyl 4 - ( ( 6- ( difluoromethoxy ) pyridin - 3 - yl ) ( 4 - methoxypyridin - 3 - yl ) amino ) piperidine - 1 - carboxylate 111 N ` N F BOC PCT / US2024 / 0440 [ 326 ] A mixture of tert - butyl 4 - [ ( 6 - hydroxy - 3 - pyridyl ) - ( 4 - methoxy - 3 - pyridyl ) amino ] piperidine - 1- carboxylate ( 700 mg , 1.29 mmol , 74 % purity ) was dissolved in CH3CN ( 6 mL ) , KOH ( 6 M , 2.58 mL ) , difluoromethyl trifluoromethanesulfonate ( 776 mg , 3.88 mmol ) , and then the mixture was stirred at ° C for 0.03 hr . The reaction mixture was diluted with brine ( 20 mL ) and extracted with ethyl acetate ( mL x 3 ) . The combined organic layers was washed with brine , dried over Na2SO4 , filtered and concentrated under reduced pressure . The residue was purified by flash silica gel chromatography ( Eluent of 0-60 % Ethyl acetate / Petroleum ether ) and then purified by prep - TLC ( Petroleum ether / Ethyl acetate / ETOH = 4 / 3 / 1 ) to provide title compound ( 240 mg , 41 % yield ) . LCMS ( ESI ) [ M + H ] + = 451.1 . Step 4 : 6- ( Difluoromethoxy ) -N- ( 4 - methoxypyridin - 3 - yl ) -N- ( piperidin - 4 - yl ) pyridin - 3 - amine [ 327 ] hydrochloride F NH [ 328 ] To a solution of tert - butyl 4 - [ [ 6- ( difluoromethoxy ) -3 - pyridyl ] - ( 4 - methoxy - 3 - pyridyl ) amino ] piperidine - 1 - carboxylate ( 215.07 mg , 477.42 lomµ ) in dioxane ( 2 mL ) was added HCl / dioxane ( M , 2 mL ) at 25 ° C and the mixture was stirred at 25 ° C for 1 hr . The reaction was concentrated under reduced pressure to provide the title compound ( 184 mg , 475.67 lomµ , 99.63 % yield , HCl salt ) . LCMS ( ESI ) [ M + H ] + = 351.1 . [ 329 ] Step 5 : 2- ( 4 - ( ( 6- ( Difluoromethoxy ) pyridin - 3 - yl ) ( 4 - methoxypyridin - 3 - yl ) amino ) piperidin - 1- yl ) pyrimidine - 5 - carbonitrile ( Compound 25 ) : 112 WO 2025/049495 PCT / US2024 / 0440 F [ 330 ] A mixture of 6- ( difluoromethoxy ) -N- ( 4 - methoxy - 3 - pyridyl ) -N- ( 4 - piperidyl ) pyridin - 3 - aminc ( 40 mg , 103.41 lomμ , HCl salt ) , 2 - chloropyrimidine - 5 - carbonitrile ( 17.32 mg , 124.09 lomµ ) and DIEA ( 40.09 mg , 310.22 lomµ ) in DMF ( 2.0 mL ) and then the mixture was stirred at 0 ° C for 1 hr . The reaction mixture was diluted with water ( 10 ml ) and extracted with ethyl acetate ( 20 mL X 3 ) . The combined organic layers was washed with brine ( 30 mLX3 ) , dried over Na2SO4 , filtered and concentrated under reduced pressure to give the crude residue . The residue was purified by flash silica gel chromatography ( Eluent of 0-5 % methanol in dichloromethane ) to provide the title compound ( 34 mg , 72.73 lomμ , 70.34 % yield , 97 % purity ) . LCMS ( ESI ) [ M + H ] + = 454.1 . [ 331 ] = Compound 25 : ' HNMR ( 400 MHz , DMSO - do ) : 8.71 ( s , 2H ) , 8.46 ( d , J = 5.6 Hz , 1H ) , 8.( s , 1H ) , 7.54 ( s , 1H ) , 7.48 ( t , J = 74 Hz , 1H ) , 7.19 ( d , J = 5.6 Hz , 1H ) , 7.02 ( d , J = 3.2 Hz , 1H ) , 6.87 ( d , J = 8.8 Hz , 1H ) , 4.78 - 4.75 ( m , 2H ) , 4.34 - 4.28 ( m , 1H ) , 3.76 ( s , 3H ) , 3.19-3.14 ( m , 2H ) , 2.05-2.02 ( m , 2H ) , 1.17-1.14 ( m , 2H ) . [ 332 ] Example Z : 6- ( Difluoromethoxy ) -N- ( 4 - methoxypyridin - 3 - yl ) -N- ( 1- ( 5- ( methylsulfonyl ) pyrimidin - 2 - yl ) piperidin - 4 - yl ) pyridin - 3 - amine ( Compound 26 ) : F [ 333 ] ) . The title compound was synthesized following a procedure similar to Example Y ( Compound [ 334 ] The residue was purified by flash silica gel chromatography ( Eluent of 0 ~ 5 % methanol in 113 WO 2025/049495 PCT / US2024 / 0440 dichloromethane ) to provide the title compound ( 40 mg , 77.39 lomµ , 74.84 % yield ) . LCMS ( ESI ) [ M + H ] + = 507.1 . = [ 335 ] H¹ Compound 26 : ' H NMR ( 400 MHz , CDC13 ) 8.66 ( s , 2H ) , 8.49 ( d , J = 5.2 Hz , 1H ) , 8.25 ( s , = 1H ) , 7.58 ( s , 1H ) , 7.27 ( t , J = 75.2 Hz , 1H ) , 6.93 - 6.88 ( m , 2H ) , 6.74 ( d , J = 8.8 Hz , 1H ) , 5.03 -4.99 ( m , 2H ) , 4.15 - 4.09 ( m , 1H ) , 3.79 ( s , 3H ) , 3.09 - 3.03 ( m , 5H ) , 2.15 - 2.12 ( m , 2H ) , 1.42 - 1.34 ( m , 2H ) . [ 336 ] Example AA : N- ( 4- ( Difluoromethoxy ) phenyl ) -4 - methoxy - N- ( 1- ( 1 - methyl - 1H - pyrazol - 5- yl ) piperidin - 4 - yl ) pyridin - 3 - amine ( Compound 27 ) : [ 337 ] ) . [ 338 ] The title compound was synthesized following a procedure similar to Example C ( Compound The title compound was purified by prep - TLC ( ethanol : ethyl acetate : Petroleum ether = 1 : 3 : 4 ) to provide the title compound ( 41 mg , 92.60 lomµ , 16.18 % yield ) . LCMS ( ESI ) , [ M + H ] + = 430.2 . [ 339 ] - = Compound 27 : ' H NMR ( 400 MHz , CDC13 ) 8.53 ( d , J = 5.6 Hz , 1H ) , 8.30 ( s , 1H ) , 7.36 ( d , J = 2.0 Hz , 1H ) , 7.05 - 6.93 ( m , 3H ) , 6.59 ( s , 1H ) , 6.53 ( d , J = 9.2 Hz , 2H ) , 6.43 - 6.18 ( m , 1H ) , 5.80 ( d , J = 2.0 Hz , 1H ) , 4.01 - 3.92 ( m , 1H ) , 3.84 ( s , 3H ) , 3.66 ( s , 3H ) , 3.19 - 3.15 ( m , 2H ) , 2.86 - 2.74 ( m , 2H ) , 2.- 2.06 ( m , 2H ) , 1.58 - 1.55 ( m , 2H ) . [ 340 ] Example AB : ( 4 - ( ( 4- ( Difluoromethoxy ) phenyl ) ( 4 - methoxypyridin - 3 - yl ) amino ) piperidin- - yl ) ( pyridin - 4 - yl ) methanone ( Compound 28 ) : N [ 341 ] F The title compound was synthesized following a procedure similar to Example U ( Compound 114 WO 2025/049495 PCT / US2024 / 0440 21 ) . [ 342 ] The title compound was purified by prep - TLC ( 10 % methanol in dichloromethane ) to provide the title compound ( 129.8 mg , 285.61 lomµ , 66.52 % yield ) . LCMS ( ESI ) , [ M + H ] + = 455.2 . [ 343 ] = Compound 28 : ' H NMR ( 400 MHz , CD3OD ) 8 8.69 - 8.59 ( m , 2H ) , 8.46 ( d , J = 5.6 Hz , 1H ) , 8.18 ( s , 1H ) , 7.43 - 7.35 ( m , 2H ) , 7.22 ( d , J = 5.6 Hz , 1H ) , 7.00 -6.89 ( m , 2H ) , 6.80 - 6.39 ( m , 3H ) , 4.( d , J = 13.6 Hz , 1H ) , 4.3 . - 4.20 ( m , 1H ) , 3.83 ( s , 3H ) , 3.63 - 3.60 ( m , 1H ) , 3.39 - 3.34 ( m , 1H ) , 3.05 - 3.( m , 1H ) , 2.16 - 2.13 ( m , 1H ) , 2.05 - 1.93 ( m , 1H ) , 1.49 - 1.33 ( m , 2H ) . [ 344 ] Example AC : ( 4 - ( ( 4 - Methoxypyridin - 3 - yl ) ( 4- ( trifluoromethyl ) phenyl ) amino ) piperidin - 1- yl ) ( pyridin - 4 - yl ) methanone ( Compound 29 ) : -N- [ 345 ] ) . [ 346 ] CFThe title compound was synthesized following a procedure similar to Example U ( Compound The title compound was purified by prep - TLC ( 10 % methanol in dichloromethane ) to provide the title compound ( 135 mg . 295.75 lomμ , 69.28 % yield ) . LCMS ( ESI ) , [ M + H ] + = 457.2 . [ 347 ] Compound 29 : ' H NMR ( 400 MHz , CD3OD ) 8 8.63 ( d , J = 6.0 Hz , 2H ) , 8.51 ( d , J = 5.6 Hz , 1H ) , 8.20 ( s , 1H ) , 7.42 - 7.34 ( m , 4H ) , 7.26 ( d , J = 5.6 Hz , 1H ) , 6.64 ( d , J = 8.8 Hz , 2H ) , 4.73 - 4.69 ( m , 1H ) , 4.37 - 4.28 ( m , 1H ) , 3.85 ( s , 3H ) , 3.65 - 3.62 ( m , 1H ) , 3.40 - 3.34 ( m , 1H ) , 3.05 - 3.01 ( m , 1H ) , 2.19 - 2.16 ( m , 1H ) , 2.05 - 2.02 ( m , 1H ) , 1.42 - 1.31 ( m , 2H ) . [ 348 ] Example AD : 6- ( Difluoromethoxy ) -N- ( 4 - methoxypyridin - 3 - yl ) -N- ( 1- ( 1 - methyl - 1H- pyrazol - 5 - yl ) piperidin - 4 - yl ) pyridin - 3 - amine ( Compound 30 ) : - F WO 2025/049495 PCT / US2024 / 0440 [ 349 ] Step 1 : N- ( 1- ( 3 - Bromo - 1 - methyl - 4 - nitro - 1H - pyrazol - 5 - yl ) piperidin - 4 - yl ) -6- ( difluoromet- hoxy ) -N- ( 4 - methoxypyridin - 3 - yl ) pyridin - 3 - amine Br N₂O [ 350 ] A mixture of 6- ( difluoromethoxy ) -N- ( 4 - methoxy - 3 - pyridyl ) -N- ( 4 - piperidyl ) pyridin - 3 - amine ( 60 mg , 155.11 umol , HCl salt ) , 3,5 - dibromo - 1 - methyl - 4 - nitro - pyrazole ( 53.03 mg , 186.lomμ ) and DIEA ( 60.14 mg , 465.33 lomμ ) in CH3CN ( 2.0 mL ) and then the mixture was stirred at 80 ° C for 4 hr . The reaction mixture was concentrated under reduced pressure to give the crude residue and the residue was purified by flash silica gel chromatography ( 10 ~ 45 % ethyl acetate in petroleum ether ) to provide the title compound ( 56 mg , 101.02 lomµ ) . [ 351 ] Step 2 : N- ( 1- ( 4 - Amino - 3 - bromo - 1 - methyl - 1H - pyrazol - 5 - yl ) piperidin - 4 - yl ) -6- ( difluoro- methoxy ) -N- ( 4 - methoxypyridin - 3 - yl ) pyridin - 3 - amine Br N₂H N N ' ` N F [ 352 ] A solution of N- [ 1- ( 5 - bromo - 2 - methyl - 4 - nitro - pyrazol - 3 - yl ) -4 - piperidyl ] -6- ( difluoromethoxy ) -N- ( 4 - methoxy - 3 - pyridyl ) pyridin - 3 - amine ( 56 mg , 101.02 lomμ ) in EtOH ( mL ) and H2O ( 1 mL ) , NH4Cl ( 27.02 mg , 505.10 lomμ ) and Fe ( 28.21 mg , 505.10 lomμ ) were added in one portion and then the mixture was stirred at 80 ° C for 1 hr . The reaction mixture was cooled to room temperature and then filtered on a plug of kieselguhr and the filtrate was concentrated . The residue was diluted with ethyl acetate and the suspension was filtered . The filtrate was concentrated to provide the title compound ( 52 mg , 99.17 lomμ , 98.17 % yield ) ; it was used in next step without further purification . LCMS ( ESI ) [ M + H ] + = 513.9 . [ 353 ] Step 3 : N- ( 1- ( 3 - bromo - 1 - methyl - 1H - pyrazol - 5 - yl ) piperidin - 4 - yl ) -6- ( difluoromethoxy ) -N- ( 4- 116 methoxypyridin - 3 - yl ) pyridin - 3 - amine Br F PCT / US2024 / 0440 [ 354 ] To stirred solution of N- [ 1- ( 4 - amino - 5 - bromo - 2 - methyl - pyrazol - 3 - yl ) -4 - piperidyl ] -6- ( difluoromethoxy ) -N- ( 4 - methoxy - 3 - pyridyl ) pyridin - 3 - amine ( 52 mg , 99.17 lomμ ) in EtOH ( 6 mL ) at 0 ° C was added concentrated H2SO4 ( 103.67 mg , 1.06 mmol ) slowly . The reaction mixture was stirred at 0 ° C for 5 min and then NaNO2 ( 20.53 mg , 297.51 lomμµ ) in O₂H ( 0.4 mL ) was added dropwise . The reaction mixture was stirred at ice bath for 15 min and then heated to 100 ° C and stirred for 1 h . H3PO2 ( 128.90 mg , 991.68 lomμ , 50 % purity ) was added and the resulting reaction mixture was stirred at 0-100 ° C for 3 hr . The reaction mixture was diluted with water ( 20 ml ) and extracted with ethyl acetate ( 20 mLX3 ) . The combined organic layers was washed with brine ( 30 mLX3 ) , dried over Na2SO4 , filtered and concentrated under reduced pressure to give the crude residue . The residue was purified by flash silica gel chromatography ( Eluent of 25-45 % EE ( Ethanol / ethyl acetate ) in petroleum ether ) to provide the title compound ( 38 mg , 74.61 lomµ , 75.23 % yield ) was obtained as a white solid . LCMS ( ESI ) [ M + H ] + = 511.1 . [ 355 ] Step 4 : 6- ( Difluoromethoxy ) -N- ( 4 - methoxypyridin - 3 - yl ) -N- ( 1- ( 1 - methyl - 1H - pyrazol - 5- yl ) piperidin - 4 - yl ) pyridin - 3 - amine ( Compound 30 ) : F [ 356 ] A mixture of N- [ 1- ( 5 - bromo - 2 - methyl - pyrazol - 3 - yl ) -4 - piperidyl ] -6- ( difluoromethoxy ) -N- ( 4- methoxy - 3 - pyridyl ) pyridin - 3 - amine ( 38 mg , 74.61 lomμ ) and Pd / C ( 25 mg , 74.61 lomμ , 10 % purity ) in methanol ( 10 mL ) was degassed and purged with H2 for 3 times , and then the mixture was stirred at 28 ° C for 4 hr under ₂H ( 15 psi ) . The reaction mixture was filtered and the filter was concentrated . The crude product was purified by silica gel chromatography ( eluted with Petroleum ether / Ethyl acetate / ethanol = 4 : 3 : 1 , then purified by prep - TLC ) to provide the title compound ( 22 mg , 48.04 lomµ , 64.40 % 117 WO 2025/049495 PCT / US2024 / 0440 yield ) . LCMS ( ESI ) [ M + H ] + = 431.2 . [ 357 ] Compound 30 : ' H NMR ( 400 MHz , CDCl3 ) 8.54 ( d , J = 5.6 Hz „ , 1H ) , 8.32 ( s , 1H ) , 7.55 ( d , J = 3.2 Hz , 1H ) , 7.36 - 7.27 ( m , 2H ) , 6.96 ( d , J = 5.6 Hz , 1H ) , 6.88 ( d , J = 3.2 Hz , 1H ) , 6.73 ( d , J = 8.8 Hz , 1H ) , 5.79 ( s , 1H ) , 3.97 - 3.91 ( m , 1H ) , 3.81 ( s , 3H ) , 3.62 ( s , 3H ) , 3.19 - 3.16 ( m , 2H ) , 2.81 - 2.75 ( m , 12 ) , 2.08 2.05 ( m , 2H ) , 1.59 - 1.57 ( m , 2H ) . - [ 358 ] Example AE : ( 4 - Chlorophenyl ) ( 4 - ( ( 4- ( difluoromethoxy ) phenyl ) ( 4 - methoxypyridin - 3- yl ) amino ) piperidin - 1 - yl ) methanone ( Compound 31 ) : N F [ 359 ] ) . [ 360 ] The title compound was synthesized following a procedure similar to Example U ( Compound The title compound was purified by prep - HPLC ( column : Boston Prime C18 150 * 30mm * 5um ; mobile phase : [ water ( NH3H2O + NH4HCO3 ) -ACN ] ; B % : 50 % -80 % , 10 min ) to provide the title compound ( 125 mg , 255.16 lomμ , 44.57 % yield ) . LCMS ( ESI ) , [ M + H ] + = 488.0 . [ 361 ] Compound 31 : ' H NMR ( 400 MHz , CDCl3 ) 8 8.53 ( s , 1H ) , 8.24 ( s , 1H ) , 7.43 - 7.34 ( m , 2H ) , 7.33 7.28 ( m , 2H ) , 6.95 ( d , J = 9.2 Hz , 3H ) , 6.63 -6.17 ( m , 3H ) , 4.78 ( s , 1H ) , 4.17 - 4.03 ( m , 1H ) , 3.80 . ( s , 4H ) , 3.26-2.72 ( m , 2H ) , 2.14 - 2.02 ( m , 2H ) , 1.35- 1.30 ( m , 2H ) . - [ 362 ] Example AF : 4- ( 4 - ( ( 4- ( Difluoromethoxy ) phenyl ) ( 4 - methoxypyridin - 3 - yl ) amino ) piper- idine - 1 - carbonyl ) benzonitrile ( Compound 32 ) : [ 363 ] N N F The title compound was synthesized following a procedure similar to Example U ( Compound 118 WO 2025/049495 PCT / US2024 / 0440 21 ) . [ 364 ] The title compound was purified by prep - HPLC ( column : Boston Prime C18 150 * 30mm * 5um ; mobile phase : [ water ( NH3H2O + NH4HCO3 ) -ACN ] ; B % : 38 % -50 % , 10 min ) to provide the title compound ( 110 mg , 227.59 lomµ , 39.76 % yield ) . LCMS ( ESI ) , [ M + H ] + = 479.0 . [ 365 ] Compound 32 : ' H NMR ( 400 MHz , CDC13 ) 8 8.53 ( d , J = 4.8 Hz , 1H ) , 8.24 ( s , 1H ) , 7.70 ( d , . J = 8.0 Hz , 2H ) , 7.46 ( d , J = 8.0 Hz , 2H ) , 6.96 ( d , J = 9.2 Hz , 3H ) , 6.60 -6.18 ( m , 3H ) , 4.79 - 4.76 ( m , 1H ) , 4.13 - 4.07 ( m , 1H ) , 3.81 ( s , 3H ) , 3.75 -3.67 ( m , 1H ) , 3.20 - 3.16 ( m , 1H ) , 2.95 - 2.89 ( m , 1H ) , 2.22 - 1.93 ( m , 2H ) , 1.52 - 1.12 ( m , 2H ) . [ 366 ] Example AG : ( 4 - ( ( 4- ( Difluoromethoxy ) phenyl ) ( 4 - methoxypyridin - 3 - yl ) amino ) piperidin- - yl ) ( 4- ( methylsulfonyl ) phenyl ) methanone ( Compound 33 ) : F [ 367 ] ) . [ 368 ] The title compound was synthesized following a procedure similar to Example U ( Compound The title compound was purified by prep - HPLC ( column : Boston Prime C18 150 * 30mm * 5um ; mobile phase : [ water ( NH3H2O + NH4HCO3 ) -ACN ] ; B % : 44 % -74 % , 10 min ) to provide the title compound ( 130 mg , 242.11 lomµ , 42.29 % yield ) . LCMS ( ESI ) , [ M + H ] + = 532.0 . [ 369 ] Compound 33 : ' H NMR ( 400 MHz , CDCl3 ) 8 8.53 ( d , J = 5.2 Hz , 1H ) , 8.25 ( s , 1H ) , 7.99 ( d , J = 8.4 Hz , 2H ) , 7.54 ( d , J = 8.4 Hz , 2H ) , 6.96 ( d , J = 8.8 Hz , 3H ) , 6.61 - 6.19 ( m , 3H ) , 4.81 - 4.76 ( m , 1H ) , 4.15 -4.10 ( m , 1H ) , 3.81 ( s , 3H ) , 3.68 - 3.64 ( m , 1H ) , 3.19-3.07 ( m , 1H ) , 3.07 ( s , 3H ) , 2.93 - 2.89 ( m , 1H ) , 2.21 1.93 ( m , 2H ) , 1.52 - 1.21 ( m , 2H ) . - [ 370 ] Example AH : 6- ( 4 - ( ( 4- ( Difluoromethoxy ) phenyl ) ( 4 - methoxypyridin - 3 - yl ) amino ) piper- idin - 1 - yl ) nicotinonitrile ( Compound 34 ) : 119 ﻢﺤﻣﻭﺩ F.

PCT / US2024 / 0440 [ 371 ] ) . [ 372 ] The title compound was synthesized following a procedure similar to Example R ( Compound The title compound was purified by prep - HPLC ( column : Boston Prime C18 150 * 30mm * 5um ; mobile phase : [ water ( NH3H2O + NH4HCO3 ) -ACN ] ; B % : 55 % -85 % , 10 min ) to provide the title compound ( 104 mg , 223.45 lomμ , 39.03 % yield ) . LCMS ( ESI ) , [ M + H ] + = 452.0 . [ 373 ] Compound 34 : ' H NMR ( 400 MHz , CDC13 ) 8 8.53 ( d , J = 4.8 Hz , 1H ) , 8.24 ( s , 1H ) , 7.70 ( d , J = 8.0 Hz , 2H ) , 7.46 ( d , J = 8.0 Hz , 2H ) , 6.96 ( d , J = 9.2 Hz , 3H ) , 6.60 - 6.18 ( m , 3H ) , 4.81 - 4.76 ( s , 1H ) , 4.14 - 4.09 ( m , 1H ) , 3.81 ( s , 3H ) , 3.69 - 3.66 ( m , 1H ) , 3.21 - 3.18 ( m , 1H ) , 2.94 - 2.88 ( m , 1H ) , 2.22 - 1.( m , 2H ) , 1.52 - 1.12 ( m , 2H ) . [ 374 ] Example AI : Cyclobutyl ( 4 - ( ( 4- ( difluoromethoxy ) phenyl ) ( 4 - methoxypyridin - 3 - yl ) amino ) piperidin - 1 - yl ) methanone ( Compound 35 ) : N F [ 375 ] ) . [ 376 ] The title compound was synthesized following a procedure similar to Example U ( Compound The title compound was purified by prep - HPLC ( column : Boston Prime C18 150 * 30mm * 5um ; mobile phase : [ water ( NH3H2O + NH4HCO3 ) -ACN ] ; B % : 50 % -80 % , 10 min ) to provide the title compound ( 115.0 mg , 261.20 lomμ , 45.63 % yield ) . LCMS ( ESI ) , [ M + H ] + = 432.2 . [ 377 ] Compound 35 : ' H NMR ( 400 MHz , CD3OD ) 8 8.43 ( d , J = 5.6 Hz , 1H ) , 8.14 ( s , 1H ) , 7.19 ( d , J = 5.6 Hz , 1H ) , 6.93 ( d , J = 9.2 Hz , 2H ) , 6.79 - 6.39 ( m , 3H ) , 4.57 - 4.46 ( m , 120 WO 2025/049495 PCT / US2024 / 0440 [ 378 ] 1H ) , 4.22-4.13 ( m , 1H ) , 3.91 3.77 ( m , 4H ) , 3.41 3.33 ( m , 1H ) , 3.223.08 ( m , 1H ) , 2.78- - 2.70 ( m , 1H ) , 2.23 - 1.92 ( m , 7H ) , 1.86 - 1.72 ( m , 1H ) , 1.28 - 1.08 ( m , 2H ) . [ 379 ] Example AJ : Cyclobutyl ( 4 - ( ( 4 - methoxypyridin - 3 - yl ) ( 4- ( trifluoromethyl ) phenyl ) amino ) piperidin - 1 - yl ) methanone ( Compound 36 ) : N F [ 380 ] The title compound was synthesized following a procedure similar to Example U ( Compound ) . [ 381 ] The title compound was purified by prep - HPLC ( column : Boston Prime C18 150 * 30mm * 5um ; mobile phase : [ water ( NH3H2O + NH4HCO3 ) -ACN ] ; B % : 50 % -80 % , 10 min ) to provide the title compound ( 131.8 mg , 304.06 lomμ , 53.42 % yield ) . LCMS ( ESI ) , [ M + H ] + = 434.1 . [ 382 ] Compound 36 : ' H NMR ( 400 MHz , CD3OD ) 8 8.56 - 8.44 ( m , 1H ) , 8.25 -8.12 ( m , 1H ) , 7.( d , J = 8.8 Hz , 2H ) , 7.30 - 7.21 ( m , 1H ) , 6.70 - 6.57 ( m , 2H ) , 4.63 - 4.54 ( m , 1H ) , 4.36 - 4.26 ( m , 1H ) , 3.- 3.89 ( M , 1H ) , 3.86 ( s , 3H ) , 3.44 - 3.36 ( m , 1H ) , 3.25 - 3.12 ( m , 1H ) , 2.83 - 2.72 ( m , 1H ) , 2.29 - 2.05 ( m , 6H ) , 2.03 - 1.91 ( m , 1H ) , 1.87 - 1.74 ( m , 1H ) , 1.32 - 1.14 ( m , 2H ) . [ 383 ] Example AK : ( 4 - Fluoro - 2- ( methylsulfonyl ) phenyl ) ( 4 - ( ( 4 - methoxypyridin - 3 - yl ) ( 4- ( tri- fluoromethyl ) phenyl ) amino ) piperidin - 1 - yl ) methanone ( Compound 37 ) : [ 384 ] N HC₂OS • N • F Step 1 : Preparation of tert - Butyl 4 - ( ( 4 - methoxypyridin - 3 - yl ) amino ) piperidine - 1 - carboxylate : NBoc WO 2025/049495 PCT / US2024 / 0440 [ 385 ] To a stirred solution of tert - Butyl 4 - oxopiperidine - 1 - carboxylate ( 12.03 g , 60.41 mmol , 1.eq . ) in anhydrous Dichloromethane ( 75 mL ) was added 4 - Methoxypyridin - 3 - amine ( 5.0 g , 40.27 mmol , 1.eq ) , Acetic acid ( 2.53 mL , 44.30 mmol , 1.1 eq ) and Sodium triacetoxyborohydride ( 12.80 g , 60.41 mmol , 1.5 eq ) sequentially at room temperature . The resulted reaction mixture was stirred at reflux for 20 h . The progress of the reaction was monitored by TLC and UPLC - MS which indicated product formation along with complete consumption of starting materials . Then , the reaction mixture was cooled to room temperature and adjusted the pH up to ~ 8 with 2M aqueous sodium hydroxide solution ( 100 mL ) and extracted with Dichloromethane ( 2 × 200 mL ) . The combined organic layers were dried over anhydrous Na2SO4 , filtered the drying agent and concentrated the solution under reduced pressure to obtain crude residue . The crude material was purified by combi flash chromatography using silica gel by eluted with EtOAc and pure fractions are concentrated under reduced pressure to afford tert - Butyl 4 - ( ( 4- methoxypyridin - 3 - yl ) amino ) piperidine - 1 - carboxylate ( 7.80 g , 63 % ) . MS ( ESI ) : mass calculated for C16H25N3O3 , 307.39 ; m / z found , 308.2 [ M + H ] * . [ 386 ] ' H NMR ( 400 MHz , CDCl3 ) 87.88 ( s , 1H ) , 7.76 ( d , J = 5.2 Hz , 1H ) , 6.83 ( d , J = 5.2 Hz , 1H ) , 4.61 ( d , J = 8.4 Hz , 1H ) , 3.90 ( d , J = 12.4 Hz , 2H ) , 3.82 ( s , 3H ) , 3.50 ( br s , 1H ) , 2.86 ( br s , 2H ) , 1.90 - 1.( m , 2H ) , 1.40 ( s , 9H ) , 1.34 -1.26 ( m , 2H ) . [ 387 ] Step 2 : Preparation of tert - Butyl 4 - ( ( 4 - methoxypyridin - 3 - yl ) ( 4- ( trifluoromethyl ) phenyl ) amino ) piperidine - 1 - carboxylate : N ' N ' NBoc [ 388 ] F F The sealed tube was charged with tert - Butyl 4 - ( ( 4 - methoxypyridin - 3 - yl ) amino ) piperidine - 1- carboxylate ( 7.80 g , 25.37 mmol , 1.0 eq ) , 1 - Bromo - 4- ( trifluoromethyl ) benzene ( 5.71 g , 25.37 mmol , 1.eq ) , Sodium tert - butoxide ( 4.80 g , 50.74 mmol , 2.0 eq ) and toluene ( 150 mL ) at room temperature under argon atmosphere . The resulting mixture was degassed using argon balloon for 10 min , then added Ruphos- Pd - G3 ( 1.06 g , 1.26 mmol , 0.05 eq ) under argon . Then , sealed the tube and stirred for 16 h at 120 ° C . The reaction was monitored by TLC and UPLC - MS which indicated product formation . The reaction mixture was cooled to room temperature , passed through a pad of celite . The filtrate was concentrated under reduced pressure to obtain crude material . The obtained crude material was purified by combi flash chromatography using silica gel by eluted with 80 % EtOAc in hexanes and pure fractions were concentrated under reduced pressure to afford tert - Butyl 4 - ( ( 4 - methoxypyridin - 3 - yl ) ( 4- ( trifluoromethyl ) phenyl ) amino ) piperidine - 1- 122 WO 2025/049495 PCT / US2024 / 0440 carboxylate ( 5 , 4.40 g , 38 % ) . MS ( ESI ) : mass calculated for C23H28F3N3O3 , 451.49 ; m / z found , 452.[ M + H ] + . [ 389 ] = ' H NMR ( 400 MHz , CDCl3 ) 8 8.54 ( d , J = 5.6 Hz , 1H ) , 8.21 ( s , 1H ) , 7.36 ( d , J = 8.8 Hz , 2H ) , 6.96 ( d , J = 6.0 Hz , 1H ) , 6.47 ( d , J = 8.8 Hz , 2H ) , 4.18 ( br s , 2H ) , 4.06 - 3.97 ( tt , J = 11.6 Hz , J = 3.6 Hz , IH ) , 3.79 ( s , 3H ) , 2.81 ( m , 2H ) , 1.32 -1.25 ( td , J = 12.4 Hz , J = 4.0 Hz , 2H ) , 1.42 ( s , 9H ) , 1.32 - 1.25 ( td , J = 12.4 Hz . J = 4.0 Hz , 2H ) . [ 390 ] Step 3 : Preparation of 4 - Methoxy - N- ( piperidin - 4 - yl ) -N- ( 4- ( trifluoromethyl ) phenyl ) pyri - din - 3- amine hydrochloride : N • N • NH [ 391 ] F F To a solution of tert - Butyl 4 - ( ( 4 - methoxypyridin - 3 - yl ) ( 4- ( trifluoromethyl ) phenyl ) amino ) piperidine - 1 - carboxylate ( 4.40 g , 9.74 mmol , 1.0 eq ) in 2,2,2 - Trifluoroethanol ( 25.0 mL ) at 0 ° C was added Chlorotrimethylsilane ( 6.80 mL ) dropwise and stirred at room temperature for 1 h . The progress of the reaction was monitored by TLC which showed complete consumption of starting material . The volatiles were removed under reduced pressure to obtain the crude material . Trituration of crude product using Acetonitrile ( 10.0 mL ) to afford 4 - Methoxy - N- ( piperidin - 4 - yl ) -N- ( 4- ( trifluoromethyl ) phenyl ) pyridin - 3 - amine hydrochloride ( 3.10 g ( crude ) ) . MS ( ESI ) : mass calculated for C18H20F3N30 , 351.16 ; m / z found , 352.1 [ M + H ] * . [ 392 ] ' H NMR ( 400 MHz , DMSO - do ) 89.11 ( d , J = 8.8 Hz , 1H ) , 8.92 - 8.90 ( m , 2H ) , 8.74 ( s , 1H ) , 7.79 ( d , J = 6.4 Hz , 1H ) , 7.46 ( d , J = 8.4 Hz , 2H ) , 6.78 ( d , J = 8.4 Hz , 2H ) , 4.43 ( t , J = 11.6 Hz , 1H ) , 4.( s , 3H ) , 3.25 ( d , J = 12.0 Hz , 2H ) , 3.11 - 3.02 ( m , 2H ) , 2.03 ( d , J = 12.8 Hz , 2H ) , 1.68 - 1.59 ( m , 2H ) . [ 393 ] Step 4 : Preparation of 4 - Fluoro - 2- ( methylsulfonyl ) benzoic acid ( 7 ) H₂OC F SO2CH[ 394 ] To a solution of 2 - Bromo - 4 - fluorobenzoic acid ( 0.25 g , 1.14 mmol , 1.0 eq ) in Dimethyl sulfoxide ( 15.0 mL ) was added Sodium methanesulfonate ( 0.47 g , 3.99 mmol , 3.5 eq ) , CuI ( 0.86 g , 4.mmol , 4.0 eq ) and Sodium hydroxide ( 5N in O₂H , 0.22 mL , 1.14 mmol , 1.0 eq ) at room temperature and stirred at 120 ° C for 2 h . The progress of the reaction was monitored by TLC which showed complete consumption of starting material . The reaction mixture was cooled to room temperature , diluted with water 123 WO 2025/049495 PCT / US2024 / 0440 ( 20.0 mL ) and washed with EtOAc ( 2 × 10 mL ) . The aqueous layer was acidified with 2N aq . HCl solution ( 2.0 mL ) and extracted with EtOAc ( 2 × 20 mL ) . The combined organic layers were dried over anhydrous Na2SO4 , filtered the drying agent and concentrated the solution under reduced pressure to obtain 4 - Fluoro- 2- ( methylsulfonyl ) benzoic acid ( 0.15 g , Crude ) . MS ( ESI ) : mass calculated for C3H7FO4S , 218.00 ; m / z found , 216.98 [ M - H ] . [ 395 ] [ 396 ] ' H NMR ( 400 MHz , DMSO - d6 ) 8 7.93 - 788 ( m , 2H ) , 7.40 -7.37 ( m , 1H ) , 3.44 ( s , 3H ) . Step 5 : Preparation of ( 4 - Fluoro - 2- ( methylsulfonyl ) phenyl ) ( 4 - ( ( 4 - methoxypyridin - 3 - yl ) ( 4- ( trifluoromethyl ) phenyl ) amino ) piperidin - 1 - yl ) methanone ( Compound 37 ) : HC₂OS 20N F F [ 397 ] To a stirred solution of 4 - Methoxy - N- ( piperidin - 4 - yl ) -N- ( 4- ( trifluoromethyl ) phenyl ) pyridin- - amine hydrochloride ( 0.10 g , 0.25 mmol , 1.0 eq . ) and 4 - Fluoro - 2- ( methylsulfonyl ) benzoic acid ( 0.06 g , 0.30 mmol , 1.2 eq . ) in N.N - Dimethylformamide ( 2.0 mL ) was added Diisopropylethylamine ( 0.17 mL , 1.mmol , 4.0 eq . ) and 1- [ Bis ( dimethylamino ) methylene ] -1H - 1,2,3 - triazolo [ 4,5 - b ] pyridinium 3- oxidehexafluorophosphate ( HATU , 0.11 g , 0.30 mmol , 1.2 eq . ) at 0 ° C . Then , the resulted reaction mixture was stirred at room temperature for 8 h . The progress of the reaction was monitored by TLC and UPLC- MS which indicated the product formation along with complete consumption of starting materials . The reaction mixture was poured into ice cold water ( 5.0 mL ) . The obtained solid was collected by filtration , the solid cake was washed with excess cold water ( 5.0 mL ) and dried under vacuum to afford ( 4 - Fluoro - 2- ( methylsulfonyl ) phenyl ) ( 4 - ( ( 4 - methoxypyridin - 3 - yl ) ( 4- ( trifluoromethyl ) phenyl ) amino ) piperidin - 1- yl ) methanone ( 0.14 g , 66 % yield ) . MS ( ESI ) : mass calculated for C26H25F4N3O4S , 551.15 ; m / z found , 552.[ M + H ] + , HPLC purity : 95.77 % [ 398 ] Compound 37 : H¹ NMR ( 400 MHz , CDC13 ) of rotamers 8 8.53 ( dd , J = 18.0 Hz , J = 5.6 Hz , 1H ) , 8.17 ( d , J = 38.4 Hz , 1H ) , 7.74 - 7.60 ( m , 2H ) , 7.59 - 7.53 ( m , 1H ) , 7.40 ( d , J = 8.8 Hz , 2H ) , 7.25 ( dd , J = 16.8 Hz , J = 6.0 Hz , 1H ) , 6.62 - 6.57 ( m , 2H ) , 4.59 - 4.46 ( m , 1H ) , 4.33 - 4.24 ( dd , J = 24.0 Hz , J = 11.6 Hz , 1H ) , 3.76 ( d , J = 14.8 Hz , 3H ) , 3.26 ( d , J = 7.6 Hz , 3H ) , 3.25 -3.09 ( m , 2H ) , 2.99 - 2.86 ( m , 1H ) , 2.06 1.94 ( m , 2H ) , 1.85 - 1.68 ( d , J = 56.0 Hz , J = 12.0 Hz 1H ) , 1.48- 1.23 ( m , 2H ) . [ 399 ] - Example AL : N- ( 4- ( Difluoromethoxy ) phenyl ) -4 - methoxy - N- ( 1- ( 4- ( methylsulfonyl ) phenyl ) piperidin - 4 - yl ) pyridin - 3 - amine ( Compound 38 ) : 124 N HC₂OS PCT / US2024 / 0440 [ 400 ] OCHFStep 1 : Preparation of tert - Butyl 4 - ( ( 4- ( difluoromethoxy ) phenyl ) ( 4 - methoxypyridin - 3- yl ) amino ) piperidine - 1 - carboxylate : NBoc [ 401 ] OCHFThe sealed tube charged with tert - Butyl 4 - ( ( 4 - methoxypyridin - 3 - yl ) amino ) piperidine - 1- carboxylate ( 1.50 g , 4.88 mmol , 1.0 eq . ) , 1 - Bromo - 4- ( difluoromethoxy ) benzene ( 1.30 g , 5.86 mmol , 1.cq ) , Sodium tert - butoxide ( 0.93 g , 9.76 mmol , 2.0 cq ) and toluene ( 30.0 mL ) at room temperature under argon atmosphere . The resulting mixture was degassed by argon purging for 10 min , then added P ( 1 - Bu ) Pd - G2 ( 0.15 g , 0.29 mmol , 0.05 eq ) . Then sealed the cap and stirred at 120 ° C for 16 h . The reaction was monitored by UPLC which showed product formation . The reaction mixture was cooled to room temperature , passed through a pad of celite . The filtrate was concentrated under reduced pressure to obtain crude material . The obtained crude material was purified by combi flash chromatography using silica gel by eluted with 60 % EtOAc in hexanes , pure fractions were concentrated under reduced pressure to afford tert - Butyl 4 - ( ( 4- ( difluoromethoxy ) phenyl ) ( 4 - methoxypyridin - 3 - yl ) amino ) piperidine - 1 - carboxylate ( 0.g , 17 % yield ) . MS ( ESI ) : mass calculated for C23H29F2N3O4 , 449.21 ; m / z found , 450.2 [ M + H ] * . [ 402 ] ' H NMR ( 400 MHz , DMSO - d6 ) 8 8.48 ( d , J = 5.6 Hz , 1H ) , 8.15 ( s , 1H ) , 7.21 ( d , J = 7.2 Hz , 1H ) , 7.16 - 6.97 ( t , J = 75 Hz , 1H ) , 6.96 - 6.93 ( d , J = 9.2 Hz , 2H ) , 6.45 ( d , J = 9.2 Hz , 2H ) , 4.09 - 4.05 ( m , IH ) , 3.93 ( br s , 2H ) , 3.76 ( s , 3H ) , 2.86 ( br s , 2H ) , 1.88 ( d , J = 12.0 Hz , 2H ) , 1.33 ( s , 9H ) , 1.10 1.08 ( m , 2H ) . [ 403 ] Step 2 : Preparation of N- ( 4- ( Difluoromethoxy ) phenyl ) -4 - methoxy - N- ( piperidin - 4 - yl ) pyridin- - amine hydrochloride ( 11 ) 125 ` N · NH OCHF PCT / US2024 / 0440 [ 404 ] To a solution of tert - Butyl 4 - ( ( 4- ( difluoromethoxy ) phenyl ) ( 4 - methoxypyridin - 3 - yl ) amino ) piperidine - 1 - carboxylate ( 0.40 g , 0.89 mmol , 1.0 eq , ) in 2,2,2 - Trifluoroethanol ( 3.0 mL ) was added Chlorotrimethylsilane ( 0.70 mL ) dropwise at 0 ° C . Then , the reaction mixture was stirred for 1 h at room temperature . The volatiles were removed under reduced pressure to obtain the crude material . The obtained crude material was triturated with Acetonitrile ( 10.0 mL ) to afford N- ( 4- ( Difluoromethoxy ) phenyl ) -4- methoxy - N- ( piperidin - 4 - yl ) pyridin - 3 - amine hydrochloride ( crude , 0.25 g ) . MS ( ESI ) : mass calculated for C18H21F2N3O2 , 349.16 ; m / z found , 350.1 [ M + H ] * [ 405 ] ' H NMR ( 400 MHz , DMSO - do ) 8 9.14 ( d , J = 9.2 Hz , 1H ) , 8.84 - 8.82 ( m , 2H ) , 8.69 ( s , 1H ) , 7.73 ( d , J = 6.8 Hz , 1H ) , 7.25 - 6.88 ( t , J = 75 Hz , 1H ) , 7.01 ( d , J = 9.2 Hz , 2H ) , 6.74 ( d , J = 12 Hz , 2H ) , - 4.31 4.25 ( m , 1H ) , 3.97 ( s , 3H ) , 3.25 ( d , J = 12 Hz , 2H ) , 3.08 -2.99 ( m , 2H ) , 2.01 ( d , J = 12.4 Hz , 2H ) , 1.67 1.58 ( m , 2H ) . [ 406 ] Step 3 : Preparation of N- ( 4- ( Difluoromethoxy ) phenyl ) -4 - methoxy - N- ( 1- ( 4- ( methylsulfonyl ) phenyl ) piperidin - 4 - yl ) pyridin - 3 - amine ( Compound 38 ) N 3HC₂OS N [ 407 ] OCHFThe sealed tube was charged with N- ( 4- ( Difluoromethoxy ) phenyl ) -4 - methoxy - N- ( piperidin - 4- yl ) pyridin - 3 - amine hydrochloride ( 0.21 g , 0.54 mmol , 1.0 eq , ) , 1 - Bromo - 4- ( methylsulfonyl ) benzene ( 0.g , 0.81 mmol , 1.5 eq ) , Sodium tert - butoxide ( 0.15 g , 1.62 mmol , 3.0 eq ) and dry 1,4 - dioxane ( 10.0 mL ) at room temperature under argon atmosphere . The reaction mixture was degassed with argon for 10 min , then added Ruphos - Pd - G3 ( 0.02 g . 0.027 mmol , 0.05 eq ) under argon . Sealed the tube with cap and stirred at 110 ° C for 16 h . The reaction mixture was cooled to room temperature , passed through a pad of celite and the filtrate was concentrated under reduced pressure to obtain crude material . The obtained crude material was purified by combi flash chromatography using silica gel by eluted with 60 % EtOAc in hexanes to afford N- ( 4- ( Difluoromethoxy ) phenyl ) -4 - methoxy - N- ( 1- ( 4- ( methylsulfonyl ) phenyl ) piperidin - 4 - yl ) pyri- 126 WO 2025/049495 PCT / US2024 / 0440 din - 3 - amine ( 0.08 g . 22 % yield ) . MS ( ESI ) : mass calculated for C25H27F2N3O4S , 503.56 ; m / z found , 504.[ M + H ] * , HPLC purity : 98.27 % . [ 408 ] Compound 38 : ' H NMR ( 400 MHz , DMSO - do ) 8 8.46 ( d , J = 5.6 Hz , 1H ) , 8.16 ( s , 1H ) , 7.( d , J = 9.2 Hz , 2 H ) , 7.20 ( d , J = 5.6 Hz , 1H ) , 7.17 ( t , J = 75 Hz , 1H ) , 7.02 - 7.00 ( d , J = 9.2 Hz , 2H ) , 6.- 6.94 ( d , J = 9.2 Hz , 2H ) , 6.49 ( d , J = 9.2 Hz , 2H ) , 4.20 -4.14 ( m , 1H ) , 3.97 ( d , J = 13.2 Hz , 2H ) , 3.75 ( s , 3H ) , 3.02 2.99 ( m , 5H ) , 1.98 ( d , J = 11.6 Hz , 2H ) , 1.29 - 1.21 ( m , 2H ) . [ 409 ] Example AM : N- ( 1- ( 5- ( Difluoromethyl ) pyridin - 2 - yl ) piperidin - 4 - yl ) -4 - methoxy - N- ( 4- ( trifluoromethyl ) phenyl ) pyridin - 3 - amine ( Compound 39 ) : CF2H [ 410 ] The microwave tube was charged with 4 - Methoxy - N- ( piperidin - 4 - yl ) -N- ( 4- ( trifluoromethyl ) phenyl ) pyridin - 3 - amine hydrogen chloride ( 0.60 g , 1.54 mmol , 1.0 eq ) , 2 - Chloro - 5- ( difluoromethyl ) pyridine ( 0.25 g , 1.54 mmol , 1.3 eq ) , Sodium tert - butoxide ( 0.297 g , 3.09 mmol , 2.0 eq ) and Toluene ( 5.0 mL ) at room temperature under argon atmosphere . Then , the resulting mixture was degassed with argon for 10 min , added Ruphos - Pd - G3 ( 0.06 g , 0.077 mmol , 0.05 eq ) under argon . Sealed the microwave tube with cap and stirred at 130 ° C under microwave for 2 h . The progress of the reaction was monitored by TLC and complete consumption of starting material was observed . The reaction mixture was cooled to room temperature , passed through a pad of celite and the filtrate was concentrated under reduced pressure to obtain crude material . The obtained crude material was purified by combi flash chromatography using silica gel by eluted with 100 % EtOAc in hexanes to afford N- ( 1- ( 5- ( Difluoromethyl ) pyridin - 2 - yl ) piperidin - 4 - yl ) -4 - methoxy - N- ( 4- ( trifluoromethyl ) phenyl ) pyridin - 3 - amine ( 0.23 g , 31 % yield ) . MS ( ESI ) : mass calculated for C24H23F5N40 , 478.47 ; m / z found , 479.3 [ M + H ] + , HPLC purity : 95.15 % . [ 411 ] Compound 39 : ' H NMR ( 400 MHz , DMSO - d6 ) 8 8.49 ( d , J = 5.6 Hz , 1H ) , 8.20 ( d , J = 8.Hz , 1H ) , 8.18 ( s , 1H ) , 7.61 ( dd , J = 9.2 Hz , J = 2.4 Hz , 1H ) , 7.42 ( d , J = 8.8 Hz , 2H ) , 7.23 ( d , J = 5.6 Hz , IH ) , 7.06 - 6.74 ( t , J = 50 Hz , 1H ) , 6.89 - 6.87 ( m , 1H ) , 6.61 ( d , J = 8.8 Hz , 2H ) , 4.44 ( d , J = 13.6 Hz , 2H ) , 4.36 4.31 ( m , 1H ) , 3.76 ( s , 3H ) , 3.07 - 3.01 ( m , 2H ) , 2.10 ( d , J = 12.0 Hz , 2H ) , 1.23 - 1.16 ( m , 2H ) . - [ 412 ] Example AN : 6- ( 4 - ( ( 4 - Methoxypyridin - 3 - yl ) ( 4- ( trifluoromethyl ) phenyl ) amino ) piperidin- 127 1 - yl ) -1 - methylpyridin - 2 ( 1H ) -one ( Compound 40 ) : [ 413 ] ' N ' ' N ' Step 1 : Preparation of 6 - bromo - 1 - methylpyridin - 2 ( 1H ) -one PCT / US2024 / 0440 [ 414 ] Br To a solution of 6 - bromopyridin - 2 - ol ( 0.25 g , 1.43 mmol , 1.0 eq ) in N , N- Dimethylformamide ( 5.0 mL ) was added K2CO3 ( 0.99 g , 7.18 mmol , 5.0 eq ) , I³HC ( 0.44 mL , 7.18 mmol , 5.0 eq ) at room temperature . Then the reaction mixture was stirred at room temperature for 18 h . The progress of the reaction was monitored by TLC which showed complete consumption of starting material . The reaction mixture was quenched with water ( 5.0 mL ) and extracted with EtOAc ( 2 × 10 mL ) . The combined organic layers were dried over anhydrous Na2SO4 , filtered the drying agent and concentrated the solution under reduced pressure to obtain crude material . The obtained crude material was purified by combi flash chromatography using silica gel by eluted with 30-35 % EtOAc in hexanes , pure fractions were concentrated under reduced pressure to afford 6 - bromo - 1 - methylpyridin - 2 ( 1H ) -one ( 0.23 g . 31 % yield ) . [ 415 ] ' H NMR ( 400 MHz , CDC13 ) 8 7.16 - 7.12 ( dd , J = 9.2 Hz , J = 7.2 Hz , 1H ) , 6.53 - 6.48 ( m , 2H ) , 6.68 ( d , J = 8.0 Hz , 1H ) . 3.74 ( s , 3H ) . [ 416 ] Step 2 : Preparation of 6- ( 4 - ( ( 4 - Methoxypyridin - 3 - yl ) ( 4- ( trifluoromethyl ) phenyl ) amino ) piperidin - 1 - yl ) -1 - methylpyridin - 2 ( 1H ) -one ( Compound 40 ) : [ 417 ] The microwave tube was charged with 4 - Methoxy - N- ( piperidin - 4 - yl ) -N- ( 4- 128 WO 2025/049495 PCT / US2024 / 0440 ( trifluoromethyl ) phenyl ) pyridin - 3 - amine hydrochloride ( 0.15 g , 0.38 mmol , 1.0 eq Curia lot # IN - NRM- G - 39 ) , 6 - Bromo - 1 - methylpyridin - 2 ( 1H ) -one ( 0.07 g , 0.42 mmol , 1.1 eq ) , Sodium tert - butoxide ( 0.11 g , 1.15 mmol , 3.0 eq ) and dry Toluene ( 3.0 mL ) at room temperature under argon atmosphere . The resulting mixture was degassed with argon for 10 min , added Ruphos - Pd - G3 ( 0.016 g , 0.01 mmol , 0.05 eq ) under argon . The microwave tube was sealed with cap and stirred at 120 ° C under microwave for 2 h . The progress of the reaction was monitored by TLC & UPLC - MS which showed product formation . The reaction mixture was cooled to room temperature , passed through a pad of celite and the filtrate was concentrated under reduced pressure to obtain crude material . The obtained crude material was purified by combi flash chromatography using silica gel by eluted with 4 % MeOH in CH2Cl2 , the pure fractions were concentrated under reduced pressure to afford 6- ( 4 - ( ( 4 - Methoxypyridin - 3 - yl ) ( 4- ( trifluoromethyl ) phenyl ) amino ) piperidin - 1 - yl ) -1 - methylpyridin - 2 ( 1H ) -one ( 0.15 g , 51 % yield ) . MS ( ESI ) : mass calculated for C24H25F3N402 , 458.49 ; m / z found , 459.2 [ M + H ] * . HPLC purity : 99.73 % . [ 418 ] Compound 40 : ' H NMR ( 400 MHz , DMSO - do ) 8 8.55 ( d , J = 5.6 Hz , 1H ) , 8.26 ( s , 1H ) , 7.( d , J = 8.8 Hz , 2H ) , 7.35 - 7.28 ( m , 2H ) , 6.60 ( d , J = 8.8 Hz , 2H ) , 6.08 ( d , J = 8.4 Hz , 1H ) , 5.83 - 5.81 ( m , 1H ) , 4.224.16 ( m , 1H ) , 3.80 ( s , 3H ) , 3.27 ( s , 3H ) , 3.16 ( d , J = 12.0 Hz , 2H ) , 2.83 ( t , J = 11.6 Hz , 2H ) , 2.03 ( d , J = 12.0 Hz , 2H ) , 1.47 - 1.39 ( m , 2H ) . [ 419 ] Example AO : Bicyclo [ 1.1.1 ] pentan - 1 - yl ( 4 - ( ( 4- ( difluoromethoxy ) phenyl ) ( 4 - methoxy- pyridin - 3 - yl ) amino ) piperidin - 1 - yl ) methanone ( Compound 41 ) : F [ 420 ] ) . The title compound was synthesized following a procedure similar to Example U ( Compound [ 421 ] The title compound was purified by prep - HPLC ( column : Welch Xtimate C150 * 30mm * 5um ; mobile phase : [ water ( FA ) -ACN ] ; B % : 22 % -52 % , 7min ) to provide the title compound ( 49.4 mg , 109.16 lomμ , 84.24 % yield ) . LCMS ( ESI ) , [ M + H ] + = 444.1 . [ 422 ] Compound 41 : ' H NMR ( 400 MHz , CD3OD ) 8 8.59 ( d , J = 6.4 Hz , 1H ) , 8.49 ( s , 1H ) , 7.58 ( d , J = 6.8 Hz , 1H ) , 7.02 ( d , J = 9.2 Hz , 2H ) , 6.88 - 6.45 ( m , 3H ) , 4.52 - 4.48 ( m , 1H ) , 4.35 - 4.31 ( m , 1H ) , 4.27 4.16 ( m , 1H ) , 3.99 ( s , 3H ) , 3.26 - 3.23 ( m , 1H ) , 2.84 - 2.71 ( m , 1H ) , 2.45 ( s , 1H ) , 2.16 - 2.11 ( m , - 129 6H ) , 2.10 -1.96 ( m , 2H ) , 1.36 - 1.21 ( m , 2H ) .

PCT / US2024 / 0440 [ 423 ] Example AP : ( 4 - ( ( 4- ( Difluoromethoxy ) phenyl ) ( 4 - methoxypyridin - 3 - yl ) amino ) piperidin- - yl ) ( 3 - fluorobicyclo [ 1.1.1 ] pentan - 1 - yl ) methanone ( Compound 42 ) : N ` N F F [ 424 ] ) . [ 425 ] The title compound was synthesized following a procedure similar to Example U ( Compound The title compound was purified purified by prep - HPLC ( column : Phenomenex C80 * 40mm * 3um ; mobile phase : [ water ( NH3H2O + NH4HCO3 ) -ACN ] ; B % : 50 % -80 % , 7min ) to provide the title compound ( 26 mg , 55.05 lomμ , 70.79 % yield ) . LCMS ( ESI ) , [ M + H ] + [ 426 ] = 462.0 . Compound 42 : ' H NMR ( 400 MHz , CD3OD ) 8 8.45 ( s , 1H ) , 8.16 ( s , 1H ) , 7.20 ( d , J – 4.4 Hz , 1H ) , 6.93 ( d , J = 9.2 Hz , 2H ) , 6.81 - 6.39 ( m , 4H ) , 4.53 - 4.50 ( m , 1H ) , 4.26 - 4.18 ( m , 1H ) , 4.13 -4.09 ( m , 1H ) , 3.82 ( s , 3H ) , 3.29 - 3.22 ( m , 1H ) , 2.88 2.74 ( m , 1H ) , 2.36 ( s . 6 H ) , 2.13 2.09 ( m , 1H ) , 2.08 - 2.( m , 1H ) , 1.33 1.09 ( m , 3H ) . - - [ 427 ] Example AQ : 3- ( 4 - ( ( 4- ( Difluoromethoxy ) phenyl ) ( 4 - methoxypyridin - 3 - yl ) amino ) piperidine - 1 - carbonyl ) bicyclo [ 1.1.1 ] pentane - 1 - carbonitrile ( Compound 43 ) : N ' N ' F N [ 428 ] ) . The title compound was synthesized following a procedure similar to Example U ( Compound [ 429 ] The title compound was purified by prep - HPLC ( column : Welch Xtimate C150 * 30mm * 5um ; mobile phase : [ water ( FA ) -ACN ] ; B % : 20 % -50 % , 7min ) to provide the title compound 130 WO 2025/049495 PCT / US2024 / 0440 ( 56.6 mg , 118.40 lomμ , 91.36 % yield ) . LCMS ( ESI ) , [ M + H ] + = 469.0 . [ 430 ] Compound 43 : ' H NMR ( 400 MHz , CD3OD ) 8 8.60 ( d , J = 6.4 Hz , 1H ) , 8.51 ( s , 1H ) , 7.61 ( d , J = 6.8 Hz , 1H ) , 7.03 ( d , J = 9.2 Hz , 2H ) , 6.94 - 6.43 ( m , 3H ) , 4.49 - 4.46 ( m , 1H ) , 4.31 - 4.09 ( m , 2H ) , 4.00 ( s , 3H ) , 3.29 - 3.21 ( m , 1H ) , 2.81 - 2.78 ( m , 1H ) , 2.56 ( s , 6H ) , 2.15 - 1.97 ( m , 2H ) , 1.42 - 1.22 ( m , 2H ) . [ 431 ] Example AR : 4 - Methoxy - N- ( 1- ( pyrazin - 2 - yl ) piperidin - 4 - yl ) -N- ( 4- ( trifluoromethyl ) phenyl ) pyridin - 3 - amine ( Compound 44 ) : F ' N ' ` N ' [ 432 ] ) . The title compound was synthesized following a procedure similar to Example C ( Compound [ 433 ] = The title compound was purified by prep - TLC ( SiO2 , Dichloromethane Methanol 10 : 1 ) to provide the title compound ( 129.2 mg , 288.82 lomμ , 50.74 % yield ) . LCMS ( ESI ) , [ M + H ] + [ 434 ] = 430.1 . Compound 44 : ' H NMR ( 400 MHz , CD3OD ) 8 8.47 ( d , J = 6.0 Hz , 1H ) , 8.16 ( d , J = 4.4 Hz , 2H ) , 8.04 - 8.03 ( m , 1H ) , 7.71 ( d , J = 2.4 Hz , 1H ) , 7.39 ( d , J = 8.8 Hz , 2H ) , 7.23 ( d , J = 5.6 Hz , 1H ) , 6.( d , J = 8.8 Hz , 2H ) , 4.47 - 4.44 ( m , 2H ) , 4.37 - 4.29 ( m , 1H ) , 3.83 ( s , 3H ) , 3.113.00 ( m , 2H ) , 2.15 -2.( m , 2H ) , 1.43 - 1.33 ( m , 2H ) . : [ 435 ] Example AS : Bicyclo [ 1.1.1 ] pentan - 1 - yl ( 4 - ( ( 4 - methoxypyridin - 3 - yl ) ( 4- ( trifluoromethyl ) phenyl ) amino ) piperidin - 1 - yl ) methanone ( Compound 45 ) : N [ 436 ] ) .

H CFThe title compound was synthesized following a procedure similar to Example U ( Compound 131 WO 2025/049495 PCT / US2024 / 0440 [ 437 ] The title compound was purified by prep - HPLC ( column : Welch Xtimate C150 * 30mm * 5um ; mobile phase : [ water ( FA ) -ACN ] ; B % : 26 % -56 % , 7 min ) to provide the title compound ( 56 mg , 125.71 lomμ , 97.51 % yield ) . LCMS ( ESI ) , [ M + H ] + = 446.1 . [ 438 ] Compound 45 : ' H NMR ( 400 MHz , CD3OD ) 8 8.60 ( d , J = 6.0 Hz , 1H ) , 8.35 ( s , 1H ) , 7.45 - 7.39 ( m , 3H ) , 6.70 ( d , J = 8.8 Hz , 2H ) , 4.57 - 4.49 ( m , 1H ) , 4.38 -4.31 ( m , 2H ) , 3.93 ( s , 3H ) , 3.28 - 3.( m , 1H ) , 2.79 2.76 ( m , 1H ) , 2.45 ( s , 1H ) , 2.14 2.02 ( m , 8H ) , 1.31 - 1.23 ( m , 2H ) . - [ 439 ] Example AT : ( 3 - Fluorobicyclo [ 1.1.1 ] pentan - 1 - yl ) ( 4 - ( ( 4 - methoxypyridin - 3 - yl ) ( 4- ( trifluoromethyl ) phenyl ) amino ) piperidin - 1 - yl ) methanone ( Compound 46 ) : F [ 440 ] ) . [ 441 ] CFThe title compound was synthesized following a procedure similar to Example U ( Compound The title compound was purified by prep - HPLC ( column : Welch Xtimate C150 * 30mm * 5um ; mobile phase : [ water ( FA ) -ACN ] ; B % : 26 % -56 % , 7 min ) to provide the title compound ( 69.9 mg , 150.82 lomµ , 97.49 % yield ) . LCMS ( ESI ) , [ M + H ] + = 464.1 . [ 442 ] Compound 46 : ' H NMR ( 400 MHz , CD3OD ) 8 8.76 - 8.74 ( m , 1H ) , 8.60 ( s , 1H ) , 7.71 ( d , J = 7.2 Hz , 1H ) , 7.46 ( d , J = 8.8 Hz , 2H ) , 6.79 ( d , J = 8.8 Hz , 2H ) , 4.61 - 4.55 ( m , 1H ) , 4.42 - 4.33 ( m , 1H ) , 4.17 4.13 ( m , 1H ) , 4.05 ( s , 3H ) , 3.29 - 3.23 ( m , 1H ) , 2.83 -2.82 ( m , 1H ) , 2.38 ( s , 6H ) , 2.18 - 2.05 ( m , 2H ) , 1.36 - 1.25 ( m , 2H ) . [ 443 ] Example AU : 3- ( 4 - ( ( 4 - Methoxypyridin - 3 - yl ) ( 4- ( trifluoromethyl ) phenyl ) amino ) piperidine - 1 - carbonyl ) bicyclo [ 1.1.1 ] pentane - 1 - carbonitrile ( Compound 47 ) : CF CN WO 2025/049495 PCT / US2024 / 0440 [ 444 ] ) . [ 445 ] The title compound was synthesized following a procedure similar to Example U ( Compound The title compound was purified by prep - HPLC ( column : Welch Xtimate C150 * 30mm * 5um ; mobile phase : [ water ( FA ) -ACN ] ; B % : 25 % -55 % , 7 min ) to provide the title compound ( 65 mg , 125.72 lomμ , 97.52 % yield ) . LCMS ( ESI ) , [ M + H ] + = 471.1 . [ 446 ] Compound 47 : ' H NMR ( 400 MHz , CD3OD ) 8 8.75 ( dd , J = 0.8 , 6.8 Hz , 1H ) , 8.60 ( d , J = 0.Hz , 1H ) , 7.71 ( d , J = 6.8 Hz , 1H ) , 7.46 ( d , J = 8.8 Hz , 2H ) , 6.79 ( d , J = 8.8 Hz , 2H ) , 4.61 - 4.55 ( m , 1H ) , - 4.42 4.33 ( m , 1H ) , 4.17 - 4.13 ( m , 1H ) , 4.05 ( s , 3H ) , 3.29 - 3.23 ( m , 1H ) , 2.83 - 2.82 ( m , 1H ) , 2.38 ( s , 6H ) , 2.18 - 2.05 ( m , 2H ) , 1.36 - 1.25 ( m , 2H ) . [ 447 ] Example AV : ( 4 - ( ( 4- ( Trifluoromethyl ) phenyl ) ( 4 - methoxypyridin - 3 - yl ) amino ) piperidin- - yl ) ( 3- ( trifluoromethyl ) bicyclo [ 1.1.1 ] pentan - 1 - yl ) methanone ( Compound 48 ) : [ 448 ] ) . [ 449 ] The title compound was synthesized following a procedure similar to Example U ( Compound The title compound was purified by prep - HPLC ( column : Welch Xtimate C150 * 30mm * 5um ; mobile phase : [ water ( FA ) -ACN ] ; B % : 33 % - 63 % , 7 min ) to provide the title compound ( 74.2 mg , 141.62 lomµ , 82.93 % yield ) as white solid . LCMS ( ESI ) , [ M + H ] + = 514.1 . [ 450 ] = = Compound 48 : ' H NMR ( 400 MHz , CD3OD ) 88.52 ( d , J = 7.6 Hz , 1H ) , 8.19 ( s , 1H ) , 7.39 ( d , J = 8.8 Hz , 2H ) , 7.27 ( d , J = 6.0 Hz , 1H ) , 6.63 ( d , J = 8.8 Hz , 2H ) , 4.55 -4.52 ( m , 1H ) , 4.35 - 4.30 ( m , 1H ) , 4.23 - 4.20 ( m , 1H ) , 3.85 ( s , 3H ) , 3.26 - 3.24 ( m , 1H ) , 2.86 - 2.78 ( m , 1H ) , 2.33 ( s , 6H ) , 2.20 - 2.( m , 2H ) , 1.30 -1.22 ( m , 2H ) . [ 451 ] Example AW : ( 4 - ( ( 4- ( Difluoromethoxy ) phenyl ) ( 4 - methoxypyridin - 3 - yl ) amino ) piperidin- - yl ) ( 3- ( trifluoromethyl ) bicyclo [ 1.1.1 ] pentan - 1 - yl ) methanone ( Compound 49 ) : 133 F ' N ' F F PCT / US2024 / 0440 [ 452 ] ) . [ 453 ] The title compound was synthesized following a procedure similar to Example U ( Compound The title compound was purified by prep - HPLC ( column : Welch Xtimate C150 * 30mm * 5um ; mobile phase : [ water ( FA ) -ACN ] ; B % : 29 % - 59 % , 7 min ) to provide the title compound ( 56.45 mg , 110.37 lomµ , 77.12 % yield ) . LCMS ( ESI ) , [ M + H ] + = 512.0 . [ 454 ] Compound 49 : ' H NMR ( 400 MHz , CD3OD ) 8 8.59 ( d , J = 6.8 , 1H ) , 8.511 ( s , 1H ) , 7.61 ( d , J = 6.8 Hz , 1H ) , 7.03 ( d , J = 8.8 , 2H ) , 6.87 - 6.50 ( m , 3H ) , 4.57 - 4.47 ( m , 1H ) , 4.23 - 4.19 ( m , 2H ) , 3.99 ( s , 3H ) , 3.31 3.26 ( m , 1H ) , 2.88 - 2.72 ( m , 1H ) , 2.31 ( s , 6H ) , 2.16 - 2.07 ( m , 1H ) , 2.06 - 1.97 ( m , 1H ) , 1.43 - 1.29 ( m , 2H ) . [ 455 ] Example AX : 4 - Methoxy - N- ( 1- ( 5 - methylpyrazin - 2 - yl ) piperidin - 4 - yl ) -N- ( 4- ( trifluoromethyl ) phenyl ) pyridin - 3 - amine ( Compound 50 ) : N F N ' N [ 456 ] ) . [ 457 ] The title compound was synthesized following a procedure similar to Example C ( Compound The title compound was purified by reversed - phase HPLC ( column : Boston Green ODS 150 * 30mm * 5um ; mobile phase : [ water ( FA ) -ACN ] ; B % : 32 % -62 % , 6min ) to provide the title compound ( 136.4mg , 298.35 lomμ , 52.42 % yield ) . LCMS ( ESI ) , [ M + H ] + = 444.1 . [ 458 ] Compound 50 : ' H NMR ( 400 MHz , CD3OD ) 8 8.47 ( d , J = 4.4 Hz , 1H ) , 8.17 ( s , 1H ) , 8.05 ( s , 1H ) , 7.95 ( s , 1H ) , 7.39 ( d , J = 7.6 Hz , 2H ) , 7.23 ( d , J = 4.0 Hz , 1H ) , 6.64 ( d , J = 8.0 Hz , 2H ) , 4.39 - 4.( m , 1H ) , 3.84 ( s , 3H ) , 3.08 - 2.97 ( m , 2H ) , 2.34 ( s , 3H ) , 2.17 - 2.09 ( m , 2H ) , 1.43 - 1.31 ( m , 2H ) . 134 WO 2025/049495 PCT / US2024 / 0440 [ 459 ] Example AY : 4 - Methoxy - N- ( 1- ( pyrimidin - 5 - yl ) piperidin - 4 - yl ) -N- ( 4- ( trifluoromethyl ) phenyl ) pyridin - 3 - amine ( Compound 51 ) : N [ 460 ] ) . [ 461 ] The title compound was synthesized following a procedure similar to Example C ( Compound The title compound was purified by reversed - phase HPLC ( column : Boston Green ODS 150 * 30mm * 5um ; mobile phase : [ water ( FA ) -ACN ] ; B % : 32 % -62 % , 6min ) to provide the title compound ( 156.6 mg , 364.66 lomµ , 64.07 % yield ) . LCMS ( ESI ) , [ M + H ] + = 430.1 . = [ 462 ] Compound 51 : ' H NMR ( 400 MHz , CD3OD ) 8 8.54 - 8.46 ( m , 2H ) , 8.44 ( s , 2H ) , 8.22 ( s , 1H ) , 7.39 ( d , J = 8.8 Hz , 2H ) , 7.25 ( d , J = 6.0 Hz , 1H ) , 6.64 ( d , J = 8.8 Hz , 2H ) , 4.29 - 4.21 ( m , 1H ) , 3.93 -3.( m , 2H ) , 3.85 ( s , 3H ) , 3.07 - 2.98 ( m , 2H ) , 2.18 - 2.15 ( m , 2H ) , 1.54 - 1.48 ( m , 2H ) . [ 463 ] Example AZ : 4 - Methoxy - N- ( 1- ( 2 - methylpyrimidin - 5 - yl ) piperidin - 4 - yl ) -N- ( 4- ( trifluoro- methyl ) phenyl ) pyridin - 3 - amine ( Compound 52 ) : ' N ' ` N ' [ 464 ] ) . [ 465 ] The title compound was synthesized following a procedure similar to Example C ( Compound The title compound was purified by reversed - phase HPLC ( column : Boston Green ODS 150 * 30mm * 5um ; mobile phase : [ water ( FA ) -ACN ] ; B % : 30 % -60 % , 6min ) to provide the title compound ( 126.6 mg , 279.77 umol , 49.15 % yield ) . LCMS ( ESI ) . [ M + H ] + = 444.1 . [ 466 ] Compound 52 : ' H NMR ( 400 MHz , CD3OD ) 8 8.49 ( d , J = 6.0 Hz , 1H ) , 8.35 ( s , 2H ) , 8.22 - 135 WO 2025/049495 PCT / US2024 / 0440 8.20 ( m , 1H ) , 7.41 - 7.38 ( m , 2H ) , 7.26 - 7.25 ( m , 1H ) , 6.65 - 6.63 ( m , 2H ) , 4.25 -4.22 ( m , 1H ) , 3.86 ( s , 3H ) , 3.84 - 3.81 ( m , 2H ) , 3.01 - 2.94 ( m , 2H ) , 2.56 - 2.55 ( m , 3H ) , 2.17 - 2.14 ( m , 2H ) , 1.58 - 1.50 ( m , 2H ) . [ 467 ] Example BA : 5- ( 4 - ( ( 4 - Methoxypyridin - 3 - yl ) ( 4- ( trifluoromethyl ) phenyl ) amino ) piperidin- - yl ) pyrimidine - 2 - carbonitrile ( Compound 53 ) : F N N [ 468 ] ) . The title compound was synthesized following a procedure similar to Example L ( Compound [ 469 ] The title compound was purified by flash silica gel chromatography ( ®hsalFapeS Silica Flash Column , Eluent of 0-50 % Ethyl acetate / Petroleum ether , 40 mL / min ) to provide the title compound ( 164.mg , 328.80 lomμ , 63.76 % yield ) . LCMS ( ESI ) , [ M + H ] + = 455.1 . [ 470 ] – Compound 53 : ' H NMR ( 400 MHz , CD3OD ) 8 8.48 ( d , J = 5.6 Hz , 1H ) , 8.44 ( s , 2H ) , 8.19 ( s , 1H ) , 7.39 ( d , J = 8.8 Hz , 2H ) , 7.24 ( d , J = 5.6 Hz , 1H ) , 6.65 ( d , J = 8.8 Hz , 2H ) , 4.37 - 4.31 ( m , 1H ) , 4.- 4.08 ( m , 2H ) , 3.86 ( s , 3H ) , 3.20 -3.13 ( m , 2H ) , 2.19 - 2.13 ( m , 2H ) , 1.53 1.43 ( m , 2H ) . [ 471 ] Example BB : 4 - Methoxy - N- ( 4- ( trifluoromethyl ) phenyl ) -N- ( 1- ( 2- ( trifluoromethyl ) pyrimidin - 5 - yl ) piperidin - 4 - yl ) pyridin - 3 - amine ( Compound 54 ) : F F [ 472 ] ) . [ 473 ] The title compound was synthesized following a procedure similar to Example C ( Compound The title compound was purified by reversed - phase HPLC ( column : Boston Green ODS 150 * 30mm * 5um ; mobile phase : [ water ( FA ) -ACN ] ; B % : 40 % -70 % , 6min ) to provide the title compound 136 WO 2025/049495 PCT / US2024 / 0440 ( 160 mg , 308.78 lomμ , 54.25 % yield ) . LCMS ( ESI ) , [ M + H ] + = 498.1 . [ 474 ] Compound 54 : ' H NMR ( 400 MHz , CD3OD ) 8 8.49 - 8.48 ( m , 3H ) , 8.20 ( s , 1H ) , 7.39 ( d , J = 8.4 Hz , 2H ) , 7.25 ( d , J = 6.0 Hz , 1H ) , 6.65 ( d , J = 8.4 Hz , 2H ) , 4.35 - 4.27 ( m , 1H ) , 4.08 -4.04 ( m , 2H ) , 3.84 ( s , 3H ) , 3.16 - 3.10 ( m , 2H ) , 2.20 - 2.16 ( m , 2H ) , 1.56 - 1.49 ( m , 2H ) . [ 475 ] Example BC : N- ( 4- ( Difluoromethoxy ) phenyl ) -4 - methoxy - N- ( 1- ( pyrazin - 2 - yl ) piperidin- - yl ) pyridin - 3 - amine ( Compound 55 ) : F.

' N ' N [ 476 ] ) . [ 477 ] The title compound was synthesized following a procedure similar to Example C ( Compound The title compound was purified by reversed - phase HPLC ( column : Boston Green ODS 150 * 30mm * 5um ; mobile phase : [ water ( FA ) -ACN ] ; B % : 40 % - 70 % , 6min ) to provide the title compound ( 0.20 g , 459.77 lomµ , 80.32 % yield ) . LCMS ( ESI ) , [ M + H ] + = 428.0 . [ 478 ] Compound 55 : ' H NMR ( 400 MHz , CD3OD ) 8 8.41 ( d , J = 5.6 Hz , 1H ) , 8.14 ( d , J = 5.6 Hz , 2H ) , 8.02 ( s , 1H ) , 7.69 ( s , 1H ) , 7.17 ( d , J = 5.6 Hz , 1H ) , 6.93 ( d , J = 5.6 Hz , 2H ) , 6.78 ( d , J = 5.6 Hz , 2H ) , - 6.59 6.41 ( m , 3H ) , 4.43 - 4.39 ( m , 2H ) , 4.25 -4.15 ( m , 1H ) , 3.80 ( s , 3H ) , 3.06 - 2.99 ( m , 2H ) , 2.11 -2.( m , 2H ) , 1.37 1.33 ( m , 2H ) . [ 479 ] Example BD : N- ( 4- ( Difluoromethoxy ) phenyl ) -4 - methoxy - N- ( 1- ( 5 - methylpyrazin - 2 - yl ) piperidin - 4 - yl ) pyridin - 3 - amine ( Compound 56 ) : N ' N 137 WO 2025/049495 PCT / US2024 / 0440 [ 480 ] ) . [ 481 ] The title compound was synthesized following a procedure similar to Example C ( Compound The title compound was purified by reversed - phase HPLC ( column : Boston Green ODS 150 * 30mm * 5um ; mobile phase : [ water ( FA ) -ACN ] ; B % : 23 % - 53 % , 7 min ) to provide the title compound ( 113.62 mg , 257.37 lomμ , 44.96 % yield ) . LCMS ( ESI ) , [ M + H ] + = 442.3 . [ 482 ] Compound 56 : ' H NMR ( 400 MHz , CD3OD ) 8 8.41 ( d , J = 5.6 Hz , 1H ) , 8.26 ( s , 1H ) , 8.09 ( s , 1H ) , 7.95 ( s , 1H ) , 7.24 ( d , J = 5.6 Hz , 1H ) , 6.82 ( d , J = 8.8 Hz , 2H ) , 6.65 - 6.35 ( m , 3H ) , 4.44 - 4.32 ( m , - 2H ) , 4.19 - 4.09 ( m , 1H ) , 3.81 ( s , 3H ) , 3.12 - 2.99 ( m , 2H ) , 2.33 ( s , 3H ) , 2.18 - 2.10 ( m , 2H ) , 1.43 - 1.( m , 2H ) . [ 483 ] Example BE : N- ( 4- ( Difluoromethoxy ) phenyl ) -4 - methoxy - N- ( 1- ( pyrimidin - 5- yl ) piperidin - 4 - yl ) pyridin - 3 - amine ( Compound 57 ) : N F. [ 484 ] ) . [ 485 ] The title compound was synthesized following a procedure similar to Example C ( Compound The title compound was purified by reversed - phase HPLC ( column : Boston Green ODS 150 * 30mm * 5um ; mobile phase : [ water ( FA ) -ACN ] ; B % : 15 % - 45 % , 7 min ) to provide the title compound ( 238.4 mg , 557.73 lomµ , 97.43 % yield ) . LCMS ( ESI ) , [ M + H ] + = 428.0 . [ 486 ] Compound 57 : ' H NMR ( 400 MHz , CD3OD ) 8 8.55 ( s , 1H ) , 8.50 ( s , 3H ) , 8.21 ( s , 1H ) , 7.( d , J = 6.0 Hz , 1H ) , 6.96 ( d , J = 8.8 Hz , 2H ) , 6.72 - 6.45 ( m , 3H ) , 4.29 - 4.21 ( m , 1H ) , 3.93 - 3.89 ( m , 2H ) , 3.85 ( s , 3H ) , 3.07 - 2.98 ( m , 2H ) , 2.18 - 2.15 ( m , 2H ) , 1.54 - 1.48 ( m , 2H ) . [ 487 ] Example BF : 5- ( 4 - ( ( 4- ( Difluoromethoxy ) phenyl ) ( 4 - methoxypyridin - 3- yl ) amino ) piperidin - 1 - yl ) pyrimidine - 2 - carbonitrile ( Compound 58 ) : 138 N N PCT / US2024 / 0440 [ 488 ] ) . The title compound was synthesized following a procedure similar to Example L ( Compound [ 489 ] The title compound was purified was purified by reversed - phase HPLC ( column : Boston Green ODS 150 * 30mm * 5um ; mobile phase : [ water ( FA ) -ACN ] ; B % : 25 % -55 % , 7 min ) to provide the title compound ( 96.63 mg , 213.57 lomμ , 37.31 % yield ) . LCMS ( ESI ) , [ M + H ] + 455.1 . [ 490 ] = Compound 58 : ' H NMR ( 400 MHz , CD3OD ) 8 8.45 - 8.41 ( m , 3H ) , 8.17 ( s , 1H ) , 7.19 ( d , J = = 5.6 Hz , 1H ) , 6.94 ( d , J = 8.8 Hz , 2H ) , 6.79 - 6.42 ( m , 3H ) , 4.26 - 4.20 ( m , 1H ) , 4.10 - 4.07 ( m , 2H ) , 3.( s , 3H ) , 3.17 3.11 ( m , 2H ) , 2.17 2.13 ( m , 2H ) , 1.50 1.43 ( m , 2H ) . [ 491 ] - - - Example BG : N- ( 4- ( Difluoromethoxy ) phenyl ) -4 - methoxy - N- ( 1- ( 2- ( trifluoromethyl ) pyrim - idin - 5 - yl ) piperidin - 4 - yl ) pyridin - 3 - amine ( Compound 59 ) : F.

N F F N F [ 492 ] ) . [ 493 ] The title compound was synthesized following a procedure similar to Example C ( Compound The title compound was purified by column chromatography ( 10 % -60 % Ethyl acetate in petroleum ether ) to provide the title compound ( 215 mg , 416.60 lomµ , 72.77 % yield ) . LCMS ( ESI ) , [ M + H ] + = 496.0 . [ 494 ] Compound 59 : ' H NMR ( 400 MHz , CD3OD ) 8 8.48 ( s , 2H ) , 8.43 ( d , J = 5.6 Hz , 1H ) , 8.18 ( s , 1H ) , 7.19 ( d , J = 5.6 Hz , 1H ) , 6.96 ( d , J = 8.8 , 2H ) , 6.60 - 6.58 ( m , 3H ) , 4.64 - 4.56 ( m , 1H ) , 4.26 - 4. 139 WO 2025/049495 PCT / US2024 / 0440 ( m , 1H ) , 4.06 - 4.03 ( m , 2H ) , 3.82 ( s , 3H ) , 3.16 - 3.11 ( m , 2H ) , 2.17 - 2.14 ( m , 2H ) , 1.56 - 1.42 ( m , 2H ) . [ 495 ] Example BH : ( ( 4 - Methoxypyridin - 3 - yl ) ( 4- ( trifluoromethyl ) phenyl ) amino ) piperidin - 1- yl ) ( 2 - methylpyridin - 4 - yl ) methanone ( Compound 60 ) : N ' N [ 496 ] To a stirred solution of 4 - Methoxy - N- ( piperidin - 4 - yl ) -N- ( 4- ( trifluoromethyl ) phenyl ) pyridin- - amine hydrochloride ( 0.20 g , 0.51 mmol , 1.0 eq ) and 2 - Methylisonicotinic acid ( 0.07 g , 0.56 mmol , 1.eq ) in N , N - Dimethylformamide ( DMF , 2.0 mL ) was added Diisopropylethylamine ( 0.26 g , 2.06 mmol , 4.eq ) and 0- ( 7 - azabenzotriazol - 1 - yl ) -N , N , N ' , N'- tetramethyluronium hexafluorophosphate ( HATU , 0.29 g , 0.77 mmol , 1.5 eq ) at 0 ° C . Then the reaction mixture was stirred at room temperature for 8 h . The progress of the reaction was monitored by TLC & UPLC - MS which showed product formation . The crude material was purified by combi flash chromatography using silica gel by eluted with 72 % EtOAc in hexanes and pure fractions were concentrated under reduced pressure to afford ( 4 - ( ( 4 - Methoxypyridin - 3 - yl ) ( 4- ( trifluoromethyl ) phenyl ) amino ) piperidin - 1 - yl ) ( 2 - methylpyridin - 4 - yl ) methanone ( 0.16 g , 66 % yield ) . MS ( ESI ) : mass calculated for C25H25F3N4O2 , 470.50 ; m / z found , 471.5 [ M + H ] * , HPLC purity : 99.90 % . [ 497 ] = = Compound 60 : ' H NMR ( 400 MHz , CDC13 ) 8 8.55 ( dd , J = 13.6 , 5.6 Hz , 2H ) , 8.22 ( s , 1H ) , 7.37 ( d , J 8.8 Hz , 2H ) , 7.09 ( s , 1H ) , 7.00 -6.97 ( m , 2H ) , 6.50 ( d , J = 8.8 Hz , 2H ) , 4.81 ( d , J = 12.4 Hz , 1H ) , 4.19 - 4.14 ( m , 1H ) , 3.80 ( s , 3H ) , 3.70 ( d , J = 12.4 Hz , 1H ) , 3.21 - 3.15 ( m , 1H ) , 2.90 - 2.84 ( m , 1H ) , 2.57 ( s , 3H ) , 2.17 ( d , J = 11.6 Hz , 1H ) , 1.99 ( d , J = 10.4 Hz , 1H ) , 1.43 -1.25 ( m , 2H ) . [ 498 ] Example BI : 4 - ( ( 4 - Methoxypyridin - 3 - yl ) ( 4- ( trifluoromethyl ) phenyl ) amino ) piperidin - 1- yl ) ( 2- ( trifluoromethyl ) pyridin - 4 - yl ) methanone ( Compound 61 ) : N CF [ 499 ] ' N F F To a stirred solution of 4 - Methoxy - N- ( piperidin - 4 - yl ) -N- ( 4- ( trifluoromethyl ) phenyl ) pyridin- 140 WO 2025/049495 PCT / US2024 / 0440 3 - amine hydrochloride ( 0.28 g , 0.51 mmol , 1.0 eq ) and 2- ( Trifluoromethyl ) isonicotinic acid ( 0.11 g , 0.mmol , 1.2 eq ) in N , N - Dimethylformamide ( DMF , 2.0 mL ) was added Diisopropylethylamine ( 0.33 mL , 2.06 mmol , 4.0 eq ) and 0- ( 7 - azabenzotriazol - 1 - yl ) -N , N , N ' , N'- tetramethyluronium hexafluorophosphate ( HATU , 0.29 g , 0.77 mmol , 1.5 eq ) at 0 ° C . Then , the reaction mixture was stirred at room temperature for h . The progress of the reaction was monitored by TLC & UPLC - MS and complete consumption of starting materials was observed . The reaction mixture was poured into cold water ( 5.0 mL ) . The obtained solid was collected by filtration and solid cake was washed with excess cold water ( 5.0 mL ) . The solid was dried under vacuum to afford ( 4 - ( ( 4 - Methoxypyridin - 3 - yl ) ( 4- ( trifluoromethyl ) phenyl ) amino ) piperidin - 1 - yl ) ( 2- ( trifluoromethyl ) pyridin - 4 - yl ) methanone ( 0.18 g , 67 % yield ) . MS ( ESI ) : mass calculated for C25H22F6N4O2 , 524.47 ; m / z found , 525.1 [ M + H ] * , HPLC purity : 99.76 % . [ 500 ] Compound 61 : ' H NMR ( 400 MHz , CDCl3 ) 8 8.79 ( d , J = 4.8 Hz , 1H ) , 8.58 ( d , J = 5.6 Hz , IH ) , 8.22 ( s , 1H ) , 7.64 ( s , 1H ) , 7.42 ( d , J = 4.8 Hz , 1H ) , 7.38 ( d , J = 8.8 Hz , 2H ) , 6.99 ( d , J = 5.6 Hz , 1H ) , 6.50 ( d , J 8.8 Hz , 2H ) , 4.82 ( d , J = 13.2 Hz , 1H ) , 4.22 - 4.14 ( m , 1H ) , 3.80 ( s , 3H ) , 3.63 ( d , J = 8.4 Hz , 1H ) , 3.29 -3.23 ( m , 1H ) , 2.95 - 2.80 ( m , 1H ) , 2.19 ( d , J = 11.2 Hz , 1H ) , 2.04 - 2.02 ( m , 1H ) , 1.50 -1.( m , 2H ) . = [ 501 ] Example BJ : 4 - ( ( 4- ( Difluoromethoxy ) phenyl ) ( 4 - methoxypyridin - 3 - yl ) amino ) piperi - din- - yl ) ( 2 - methylpyridin - 4 - yl ) methanone ( Compound 62 ) : N gora OCHF[ 502 ] To a stirred solution of N- ( 4- ( Difluoromethoxy ) phenyl ) -4 - methoxy - N- ( piperidin - 4 - yl ) pyridin- - amine hydrochloride ( 0.15 g , 0.38 mmol , 1.0 eq , ) in dry N , N - Dimethylformamide ( DMF , 2.0 mL ) was added Diisopropylethylamine ( 0.27 mL , 1.55 mmol , 4.0 eq ) , 2 - Methylisonicotinic acid ( 0.05 g , 0.42 mmol , 1.1 eq ) and 0- ( 7 - azabenzotriazol - 1 - yl ) -N , N , N ' , N ' - tetramethyluronium hexafluorophosphate ( HATU , 0.g , 0.58 mmol , 1.50 eq ) at 0 ° C . The resulted mixture was stirred at room temperature for 8 h . The reaction mixture was diluted with ice cold water ( 10.0 mL ) and extracted with Ethylacetate ( 2 × 10.0 mL ) . The combined organic layers were dried over anhydrous Na2SO4 and concentrated under reduced pressure to obtain crude material . The obtained crude material was purified by combi flash chromatography using silica gel , and eluted with 72 % EtOAc in hexanes to afford ( 4 - ( ( 4- ( Difluoromethoxy ) phenyl ) ( 4 - methoxypyridin- - yl ) amino ) piperidin - 1 - yl ) ( 2 - methylpyridin - 4 - yl ) methanone ( 0.07 g , 39 % yield ) . MS ( ESI ) : mass 141 WO 2025/049495 PCT / US2024 / 0440 calculated for C25H26F2N4O3 , 468.50 ; m / z found , 469.4 [ M + H ] * , HPLC purity : 98.95 % . [ 503 ] 7.09 - Compound 62 : ' H NMR ( 400 MHz , CDC13 ) 8 8.52 ( s , 2H ) , 8.22 ( s , 1H ) , 7.09 ( s , 1H ) , 6.93 ( m , 4H ) , 6.56 - 6.19 ( t , J = 75 Hz , 1H ) , 6.47 ( d , J = 8.8 Hz , 2H ) , 4.78 ( d , J = 11.6 Hz , 1H ) , 4.11-4.( m , 1H ) , 3.79 ( s , 3H ) , 3.70 - 3.67 ( m , 1H ) , 3.26 - 3.16 ( m , 1H ) , 2.90 - 2.87 ( m , 1H ) , 2.57 ( s , 3H ) , 2.16 ( d , J = 10.8 Hz , 1H ) , 1.97 ( d , J = 12.8 Hz , 1H ) , 1.68 - 1.25 ( m , 2H ) . [ 504 ] Example BK : 4 - Methoxy - N- ( 1- ( 4- ( methylsulfinyl ) phenyl ) piperidin - 4 - yl ) -N- ( 4- ( trifluoro- methyl ) phenyl ) pyridin - 3 - amine ( Compound 63 ) : -CH [ 505 ] F with The sealed tube was charged 4 - Methoxy - N- ( piperidin - 4 - yl ) -N- ( 4- ( trifluoromethyl ) phenyl ) pyridin - 3 - amine hydrochloride ( 0.25 g , 0.64 mmol , 1.0 eq ) , 1 - Bromo - 4- ( methylsulfinyl ) benzene ( 0.18 g , 0.83 mmol , 1.3 eq ) , Sodium tert - butoxide ( 0.18 g , 1.92 mmol , 3.0 eq ) and dry 1,4 - dioxane ( 10.0 mL ) at room temperature under argon atmosphere . The reaction mixture was degassed with argon for 10 min , then added Ruphos - Pd - G3 ( 0.026 g , 0.032 mmol , 0.05 eq ) under argon . Sealed the tube with cap and stirred at 110 ° C for 16 h . The reaction mixture was cooled to room temperature , passed through a pad of celite and the filtrate was concentrated under reduced pressure to obtain crude material . The obtained crude material was purified by combi flash chromatography using silica gel , and eluted with 10 % MeOH in EtOAc to afford 4 - Methoxy - N- ( 1- ( 4- ( methylsulfinyl ) phenyl ) piperidin- - yl ) -N- ( 4- ( trifluoromethyl ) phenyl ) pyridin - 3 - amine ( 0.18 g , 48 % yield ) . MS ( ESI ) : mass calculated for C25H26F3N3O2S , 489.56 ; m / z found , 490.5 [ M + H ] * , HPLC purity : 98.39 % . [ 506 ] Compound 63 : ' H NMR ( 400 MHz , DMSO - d6 ) 8 8.52 ( d , J = 5.6 Hz , 1H ) , 8.21 ( s , 1H ) , 7.-7.41 ( m , 4H ) , 7.25 ( d , J = 5.6 Hz , 1H ) , 7.04 ( d , J = 9.2 Hz , 2H ) , 6.60 ( d , J = 8.8 Hz , 2H ) , 4.26 - 4.21 ( m , 1H ) , 3.87 ( d , J = 12.8 Hz , 2H ) , 3.77 ( s , 3H ) , 2.98 - 2.93 ( m , 2H ) , 2.64 ( s , 3H ) , 2.07 - 1.99 ( m , 2H ) , 1.36 - 1.23 ( m , 2H ) . [ 507 ] Example BL : N- ( 1- ( 2 - Fluoro - 4- ( methylsulfonyl ) phenyl ) piperidin - 4 - yl ) -4 - methoxy - N- ( 4- ( tri - fluoromethyl ) phenyl ) pyridin - 3 - amine ( Compound 64 ) : 142 CH FF PCT / US2024 / 0440 [ 508 ] The microwave tube was charged with - Methoxy - N- ( piperidin - 4 - yl ) -N- ( 4- ( trifluoromethyl ) phenyl ) pyridin - 3 - amine hydrochloride ( 0.25 g , 0.64 mmol , 1.0 eq ) , 1 - Bromo - 2 - fluoro - 4- ( methylsulfonyl ) benzene ( 0.21 g , 0.83 mmol , 1.3 eq ) , Sodium tert - butoxide ( 0.18 g , 1.92 mmol , 3.0 eq ) and dry 1,4 - dioxane ( 10.0 mL ) at room temperature under argon atmosphere . The resulting mixture was degassed with argon for 10 min , added Ruphos - Pd - G3 ( 0.026 g , 0.032 mmol , 0.05 eq ) under argon . The microwave tube was sealed with cap and stirred at 120 ° C under microwave for 2 h . The progress of the reaction was monitored by TLC & UPLC - MS which showed product formation . The reaction mixture was cooled to room temperature , passed through a pad of celite and the filtrate was concentrated under reduced pressure to obtain crude material . The obtained crude material was purified by combi flash chromatography using silica gel and eluted with 80 % EtOAc in hexanes EtOAc in hexanes to afford N- ( 1- ( 2 - Fluoro - 4- ( methylsulfonyl ) phenyl ) piperidin - 4 - yl ) -4 - methoxy - N- ( 4- ( trifluoromethyl ) phenyl ) pyridin - 3 - amine ( 0.18 g , % yield ) as an off - white solid . MS ( ESI ) : mass calculated for C25H25F4N3O3S , 523.55 ; m / z found , 524.[ M + H ] * , HPLC purity : 99.52 % . [ 509 ] Compound 64 : ' H NMR ( 400 MHz , DMSO - d6 ) 8 8.52 ( d , J = 5.6 Hz , 1H ) , 8.21 ( s , 1H ) , 7.( bs , 1H ) , 7.59 ( s , 1H ) , 7.43 ( d , J = 8.8 Hz , 2H ) , 7.28 ( d , J = 5.6 Hz , 1H ) , 7.19 ( t , J = 8.4 Hz , 1H ) , 6.61 ( d , J = 8.4 Hz , 2H ) , 4.27 - 4.21 ( m , 1H ) , 3.79 ( s , 3H ) , 3.57 ( d , J = 12.4 Hz , 2H ) , 3.17 ( s , 3H ) , 3.03 ( t , J = 11.Hz , 2H ) , 2.03 ( d , J = 12.4 Hz , 2H ) , 1.45 - 1.36 ( m , 2H ) . [ 510 ] Example BM : 2- ( 4 - ( ( 4 - Fluorophenyl ) ( 4 - methoxypyridin - 3 - yl ) amino ) piperidin - 1- yl ) pyrim - idine - 5 - carbonitrile ( Compound 65 ) : [ 511 ] CN Step 1 : Preparation of tert - Butyl 4 - ( ( 4 - fluorophenyl ) ( 4 - methoxypyridin - 3 - yl ) amino ) 143 piperidine - 1 - carboxylate ( 22 ) N NBoc PCT / US2024 / 0440 [ 512 ] The microwave tube was charged with tert - Butyl 4 - ( ( 4 - methoxypyridin - 3- yl ) amino ) piperidine - 1 - carboxylate ( 0.45 g , 1.46 mmol , 1.0 eq ) , 1 - Bromo - 4 - fluorobenzene ( 0.30 g , 1.mmol , 1.2 eq ) , Sodium tert - butoxide ( 0.28 g , 2.92 mmol , 2.0 eq ) and Toluene ( 5.0 mL ) at room temperature under argon atmosphere . The resulting mixture was degassed with argon for 10 min , added Ruphos - Pd - G( 0.06 g , 0.07 mmol , 0.05 eq ) under argon . Sealed the tube with cap and stirred under microwave at 130 ° C for 2 h . TLC examination showed new non - polar spot along with some unreacted starting materials . The reaction mixture was cooled to room temperature , passed through a pad of celite and the filtrate was concentrated under reduced pressure to obtain crude material . The obtained crude material was purified by combi flash chromatography using silica gel , and eluted with 60- 65 % EtOAc in hexanes to afford tert- Butyl 4 - ( ( 4 - fluorophenyl ) ( 4 - methoxypyridin - 3 - yl ) amino ) piperidine - 1 - carboxylate ( 0.30 g . 35 % yield ) . MS ( ESI ) : mass calculated for C22H28FN3O3 , 401.48 ; m / z found , 402.2 [ M + H ] * . [ 513 ] ' H NMR ( 400 MHz , CDC13 ) 8 8.47 ( d , J = 5.6 Hz , 1H ) , 8.22 ( s , 1H ) , 6.90 ( d , J = 5.6 Hz , 1H ) , 6.87 6.83 ( m , 2H ) , 6.47 - 6.44 ( m , 2H ) , 4.16 - 4.11 ( m , 2H ) , 3.92 ( tt , J = 3.6 Hz , 1H ) , 3.77 ( s , 3H ) , 2.83 - 2.77 ( m , 2H ) , 1.96 ( d , J = 12 Hz , 2H ) , 1.42 ( s , 9H ) , 1.34 - 1.25 ( m , 2H ) . [ 514 ] hydrochloride Step 2 : Preparation of N- ( 4 - Fluorophenyl ) -4 - methoxy - N- ( piperidin - 4 - yl ) pyridin - 3 - amine NH ' N ' [ 515 ] To a solution of tert - Butyl 4 - ( ( 4 - fluorophenyl ) ( 4 - methoxypyridin - 3 - yl ) amino ) piperidine - 1- carboxylate ( 0.30 g , 0.77 mmol , 1.0 eq ) in 2,2,2 - Trifluoroethanol ( 2.0 mL ) at 0 ° C was added Chlorotrimethylsilane ( 0.45 mL ) dropwise at room temperature . Then the reaction mixture was stirred at room temperature for 1 h . TLC examination showed new polar spot along with complete conversion of starting material . The volatiles were removed under reduced pressure to obtain the crude material . The obtained crude material was triturated with ACN ( 10.0 mL ) to afford N- ( 4 - Fluorophenyl ) -4 - methoxy - N- 144 WO 2025/049495 PCT / US2024 / 0440 ( piperidin - 4 - yl ) pyridin - 3 - amine hydrochloride ( 0.21 g , 81 % yield ) . MS ( ESI ) : mass calculated for C17H20FN3O , 301.37 ; m / z found , 302.1 [ M + H ] * . [ 516 ] ' H NMR ( 400 MHz , DMSO - d6 ) 8 9.10 ( d , J = 10 Hz , 1H ) , 8.81 - 8.79 ( m , 2H ) , 8.64 ( s , 1H ) , 7.70 ( d , J = 6.8 Hz , 1H ) , 7.04 ( t , J = 8.8 Hz , 2H ) , 6.79 - 6.75 ( m , 2H ) , 4.28 - 4.22 ( m , 1H ) , 3.94 ( s , 3H ) , 3.25 ( d , J = 14.4 Hz , 2H ) , 3.07 - 2.98 ( m , 2H ) , 2.02 1.99 ( m , 2H ) , 1.65 - 1.58 ( m , 2H ) . [ 517 ] - Step 3 : Preparation of 2- ( 4 - ( ( 4 - Fluorophenyl ) ( 4 - methoxypyridin - 3 - yl ) amino ) piperidin - 1- yl ) pyrimidine - 5 - carbonitrile ( Compound 65 ) : CN N N N [ 518 ] To a stirred solution of N- ( 4 - Fluorophenyl ) -4 - methoxy - N- ( piperidin - 4 - yl ) pyridin - 3 - amine hydrochloride ( 0.15 g , 0.44 mmol , 1.0 eq ) in dry N.N - Dimethylformamide ( DMF , 2.0 mL ) was added Diisopropylethylamine ( 0.31 mL , 1.77 mmol , 2.0 eq ) , and 2 - Chloropyrimidine - 5 - carbonitrile ( 0.07 g , 0.mmol , 1.0 eq ) at room temperature and was stirred at 90 ° C for 4 h . TLC examination showed new non polar spot along with complete conversion of starting materials . The reaction mixture was cooled to room temperature , diluted with ice cold water ( 10.0 mL ) and extracted with Ethyl acetate ( 2 × 10.0 mL ) . The combined organic layers were dried over anhydrous Na2SO4 , filtered the drying agent and the filtrate was concentrated under reduced pressure to obtain crude material . The crude material was purified by combi flash chromatography using silica gel , and eluted with 65-70 % EtOAc in hexanes to afford 2- ( 4 - ( ( 4- Fluorophenyl ) ( 4 - methoxypyridin - 3 - yl ) amino ) piperidin - 1 - yl ) pyrimidine - 5 - carbonitrile ( 0.12 g , 51 % yield ) . MS ( ESI ) : mass calculated for C22H21FN6O , 404.45 ; m / z found , 405.1 [ M + H ] * , HPLC purity : 98.93 % . [ 519 ] Compound 65 : ' H NMR ( 400 MHz , CDCI3 ) 88.46 ( d , J = 5.6 Hz , 1H ) , 8.44 ( s , 2H ) , 8.22 ( s , IH ) , 6.90 -6.85 ( m , 3H ) , 6.51-6.48 ( m , 2H ) , 4.94 - 4.90 ( m , 2H ) , 4.16 - 4.09 ( m , 1H ) , 3.77 ( s , 3H ) , 3.07 - 3.00 ( m , 2H ) , 2.12 ( d , J = 13.2 Hz , 2H ) , 1.42 - 1.29 ( m , 2H ) . [ 520 ] Example BN : 4 - Cyclopropoxy - N- ( 4- ( difluoromethoxy ) phenyl ) -N- ( 1- ( 1 - methyl - 1H- pyrazol - 5 - yl ) piperidin - 4 - yl ) pyridin - 3 - amine ( Compound 66 ) : 145 N N PCT / US2024 / 0440 The title compound was synthesized following a procedure similar to Example AD [ 521 ] ( Compound 30 ) . [ 522 ] The title compound was purified by column chromatography ( 10 % -80 % Ethyl acetate in petroleum ether ) to provide the title compound ( 110.7 mg , 243.03 lomμ , 44.78 % yield ) . LCMS ( ESI ) , [ M + H ] + = 456.2 . [ 523 ] = Compound 66 : ' H NMR ( 400 MHz , CD3OD ) 8 8.45 ( d , J = 5.6 Hz , 1H ) , 8.21 ( s , 1H ) , 7.50 ( d , J = 5.6 Hz , 1H ) , 7.29 ( s , 1H ) , 6.93 ( d , J = 8.8 Hz , 2H ) , 6.79 - 6.41 ( m , 3H ) , 5.89 ( s , 1H ) , 4.06 - 4.03 ( m , 1H ) , 3.94 - 3.92 ( m , 1H ) , 3.62 ( s , 3H ) , 3.20 - 3.17 ( m , 2H ) , 2.88 - 2.82 ( m , 2H ) , 2.08 - 2.05 ( m , 2H ) , 1.59 - 1.54 ( m , 2H ) , 0.80 - 0.76 ( m , 2H ) , 0.52 - 0.49 ( m , 2H ) . [ 524 ] Example BO : 4 - Cyclopropoxy - N- ( 1- ( 1 - methyl - 1H - pyrazol - 5 - yl ) piperidin - 4 - yl ) -N- ( 4- ( trifluoromethyl ) phenyl ) pyridin - 3 - amine ( Compound 67 ) : N N [ 525 ] F The title compound was synthesized following a procedure similar to Example AD ( Compound 30 ) . [ 526 ] The title compound was purified by column chromatography ( 10 % -80 % Ethyl acetate in petroleum ether ) to provide the title compound ( 70.1 mg , 153.23 lomμ , 43.26 % yield ) . LCMS ( ESI ) , [ M + H ] + = 458.2 . [ 527 ] = Compound 67 : ' H NMR ( 400 MHz , CD3OD ) 8.51 ( d , J = 5.6 Hz , 1H ) , 8.24 ( s , 1H ) , 7.56 ( d , J = 5.6 Hz , 1H ) , 7.38 ( d , J = 8.8 Hz , 2H ) , 7.30 ( d , J = 2.4 Hz , 1H ) , 6.61 ( d , J = 8.8 Hz , 2H ) , 5.90 ( s , 1H ) , 4.09 - 4.05 ( m , 1H ) , 3.96 - 3.89 ( m , 1H ) , 3.62 ( s , 3H ) , 3.22 - 3.18 ( m , 2H ) , 2.91 - 2.85 ( m , 2H ) , 2.10 - 2. 146 ( m , 2H ) , 1.59 1.55 ( m , 2H ) , 0.82 - 0.76 ( m , 2H ) , 0.53 -0.48 ( m , 2H ) .

PCT / US2024 / 0440 [ 528 ] Example BP : 6- [ 4- [ N- [ 4- ( Cyclopropoxy ) -3 - pyridyl ] -4- ( difluoromethoxy ) anilino ] -1- piperidyl ] pyridine - 3 - carbonitrile ( Compound 68 ) : [ 529 ] ) . [ 530 ] The title compound was synthesized following a procedure similar to Example R ( Compound = The title compound was purified by Silica Flash Column ( 10-50 % Ethyl acetate in Petroleum ether ) to provide the title compound ( 162.9 mg , 320.68 lomµ , 60.19 % yield ) . LCMS ( ESI ) , [ M + H ] + 478.1 . [ 531 ] Compound 68 : ' H NMR ( 400 MHz , CD3OD ) 88.40 ( d , J = 5.6 Hz , 1H ) , 8.33 ( s , 1H ) , 8.15 ( s , 1H ) , 7.65 ( d , J = 2.0 Hz , 1H ) , 7.44 ( d , J = 5.6 Hz , 1H ) , 6.93 ( d , J = 8.8 Hz , 2H ) , 6.83 - 6.79 ( m , 1H ) , 6.- 6.41 ( m , 3H ) , 4.55 - 4.52 ( m , 2H ) , 4.26 - 4.22 ( m , 1H ) , 3.89 - 3.87 ( m , 1H ) , 3.12 - 3.06 ( m , 2H ) , 2.08 - 2.05 ( m , 2H ) , 1.31 - 1.27 ( m , 2H ) , 0.79 - 0.73 ( m , 2H ) , 0.46 - 0.42 ( m , 2H ) . [ 532 ] Example BQ : ( 4 - ( ( 4 - Methoxypyridin - 3 - yl ) ( 4- ( trifluoromethyl ) phenyl ) amino ) piper - idin- - yl ) ( 3- ( trifluoromethyl ) bicyclo [ 1.1.1 ] pentan - 1 - yl ) methanone ( Compound 69 ) : N F [ 533 ] ) . [ 534 ] The title compound was synthesized following a procedure similar to Example L ( Compound The title compound was purified by reversed - phase HPLC ( Welch Xtimate C150 * 30mm * 5um ; mobile phase : [ water ( FA ) -ACN ] ; B % : 32 % -62 % , 7 min ) to provide the title compound 147 WO 2025/049495 PCT / US2024 / 0440 ( 73.5 mg , 150.54 lomμ , 28.26 % yield ) . LCMS ( ESI ) , [ M + H ] + = 479.2 . [ 535 ] Compound 69 : ' H NMR ( 400 MHz , CD3OD ) 8 8.54 ( s , 2H ) , 8.41 ( d , J = 5.6 Hz , 1H ) , 8.16 ( s , 1H ) , 7.46 ( d , J = 5.6 Hz , 1H ) , 6.94 ( d , J = 8.8 Hz , 2H ) , 6.60 - 6.42 ( m , 3H ) , 4.60 - 4.59 ( m , 2H ) , 4.29 - 4.22 ( m , 1H ) , 3.92 - 3.88 ( m , 1H ) , 3.15 - 3.06 ( m , 2H ) , 2.11 -2.07 ( m , 2H ) , 1.29 - 1.24 ( m , 2H ) , 0.79 -0.( m , 2H ) , 0.47-0.43 ( m , 2H ) . [ 536 ] Example BR : N- ( 1- ( 1,2,4 - Oxadiazol - 3 - yl ) piperidin - 4 - yl ) -4 - cyclopropoxy - N- ( 4- ( trifluoro- methyl ) phenyl ) pyridin - 3 - amine ( Compound 70 ) : [ 537 ] carbonitrile Step 1 : N ' N ' N - O 4 - ( ( 4 - Cyclopropoxypyridin - 3 - yl ) ( 4- ( trifluoromethyl ) phenyl ) amino ) piperidine - 1- N N = N F [ 538 ] To a solution of 4- ( cyclopropoxy ) -N- ( 4 - piperidyl ) -N- [ 4- ( trifluoromethyl ) phenyl ] pyridin - 3- amine ( 400 mg , 966.50 lomµ , HCl salt ) in dichloromethane ( 4.0 mL ) was added NaHCO3 ( 405.96 mg , 4.mmol ) in H2O ( 1 mL ) at ° C . Then carbononitridic bromide ( 1.1 g , 10.39 mmol ) was addedand stirred at ° C for 1 hr . Sodium carbonate ( 2 g ) was added in order to ensure the completion of neutralization . MgSO( 5 g ) was added and the mixture was stirred vigorously for 15 minutes . The resulting suspension was filtered , rinsing with dichloromethane ( 50 mL x2 ) . The organic layers was concentrated under reduced pressure and the residue was purified by flash silica gel chromatography ( Eluent of 0-85 % Ethyl acetate in Petroleum ether ) to provide the title compound ( 200 mg , 497.00 lomµ , 51.42 % yield ) . LCMS ( ESI ) , [ M + H ] + = 403.1 . [ 539 ] Step 2 : ( E ) -4 - ( ( 4 - Cyclopropoxypyridin - 3 - yl ) ( 4- ( trifluoromethyl ) phenyl ) amino ) -N ' - hydroxy piperidine - 1 - carboximidamide 148 N ' N ' N - OH NH PCT / US2024 / 0440 [ 540 ] To a solution of 4- [ N- [ 4- ( cyclopropoxy ) -3 - pyridyl ] -4- ( trifluoromethyl ) anilino ] piperidine - 1- carbonitrile ( 200 mg , 497.00 lomμ ) in THF ( 5 mL ) was added HO₂HN ( 164.01 mg , 2.49 mmol , 50 % purity in water ) and the mixture was stirred at 25 ° C for 1 hr . The reaction mixture was concentrated under reduced pressure and the residue was purified by lash silica gel chromatography ( Elucnt of 30 ~ 100 % Ethyl acetate in Petroleum ether ) to provide the title compound ( 190 mg , 436.34 lomµ , 87.79 % yield ) . LCMS ( ESI ) , [ M + H ] + = 436.[ 541 ] Step 3 : N- ( 1- ( 1,2,4 - oxadiazol - 3 - yl ) piperidin - 4 - yl ) -4 - cyclopropoxy - N- ( 4- ( trifluoromethyl ) phenyl ) pyridin - 3 - amine ( Compound 70 ) : F F N - O [ 542 ] To a solution of 4- [ N- [ 4- ( cyclopropoxy ) -3 - pyridyl ] -4- ( trifluoromethyl ) anilino ] -N ' - hydroxy- piperidine - 1 - carboxamidine ( 190 mg , 436.34 lomμ ) in triethoxymethane ( 5 mL ) was added diethoxymethoxyethane ( 129.33 mg , 872.68 lomµ ) , then HCl ( 12 M , Lµ63.63 ) was added . The resulting mixture was stirred at 110 ° C for 0.5 hr . Sodium carbonate ( 2 g ) was added in order to ensure the completion of neutralization . The reaction mixture was filtered and concentrated under reduced pressure and the residue was purified by flash silica gel chromatography ( Eluent of 0-60 % Ethyl acetate in Petroleum ether ) to provide ( 80.5 mg , 180.72 lomµ , 41.42 % yield ) . LCMS ( ESI ) , [ M + H ] + = 446.[ 543 ] Compound 70 : ' H NMR ( 400 MHz , CD3OD ) § 8.72 ( s , 1H ) , 8.48 ( d , J = 5.6 Hz , 1H ) , 8.18 ( s , 1H ) , 7.52 ( d , J = 5.6 Hz , 1H ) , 7.38 ( d , J = 8.8 Hz , 2H ) , 6.62 ( d , J = 8.8 Hz , 2H ) , 4.27 - 4.19 ( m , 1H ) , 4.- 4.03 ( m , 2H ) , 3.94 - 3.92 ( m , 1H ) , 3.17 - 3.11 ( m , 2H ) , 2.07 - 2.03 ( m , 2H ) , 1.41 - 1.37 ( m , 2H ) , 0.81 - 0.77 ( m , 2H ) , 0.53 -0.49 ( m , 2H ) . 149 WO 2025/049495 PCT / US2024 / 0440 [ 544 ] Example BS : 6- ( 4 - ( ( 4 - Cyclopropoxypyridin - 3 - yl ) ( 4- ( trifluoromethyl ) phenyl ) amino ) piper - idin - 1 - yl ) nicotinonitrile ( Compound 71 ) : ./V ﻢﺻﻭﺭﺓ [ 545 ] ) . [ 546 ] The title compound was synthesized following a procedure similar to Example R ( Compound The title compound was purified by Silica Flash Column ( 10 ~ 40 % Ethyl acetate in Petroleum ether , 40 mL / min ) to provide the title compound ( 114.5 mg , 224.46 lomµ , 42.36 % yield ) . LCMS ( ESI ) , [ M + H ] + = 480.1 . [ 547 ] Compound 71 : ' H NMR ( 400 MHz , CD3OD ) 88.46 ( d , J = 5.6 Hz , 1H ) , 8.33 ( d , J = 1.6 Hz , 1H ) , 8.15 ( s , 1H ) , 7.68 - 7.65 ( m , 1H ) , 7.50 ( d , J = 5.6 Hz , 1H ) , 7.38 ( d , J = 8.8 Hz , 2H ) , 6.83 - 6.81 ( m , 1H ) , 6.63 ( d , J = 8.8 Hz , 2H ) , 4.59 - 4.55 ( m , 2H ) , 4.38 - 4.35 ( m , 1H ) , 3.93 - 3.89 ( m , 1H ) , 3.14 - 3.08 ( m , 2H ) , 2.11 -2.07 ( m , 2H ) , 1.32 - 1.28 ( m , 2H ) , 0.81 - 0.76 ( m , 2H ) , 0.49 - 0.45 ( m , 2H ) . [ 548 ] Example BT : 2- ( 4 - ( ( 4 - Cyclopropoxypyridin - 3 - yl ) ( 4- ( trifluoromethyl ) phenyl ) amino ) piper - idin - 1 - yl ) pyrimidine - 5 - carbonitrile ( Compound 72 ) : N ` N [ 549 ] ) . [ 550 ] · F The title compound was synthesized following a procedure similar to Example L ( Compound The title compound was purified by reversed - phase HPLC ( Welch Xtimate C150 * 30mm * 5um ; mobile phase : [ water ( FA ) -ACN ] ; B % : 35 % - 65 % , 7 min ) to provide the title compound 150 WO 2025/049495 PCT / US2024 / 0440 ( 130.3 mg , 271.18 lomμ , 56.12 % yield ) . LCMS ( ESI ) , [ M + H ] + = 481.2 . [ 551 ] = Compound 72 : ' H NMR ( 400 MHz , CD3OD ) 88.54 ( s , 2H ) , 8.47 ( d , J = 6.0 Hz , 1H ) , 8.17 ( s , 1H ) , 7.50 ( d , J = 6.0 Hz , 1H ) , 7.39 ( d , J = 8.4 Hz , 2H ) , 6.63 ( d , J = 8.4 Hz , 2H ) , 4.61 - 4.59 ( m , 2H ) , 4.- 4.37 ( m , 1H ) , 3.95 - 3.92 ( m , 1H ) , 3.18 - 3.09 ( m , 2H ) , 2.15 - 2.08 ( m , 2H ) , 1.32 - 1.23 ( m , 2H ) , 0.81 - 0.76 ( m , 2H ) , 0.51 -0.45 ( m , 2H ) . [ 552 ] Example BU : N- ( 1- ( 1,2,4 - Oxadiazol - 3 - yl ) piperidin - 4 - yl ) -4 - cyclopropoxy - N- ( 4- ( difluoromethoxy ) phenyl ) pyridin - 3 - amine ( Compound 73 ) : N F.

' N ' N - O [ 553 ] ) . [ 554 ] The title compound was synthesized following a procedure similar to Example BS ( Compound The title compound was purified by Silica Flash Column ( 10 ~ 40 % Ethyl acetate in Petroleum ether , 40 mL / min ) to provide the title compound ( 67.5 mg , 152.22 lomµ , 21.28 % yield ) . LCMS ( ESI ) , [ M + H ] + = 444.1 . [ 555 ] Compound 73 : ' H NMR ( 400 MHz , CD3OD ) 8 8.71 ( s , 1H ) , 8.42 ( d , J = 5.6 Hz , 1H ) , 8.17 ( s , 1H ) , 7.47 ( d , J = 5.6 Hz , 1H ) , 6.94 ( d , J = 8.8 Hz , 2H ) , 6.79 - 6.41 ( m , 3H ) , 4.18 - 4.14 ( m , 1H ) , 4.05 - 4.02 ( m , 2H ) , 3.91 - 3.89 ( m , 1H ) , 3.15 - 3.07 ( m , 2H ) , 2.04 - 2.01 ( m , 2H ) , 1.39 - 1.32 ( m , 2H ) , 0.79 - 0.( m , 2H ) , 0.49 -0.47 ( m , 2H ) . [ 556 ] Example BV : 2- ( 4 - ( ( 4- ( Difluoromethoxy ) -3 - fluorophenyl ) ( 4 - methoxypyridin - 3 - yl ) amino ) piperidin - 1 - yl ) pyrimidine - 5 - carbonitrile ( Compound 74 ) : 151 F N PCT / US2024 / 0440 [ 557 ] ) . [ 558 ] The title compound was synthesized following a procedure similar to Example L ( Compound The title compound was purified by reversed - phase HPLC ( Welch Xtimate C18 150 * mm * 5um ; mobile phase : [ water ( FA ) -ACN ] ; B % : 28 % - 58 % , 7 min ) to provide the title compound ( 153.mg , 319.34 lomμ , 64.48 % yield ) . LCMS ( ESI ) , [ M + H ] + = 471.2 . [ 559 ] Compound 74 : ' H NMR ( 400 MHz , CD3OD ) 8 8.55 ( s , 2H ) , 8.47 ( d , J = 5.6 Hz , 1H ) , 8.18 ( s , 1H ) , 7.23 ( d , J = 5.6 Hz , 1H ) , 7.05 -7.03 ( m , 1H ) , 6.64 ( t , J = 74 Hz , 1H ) , 6.44 - 6.39 ( m , 1H ) , 6.33 - 6.( m , 1H ) , 4.61 - 4.59 ( m , 2H ) , 4.32 -4.28 ( m , 1H ) , 3.86 ( s , 3H ) , 3.16 - 3.10 ( m , 2H ) , 2.14 - 2.11 ( d , J = Hz , 2H ) , 1.32 - 1.22 ( m , 2H ) . = [ 560 ] Example BW : N- ( 4- ( Difluoromethoxy ) phenyl ) -4 - methoxy - N- ( 1- ( 5- ( methylsulfonyl ) pyridin - 2 - yl ) piperidin - 4 - yl ) pyridin - 3 - amine ( Compound 75 ) : ﻝا [ 561 ] ) . [ 562 ] The title compound was synthesized following a procedure similar to Example C ( Compound The title compound was purified by reversed - phase HPLC ( column : Boston Green ODS 150 * 30mm * 5um ; mobile phase : [ water ( FA ) -ACN ] ; B % : 15 % - 45 % , 7 min ) to provide the title compound ( 238.4 mg , 435.42 lomµ , 76.06 % yield ) . LCMS ( ESI ) . [ M + H ] + = 505.2 . [ 563 ] Compound 75 : ' H NMR ( 400 MHz , CD3OD ) 8 8.59 ( d , J = 2.4 Hz , 1H ) , 8.48 ( d , J = 5.6 Hz , 152 WO 2025/049495 PCT / US2024 / 0440 1H ) , 8.24 ( s , 1H ) , 7.82 ( d , J = 5.6 Hz , 1H ) , 6.98 - 6.93 ( m , 3H ) , 6.62 ( d , J = 9.2 Hz , 1H ) , 6.53 ( d , J = 8.Hz , 2H ) , 6.40 ( t , J = 74 Hz , 1H ) , 4.59 - 4.51 ( m , 2H ) , 4.18 - 4.14 ( m , 1H ) , 3.80 ( s , 3H ) , 3.18 - 3.6 ( m , 2H ) , 3.03 ( s , 3H ) , 2.15 - 2.10 ( m , 2H ) , 1.42 - 1.38 ( m , 2H ) . [ 564 ] Example BX : 4 - Methoxy - N- ( 1- ( 5- ( methylsulfonyl ) pyridin - 2 - yl ) piperidin - 4 - yl ) -N- ( 4- ( tri- fluoromethyl ) phenyl ) pyridin - 3 - amine ( Compound 76 ) : ' N ' ` ⋅N FL F 0 = [ 565 ] ) . The title compound was synthesized following a procedure similar to Example C ( Compound [ 566 ] The title compound was purified by reversed - phase HPLC ( column : Boston Green ODS 150 * 30mm * 5um ; mobile phase : [ water ( FA ) -ACN ] ; B % : 7 % - 37 % , 7 min ) to provide the title compound ( 153.9 mg , 300.79 lomμ , 48.04 % yield ) . LCMS ( ESI ) , [ M + H ] + = 507.6 . [ 567 ] Compound 76 : ' H NMR ( 400 MHz , CD3OD ) 8 8.48 ( d , J = 5.6 Hz , 1H ) , 8.43 ( s , 1H ) , 8.18 ( s , 1H ) , 7.82 ( d , J = 8.0 Hz , 1H ) , 7.42 ( d , J = 8.8 Hz , 2H ) , 7.23 ( d , J = 5.6 Hz , 1H ) , 6.92 ( d , J = 9.2 Hz , 1H ) , 6.61 ( d , J = 8.8 Hz , 2H ) , 4.55 - 4.52 ( m , 2H ) , 4.41 - 4.35 ( m , 1H ) , 3.76 ( s , 3H ) , 3.15 - 3.09 ( m , 5H ) , 2.04 - 2.01 ( m , 2H ) , 1.23 - 1.13 ( s , 2H ) . [ 568 ] Example BY : ( ( Trans ) -4 - ( ( 4- ( Difluoromethoxy ) phenyl ) ( 4 - methoxypyridin - 3 - yl ) amino ) cyclohexyl ) ( morpholino ) methanone ( Compound 77 ) : N F.

' N ' WO 2025/049495 PCT / US2024 / 0440 [ 569 ] carboxylate Step 1 : Ethyl 4 - ( ( 4- ( difluoromethoxy ) phenyl ) ( 4 - methoxypyridin - 3 - yl ) amino ) cyclo - hexane - 1- F [ 570 ] A mixture of ethyl 4 - [ ( 4 - methoxy - 3 - pyridyl ) amino ] cyclohexanecarboxylate ( 200 mg , 718.lomμ ) , 1 - bromo - 4- ( difluoromethoxy ) benzene ( 320.49 mg , 1.44 mmol ) , t - PзuB ( 581.48 mg , 287.41 lomµ , Lμ85.476 , 10 % purity ) , Pd ( OAc ) 2 ( 32.26 mg , 143.71 lomμ ) and BuONa ( 207.16 mg , 2.16 mmol ) in toluene ( 8 mL ) was degassed and purged with N2 for 3 times , and then the mixture was stirred at 120 ° C for 24 hr under N2 atmosphere . The reaction mixture was concentrated under reduced pressure and the residue was purified by Silica Flash Column ( 0 ~ 30 % Ethyl acetate in Petroleum ether ) to provide the title compound ( 136 mg , 322.51 lomμ , 45 % yield ) . LCMS ( ESI ) , [ M + H ] + = 421.3 . [ 571 ] Step 2 : 4 - ( ( 4- ( Difluoromethoxy ) phenyl ) ( 4 - methoxypyridin - 3 - yl ) amino ) cyclohexane - 1 - car- boxylic acid F.

OH ' N ' [ 572 ] To a solution of ethyl 4- [ 4- ( difluoromethoxy ) -N- ( 4 - methoxy - 3 - pyridyl ) anilino ] cyclohex- anecarboxylate ( 403 mg , 958.50 lomμ ) in THF ( 5 mL ) and methanol ( 5 mL ) was added Lithium hydroxide monohydrate ( 201.11 mg , 4.79 mmol ) in H2O ( 5 mL ) and the mixture was stirred at 25 ° C for 2 hr . The reaction mixture was concentrated under reduced pressure and the residue was adjusted with HCl ( 4M ) to pH 6. The resulting mixture was extracted with ethyl acetate ( 25 mL x3 ) and the combined organics was dried over Na2SO4 , filtered . The filtrate was concentrated under reduced pressure to provide the title compound ( 376.11 mg , 958.50 lomμ , 100.00 % yield ) . LCMS ( ESI ) , [ M + H ] + = 393.1 . [ 573 ] Step 3 : ( ( Trans ) -4 - ( ( 4- ( Difluoromethoxy ) phenyl ) ( 4 - methoxypyridin - 3 - yl ) amino ) cyclohe- xyl ) ( morpholino ) methanone ( Compound 77 ) & ( ( Cis ) -4 - ( ( 4- ( difluoromethoxy ) phenyl ) ( 4 - methoxy- 154 pyridin - 3 - yl ) amino ) cyclohexyl ) ( morpholino ) methanone F.

' ` N " ' ' F.

' N ' ' PCT / US2024 / 0440 [ 574 ] To a solution of 4- [ 4- ( difluoromethoxy ) -N- ( 4 - methoxy - 3 - pyridyl ) anilino ] cyclo- hexanecarboxylic acid ( 200 mg , 437.82 lomμ ) and morpholine ( 57.21 mg , 656.74 lomμ ) in dichloromethane ( 4 mL ) was added DIEA ( 169.75 mg , 1.31 mmol ) and HATU ( 332.95 mg , 875.65 lomµ ) at 0 ° C and the mixture was stirred at 0 ° C for 2 hr . The reaction mixture was concentrated under reduced pressure and the residue was purified by prep - HPLC ( column : Welch Xtimate C18 150 * 30 mm * 5um ; mobile phase : [ water ( NH3H2O + NH4HCO3 ) -ACN ] ; B % : 40 % -70 % , 7 min ) to provide the title compound - 1 ( Peak 1 on HPLC , Compound 77 , 31.9 mg , 68.63 lomµ , 15.67 % yield ) and compound - 2 ( Peak 2 on HPLC , isomer of compound 77 , 64.3 mg , 136.29 lomµ , 31.13 % yield ) . LCMS ( ESI ) , [ M + H ] + = 462.2 . Only the trans isomer , Compound 77 , displayed activity . [ 575 ] Compound 77 : ' H NMR ( 400 MHz , CD3OD ) 8 8.41 ( d , J = 5.6 Hz , 1H ) , 8.15 ( s , 1H ) , 7.18 ( d , J = 5.6 Hz , 1H ) , 6.90 ( d , J = 9.2,2H ) , 6.76 - 6.38 ( m , 3H ) , 3.98 - 3.86 ( m , 1H ) , 3.81 ( s , 3H ) , 3.62 - 3.( m , 8H ) , 2.60 - 2.44 ( m , 1H ) , 2.11 - 2.09 ( m , 2H ) , 1.87 - 1.74 ( m , 2H ) , 1.74 - 1.60 ( m , 2H ) , 1.26 - 1.22 ( m , 2H ) . [ 576 ] § Compound 77 cis - isomer : ' H NMR ( 400 MHz , CD3OD ) 8 8.38 ( d , J = 5.6 Hz , 1H ) , 8.22 ( s , 1H ) , 7.15 ( d , J = 5.6 Hz , 1H ) , 6.91 ( d , J = 9.2,2H ) , 6.78 - 6.41 ( m , 3H ) , 3.96 - 3.93 ( m , 1H ) , 3.81 ( s , 3H ) , 3.61 - 3.46 ( m , 8H ) , 2.86 - 2.84 ( m , 1H ) , 1.90 - 1.67 ( m , 8H ) . [ 577 ] Example BZ : ( Cis ) -4 - ( ( 4 - Methoxypyridin - 3 - yl ) ( 4- ( trifluoromethyl ) phenyl ) am- ino ) cyclohexyl ) ( morpholino ) methanone ( Compound 78 ) : 155 N ' N ' goto F F PCT / US2024 / 0440 [ 578 ] ) . [ 579 ] The title compound was synthesized following a procedure similar to Example BY ( Compound The title compounds were purified by reversed - phase HPLC ( column : Welch Xtimate C18 1* 30 mm * 5um ; mobile phase : [ water ( NH3H2O + NH4HCO3 ) -ACN ] ; B % : 40 % -70 % , 7 min ) to provide the title compound - 1 ( Peak 1 on HPLC , 125 mg , 269.69 lomµ , 66.48 % yield ) and compound - 2 ( Compound , Peak 2 on HPLC , 60 mg , 129.45 lomμ , 31.91 % yield ) . LCMS ( ESI ) , [ M + H ] + = 464.3 . Only the cis isomer , Compound 78 , displayed activity . [ 580 ] Compound 78 : ' H NMR ( 400 MHz , CD3OD ) 8 8.45 ( d , J = 5.6 Hz , 1H ) , 8.18 ( s , 1H ) , 7.35 ( d , J = 8.8 Hz , 2H ) , 7.22 ( d , J = 5.6,1H ) , 6.57 ( d , J = 5.6,2H ) , 4.01 3.98 ( m , 1H ) , 3.83 ( s , 3H ) , 3.65 - 3.( m , 4H ) , 3.52 - 3.46 ( m , 4H ) , 2.91 - 2.88 ( m , 1H ) , 1.90 - 1.86 ( m , 4H ) , 1.76 - 1.71 ( m , 4H ) . [ 581 ] = Compound 78 isomer : ' H NMR ( 400 MHz , CD3OD ) 8 8.47 ( d , J = 5.6 Hz , 1H ) , 8.18 ( s , 1H ) , 7.36 ( d , J 8.8 Hz , 2H ) , 7.22 ( d , J = 5.6 , 1H ) , 6.57 ( d , J = 8.8,2H ) , 4.27 -4.16 ( m , 1H ) , 3.84 ( s , 3H ) , 3.63- 3.60 ( m , 4H ) , 3.58 - 3.53 ( m , 4H ) , 2.59 - 2.51 ( m , 1H ) , 2.14 -2.11 ( m , 2H ) , 1.85 - 1.83 ( m , 2H ) , 1.74 - 1.( m , 4H ) . [ 582 ] Example CA : N- ( 4- ( difluoromethoxy ) phenyl ) -5 - fluoro - 4 - methoxy - N- ( 1- ( 5- ( methyl sulfonyl ) pyrimidin - 2 - yl ) piperidin - 4 - yl ) pyridin - 3 - amine ( Compound 79 ) : N F [ 583 ] Step 1 : 3 - bromo - 5 - fluoro - 4 - methoxypyridine Br PCT / US2024 / 0440 [ 584 ] To a solution of 3 - bromo - 4 - chloro - 5 - fluoropyridine ( 3.0 g , 14.26 mmol , 1 eq ) in THF ( 30 mL ) was added NaOMe ( 5.4 M , 2.64 mL , 1 eq ) . The mixture was stirred at 50 ° C for 1 h . LCMS ( 5- 95AB / 1.5min ) : RT = 0.656 min , [ M + H ] * = 206.1 , showed 58 % of desired product . The reaction was diulted with brine ( 50 mL ) . And the mixture was extracted with EtOAc ( 50 mL × 2 ) . The combined organic layers were washed with brine ( 50 mL × 2 ) , dried over anhydrous Na2SO4 , filtered and concentrated under reduced pressure to give a residue . The residue was purified by flash chromatography on silica gel ( 0 - 12.5 % ethyl acetate in petroleum ether ) to provide the title compound ( 760 mg , 26 % ) . [ 585 ] ' H NMR ( 400 MHz , CDC13 ) : 8 8.44 ( s , 1H ) , 8.34 ( d , J = 2.8 Hz , 1H ) , 4.21 ( d , J = 4.4 Hz , 3H ) ; LCMS ( ESI ) : m / z 206.1 ( M + H ) * . [ 586 ] [ 587 ] Step 2 : tert - butyl 4 - ( ( 5 - fluoro - 4 - methoxypyridin - 3 - yl ) amino ) piperidine - 1 - carboxylate Boc ° N H = The mixture of 3 - bromo - 5 - fluoro - 4 - methoxypyridine ( 850 mg , 4.13 mmol , 1 eq ) , tert - butyl 4- aminopiperidine - 1 - carboxylate ( 992 mg , 4.95 mmol , 1.2 eq ) , Pd ( OAc ) 2 ( 93 mg , 412.60 lomµ , 0.1 eq ) , BINAP ( 514 mg , 825.19 lomµ , 0.2 eq ) and t - BuONa ( 1.19 g , 12.38 mmol , 3 eq ) in toluene ( 20 mL ) was was stirred at 100 ° C for 12 h under N2 atmosphere . LCMS ( 5-95AB / 1.5min ) : RT = 0.655 min , [ M + H ] * 326.3 , showed 57 % of desired product . The reaction was diulted with brine ( 50 mL ) , the mixture was extracted with EtOAc ( 50 mL × 2 ) . The combined organic layers were washed with brine ( 50 mL × 2 ) , dried over anhydrous Na2SO4 , filtered and concentrated under reduced pressure to give a residue . The residue was purified by prep - TLC ( SiO2 , Petroleum ether : Ethyl acetate = 2 : 1 ) to provide the title compound ( 830 mg , 62 % ) . LCMS ( ESI ) : m / z 326.3 ( M + H ) * . [ 588 ] Step 3 : tert - butyl 4 - ( ( 4- ( difluoromethoxy ) phenyl ) ( 5 - fluoro - 4 - methoxypyridin - 3- yl ) amino ) piperidine - 1 - carboxylate 157 N Boc ` N PCT / US2024 / 0440 [ 589 ] OCHFThe mixture of tert - butyl 4 - ( ( 5 - fluoro - 4 - methoxypyridin - 3 - yl ) amino ) piperidine - 1 - carboxylate ( 250 mg , 768.34 lomμ , 1 eq ) , 1 - bromo - 4- ( difluoromethoxy ) benzene ( 343 mg , 1.54 mmol , 210.12 Lμ , 2 eq ) , t - Bu3P - Pd - G2 ( 79 mg , 153.67 lomµ , 0.2 eq ) , t - BuONa ( 222 mg , 2.31 mmol , 3 eq ) in toluene ( 5 mL ) was stirred at 120 ° C for 16 h under N2 atmosphere . LCMS ( 5-95AB / 1.5min ) : RT = 0.885 min , [ M + H ] * = 468.showed 46 % of desired product . The reaction was diulted with brine ( 50 mL ) , the mixture was extracted with EtOAc ( 50 mL × 2 ) . The combined organic layers were washed with brine ( 50 mL × 2 ) , dried over anhydrous Na2SO4 , filtered and concentrated under reduced pressure to give a residue . The residue was purified by flash chromatography on silica gel ( 0 - 5 % EE ( ethanol : EtOAc = 1 : 3 ) in Petroleum ether ) to provide the title compound ( 350 mg , crude ) . LCMS ( ESI ) : m / z 468.3 ( M + H ) * . [ 590 ] Step 4 : N- ( 4- ( difluoromethoxy ) phenyl ) -5 - fluoro - 4 - methoxy - N- ( piperidin - 4 - yl ) pyridin - 3- amine hydrochloride N NH N HCI OCHF[ 591 ] To a solution of tert - butyl 4 - ( ( 4- ( difluoromethoxy ) phenyl ) ( 5 - fluoro - 4 - methoxypyridin - 3- yl ) amino ) piperidine - 1 - carboxylate ( 350 mg , 748.69 lomμ , 1 eq ) in dioxane ( 0.5 mL ) was added HCl / dioxane ( 4 M , 5 mL , 26.71 eq ) . The mixture was stirred at 25 ° C for 1 h . LCMS ( 5-95AB / 1.5min ) : RT 0.747 min , [ M + H ] * 368.2 , showed 94 % of desired product . The mixture was concentrated under reduced pressure to provide the title compound ( 275 mg , crude , HCl salt ) . The crude was used directly for next step . LCMS ( ESI ) : m / z 368.2 ( M + H ) * . = [ 592 ] = Step 5 : N- ( 4- ( difluoromethoxy ) phenyl ) -5 - fluoro - 4 - methoxy - N- ( 1- ( 5- ( methylsulfonyl ) pyrimidin - 2 - yl ) piperidin - 4 - yl ) pyridin - 3 - amine ( Compound 79 ) 158 ` N F PCT / US2024 / 0440 [ 593 ] To solution = of N- ( 4- ( difluoromethoxy ) phenyl ) -5 - fluoro - 4 - methoxy - N- ( piperidin - 4- yl ) pyridin - 3 - amine hydrochloride ( 132 mg , 359.32 lomμ , 1 eq ) and 2 - chloro - 5- ( methylsulfonyl ) pyrimidine ( 70 mg , 359.32 lomμ , 1 eq ) in MeCN ( 5 mL ) was added TEA ( 181.79 mg , 1.80 mmol , 250.06 Lµ , 5 eq ) at ° C . The mixture was stirred at 0 ° C for 1 h . LCMS ( 5-95AB / 1.5min ) : RT = 0.811 min , [ M + H ] + 524.2 , showed 70 % of desired product . The mixture was concentrated under reduced pressure to give a residue . The residue was purified by flash chromatography on silica gel ( 0 - 45 % EtOAc in Petroleum ether ) to provide the title compound ( 97.68 mg , 52 % ) . [ 594 ] = Compound 79 : ' H NMR ( 400 MHz , CD3OD ) : 8 8.65 ( s , 2H ) , 8.38 ( d , J = 3.2 Hz , 1H ) , 8.( s , 1H ) , 7.00 ( d , J = 9.2 Hz , 2H ) , 6.84 - 6.39 ( m , 3H ) , 5.01 - 4.97 ( m , 2H ) , 4.33 - 4.30 ( m , 1H ) , 3.93 ( d , J 4.4 Hz , 3H ) , 3.19 - 3.12 ( m , 2H ) , 3.11 ( s , 3H ) , 2.15 - 2.11 ( m , 2H ) , 1.37 - 1.29 ( m , 2H ) ; LCMS ( ESI ) : m / z 524.2 ( M + H ) * . [ 595 ] The following compounds were preparing following similar protocols described above with appropriate reagents . [ 596 ] Example CB : ( 4 - methyl - 3 - pyridyl ) [ p- ( trifluoromethyl ) phenyl ] { 1- [ 5- ( trifluoromethyl ) -2- pyridyl ] -4 - piperidyl } amine : N ' NH .

Boc NaBH ( OAc ) 3 . AcOH DCM , 40 ° C , 16 h ﻪﻣﺪﻣ Boc Br Boc Pd ( OAc ) 2.tBugP.tBuONa PhMe , 125 ° C , 12 h HCI 3.5 g used after pre - HPLC ( basic ) 2.5 g ( 27 % ) ; 50 mg used LCMS : 38 % DP , others ligand mg used mg used tBu P - Pd - G2 , tBuONa Ph Me , 125 ° C , 12 h L7 - Pd - G3 , tBuONa CPME , 80 ° C , 12 h ACIE , 2015 , 54 , 82 LCMS : 49 % DP , others ligand LCMS : 24 % DP , 18 % STM , others ligand 110 mg after column- 84 mg crude NH DIEA DMF , 95 ° C F after pre - HPLC ( FA ) and pre - TLC ﻱﺩ mg ( 86 % purity ) HNMR showed pure , but HPLC showed only 86 % purity 29.9 mg delivered after SFC purification WO 2025/049495 PCT / US2024 / 0440 [ 597 ] Compound 100 : 29.9 mg ; ' H NMR ( 400 MHz , CD3OD ) d 8.42 ( d , 1H ) , 8.25 ( m , 2H ) , 7.( d , 1H ) , 7.44 ( m , 3H ) , 6.86 ( d , 1H ) , 6.62 ( m , 2H ) , 4.50 ( m , 2H ) , 4.46 ( m , 1H ) , 3.11 ( m , 2H ) , 2.19 ( s , 3H ) , 2.12 ( m , 2H ) , 1.4 ( m , 2H ) ; LCMS ( ESI ) [ M + H ] + = 481 . [ 598 ] Example CD : 2- { 4 - [ ( 4 - methyl - 3 - pyridyl ) [ 6- ( trifluoromethyl ) -3 - pyridyl ] amino ] -1- piperidyl ) -5 - pyrimidinecarbonitrile : H 300 mg used ' N- Br Boc " N " N NH Boc F3C Pd ( OAc ) 2 , tBu3P , tBuONa PhMe , 125 ° C , 12 h DIEA HCI DMF , 80 ° C F N N 280 mg ( 62 % ) -200 mg crude ; 20 mg used LMCS : major BP mg used mg used DIEA DMF , 20 ° C LMCS : 60 % DP , 18 % BP 26.6 mg delivered [ 599 ] Compound 101 : 26.6 mg ; ' H NMR ( 400 MHz , CD3OD ) d 8.55 ( s , 2H ) , 8.47 ( d , 1H ) , 8.( s , 1H ) , 7.87 ( s , 1H ) , 7.59 ( d , 1H ) , 7.49 ( d , 1H ) , 7.10 ( d , 1H ) , 5.00 ( m , 2H ) , 4.53 ( m , 1H ) , 3.17 ( m , 2H ) , 2.21 ( s , 3H ) , 2.17 ( m , 2H ) , 1.37 ( m , 2H ) LCMS ( ESI ) [ M + H ] + = 440 . [ 600 ] Example CE : 2- { 4 - [ ( 4 - chloro - 3 - pyridyl ) [ 6- ( trifluoromethyl ) -3 - pyridyl ] amino ] -1- piperidyl ) -5 - pyrimidinecarbonitrile : Boc HCI / dioxane ° C , 2 h NH DIEA N DMF , 0 ° C , 1 h N 250 mg used [ 601 ] 170 mg ( crude ) all used mg Compound 102 : 95 mg ; ' H NMR ( 400 MHz , CDCl3 ) d 8.58 ( m , 1H ) , 8.48 ( m , 3H ) , 8.( s , 1H ) , 7.54 ( dd , 2H ) , 6.84 ( d , 1H ) , 5.03 ( m , 2H ) , 4.30 ( m , 1H ) , 3.08 ( m , 2H ) , 2.22 ( m , 2H ) , 1.41-1.50 ( br . m , 2H ) ; LCMS ( ESI ) [ M + H ] + = 460 . [ 602 ] Example CF : ( p - difluoromethoxyphenyl ) ( 4 - methoxy - 3 - pyridyl ) [ 1- ( 2 - methyl - 5- pyrimidinyl ) -4 - piperidyl ] amine : 160 WO 2025/049495 PCT / US2024 / 0440 Boc N Br Boc N ﮎ ﮦﻭ ﺐﮨﻭ ﮦﻭ ۔ NH NH Br Amberlyst A - 26 ( OH ) HCI MeOH , rt , 1 h RuPhos Pd G3 , tBuONa dioxane , 120 ° C , 12 h OCHF₂FHCO OCHF HCI / Dioxane dioxane , 20 ° C , 2 h OCHF tBuz P Pd G2 , tBuONa PhMe , 120 ° C , 12 h 2 g used [ 603 ] 1.6 g ( 55 % ) 1.37 g crude 1.24 g 538.41 mg Compound 103 : 538 mg ; ' H NMR ( 400 MHz , CD3OD ) d 8.44 ( d , 1H ) , 8.43 ( s , 2H ) , 8.42 ( s , 1H ) , 6.97 ( m , 1H ) , 6.96 ( m , 2H ) , 6.92 ( m , 3H ) , 4.11 ( m , 1H ) , 3.84 ( s , 3H ) , 3.83 ( m , 2H ) , 2.98 ( m , 2H ) , 2.20 ( s , 3H ) , 2.14 ( m , 2H ) , 1.5 ( m , 2H ) ; LCMS ( ESI ) [ M + H ] + = 442 . [ 604 ] Example CG : 5- { 4 - [ ( p - difluoromethoxyphenyl ) ( 4 - methoxy - 3- pyridyl ) amino ] cyclohexyloxy } -2 - pyridinecarbonitrile : N OH N CN N OCHF NaBHMeOH / THF NaH DMSO , 0 ° C Peak WO2020 / 132636 , 2020 , AOCHFOCHF7.5 mg 100 mg used 120 mg crude ; 20 mg used- -400 mg crude ; 200 mg used 400 mg used [ 605 ] Compound 104 - isomer 1 : 7.5 mg ; ' H NMR ( 400 MHz , CD3OD ) d 8.5 ( d , 1H ) , 8.3 ( d , 1H ) , 8.2 ( d , 1H ) , 7.8 ( d , 1h ) , 7.5 ( d , 1H ) , 7.2 ( d , 1H ) , 6.9 ( d , 2H ) , 6.4-6.6 ( m , 3H ) , 4.6 ( m , 1H ) , 4.1 ( m , 1H ) , 3.( s , 3H ) , 2.15 ( m , 2H ) , 1.9 ( br . m , 4H ) , 1.6 ( m , 2H ) ; LCMS ( ESI ) [ M + H ] + = 467 . N OH CN Peak OCHF NaBHMeOH / THF OCHF NaH DMSO , 0 ° C WO2020 / 132636 , 2020 , AOCHF51.2 mg 100 mg used . 120 mg crude ; 20 mg used 400 mg used -400 mg crude ; 200 mg used- [ 606 ] Compound 104 - isomer 2 : 51 mg ; ' H NMR ( 400 MHz , CD3OD ) d 8.6 ( d , 1H ) , 8.30 ( d , 1H ) , 8.20 ( s , 1H ) , 7.75 ( d , 1H ) , 7.50 ( d , 1H ) , 7.20 ( s , 1H ) , 6.9 ( d , 2H ) , 6.3-6.7 ( m , 3H ) , 4.3 ( m , 1H ) , 4.05 ( m , 1H ) , 3.8 ( s , 3H ) , 2.2 ( m , 4H ) , 1.7 ( m , 2H ) , 1.4 ( m , 2H ) ; LCMS ( ESI ) [ M + H ] + = 467 . [ 607 ] Example CH : 5- { 4 - [ ( 4 - methoxy - 3 - pyridyl ) [ p- ( trifluoromethyl ) phenyl ] amino ] cyclohexyloxy } -2 - pyridinecarbonitrile : , 161 WO 2025/049495 PCT / US2024 / 0440 OH CN go - gore gord NaBHMeOH / THF , 0 ° C , 1 h NaH DMSO , 0 ° C WO2020 / 132636 , 2020 , ACF 178 mg , crude 200 mg used used directly Peak N [ 608 ] mg used 108 mg used CFAfter column purification , 170 mg HPLC shows two peaks with the ratio of : 8 ) then separated peak 1 by HPLC ( basic ) 9.3 mg Compound 105 - isomer 1 : 9.3 mg ; ' H NMR ( 400 MHz , CDCl3 ) d 8.28 ( d , 1H ) , 7.59 ( d , 1H ) , 7.38 ( d , 2H ) , 7.2-7.3 ( br . m , 4H ) , 4.67 ( m , 1H ) , 4.0 ( m , 1H ) , 3.81 ( s , 3H ) , 2.17 ( m , 2H ) , 1.93 ( m , 2H ) , 1.77 ( m , 2H ) , 1.6 ( m , 2H ) ; LCMS ( ESI ) [ M + H ] + = 469 . N OH N CN NaH DMSO , 0 ° C WO2020 / 132636 , 2020 , A NaBHMeOH / THF , 0 ° C , 1 h CFCF178 mg , crude 200 mg used used directly mg used N Peak [ 609 ] 108 mg used After column purification , 170 mg , HPLC showed two peaks with the ratio of : Peak 2 was purified by HPLC ( basic ) 68.3 mg delivered Compound 105 - isomer 2 : 68 mg ; ' H NMR ( 400 MHz , CDC13 ) d 8.6 ( br . s , 1H ) , 8.35 ( s , 1H ) , 8.30 ( br . s , 1H ) , 7.6 ( d , 1H ) , 7.4 ( d , 2H ) , 7.15 ( m , 1H ) , 7.0 ( m , 1H ) , 6.5 ( d , 2H ) 4.2 ( m , 1H ) , 4.0 ( m , 1H ) , 3.80 ( s , 3H ) , 2.2 ( m , 4H ) , 1.7 ( m , 2H ) , 1.3 ( m , 2H ) LCMS ( ESI ) [ M + H ] + = 469 . [ 610 ] Example CI : ( p - difluoromethoxyphenyl ) ( 4 - methoxy - 3 - pyridyl ) { 1- [ p- ( methylsulfinyl ) phenyl ] -4 - piperidyl } amine : -Br N F NBoc NBoc Naot By GP ( t - Bu ) toluene , 130 ° C , 2h TMSCI HO₂HCC3F , 0 ° C , 1 h 50 mg 150 mg Br • HCI NH NaOt - Bu , RuPhos - Pd - G1,4 - dioxane , 120 ° C , 2 h 150 mg CH3 WO 2025/049495 PCT / US2024 / 0440 [ 611 ] Compound 106 : 150 mg ; ' H NMR ( 400 MHz , DMSO - d6 ) d 8.48 ( m , 1H ) , 8.20 ( s , 1H ) , 7.( m , 2H ) , 7.2 ( m , 1H ) , 6.8-7.1 ( m , 5H ) , 6.5 ( m , 2H ) , 4.15 ( m , 1H ) , 3.85 ( m , 2H ) , 3.75 ( s , 3H ) , 2.95 ( m , 2H ) , 2.68 ( s , 3H ) , 2.0 ( m , 2H ) , 1.3 ( m , 2H ) ; LCMS ( ESI ) [ M + H ] + = 488 . [ 612 ] Example CJ : p - difluoromethoxyphenyl ) [ 1- ( 2 - fluoro - 4 - mesylphenyl ) -4 - piperidyl ] ( 4- methoxy - 3 - pyridyl ) amine : NBoc Br N NBoc NaOt - Bu , P ( t - Bu ) 3Pd - Gtoluene , 130 ° C , 2h TMSCI HO₂HCC3F , 0 ° C , 1 h 50 mg 150 mg • HCI NH Br NaOt - Bu , RuPhos - Pd - G1,4 - dioxane , 120 ° C , 2h 150 mg CH [ 613 ] Compound 107 : 150 mg ; ' H NMR ( 400 MHz , DMSO - d6 ) d 8.50 ( d , 1H ) , 8.20 ( s , 1H ) , 7.( m , 2H ) , 6.8-7.3 ( m , 5H ) , 6.5 ( m , 2H ) , 4.15 ( m , 1H ) , 3.80 ( s , 3H ) , 3.55 ( m , 2H ) , 3.20 ( s , 3H ) , 3.00 ( m , 2H ) , 2.0 ( m , 2H ) , 1.4 ( m , 2H ) ; LCMS ( ESI ) [ M + H ] + = 522 . [ 614 ] Example CK : 5- { 4 - [ ( p - difluoromethoxyphenyl ) ( 4 - methoxy - 3- pyridyl ) amino ] cyclohexyl } -2 - pyridinecarbonitrile : Br N CN NHTS HO . HÓ Cs - COdioxane , 110 ° C CS2CO3 , CSF dioxane , 1J.Chem . Res . 2018 , OCHFBu 3P - Pd - G2 , tBuONa Ph Me , 120 ° C , 16h HCI ( 4N ) Dioxane , 40 ° C TINHNH , MeOH , rt , 4 h H OCHFOCHF2 OCHF780 mg used 720 mg ( 60 % ) 630 mg used 940 mg crude ; 100 mg used 1.6 g used 1.74 g ( 71 % ) 1.55 g , crude 1.6 g used 1.82 g ( 74 % ) 1.62 g crude ; 300 mg used 450 mg crude ; 50 mg used 100 mgx4 used .

OCHF Mixture of Diasteromers 1 : 21.4 mg [ 615 ] Compound 108 : 21.4 mg ( 1 : 1 mixture of diastereomers ) ; ' H NMR ( 400 MHz , CD3OD ) d 8.65 ( m , 1H ) , 8.25-8.5 ( m , 2H ) , 7.8-7.9 ( m , 2H ) , 7.1-7.2 ( m , 1H ) , 6.9 ( m , 2H ) , 6.4-6.7 ( m , 3H ) , 4.0-4.( m , 1H ) , 3.80 ( s . 3H ) , 2.6-2.95 ( m , m , 1H ) , 2.2 ( m , 1H ) , 2.0 ( m , 2H ) , 1.7-1.9 ( m , 5H ) ; LCMS ( ESI ) [ M + H ] + = 4[ 616 ] Example CL : ( p - difluoromethoxyphenyl ) ( 4 - methoxy - 3 - pyridyl ) [ 1- ( 4 - pyridyl ) -4- piperidyl ] amine : 163 NH NH Amberlyst A - 26 ( OH ) I / Br RuPhos Pd G3 , tBuONa HCI MeOH , rt , 1 h dioxane , 120 ° C , 12 h OCHF2 OCHFOCHF970 mg used 920 mg free base each 200 mg used 151.65 mg PCT / US2024 / 0440 [ 617 ] Compound 109 : 152 mg ; H¹ NMR ( 400 MHz , CD3OD ) d 8.45 ( s , 1H ) , 8.2 ( s , 1H ) , 8.10 ( d , 2H ) , 7.2 ( d , 1H ) , 6.9 ( m , 4H ) , 6.6 ( m , 3H ) , 4.25 ( m , 1H ) 4.1 ( m , 2H ) , 3.80 ( s , 3H ) , 3.1 ( m , 2H ) , 2.1 ( m , 2H ) , 1.4 ( m , 2H ) LCMS ( ESI ) [ M + H ] + = 427 . [ 618 ] Example CM : ( 4 - methoxy - 3 - pyridyl ) [ 1- ( 4 - pyridyl ) -4 - piperidyl ] [ p- ( trifluoromethyl ) phenyl ] amine : NH ' NH ' N ' Amberlyst A - 26 ( OH ) HCI MeOH , rt , 1 h I / Br ' N RuPhos Pd G3 , tBuONa dioxane , 120 ° C , 12 h [ 619 ] 2.3 g used g ( 91 % ) 200 mg used 158.54 mg Compound 110 : 159 mg ; ' H NMR ( 400 MHz , CD3OD ) d 8.5 ( m , 1H ) , 8.2 ( s , 1H ) , 8.15 ( d , 2H ) , 7.45 ( d , 2H ) , 7.25 ( s , 1H ) , 6.95 ( d , 2H ) , 6.65 ( d , 2H ) 4.4 ( m , 1H ) , 4.15 ( m , 2H ) , 3.80 ( s , 3H ) , 3.2 ( m , 2H ) , 2.2 ( m , 2H ) , 1.4 ( m , 2H ) ; LCMS ( ESI ) [ M + H ] + = 429 . [ 620 ] Example CN : 5- { 4 - [ ( 4 - methoxy - 3 - pyridyl ) [ p- ( trifluoromethyl ) phenyl ] amino ] cyclohexyl } -2 - pyridinecarbonitrile : Br & ₂HN NaBH ( OAc ) 3 . TFA Isopropylacetate , rt . 24 h CFBu P - Pd - G2 , tBuONa PhMe , 120 ° C , 16 h HCI ( 4N ) Dioxane , TINHNH , MeOH , rt , 4 h CN NHTS HO 3OC₂sC dioxane , 110 " C H CFCF1.98 g ( 93 % ) ; 796 mg ( 64 % ) 710 mg used 1.0 g crude ; 50 mg used 800 mg used 1.28 g 860 mg crude 50 mg used 3OC₂sC , CSF dioxane , 120 C ₂OC₂K . CsF dioxane . 120 ° C LCMS : 20 % DP , 35 % BP LCMS : 48 % DP , 11 % BP 350 mg used K2CO3 . CsF dioxane , 120 ° C LCMS : 8 % DP , 15 % BP , messy 200 mg used 200 mg 50 mg used x 1.0 g used gu 4.0 g used 7.05 g ( 83 % ) 1.5 g used Mixture of Diasteromers 1 : 34.2 mg WO 2025/049495 PCT / US2024 / 0440 [ 621 ] Compound 111 : 34.2 mg ( 41:59 mixture of diastereomers ) ; ' H NMR ( 400 MHz , CD3OD ) d 8.65 ( m , 1H ) , 8.4 ( m , 1H ) , 7.9 ( m , 1H ) , 7.8 ( m , 1H ) , 7.35-7.55 ( m , 4H ) , 6.65 ( d , 2H ) , 4.2-4.3 ( br . m , 1H ) , 3.85 , 3.95 ( s , s , 3H ) , 2.6-3.1 ( m , m , 1H ) , 2.4 ( br . s , 2H ) , 1.4-2.25 ( m , 6H ) ; LCMS ( ESI ) [ M + H ] + = 453 . [ 622 ] Example CO : ( 4 - cyclopropoxy - 3 - pyridyl ) [ 1- ( 2 - methyl - 5 - pyrimidinyl ) -4 - piperidyl ] [ p- ( trifluoromethyl ) phenyl ] amine : NH HCI Amberlyst A - 26 ( OH ) MeOH , rt , 1 h NH Br RuPhos Pd G3 , tBuONa dioxane , 120 ° C , 12 h [ 623 ] 0.8 g used 680 mg free base each 200 mg used 95.5 mg Compound 112 : 96 mg ; ' H NMR ( 400 MHz , CD3OD ) d 8.2-8.55 ( m , 4H ) , 7.55 ( d , 1H ) , 7.( d , 2H ) , 6.62 ( d , 2H ) , 4.2 ( m , 1H ) , 3.95 ( m , 1H ) , 3.80 ( m , 2H ) , 3.0 ( m , 2H ) , 2.55 ( s , 3H ) , 2.15 ( m , 2H ) , 1.55 ( m , 2H ) , 0.83 ( m , 2H ) , 0.55 ( m , 2H ) ; LCMS ( ESI ) [ M + H ] + = 470 . [ 624 ] Example CP : 3- { 4 - [ ( 4 - methoxy - 3 - pyridyl ) [ p- ( trifluoromethyl ) phenyl ] amino ] -1- piperidyl bicyclo [ 1.1.1 ] pentane - 1 - carbonitrile : CN N₂H CI Na2COMeOH , 60 ° C , 1 h 100 mg used 10mused 780 mg used 600 mg ( 44 % ) 260 mg used Br " NH2 CN CFCN TMSCI , BH 3 - THF DMF , 0 ° C , 30 min tBu3P - Pd - G2 , tBuONa toluene , 120 ° C , 16 h H 240 mg ( 58 % ) ; 20 mg used mg used CN LCMS : major DP 10.10 mg no STM remained [ 625 ] Compound 113 : 10 mg ; ' H NMR ( 400 MHz , CD3OD ) d 8.53 ( d , 1H ) , 8.24 ( s , 1H ) , 7.38 ( d , 2H ) , 7.32 ( d , 1H ) , 6.60 ( d , 2H ) , 4.04 ( m , 1H ) , 3.87 ( s , 3H ) , 2.37 ( m , 2H ) , 2.31 ( m , 2H ) , 2.27 ( s , 6H ) , 2.( m , 2H ) , 1.38 ( m , 2H ) LCMS ( ESI ) [ M + H ] + = 443 . [ 626 ] Example CQ : 2- { 4 - [ ( p - difluoromethoxyphenyl ) ( 4 - methoxy - 3- pyridyl ) amino ] cyclohexyloxy } -5 - pyrimidinecarbonitrile 165 OH Br OCHF NaH THF , 0 ~ 60 ° C 50 mg used OCHF33 mg ( 46 % ) ; all used K4 [ Fe ( CN ) 6 ] 3H2O , KOAC Br tBuXPhos , tBuXPhos Pd GDioxane / O₂H , 100 ° C , 16 h ACIE 2013 , 52 , 100 PCT / US2024 / 0440 OCHF40.28 mg 230 mg used [ 627 ] 158 mg ( 48 % ) ; all used Compound 114 : 40 mg ; ' H NMR ( 400 MHz , CD3OD ) d 8.87 ( d , 2H ) , 8.44 ( d , 1H ) , 8.18 ( s , 1H ) , 7.22 ( d , 1H ) , 6.91 ( d , 2H ) , 6.52 ( m , 3H ) , 4.95 ( m , 1H ) , 4.03 ( m , 1H ) , 4.02 ( s , 3H ) , 2.16 ( m , 4H ) , 1.( m , 2H ) , 1.33 ( m , 2H ) LCMS ( ESI ) [ M + H ] + = 468 . - [ 628 ] Example CR : 4 - methyl - 3 - pyridyl ) [ 1- ( 2 - methyl - 5 - pyrimidinyl ) -4 - piperidyl ] [ p- ( trifluoromethyl ) phenyl ] amine : CF NH NH Amberlyst A - 26 ( OH ) Br RuPhos Pd G3 , tBuONa ' N HCI MeOH , rt , 1 h dioxane , 120 ° C , 12 h CF 2.88 g used [ 629 ] 2.2 g free base each 200mg used 126 mg Compound 115 : 126 mg ; ' H NMR ( 400 MHz , CD3OD ) d 8.45 ( d , 1H ) , 8.30 ( m , 3H ) , 7.( d , 1H ) , 7.43 ( d , 2H ) , 6.61 ( d , 2H ) , 4.3 ( m , 1H ) , 3.84 ( m , 2H ) , 2.99 ( m , 2H ) , 2.54 ( s , 3H ) , 2.20 ( s , 3H ) , 2.13 ( m , 2H ) , 1.56 ( m , 2H ) ; LCMS ( ESI ) [ M + H ] + = 428 . [ 630 ] Example CS : ( p - difluoromethoxyphenyl ) ( 4 - methyl - 3 - pyridyl ) [ 1- ( 2 - methyl - 5- pyrimidinyl ) -4 - piperidyl ] amine : NH NH Amberlyst A - 26 ( OH ) Br RuPhos Pd G3 , tBuONa HCI MeOH , rt , 1 h dioxane , 120 ° C , 12 h OCHF 1.8 g used OCHFOCHF1.62 g free base 48.1 mg each 200 mg [ 631 ] Compound 116 : 48 mg ; ' H NMR ( 400 MHz , CD3OD ) d 8.35 ( br . m , 4H ) , 7.45 ( s , 1H ) , 6.( s , 2H ) , 6.55 ( m , 3H ) , 4.2 ( m , 1H ) , 3.85 ( m , 2H ) , 3.0 ( m , 2H ) , 2.55 ( s , 3H ) , 2.20 ( s , 3H ) , 2.05 ( m , 2H ) , 1.55 ( m , 2H ) ; LCMS ( ESI ) [ M + H ] + = 426 . 166 WO 2025/049495 PCT / US2024 / 0440 [ 632 ] Example CT : { 1- [ 2- ( methoxymethyl ) -5 - pyrimidinyl ] -4 - piperidyl } ( 4 - methoxy - 3- pyridyl ) [ p- ( trifluoromethyl ) phenyl ] amine : ' N ' CF NH Br N RuPhos Pd G3 , tBuONa dioxane , 120 ° C , 12 h | [ 633 ] 150 mg used 142 mg Compound 117 : 142 mg ; ' H NMR ( 400 MHz , CD3OD ) d 8.4-8.55 ( m , 3H ) , 8.21 ( s , 1H ) , 7.45 ( m , 2H ) , 7.25 ( d , 1H ) , 6.65 ( m , 2H ) , 4.5 ( m , 2H ) , 4.25 ( m , 1H ) . 3.90 ( m , 2H ) , 3.85 ( s , 3H ) , 3.42 ( s , 3H ) , 3.05 ( m , 2H ) , 2.15 ( m , 2H ) , 1.50 ( m , 2H ) ; LCMS ( ESI ) [ M + H ] + = 474 . [ 634 ] Example CU : ( 4 - cyclopropyl - 3 - pyridyl ) ( p - difluoromethoxyphenyl ) [ 1- ( 2 - methyl - 5- pyrimidinyl ) -4 - piperidyl ] amine : Br 500 mg used g used [ 635 ] ' N- Bo Bu PhMe , 120 ° C , 16 h OCHFP - Pd - G2 , tBuONa 16 ( 23 ) 542 mg ( 37 % ) * 200 mg + 260 mg used OH HO - B Boc Pd ( ₂dAPuBnO ' 2COPhMe / O₂H , MW , 1 230 mg OCHF 445 mg used Boc HCI / dioxane Dixane , 25 ° C , 1 h OCHF NH Br RuPhos Pd G3 , tBuONa dioxane , 120 ° C , 12 h 8 348 mg crude each 174 mg used 124.5 mg Compound 118 : 125 mg ; ' H NMR ( 400 MHz , CD3OD ) d 8.35 ( m , 3H ) , 8.20 ( s , 1H ) , 7.0 ( m , 3H ) , 6.56 ( m , 3H ) , 4.25 ( m , 1H ) , 3.85 ( m , 2H ) , 3.0 ( m , 2H ) , 2.55 ( s , 3H ) , 2.25 ( m , 2H ) , 2.05 ( m , 1H ) , 1.( m , 2H ) , 1.05 ( m , 2H ) , 0.85 ( m , 2H ) LCMS ( ESI ) [ M + H ] + = 452 . [ 636 ] Example CV : ( 4 - cyclopropyl - 3 - pyridyl ) [ 1- ( 2 - methyl - 5 - pyrimidinyl ) -4 - piperidyl ] [ p- ( trifluoromethyl ) phenyl ] amine : 167 WO 2025/049495 PCT / US2024 / 0440 ' N- Boc ° H HO - B OH Pd ( ₂dAPuBnO Boc Br N- Boc o go a goo HCl / dioxane . 2CON H tBu PhMe / O₂H , MW . 120 ° C 3P - Pd - G2 , tBuONa PhMe , 120 ° C , 16 h - Dixane , 25 ° C , 1hCF RuPhos Pd G3 , tBuONa dioxane , 120 ° C , 12 h CF 500 mg used 450 mg crude all used 285 mg ( mixture of 49 % DP and 46 % BP2 on LCMS ( 220 nm ) 500 mg used- 367 mg crude each 183 mg used 78 mg [ 637 ] Compound 119 : 78 mg ; ' H NMR ( 400 MHz , CD3OD ) d 8.2-8.4 ( m , 4H ) , 7.45 ( d , 2H ) , 7.( d , 1H ) , 6.65 ( d , 2H ) , 4.35 ( m , 1H ) , 3.85 ( m , 2H ) , 3.05 ( m , 2H ) , 2.55 ( s , 3H ) , 2.25 ( m , 2H ) , 2.0 ( m , 1H ) , 1.55 ( m , 2H ) , 1.05 ( m , 2H ) , 0.85 ( m , 2H ) ; LCMS ( ESI ) [ M + H ] + = 454 . [ 638 ] Example CW : 2- { 4 - [ ( 4 - methoxy - 3 - pyridyl ) [ p- ( trifluoromethyl ) phenyl ] amino ] cyclohexyloxy } -5 - pyrimidinecarbonitrile : N NaBHMeOH / THF .OH Br N N NaH DMF , 0-60 ° C CF K4 [ Fe ( CN ) 6 ] 3H2O , KOAC BrtBuXPhos , tBuXPhos Pd GDioxane / O₂H , 100 ° C , 16 h ACIE 2013 , 52 , 100400 mg used . 400 mg crude ; 50 mg used . mg crude ; all used mg used mg used . THF , 0-60 ° C DMSO , rt . LCMS : 26 % STM - 5,25 % DP . 150 mg used 64 mg ( 30 % ) tBuOK ( 3eq . ) 500 mg used . 436 mg crude : 20 mg used 150 mg used 260 mg used . [ 639 ] THF , 90 ° C , MW , 1h 150 mg ( 25 % ) ; all used .78 mg Compound 120 : 26 mg ; ' H NMR ( 400 MHz , CD3OD ) d 8.89 ( s , 2H ) , 8.54 ( br . s , 1H ) , 8.( br . s , 1H ) , 7.39 ( d , 2H ) , 7.33 ( m , 1H ) , 6.60 ( d , 2H ) , 4.95 ( s , 1H ) , 4.60 ( m , 1H ) , 4.12 ( s , 3H ) , 2.17 ( m , 4H ) , 1.76 ( m , 2H ) , 1.29 ( m , 2H ) ; LCMS ( ESI ) [ M + H ] + = 470 . [ 640 ] Example CX : ( 4 - ethyl - 3 - pyridyl ) [ 1- ( 2 - methyl - 5 - pyrimidinyl ) -4 - piperidyl ] [ p- ( trifluoromethyl ) phenyl ] amine : 168 Br N Boc ' N- Pd ( OA ) > ' n BuPAd 3OC₂sC H PhMe / O₂H , H MW , 120 ' C N Boc ' N- tBu3P Pd G2 , tBuONa PhMe , 120 ° C , 12 h CF200 mg used LCMS : 64 % DP , 24 % BP g x 2 used 1.3 g mixture 74 % DP and 22 % BP 100 mg used N Boc ' N- NH Br 1.HCl / dioxane 2. basic resin LCMS : 55 % DP , 12 % STM - PCT / US2024 / 0440 RuPhos Pd G3 , tBuO Na dioxane , 120 ° C , 12 h [ 641 ] 500 mg used 680 mg ( 92 % ) all used 390 mg crude each 195 mg used mg Compound 121 : 83 mg ; ' H NMR ( 400 MHz , CD3OD ) d 8.25-8.65 ( m , 4H ) , 7.55 ( m , 1H ) , 7.4 ( m , 2H ) , 6.65 ( m , 2H ) , 4.31 ( m , 1H ) , 3.85 ( m , 2H ) , 3.0 ( m , 2H ) , 2.55 ( m , 2H ) , 2.50 ( s , 3H ) , 2.15 ( m , 2H ) , 1.55 ( q , 2H ) , 1.15 ( t , 3H ) ; LCMS ( ESI ) [ M + H ] + = 442 . [ 642 ] Example CY : 2- { 4 - [ ( 4 - cyclopropyl - 3 - pyridyl ) [ 6- ( difluoromethyl ) -3 - pyridyl ] amino ] -1- piperidyl } -5 - pyrimidinecarbonitrile : HO - B OH Boc Pd ( OA ) ₂dAPuBn'20 ° H 500 mg used ₂OC₂sC PhMe / O₂H , MW , 120 ° C H 0.3 g ( 59 % ) all used Br Boc N- Boc tBu 3P - Pd - G2 , tBuONa PhMe , 120 ° C , 16h 0.3 g ( 71 % ) all used N NH CI HCl / dioxane Dioxane , 25 ° C , 1 h Et3N HCI CH & CN , 0 ° C , 1 h 232 mg crude all used 157 mg N : N [ 643 ] Compound 122 : 157 mg ; ' H NMR ( 400 MHz , CD3OD ) d 8.75 ( s , 2H ) , 8.42 ( m , 1H ) , 8.25 ( s , 1H ) , 7.85 ( m , 1H ) , 7.52 ( m , 1H ) , 7.20 ( m , 1H ) , 6.95 ( m , 1H0 , 6.65 ( m , 1H ) , 5.05 ( m , 2H ) , 4.55 ( m , 1H ) . 3.20 ( m , 2H ) , 2.25 ( m , 2H ) , 1.95 ( m , 1H ) , 0.85-1.545 ( br . m , 6H ) LCMS ( ESI ) [ M + H ] + = 448 . [ 644 ] Example CZ : ( p - difluoromethoxyphenyl ) ( 4 - ethyl - 3 - pyridyl ) [ 1- ( 2 - methyl - 5 - pyrimidinyl ) - - piperidyl ] amine : Br ° Boc Boc Pd ( OA ) ₂dAPuBn'CS.CO " N ~ ₂FHCO tBu3P Pd G2 , aNOúBt H PhMe / H - O , H MW , 120 ° C PhMe . 120 ° C , 12 h OCHF200 mg used LCMS : 64 % DP , 24 % BP g x 2 used 1.3 g mixture 74 % DP and 22 % BP 100 mg used 600 mg used Boc NH R 1.HCl / dioxane RuPhos Pd G3 , tBuONa 2. basic resin dioxane , 120 ° C , 12 h OCHFOCHFLCMS : 48 % DP , 12 % STM - 550 mg ( 62 % ) all used 320 mg free base after column and Prep - TLC purification , then HPLC purification 49.16 mg each 160 mg used WO 2025/049495 PCT / US2024 / 0440 [ 645 ] Compound 123 : 49 mg ; ' H NMR ( 400 MHz , CD3OD ) d 8.25-8.5 ( m , 4H ) , 7.55 ( s , 1H ) , 7.( m , 2H ) , 6.4-6.8 ( m , 3H ) , 4.2 ( m , 1H ) , 3.85 ( m , 2H ) , 2.95 ( m , 2H ) , 2.55 ( s , 3H ) , 2.10 ( q , 2H ) , 1.55 ( m , 2H ) , 1.4 ( m , 2H ) , 1.15 ( t , 3H ) ; LCMS ( ESI ) [ M + H ] + = 440 . [ 646 ] Example DA : 2- ( 4 - { [ 6- ( difluoromethyl ) -3 - pyridyl ] ( 4 - ethyl - 3 - pyridyl ) amino } -1- piperidyl ) -5 - pyrimidinecarbonitrile : Boc Pd ( OA ₂dAPuBn THF , MW , 110 ° C . 1 h H Br Boc ' N- tBu3P Pd G2 , tBuONa Ph Me , 120 ° C , 12h F Boc N NH N HCI / dioxane dioxane , rt . 2 h HCI N₂tE CH3CN , 0 ° C , 0.5 h 0.1 g +0.8 g used 0.72 g ( 7 % BP included ) 100 mg used 380 mg DP 620 mg used 280 mg used 280 mg STM recovered 185 mg DP used directly CHF 102 mg CN [ 647 ] Compound 124 : 102 mg ; ' H NMR ( 400 MHz , CD3OD ) d 8.60 ( s , 2H ) , 8.50 ( m , 1H ) , 8.30 ( s , 1H ) , 7.85 ( d , 1H ) , 7.60 ( d , 1H ) , 7.50 ( d , 1H ) , 7.15 ( d , 1H ) , 6.60 ( m , 1H ) , 5.05 ( m , 2H ) , 4.55 ( m , 1H ) , 3.( m , 2H ) , 2.6 ( m , 2H ) , 2.15 ( m , 2H ) , 1.35 ( m , 2H ) , 1.15 ( t , 3H ) ; LCMS ( ESI ) [ M + H ] + = 436 . [ 648 ] Example DB : ( R ) -4- { 4 - [ ( p - difluoromethoxyphenyl ) ( 4 - methoxy - 3 - pyridyl ) amino ] -1- piperidyl ) -1 - ethyl - 2 - pyrrolidinone : ₂HN HCI HATU , DIEA S iR ) Bn " OH NHBoc DCM , 0 ° C , 1 h NHBoc Bn P2STHF , rt , 4 h Bn i . NaBH4 , NICI O₂HEtOH / THF , rt , 2.5 days HCI / dioxane Na2CONHBOC ii . PhMe , 120 C˚ . 16 h O MeOH , 60 ° C , 1-2.5 h BocHN HNR ) g used g used US2008039517A1 US2008039517A1 US2008039517Ano DP 5.2 g ; 3 g used 2.2 g used US2021 / 115010 ; ( 2021 ) : ( A ) English WO2021 / 81074 : ( 2021 ) ; ( A1 ) English JACS , 2000 , 3721 - 372.6 g ; all used 1.95 g ; all used 1.26 ) 908 mg ( HCI salt ) 100 mg used 808 mg used- mg crude ; all used 745 mg crude ; all used Br • ₂HN TMSCI , BH3 - THF DMF , 0 ° C , 30 min OCHFtBu3P Pd G2 , tBuONa PhMe , 120 C , 16 h 50 mg mg used tBu P , Pd ( OAc ) 2 , tBuONa 84 mg mg used mg ; all used PhMe , 120 ° C , 16h P₂uBt Pd G2 , tBuONa OCHF [ 649 ] PhMe , 120 ° C , 16 h Compound 126 : 84 mg ; ' H NMR ( 400 MHz , CDCl3 ) d 8.50 ( d , 1H ) , 8.2 ( s , 1H ) , 6.95 ( m , 3H ) , 6.18 -6.55 ( br . m , 3H ) , 3.85 ( m , 1H ) , 3.70 ( s , 3H ) , 3.45 ( m , 2H ) , 3.30 ( m , 2H ) , 3.1 ( m , 1H ) , 2.95 ( m , 170 WO 2025/049495 PCT / US2024 / 0440 2H ) , 2.55 ( m , 1H ) , 2.40 ( m , 1H ) , 2.2 ( m , 2H ) , 2.05 ( m , 2H ) , 1.5 ( m , 2H ) , 1.1 ( t , 3H ) LCMS ( ESI ) [ M + H ] + = 461 . = [ 650 ] Example DC : [ 1- ( 5 - mesyl - 2 - pyrimidinyl ) -4 - piperidyl ] ( 4 - methyl - 3 - pyridyl ) [ p- ( trifluoromethyl ) phenyl ] amine : CF NH 3HC₂OS 3HC₂OS Et3N HCI CH3CN , 0 ° C , 0.5 h [ 651 ] 200 mg used 147 mg Compound 127 : 147 mg ; ' H NMR ( 400 MHz , DMSO - d6 ) d 8.7 ( s , 2H ) , 8.49 ( d , 1H ) , 8.3 ( s , 1H ) , 7.45 ( m , 3H ) , 6.60 ( d , 2H ) , 4.85 ( m , 2H ) , 4.50 ( m , 1H ) , 3.25 ( m , 2H ) , 3.1 ( s , 3H ) , 2.1 ( s , 3H ) , 2.( m , 2H ) , 1.25 ( m , 2H ) LCMS ( ESI ) [ M + H ] + = 492 . [ 652 ] Example DD : 5- { 4 - [ ( 4 - methyl - 3 - pyridyl ) [ p- ( trifluoromethyl ) phenyl ] amino ] -1- piperidyl } -2 - pyrimidinecarbonitrile : HCI CN N CN NH 3OC₂K DMSO , 80 ° C , 2 h 250 mg used [ 653 ] 192 mg Compound 128 : 192 mg ; ' H NMR ( 400 MHz , DMSO - d6 ) d 8.55 ( s , 2H ) , 8.3 ( m , 2H ) , 7.( m , 3H ) , 6.60 ( m , 2H ) , 4.45 ( m , 1H ) , 4.15 ( m , 2H ) , 3.15 ( m , 2H ) , 2.15 ( s , 3H ) , 2.0 ( m , 2h ) , 1.35 ( m , 2H ) ; LCMS ( ESI ) [ M + H ] + = 439 . [ 654 ] Example DE : ( S ) -1 ' - ethyl - 4 - [ ( 4 - methoxy - 3 - pyridyl ) [ p- ( trifluoromethyl ) phenyl ] amino ] [ 1,3 ' - bipiperidyl ] -6 ' - one : 171 Bn- HO ( S ) . 7 g used ₂HN HCI HN NHBoc DCM . 0 ° C , 1 h HATU , DIEA P2SS. NHBOC THF , rt , 4 h Bn Bn 7.2 g ( 95 % ) ﻢﻳں ﻢﺴﻠﻣ Na2COMeOH , 60 ° C , 1-2.5 h US2021 / 115010 : ( 2021 ) ; ( A1 ) English WO2021 / 81074 ; ( 2021 ) ; ( A1 ) English JACS , 2000 , 3721 - 37 PCT / US2024 / 0440 HN S i . NaBH4 , NiCl2 O₂H( S. EtOH / THF , rt , 2.5 days HCI / dioxane NHBOC ( 5 ) ii . PhMe , 120 ° C . 12 h BocHN N₂H sdfy free base g ( 63 % ) .1.8 g crude ; 1 g used 0.8 g used ₂HN Br TMSCI , BH - THF DMF , 0 ° C , 30 min N tBu P Pd G2 . tBuONa PhMe , 120 ° C , 12 h HO [ 655 ] 1.05 g ( 66 % ) ; 50 mg used- 0.88 g ( 69 % ) 0.95 g used + 25 ° C , 15 h LCMS ( 254nm ) : 66 % DP , 24 % STM 0.55 g ( contained BP ) after column after pre - HPLC ( basic ) 195 mg 20 mg used 150 mg used SFC : 99 % ee 208 mg after column , HNMR showed not pure after pre - HPLC ( FA ) 108 mg Compound 129 : 108 mg ; ' H NMR ( 400 MHz , DO₂DC ) d 8.55 ( d , 1H ) , 8.25 ( m , 2H ) < 7.( d , 2H ) , 7.30 ( d , 1H ) , 6.65 ( d , 2H ) , 4.2 ( m , 1H ) , 3.92 ( s , 3H ) , 3.05-3.55 ( br . m , 6H ) , 2.80 ( m , 2H ) , 2.5 ( m , 1H ) , 2.4 ( m , 1H ) , 2.05-2.2 ( m , 3H ) , 1.85 ( m , 1H ) , 1.55 ( m , 1H ) , 1.15 ( t , 3H ) LCMS ( ESI ) [ M + H ] + = 477 . [ 656 ] Example DF : [ 4- ( ³H² ) methoxy ( 2,5,6 - ³H² ) -3 - pyridyl ] [ 1- ( 2 - methyl - 5 - pyrimidinyl ) -4- piperidyl ] [ p- ( trifluoromethyl ) phenyl ] amine : D D H.N Boc Pd ( OAc ) 2 , BINAP , tBuONa Br PhMe , 100 ° C , 16 h OCD 50 mg used 200 mg used Boc D Boc Br tBu -CFtBuOND 3P - Pd - G2,3eq 1. HCl / dioxane . rt , 1 h PhMe , 120 ° C . 16h 2. Basic resin , MeOH , rt . 1 h 52 mg 54 mg ( 71 % ) 250 mg ( 77 % ) 310 mg ( 84 % ) mg crude 266 mg crude NH RuPhos - Pd - G3 , tBuONa dioxane , 120 ° C . 12 h after prep - HPLC ( basic ) -230 mg ready [ 657 ] Compound 130 : 230 mg ; H¹ NMR ( 400 MHz , CD3OD ) d 8.32 ( s , 2H ) , 7.41 ( d , 2H ) , 6.65 ( d , 2H ) , 4.21 ( m , 1H ) , 3.82 ( m , 2H ) , 3.0 ( m , 2H ) , 2.55 ( s , 3H ) , 2.15 ( m , 2H ) , 1.52 ( m , 2H ) ; LCMS ( ESI ) [ M + H ] + = 450 . [ 658 ] Example DG : ( p - difluoromethoxyphenyl ) [ 1- ( 5 - mesyl - 2 - pyrimidinyl ) -4 - piperidyl ] [ 4- ( 2H3 ) methoxy ( 2,5,6 - ³H² ) -3 - pyridyl ] amine : 172 WO 2025/049495 PCT / US2024 / 0440 3HC₂OS SO - CH₂FHCO Boc D. N Boc NH Boc Br D N₂H tBu DǝNOuBt HCI / dioxane Pd ( OAc ) 2 , BINAP , tBuONa Br PhMe , 100 ° C , 16h 3P - Pd - G2 , 4 eq PhMe , 120 ° C , 16h rt . 1 h Et3N CH3CN . 0 ° C OCDOCHFHCI OCHFOCHF 300 mg used [ 659 ] 412 mg ( 83 % ) ; 50 mg used 362 mg used 393 mg ( 65 % ) 338 mg crude after prep - HPLC ( basic ) -315 mg ready Compound 131 : 300 mg ; ' H NMR ( 400 MHz , CD3OD ) d 8.62 ( s , 2H ) , 6.95 ( d , 2H ) , 6.60 ( m , 3H ) , 4.95 ( m , 2H ) , 4.30 ( m , 1H ) , 3.15 ( m , 2H ) , 3.10 ( s , 3H ) , 2.12 ( m , 2H ) , 1.32 ( m , 2H ) ; LCMS ( ESI ) [ M + H ] + = 512 . [ 660 ] Example DH : [ 4- ( ³H² ) methoxy - 3 - pyridyl ] [ 1- ( 2 - methyl - 5 - pyrimidinyl ) -4 - piperidyl ] [ p- ( trifluoromethyl ) phenyl ] amine : Boc OCD Br Pd ( OAc ) 2 , BINAP , tBuONa PhMe , 100 ° C , 16h 50 mg used 200 mg used mg ( 73 % ) 219 mg ( 67 % ) Boc ' N- ' N ~ Boc tBu Br -CFP - Pd - G2 , 3eq tBuONa 1. HCl / dioxane , rt , 1 h PhMe , 120 ° C , 16 h 2. Basic resin , MeOH , rt , 1 h 78 mg ( 88 % ) 236 mg ( 73 % ) mg crude 184 mg crude NH Br RuPhos - Pd - G3 , tBuONa dioxane , 120 ° C , 12h 8 after prep - HPLC ( basic ) ~ 185 mg ready [ 661 ] Compound 132 : 185 mg ; ' H NMR ( 400 MHz , CD3OD ) d 8.5 ( d , 1H ) , 8.40 ( s , 2H ) , 8.25 ( s , IH ) , 7.45 ( d , 2H ) , 7.25 ( d , 1H ) , 6.65 ( d , 2H ) , 4.25 ( m , 1H ) , 3.82 ( m , 2H ) , 2.95 ( m , 2H ) , 2.55 ( s , 3H ) , 2.( m , 2H ) , 1.55 ( m , 2H ) ; LCMS ( ESI ) [ M + H ] + = 447 . [ 662 ] Example DI : ( p - difluoromethoxyphenyl ) [ 1- ( 5 - mesyl - 2 - pyrimidinyl ) -4 - piperidyl ] [ 4- ( 2H3 ) methoxy - 3 - pyridyl ] amine : OCDBr Boc H Pd ( OAc ) 2 , BINAP , tBuONa PhMe , 100 ° C , 16h 50 mg used 60 mg ( 73 % ) 200 mg used 219 mg ( 67 % ) 300 mg used 378 mg ( 77 % ) mg used Boc tBu OCHFBoc 3P - Pd - G2 , 3eq tBuONa PhMe , 120 ° C , 16 h NH HCI / dioxane 3HC₂OS 3HC₂OS N₂tE CH & CN . 0 ° C rt , 1 h OCHFHCI OCHFOCHF LCMS : 30 % DP , 30 % STM ; + Pd ( 0.2 eq ) , tBuONa ( 4 eq ) , 5h LCMS : major DP , no STM mg crude mg ( 76 % ) tBu mg used P - Pd - G2 , 4eq tBuONa PhMe , 120 ° C . 16 h after prep - HPLC ( basic ) LCMS : 3 % DP , 50 % STM -300 mg ready 278 mg used LCMS : 11 % DP , 51 % STM 340 mg ( 71 % ) 292 mg crude [ 663 ] Compound 133 : 300 mg ; ' H NMR ( 400 MHz , CD3OD ) d 8.85 ( s , 2H ) , 8.56 ( d , 1H ) , 8.32 ( s , 1H ) , 7.4 ( d , 1H ) , 7.15 ( d , 2H ) , 6.8 ( m , 3H ) , 5.20 ( m , 2H ) , 4.52 ( m , 1H ) , 3.35 ( m , 2H ) , 3.28 ( s , 3H ) , 2.( m , 2H ) , 1.50 ( m , 2H ) ; LCMS ( ESI ) [ M + H ] + = 509 . 173 [ 664 ] Example DJ : 2- { 1 - hydroxy - 4 - [ ( 4 - methoxy - 3 - pyridyl ) [ p- ( trifluoromethyl ) phenyl ] amino ] cyclohexyl } -5 - pyrimidinecarbonitrile : PCT / US2024 / 0440 Br Br ﮦﻮﺗا ﮦﻭ ۔ ﮦﺭ ﻦﻣﻮﺗ DCM , -75 ° C PзuBtO Pd G2 , tBuONa TFA , NaBH ( OAc ) ₂HN isopropyl acetate toluene , 125 ° C , 16 h - rt , 16 h H 3.0 g used 2.55 g ( 40 % ) ; 1.0 g used Zn ( CN ) 2 . Pd ( dba ) 3 . dppf DMF , 120 ° C CF CN Br 1.36 g ( 88 % ) 1.11 g crude : 0.45 g used three batches Park 150 pomesa : 187 mg used 150 mg Peak [ 665 ] mg ( 59 % ) Compound 134 - isomer 1 : 80 mg ; ' H NMR ( 400 MHz , CD3CN ) d 9.1 ( s , 2H ) , 8.52 ( d , 1H ) , 8.28 ( d , 1H ) , 7.40 ( d , 2H ) , 7.15 ( d , 1H ) , 6.61 ( d , 2H ) , 4.15 ( m , 1H ) , 3.85 ( m , 1H ) , 3.70 ( s , 3H ) , 2.5 ( m , 2H ) , 2.0 ( m , 2H ) , 1.85 ( m , 2H ) , 1.32 ( m , 2H ) ; LCMS ( ESI ) [ M + H ] + = 470 . Br CF NH , TFA . NaBH ( OAC ) isopropyl acetate - rt , 16 h P₂uBt Pd G2 , tBuONa toluene , 125 ° C . 16 h H 3.0 g used 2.55 g ( 40 % ) ; 1.0 g used Zn ( CN ) 2 , Pd2 ( dba ) 3 , dppf DMF , 120 ° C CN HCI ( 4N ) dioxane Br Br OHI nBuLi DCM , -75 ° C three batches 1.36 g ( 88 % ) 1.11 g crude ; 0.45 g used Pak 15 peab ?: 187 mg used 177 mg Peak [ 666 ] mg ( 50 % ) Compound 134 - isomer 2 : 78 mg ; ' H NMR ( 400 MHz , CD3CN ) d 9.1 ( s , 2H ) , 8.52 ( d , 1H ) , 8.28 ( d , 1H ) , 7.40 ( d , 2H ) , 7.15 ( d , 1H ) , 6.61 ( d , 2H ) , 4.15 ( m , 1H ) , 4.05 ( m , 1H ) , 3.80 ( s , 3H ) , 2.22 ( m , 2H ) , 2.02 ( m , 2H ) , 1.6-1.8 ( br . m , 4H ) ; LCMS ( ESI ) [ M + H ] + = 470 . 174 WO 2025/049495 PCT / US2024 / 0440 [ 667 ] Example DK : 2- { 4 - [ ( p - difluoromethoxyphenyl ) ( 4 - methoxy - 3 - pyridyl ) amino ] -1- hydroxycyclohexyl } -5 - pyrimidinecarbonitrile : ° OCHF300 mg used nBuLi THF , -75 ° C 3 batches DCM , -75 ° C Br Br N Zn ( CN ) 2 , Pd ( PPh3 ) DMF , 120 ° C OCHFPe 172 mg ( 4007Jumak2 : 95 mg ) after used mg Peak OCHF 36 mg ( 52 % ) [ 668 ] Compound 135 - isomer 1 : 36 mg ; ' H NMR ( 400 MHz , CD3OD ) d 9.1 ( s , 2H ) , 8.35 ( d , 1H ) , 8.06 ( s , 1H ) , 7.10 ( d , 1H ) , 6.9 ( m , 2H ) , 6.56 ( m , 3H ) , 4.12 ( m , 1H ) , 3.75 ( s , 3H ) , 2.66 ( m , 2H ) , 1.97 ( m , 2H ) , 1.85 ( m , 2H ) , 1.29 ( m , 2H ) ; LCMS ( ESI ) [ M + H ] + = 468 . nBuLi THF , -75 ° C OCHF300 mg used batches DCM , -75 ° C Br OCHF Br Zn ( CN ) 2 , Pd ( PPh3 ) DMF , 120 ° C 172 mg ( 40 : 95 mg ) atte'r mg used Peak OCHF 60 mg ( 58 % ) N [ 669 ] Compound 135 - isomer 2 : 60 mg ; ' H NMR ( 400 MHz , CD3OD ) d 9.01 ( s , 2H ) , 8.51 ( br . s , 1H ) , 8.32 ( br . s , 1H ) , 6.97 ( m , 3H ) , 6.2-6.6 ( br . m , 3H ) , 4.0 ( m , 2H ) , 3.8 ( s , 3H ) , 2.24 ( m , 2H ) , 2.04 ( m , 2H ) , 1.78 ( m , 4H ) ; LCMS ( ESI ) [ M + H ] + = 468 .

BIOLOGICAL ASSAY EXAMPLES Mouse OPC Preparation [ 670 ] To assess effects of treatments on OPCs , all treatments were assayed in two or more independent platings of epiblast stem cell - derived OPCs ( EpiSC ) . EpiSC - derived OPCs were obtained using in vitro differentiation protocols and culture conditions described previously ( Najm et al , 2011 , Nature Methods ) . OPCs were expanded and frozen down in aliquots . OPCs were thawed into growth conditions for at least one passage before use in further assays .

Determination of EC50 values of Compounds A : In vitro phenotypic screening of OPCs [ 671 ] Each compound's ability to induce maturation of murine OPCs into oligodendrocytes was assessed . EpiSC - derived OPCs were grown and expanded in poly - L - ornithine ( PO ) and laminin - coated 175 WO 2025/049495 PCT / US2024 / 0440 flasks in N2B27 media ( DMEM / F12 ( Gibco ) , N2 - MAX ( R & D Systems ) , B - 27 ( ThermoFisher ) , and GlutaMax ( Gibco ) ) supplemented with FGF2 ( 10 gµ / mL , R & D systems , 233 - FB - 025 ) and PDGF - AA ( gµ / mL , R & D systems , 233 - AA - 050 ) before harvesting for experiments . The cells were seeded onto poly- L - ornithine or poly - D - lysine coated CellCarrier Ultra plates ( PerkinElmer ) coated with laminin ( Sigma , L2020 ) at a density of 150,000 / ²mc in N2B27 media without growth factors . For dose - response testing , a 1000x compound stock in dimethyl sulphoxide ( DMSO ) was added to assay plates , resulting in 8 - point dose curves . Positive controls and DMSO vehicle controls were included in each assay plate . Cells were incubated under standard conditions ( 37 ° C , 5 % CO ) for 3 days and fixed with 4 % paraformaldehyde ( PFA ) in phosphate buffered saline ( PBS ) for 20 min . Fixed plates were washed with PBS , permeabilized with 0.1 % Triton X - 100 , and blocked with 10 % donkey serum ( v / v ) in PBS for 40 min . Then , cells were labelled with MBP antibodies ( Abcam , ab7349 ; 1 : 200 ) overnight at 4 ° C , washed with PBS , and stained with Alexa Fluor conjugated secondary antibodies ( 1 : 500 ) for 45 min . Nuclei were visualized by DAPI staining ( Sigma ; 1 g / ml ) , followed by further PBS washes . B : High - content imaging and analysis [ 672 ] Cells and cell culture plates were imaged on the Operetta High Content Imaging and Analysis system ( PerkinElmer ) . Analysis ( PerkinElmer Harmony and Columbus software ) began by identifying intact nuclei stained by DAPI . The peri - nuclear region of each cell was then cross - referenced with the mature myelin protein ( MBP ) stain to identify oligodendrocyte nuclei , and from this the percentage of oligodendrocytes was calculated . ECso values were calculated using The Levenberg - Marquardt algorithm to fit a Hill equation to the 8 - point dose - response curve . The results are provided in Table 3 ( OPC EC50 ) .

Determination of Potency and Enzyme Target GC / MS - based sterol profiling A : Murine Sterol Profiling Assay [ 673 ] Each compound's ability to induce accumulation of key sterol intermediates within the cholesterol biosynthesis pathway was assessed . Sterols were monitored using a modified Folch wash protocol ( Hubler et al , 2018 , Nature ) . EpiSC - derived OPCs were plated at 100,000 cells per well in PO- and laminin - coated 96 - well plates in N2B27 media without growth factors . After 24 hours , cells were rinsed with saline and plates were frozen . Cholesterol - d7 standard was then added to each well before drying under nitrogen stream and derivatization with 55 lµ of bis ( trimethylsilyl ) trifluoroacetamide . After derivatization , lμ were analyzed by gas chromatography / mass spectrometry using an Agilent 5973 Network Mass Selective Detector equipped with a 6890 gas chromatograph system and a HP - 5MS capillary column ( 30m x 0.25mm x 0.25mm ) . Samples were analyzed in full scan mode using electron impact ionization ; ion fragment peaks were integrated to calculate sterol abundance , and quantitation was relative to cholesterol- 176 WO 2025/049495 PCT / US2024 / 0440 d7 . The following ion fragments were used to quantitate each metabolite : cholesterol - d7 ( 465 ) , FF - Mas ( 482 ) , cholesterol ( 368 ) , zymostenol ( 458 ) , zymosterol ( 456 ) , Desmosterol ( 456 , 343 ) , 7- dehydrocholesterol ( 456 , 325 ) , lanosterol ( 393 ) , lathosterol ( 458 ) , 14 - dehydrozymostenol ( 456 , 351 ) , and dihydrolanosterol ( 395 ) . For reference , Table 2 shows sterol GC - MS analytes and their relationship with inhibitors of cholesterol biosynthesis . All standards were obtained from Avanti Polar Lipids unless otherwise indicated . Calibration curves were generated by injecting varying concentrations of sterol standards and maintaining a fixed amount of cholesterol - D7 . For normalized lanosterol accumulation results , the total amount of lanosterol measured after drug treatment was divided by the total amount of lanosterol accumulated after 24 hr treatment with 100 nM positive control reference . EC 50 values were calculated using The Levenberg - Marquardt algorithm to fit a Hill equation to an 8 - point dose - response curve . EC50 values for lanosterol ( Murine GCMS EC50 ) are provided in Table 3 . [ 674 ] Table 2. Sterol Analytes Analyte increased Lanosterol Dihydrolanosterol FF - MAS - dehydrozymostenol Zymosterol Zymostenol - dehydrocholesterol Cholesterol enzyme inhibited CYPCYPTM7SF2 ( Sterol 14 Reductase ) TM7SF2 ( Sterol 14 Reductase ) EBP EBP DHCR [ 675 ] B : Human Sterol Profiling Assay Each compound's ability to induce accumulation of key sterol intermediates within the cholesterol biosynthesis pathway was assessed in human cells . Sterols were monitored using a modified Folch wash protocol ( Hubler et al , 2018 , Nature ) . Human Mesenchymal stem cells ( hMSCs ) were plated at 50,000 cells per well in Nunc MicroWell 96 - well plates in hMSC High Performance Media Kit media ( RoosterBio ) . After 24 hours , cells were rinsed with saline and plates were frozen . Cholesterol - d7 standard was then added to each well before drying under nitrogen stream and derivatization with 55 lμ of bis ( trimethylsilyl ) trifluoroacetamide . After derivatization , 2 lμ were analyzed by gas chromatography / mass spectrometry using an Agilent 5973 Network Mass Selective Detector equipped with a 6890 gas chromatograph system and a HP - 5MS capillary column ( 30m x 0.25mm x 0.25mm ) . Samples were analyzed in full scan mode using electron impact ionization ; ion fragment peaks were integrated to calculate sterol abundance , and quantitation was relative to cholesterol - d7 . The following ion fragments were used to quantitate each metabolite : cholesterol - d7 ( 465 ) , FF - Mas ( 482 ) , cholesterol ( 368 ) , zymostenol ( 458 ) , 177 WO 2025/049495 PCT / US2024 / 0440 zymosterol ( 456 ) , Desmosterol ( 456 , 343 ) , 7 - dehydrocholesterol ( 456 , 325 ) , lanosterol ( 393 ) , lathosterol ( 458 ) , 14 - dehydrozymostenol ( 456 , 351 ) , and dihydrolanosterol ( 395 ) . For reference , Table 2 above shows sterol GC - MS analytes and their relationship with inhibitors of cholesterol biosynthesis . All standards were obtained from Avanti Polar Lipids unless otherwise indicated . Calibration curves were generated by injecting varying concentrations of sterol standards and maintaining a fixed amount of cholesterol - D7 . For normalized lanosterol accumulation results , the total amount of lanosterol measured after drug treatment was divided by the total amount of lanosterol accumulated after 24 hr treatment with 100 nM positive control reference . EC 50 values were calculated using The Levenberg - Marquardt algorithm to fit a Hill equation to an 8 - point dose - response curve . EC 50 values for lanosterol ( Human GCMS EC50 ) are provided in Table 3 . [ 676 ] Table 3. Assay Values Compound No. Human Mouse GC / MS GC / MS EC Mouse OPC Differentiation EC50 ( Mμ ) ( Mμ ) EC ( Mμ ) Fenarimol 53.2 > 1 0.0025 0.00469 0.032 0.0209 0.00341 0.013 0.00149 0.00318 0.014 0.00201 0.00258 0.0210 0.00244 0.00472 0.046 0.00231 0.00844 0.057 0.00273 0.00397 0.028 0.00126 0.00256 0.09 0.00397 0.0113 0.0710 0.00241 0.0047 0.0111 0.00118 0.00539 0.0212 0.00124 0.00327 0.00713 0.00136 0.00529 0.0214 0.00103 0.00368 0.00815 0.00149 0.00402 0.00816 0.00107 0.00302 0.0117 0.00312 0.0107 0.0518 0.0016 0.00383 0.0119 0.00209 0.00508 0.020 0.00237 0.00452 0.0521 0.00383 0.00913 0.122 0.00642 0.0109 0.23 0.00328 0.0112 0.2 178 WO 2025/049495 PCT / US2024 / 0440 Compound No. Human GC / MS Mouse GC / MS EC EC 50 ( Mμ ) Mouse OPC Differentiation EC ( Mµ ) ( Mμ ) 224 0.00129 0.00359 0.00825 0.00182 0.00376 0.0226 0.00292 0.00504 0.0427 0.00184 0.00526 0.0528 0.00294 0.0054 0.0629 0.00168 0.00574 0.0830 0.00161 0.0114 0.131 0.00102 0.00479 0.0332 0.00183 0.00734 0.0433 0.00218 0.0113 0.134 0.000809 0.0041 0.0135 0.00147 0.00542 0.0636 0.00157 0.0041 0.0537 0.00221 0.00795 0.0838 0.000846 0.00322 0.00639 0.00256 0.00929 0.0540 0.00207 0.00567 0.0841 0.0012 0.00463 0.0142 0.000768 0.00338 0.0143 0.00102 0.00471 0.0244 0.000754 0.00418 0.0245 0.00168 0.00461 0.0146 0.00153 0.00502 0.0147 0.00194 0.00561 0.0248 0.00148 0.00741 0.040.00111 0.00561 0.0350 0.00126 0.00517 0.0251 0.00147 0.00746 0.0552 0.00218 0.0109 0.0553 0.00141 0.00717 0.0354 0.00134 0.00565 0.0155 0.0006 0.00759 0.0256 0.00128 0.00764 0.0357 0.000731 0.0119 0.0758 0.00095 0.00947 0.0459 0.000508 0.00971 0.0360 0.00121 0.00591 0.02 179 WO 2025/049495 PCT / US2024 / 0440 Compound No. Human GC / MS Mouse GC / MS EC EC ( Mμ ) Mouse OPC Differentiation EC ( Mμ ) ( Mμ ) 0.000632 0.0037 0.020.00137 0.00529 0.030.00287 0.00764 0.000532 0.00315 0.0080.00161 0.00719 0.066 0.000961 0.00299 0.00667 0.00118 0.00346 0.0080.000841 0.00296 0.00369 0.000851 0.00162 0.00470 0.00204 0.00442 0.0171 0.00079 0.0027 0.00472 0.000588 0.00321 0.073 0.00127 0.00378 0.0174 0.000365 0.00317 0.00475 0.00050.0034 0.00676 0.00131 0.00446 0.077 0.000672 0.0074 0.0278 0.00212 0.00734 0.0279 0.00153 0.00543 0.02100 0.00248 0.0157 0.08101 0.00399 0.0269 0.1102 0.0145 0.0162 0.2103 0.00131 0.0145 0.09104 - isomer 1 0.0078 0.038 0.05104 - isomer 2 0.00302 0.0343 0.2105 - isomer 1 0.00087 0.00438 0.01105 - isomer 2 0.00637 0.0602 0.3106 0.00124 0.00546 0.01107 0.000704 0.00402 0.108 0.00156 0.00484 0.007( mixture of two isomers ) 109 0.00883 0.0155 0.06110 0.00605 0.00856 0.04111 0.0023 0.00549 0.009( mixture of two isomers ) 112 0.00175 0.00369 0.008113 0.00459 0.036 0.2 180 WO 2025/049495 PCT / US2024 / 0440 Compound No. Human GC / MS Mouse GC / MS EC EC( Mμ ) Mouse OPC Differentiation EC ( uM ) ( Mμ ) 114 0.00192 0.0152 0.0710.0050.0241 0.2116 0.00711 0.0473 0.3117 0.0039 0.0167 0.09118 0.00124 0.00539 0.01119 0.00162 0.00584 0.01120 0.00339 0.0326 0.3121 0.00182 0.00713 0.03122 0.00679 0.0083 0.09123 0.0005 0.00935 0.08124 0.00529 0.0189 0.1125 0.00442 0.0439 0.2126 0.0217 0.0356 0.3127 0.00162 0.00357 0.009128 0.0026 0.0205 0.1129 0.0175 0.0612 0.4130 0.00083 0.00391 0.03131 0.0005 0.00119 0.00510.00076 0.0034 0.03133 0.0005 0.00125 0.00134 - isomer 1 0.0145 0.0271 0.3134 - isomer 2 0.922 > 135 - isomer 135 - isomer 0.030.90.0194 0.2> [ 677 ] Efforts have been made to ensure accuracy with respect to numbers used ( e.g. , amounts , temperature , etc. ) but some experimental errors and deviations should be accounted for . [ 678 ] One skilled in the art will recognize many methods and materials similar or equivalent to those described herein , which could be used in the practicing the subject matter described herein . The present disclosure is in no way limited to just the methods and materials described . [ 679 ] Unless defined otherwise , technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this subject matter belongs , and are consistent with : Singleton et al ( 1994 ) Dictionary of Microbiology and Molecular Biology , 2nd Ed . , J. Wiley & Sons , New York , NY ; and Janeway , C. , Travers , P. , Walport , M. , Shlomchik ( 2001 ) Immunobiology , 5th Ed . , Garland Publishing , New York . 181 WO 2025/049495 PCT / US2024 / 0440 [ 680 ] Throughout this specification and the claims , the words " comprise , " " comprises , " and " comprising " are used in a non - exclusive sense , except where the context requires otherwise . It is understood that embodiments described herein include " consisting of " and / or " consisting essentially of " embodiments . [ 681 ] Where a range of values is provided , it is understood that each intervening value , to the tenth of the unit of the lower limit , unless the context clearly dictates otherwise , between the upper and lower limit of the range and any other stated or intervening value in that stated range , is encompassed . The upper and lower limits of these small ranges which may independently be included in the smaller rangers is also encompassed , subject to any specifically excluded limit in the stated range . Where the stated range includes one or both of the limits , ranges excluding either or both of those included limits are also included . [ 682 ] Many modifications and other embodiments set forth herein will come to mind to one skilled in the art to which this subject matter pertains having the benefit of the teachings presented in the foregoing descriptions and the associated drawings . Therefore , it is to be understood that the subject matter is not to be limited to the specific embodiments disclosed and that modifications and other embodiments are intended to be included within the scope of the appended claims . Although specific terms are employed herein , they are used in a generic and descriptive sense only and not for purposes of limitation . 182

Claims (90)

1. WO 2025/0494 A compound of Formula A : CLAIMS ³R PCT / US2024 / 0440 R1a ⋅N- A R1 R2a ²R , wherein . A is selected from the group consisting of ₁C - C6 alkyl , C3 - C8 cycloalkyl , phenyl , 5- to 6- membered heteroaryl and 5- to 6 - membered heterocyclyl , each of which is optionally substituted with one or more of RAI RA2 and RAAl ﻭ wherein , RAI , RA2 and RA3 are each independently selected from the group consisting of ₁C - C6 alkyl , halo - ₁C - C6 alkyl , ₁C - C6 alkoxy , halo , cyano , oxo , -C ( O ) ¸ªR- -S ( O ) -RAand -S ( O ) 2 - RA AAwherein , RA is C1 - C6 alkyl or C3 - C8 cycloalkyl , and Awherein the oxo , if present , is formed by two of RAI , RA2 and ³AR together with a carbon to which each is attached : G is -CH , C - OH , or N ; E , if present , is -C ( O ) - or -O- ; Y is -CH or N ; p is 1 , 2 or 3 ; q is 1 or 0 ; r is 1 or 0 : wherein , when r is 0 , A is other than ₁C - C6 alkyl ; ¹R is selected from the group consisting of C1 - C6 alkyl , C3 - C8 cycloalkyl and halo - ₁C - óC alkyl ; or ¹R is halo and q is 0 ; la a¹R is selected from the group consisting of hydrogen , halo , C1 - C6 alkyl ; ²R is selected from the group consisting of halo , halo - ₁C - C6 alkyl , halo - ₁C - C6 alkoxy and 183 WO 2025/049495 PCT / US2024 / 0440 -S ( O ) 2- ( C1 - C6 alkyl ) ; and , R2a is selected from the group consisting of hydrogen and halo ; ³R is hydrogen , halo , or C1 - C6 alkyl , or a pharmaceutically acceptable salt or solvate thereof .

2. The compound of claim 1 , or a pharmaceutically acceptable salt or solvate thereof , having a structure of Formula I , Formula A - i , or Formula A - ii : R1a R1a . N R -N R2a -N R1 R2a R R R ²R A A I A - i WO 2025/0494 R1a- N R RR2a R OH A PCT / US2024 / 0440 A - ii

3. The compound of claim 2 , or a pharmaceutically acceptable salt or solvate thereof , having a structure of Formula I : R R1a · ₁N R1 R2a Ho ²R A I wherein , ARA1 , RA2 and ³AR are each independently selected from the group consisting of C1 - C6 alkyl , halo- C1 - C6 alkyl , halo , cyano , oxo , -C ( O ) -RA + , -S ( O ) -RA + and -S ( O ) 2 - RA + ;

4. G is -CH or N ; and A ¹R is selected from the group consisting of ₁C - C6 alkyl , C3 - C8 cycloalkyl and halo - ₁C - C6 alkyl . The compound of claim 3 , or a pharmaceutically acceptable salt or solvate thereof , wherein G is N and having a structure of Formula I ' : 185 WO 2025/0494 R R ²R PCT / US2024 / 0440 I '

5. The compound of any one of claims 1-4 , or a pharmaceutically acceptable salt or solvate thereof , wherein q is 1 .

6. The compound of any one of claims 1-4 , or a pharmaceutically acceptable salt or solvate thereof , wherein q is 0 .

7. The compound of any one of claims 1-6 , or a pharmaceutically acceptable salt or solvate thereof , wherein ¹R is ₁C - C6 alkyl or C3 - C8 cycloalkyl .

8. The compound of claim 7 , or a pharmaceutically acceptable salt or solvate thereof , wherein ¹R is methyl , ethyl or cyclopropyl .

9. The compound of any one of claims 1-8 , or a pharmaceutically acceptable salt or solvate thereof , having a structure of Formula la , Ib or Ic : 186 WO 2025/0494 R H A R ²R -N Ho A N R R ²R A ﻭ Ic Ib PCT / US2024 / 0440 la WO 2025/049495 PCT / US2024 / 0440

10. The compound of any one of claims 1-9 , or a pharmaceutically acceptable salt or solvate thereof , wherein Y is N.

11. The compound of any one of claims 1-9 , or a pharmaceutically acceptable salt or solvate thereof , wherein Y is -CH .

12. The compound of any one of claims 1-11 , or a pharmaceutically acceptable salt or solvate thereof , wherein ²R is halo - ₁C - C6 alkyl or halo - ₁C - C6 alkoxy .

13. The compound of claim 12 , or a pharmaceutically acceptable salt or solvate thereof , wherein R2 is halo - C1 - C6 alkyl .

14. ²R is -CF3 . The compound of claim 13 , or a pharmaceutically acceptable salt or solvate thereof , wherein

15. The compound of claim 12 , or a pharmaceutically acceptable salt or solvate thereof , wherein ²R is halo - C1 - C6 alkoxy .

16. The compound of claim 15 , or a pharmaceutically acceptable salt or solvate thereof , wherein ²R is -O - CHF2 .

17. The compound of any one of claims 1-16 , or a pharmaceutically acceptable salt or solvate thereof , wherein p is 1 or 2 .

18. The compound of any one of claims 1-17 , or a pharmaceutically acceptable salt or solvate thereof , wherein p is 1 .

19. The compound of any one of claims 1-17 , or a pharmaceutically acceptable salt or solvate thereof , wherein p is 2 .

20. The compound of any one of claims 1-19 , or a pharmaceutically acceptable salt or solvate thereof , wherein ³R is ₁C - C6 alkyl . 188 WO 2025/049495 PCT / US2024 / 0440

21. ³R is methyl .

22. The compound of claim 20 , or a pharmaceutically acceptable salt or solvate thereof , wherein The compound of any one of claims 1-19 , or a pharmaceutically acceptable salt or solvate thereof , wherein ³R is hydrogen .

23. The compound of any one of claims 1-22 , or a pharmaceutically acceptable salt or solvate thereof , wherein r is 1 .

24. The compound of claim 23 , or a pharmaceutically acceptable salt or solvate thereof , wherein A is C1 - C6 alkyl .

25. The compound of claim 24 , or a pharmaceutically acceptable salt or solvate thereof , wherein A is -CH3 or -CH2CH3 .

26. The compound of any one of claims 1-22 , or a pharmaceutically acceptable salt or solvate thereof , wherein r is 0 .

27. The compound of claim 23 or 26 , or a pharmaceutically acceptable salt or solvate thereof , wherein G is -CH .

28. The compound of claim 27 , or a pharmaceutically acceptable salt or solvate thereof , wherein A is C3 - Cs cycloalkyl , optionally substituted with one or more of RAI , ²AR and ³AR .

29. A is A The compound of claim 28 , or a pharmaceutically acceptable salt or solvate thereof , wherein ﺲﻋاﺩ ﺺﻟﺎﺣ or "

30. RA The compound of claim 29 , or a pharmaceutically acceptable salt or solvate thereof , wherein RA1 is cyano or halo - ₁C - C6 alkyl . 189 WO 2025/049495 PCT / US2024 / 0440

31. RA1 is -CF3 .

32. The compound of claim 30 , or a pharmaceutically acceptable salt or solvate thereof , wherein The compound of claim 23 or 26 , or a pharmaceutically acceptable salt or solvate thereof , wherein A is phenyl , optionally substituted with one or more of RAI , ²AR and ³ªR .

33. The compound of claim 32 , or a pharmaceutically acceptable salt or solvate thereof , wherein A is phenyl , optionally substituted with one or more of RAI and RA2 .

34. A is Al The compound of claim 33 , or a pharmaceutically acceptable salt or solvate thereof , wherein RA RA

35. The compound of claim 34 , or a pharmaceutically acceptable salt or solvate thereof , wherein ¹AR is -S ( O ) 2 - RA4 ; and , RA2 is halo .

36. A is The compound of claim 33 , or a pharmaceutically acceptable salt or solvate thereof , wherein vir RA

37. The compound of claim 36 , or a pharmaceutically acceptable salt or solvate thereof , wherein RA1 is selected from the group consisting of halo , cyano , -S ( O ) 2 - RA4 and -C ( O ) ¸ªªR-

38. The compound of claim 23 or 26 , or a pharmaceutically acceptable salt or solvate thereof , wherein A is 5- to 6 - membered heterocyclyl , optionally substituted with one or more of RAI , RAZ and ³AR

39. A The compound of claim 38 , or a pharmaceutically acceptable salt or solvate thereof , wherein the heterocyclyl comprises 1 or 2 heteroatoms selected from the group consisting of N , S , and O. 190 WO 2025/049495 PCT / US2024 / 0440

40. The compound of claim 38 , or a pharmaceutically acceptable salt or solvate thereof , wherein A is 5- to 6 - membered heterocyclyl .

41. The compound of claim 40 , or a pharmaceutically acceptable salt or solvate thereof , wherein A is 5- to 6 - membered heterocyclyl comprising 1 or 2 heteroatoms selected from the group consisting of N. S and O.

42. A is The compound of claim 41 , or a pharmaceutically acceptable salt or solvate thereof , wherein 10.or

43. The compound of claim 23 or 26 , or a pharmaceutically acceptable salt or solvate thereof , wherein A is 5- to 6 - membered heteroaryl , optionally substituted with one or more of RA1 , ²AR and ³AR .

44. A The compound of claim 43 , or a pharmaceutically acceptable salt or solvate thereof , wherein A is selected from the group consisting of pyridinyl , pyridazinyl , pyrimidinyl , pyrazinyl , triazinyl , oxadiazolyl , pyrrolyl , imidazolyl , pyrazolyl , and thiazolyl , optionally substituted with one or more of RAI , RA2 and RA,

45. The compound of claim 44 , or a pharmaceutically acceptable salt or solvate thereof , wherein A is selected from the group consisting of pyridinyl , pyrimidinyl , pyrazinyl , oxadiazolyl and pyrrolyl , optionally substituted with one or more of RAI , RA2 and R3 ,

46. A The compound of claim 45 , or a pharmaceutically acceptable salt or solvate thereof , wherein A is pyridinyl , optionally substituted with one or more of RAI , RA2 and RA3 .

47. The compound of claim 46 , or a pharmaceutically acceptable salt or solvate thereof , wherein A is pyridinyl substituted with ¹AR . 191

48. A is WO 2025/049495 PCT / US2024 / 0440 The compound of claim 47 , or a pharmaceutically acceptable salt or solvate thereof , wherein RARARAEN or

49. RA The compound of claim 48 , or a pharmaceutically acceptable salt or solvate thereof , wherein RA1 is selected from the group consisting of C1 - C6 alkyl , halo - C1 - C6 alkyl , halo , cyano and -S ( O ) 2 - RA4 .

50. The compound of claim 45 , or a pharmaceutically acceptable salt or solvate thereof , wherein A is pyrimidinyl or pyrazinyl , optionally substituted with one or more of RAI , RAZ and ³AR .

51. Al A The compound of claim 50 , or a pharmaceutically acceptable salt or solvate thereof , wherein A is pyrimidinyl or pyrazinyl , optionally substituted with ¹AR .

52. A is The compound of claim 51 , or a pharmaceutically acceptable salt or solvate thereof , wherein N. RAaa RA1 RA N. N. or " N " WO 2025/049495 PCT / US2024 / 0440

53. The compound of claim 52 , or a pharmaceutically acceptable salt or solvate thereof , wherein RAI is selected from the group consisting of ₁C - C6 alkyl , halo - ₁C - C6 alkyl , halo , cyano and -S ( O ) 2 - ‍ªªR

54. The compound of claim 45 , or a pharmaceutically acceptable salt or solvate thereof , wherein A is oxadiazolyl and pyrrolyl , optionally substituted with one or more of RAI , RA2 and ³AR

55. A The compound of claim 54 , wherein or a pharmaceutically acceptable salt or solvate thereof , A is oxadiazolyl and pyrrolyl , optionally substituted with ¹AR .

56. A is The compound of claim 55 , or a pharmaceutically acceptable salt or solvate thereof , wherein +0 +or RA

57. The compound of claim 56 , or a pharmaceutically acceptable salt or solvate thereof , wherein RAI ₁C - C6 alkyl .

58. A is in The compound of claim 38 , or a pharmaceutically acceptable salt or solvate thereof , wherein ` ⋅N RARA· N ° or and RA is C1 - C6 alkyl .

59. The compound of claim 58 , or a pharmaceutically acceptable salt or solvate thereof , wherein ¹AR is ethyl .

60. The compound of claim 43 or 52 , or a pharmaceutically acceptable salt or solvate thereof , wherein RA is 3HCO₂HC . 193 WO 2025/049495 PCT / US2024 / 0440

61. The compound of claim 1 or 2 , or a pharmaceutically acceptable salt or solvate thereof , having a structure of Formula Id : R N -A Id

62. ¹R is -Cl . wherein : r and q are each 0 ; la R1a and R1b are each hydrogen ; and , ¹R is halogen . The compound of claim 61 , or a pharmaceutically acceptable salt or solvate thereof , wherein

63. The compound of claim 61 or 62 , or a pharmaceutically acceptable salt or solvate thereof , wherein ²R is CF3 .

64. The compound of any one of claims 61-63 , or a pharmaceutically acceptable salt or solvate thereof , wherein ³R is hydrogen .

65. The compound of any one of claims 61-64 , or a pharmaceutically acceptable salt or solvate thereof , wherein Y is N.

66. The compound of any one of claims 61-65 , or a pharmaceutically acceptable salt or solvate thereof , wherein G is N and p is 2 .

67. The compound of claim 1 or 2 , or a pharmaceutically acceptable salt or solvate thereof , wherein E is -O- ; r is 1 ; p is 2 ; ª¹R , ª2R , and ³R are each hydrogen , and having a structure of Formula A - i ’ : 2a 194 WO 2025/0494 N A R PCT / US2024 / 0440 A - i '

68. The compound of claim 1 or 2 , or a pharmaceutically acceptable salt or solvate thereof , wherein r is 0 ; p is 2 ; ³¹R , ª2R , and ³R are each hydrogen , and having a structure of Formula A - ii * : ﻭ R -N R OH A A - ii '

69. The compound of claim 67 or 68 , or a pharmaceutically acceptable salt or solvate thereof , wherein q is 1 and ¹R is CH3 .

70. The compound of any one of claim 67-69 , or a pharmaceutically acceptable salt or solvate thereof , wherein ²R is CF3 or OCHF2 .

71. The compound of any one of claim 67-70 , or a pharmaceutically acceptable salt or solvate thereof , wherein Y is CH . 195 WO 2025/049495 PCT / US2024 / 0440

72. The compound of any one of claims 52 and 61-71 , or a pharmaceutically acceptable salt or solvate thereof , wherein A is N. .CN

73. The compound of any one of claims 48 and 61-71 , or a pharmaceutically acceptable salt or N CN solvate thereof , wherein A is

74. The compound of any one of claims 1-73 , wherein one or more hydrogen atoms is replaced with deuterium .

75. The compound of claim 74 , having a structure of Formula A - iii : RN D -N RR2a R A - iii

76. The compound of claim 74 or 75 , or a pharmaceutically acceptable salt or solvate thereof , wherein ¹R is -CD3 .

77. The compound of claim 1 , 2 or 3 , selected from the group consisting of : 196 WO 2025/0494 Cpd . No. Structure LCF Cpd . No. N PCT / US2024 / 0440 Structure Book 8 foo | Book N , WO 2025/049495 PCT / US2024 / 0440 Cpd . No. Structure Cpd . No. Structure ﻢﻓ good ﻢﻬﻣﻮﻣ good goo F N 80 % , WO 2025/049495 PCT / US2024 / 0440 Structure Cpd . No. Structure Cpd . No. N gob F F 224 ﻞﻫ F N gola ﻭ WO 2025/049495 PCT / US2024 / 0440 Cpd . No. Structure Cpd . No. Structure === gob goa NS goby N foo F gob N F F HC₂OS N 8' N ' 3HC₂OS , OCHFH₂FC N ' N ' F ' N FF WO 2025/0494 Cpd . No. Structure Cpd . No. N 2 · N N N F ' N ' F F F N = H. CF" N PCT / US2024 / 0440 Structure CF Boba CN N -CF ' N ' • N • WO 2025/0494 Cpd . No. PCT / US2024 / 0440 Structure Cpd . No. Structure ..... N F F ' N ' N : CN 8 OCHF OCHF F F F golo OCHFﻭ F F ﻭ WO 2025/0494 Cpd . No. N Structure • N • gob LL F ' N ' CF OCHF -CH Book N N F ` N Cpd . No. N PCT / US2024 / 0440 Structure 8 goo N F goo F N , CH CN 8 203 WO 2025/0494 Cpd . No. N Structure N N Cpd . No. F ﺩﺭ O = G = O goot F or a pharmaceutically acceptable salt or solvate thereof . " N ' N ' PCT / US2024 / 0440 Structure ﻢﻠﻣﺭﺓ 20b and " goot F

78. The compound of claim 1 , selected from the group consisting of : 204 WO 2025/049495 PCT / US2024 / 0440 Cpd . No. Structure Cpd . No. Structure 1104 - b 104 - a N 105 - a OCHF gora F N 105 - b F • N • F 1 N. N OCHF F. 1N goo OCH F. WO 2025/049495 PCT / US2024 / 0440 Cpd . No. Structure Cpd . No. Structure N 108 - a ' N * 108 - b OCHF OCHF N OCHF N ﻭ 111 - a CF 111 - b 114 - a N ` N ' N ' CF N CN · N N CF 114 - b OCHF WO 2025/049495 PCT / US2024 / 0440 Cpd . No. Structure Cpd . No. Structure N N 1 CF N OCHFN Boch N CFN 120 - a 120 - b gor Bos N N N N CF N 800-8 OCHF • N • ' N ' N CF, F N OCHF ﻭ WO 2025/0494 Cpd . No. Structure CN N N ﺞﻤﻳﺮﻳ Cpd . No. D. N 1D3C- D. N D CHF 8N 11D3C N OCHF3HC₂OS N PCT / US2024 / 0440 Structure N CFHC₂OS OCHF CF CFCN N CF 8N 134 - a CFﻭ D3C N N OCHF CF 3HC₂OS CN OH WO 2025/0494 Cpd . No. Structure Cpd . No. CN OH ' N ' 134 - b 135 - a N CF OH 80 ' N ' CN 135 - b PCT / US2024 / 0440 Structure CN OHI N OCHF OCHFand , or a pharmaceutically acceptable salt or solvate thereof .

79. A pharmaceutical composition comprising a compound of any one of claims 1-78 , or a pharmaceutically acceptable salt or solvate thereof , and a pharmaceutically acceptable excipient .

80. A method of promoting myelination in a subject in need thereof , the method comprising administering to the subject in need thereof a therapeutically effective amount of a compound according to any one of claims 1-78 , or a pharmaceutically acceptable salt or solvate thereof , or the pharmaceutical composition of claim 79 .

81. A compound of any one of claims 1-78 , or a pharmaceutically acceptable salt or solvate thereof , or the pharmaceutical composition of claim 79 , for use in treating a disorder in a subject in need thereof .

82. A compound of any one of claims 1-78 , or a pharmaceutically acceptable salt or solvate thereof , or the pharmaceutical composition of claim 79 , for use in promoting myelination in a subject in need thereof .

83. Use of a compound of any one of claims 1-78 , or a pharmaceutically acceptable salt or solvate thereof , or the pharmaceutical composition of claim 79 , in the manufacture of a medicament for treating a disorder in a subject in need thereof . 209 WO 2025/049495 PCT / US2024 / 0440

84. Use of a compound of any one of claims 1-78 , or a pharmaceutically acceptable salt or solvate thereof , or the pharmaceutical composition of claim 79 , in the manufacture of a medicament for promoting myelination in a subject in need thereof .

85. The method of claim 80 , wherein the subject has a myelin - related disorder .

86. The compound for use of claim 81 or 82 , wherein the subject has a myelin - related disorder .

87. The use of claim 83 or 84 , wherein the subject has a myelin - related disorder .

88. The method of claim 85 , compound for use of claim 86 , or use of claim 87 , wherein the myelin- related disorder is multiple sclerosis ( MS ) , neuromyelitis optica ( NMO ) , optic neuritis , pediatric leukodystrophy , neonatal white matter injury , age - related dementia , schizophrenia , progressive multifocal leukoencephalopathy ( PML ) , encephalomyelitis ( EPL ) , central pontine myelolysis ( CPM ) , adrenoleukodystrophy , Alexander's disease , Pelizaeus Merzbacher disease ( PMD ) , Vanishing White Matter Disease , Wallerian Degeneration , transverse myelitis , amylotrophic lateral sclerosis ( ALS ) , Huntington's disease , Alzheimer's disease , Parkinson's disease , spinal cord injury , traumatic brain injury , post radiation injury , neurologic complications of chemotherapy , stroke , acute ischemic optic neuropathy , vitamin E deficiency , isolated vitamin E deficiency syndrome , Bassen - Kornzweig syndrome , Marchiafava - Bignami syndrome , metachromatic leukodystrophy , trigeminal neuralgia , acute disseminated encephalitis , Guillian- Barre syndrome , Charcot - Marie - Tooth disease , Bell's palsy , or radiation - induced demyelination .

89. The method of claim 85 , the compound of claim 86 , or the use of claim 87 , wherein the disorder is multiple sclerosis .

90. A method of inhibiting CYP51 ( lanosterol demethylase ) comprising , contacting CYP51 with a compound according to any one of claims 1-78 , or a pharmaceutically acceptable salt or solvate thereof , or the pharmaceutical composition of claim 79 . 210