Substituted benzimidazolone compounds

Abstract

Formula (I): TIFF2022532145000183.tif32150 [wherein G, A, R1, and n are as defined herein] Disclosed are compounds of the formula: N-oxides, or salts thereof. Also disclosed are methods of using such compounds as inhibitors of signaling through Toll-like receptors 7, 8, or 9, and pharmaceutical compositions containing such compounds. These compounds are useful for treating inflammatory and autoimmune diseases.

Description

[Technical field]

[0001] CROSS-REFERENCE TO RELATED APPLICATIONS This disclosure claims the benefit of U.S. Provisional Patent Application No. 62 / 845,339, filed May 9, 2019, the contents of which are specifically incorporated herein by reference.

[0002] The present invention relates generally to substituted benzimidazolone compounds useful as inhibitors of signaling through Toll-like receptors 7, 8 or 9 (TLR7, TLR8, TLR9) or combinations thereof. Provided herein are substituted benzimidazolone compounds, compositions comprising such compounds, and methods of using same. The present invention further relates to pharmaceutical compositions containing at least one compound according to the invention, which are useful for treating conditions associated with TLR modulation, such as inflammatory and autoimmune diseases, and methods of inhibiting the activity of TLRs in a mammal. [Background technology]

[0003] Members of the Toll / IL-1 receptor family are important regulators of inflammation and host resistance. The Toll-like receptor family recognizes molecular patterns derived from infectious microorganisms, including bacteria, fungi, parasites, and viruses (see Kawai, T. et al., Nature Immunol., 11: 373-384 (2010)). Ligand binding to the receptor induces dimerization and recruitment of adaptor molecules to a conserved cytoplasmic motif in the receptor called the Toll / IL-1 receptor (TIR) ​​domain; all TLRs recruit the adaptor molecule MyD88, except for TLR3. The IL-1 receptor family also contains a cytoplasmic TIR motif and recruits MyD88 upon ligand binding (see Sims, JE et al., Nature Rev. Immunol., 10: 89-102 (2010)).

[0004] Toll-like receptors (TLRs) are a set of evolutionarily conserved transmembrane innate immune receptors involved in primary defense. As pattern recognition receptors, TLRs protect against foreign molecules activated by pathogen-associated molecular patterns (PAMPs) or from damaged tissues activated by danger-associated molecular patterns (DAMPs). A total of 13 TLR families have been identified, 10 in humans, spread either on the cell surface or in the endosomal compartment. TLR7 / 8 / 9 is one of the set that is located in endosomes and responds to single-stranded RNA (TLR7 and TLR8) or unmethylated single-stranded DNA containing cytosine-phosphate-guanine (CpG) motifs (TLR9).

[0005] Activation of TLR7 / 8 / 9 can initiate various inflammatory responses (cytokine production, B cell activation and IgG production, type I interferon response). In autoimmune disorders, abnormal persistent activation of TLR7 / 8 / 9 leads to exacerbation of pathology. Overexpression of TLR7 in mice has been shown to exacerbate autoimmune disease, whereas knockout of TLR7 in mice was found to be protective against disease in lupus-prone MRL / lpr mice. Dual knockout of TLR7 and 9 showed further enhanced protection.

[0006] Because many conditions may benefit from treatments involving modulation of cytokines, IFN production and B cell activity, it is readily apparent that novel compounds capable of modulating TLR7 and / or TLR8 and / or TLR9, and methods employing these compounds, may provide substantial therapeutic benefit to a wide variety of patients. Summary of the Invention

[0007] The present invention relates to a series of novel substituted benzimidazolone compounds that have been found to be effective inhibitors of TLR7 / 8 / 9 mediated signaling. These compounds are provided to be useful as pharmaceuticals with desirable stability, bioavailability, therapeutic index, and toxicity values ​​that are important for their druggability.

[0008] The present invention provides compounds of formula (I) or stereoisomers, N-oxides, tautomers, pharma- ceutically acceptable salts, solvates or prodrugs thereof, which are useful as inhibitors of signaling through Toll-like receptors 7, 8 or 9 and are useful in the treatment of proliferative diseases, allergic diseases, autoimmune diseases and inflammatory diseases.

[0009] The present invention also provides pharmaceutical compositions comprising a pharma- ceutically acceptable carrier and at least one compound of the invention, or a stereoisomer, tautomer, pharma- ceutically acceptable salt, solvate, or prodrug thereof. The present invention also provides a method for inhibiting Toll-like receptors 7, 8 or 9, comprising administering to a host in need of such treatment a therapeutically effective amount of at least one compound of the present invention or a stereoisomer, tautomer, pharma- ceutically acceptable salt, solvate or prodrug thereof.

[0010] The present invention also provides methods for treating proliferative, metabolic, allergic, autoimmune and inflammatory diseases, comprising administering to a host in need of such treatment a therapeutically effective amount of at least one compound of the present invention or a stereoisomer, tautomer, pharma- ceutically acceptable salt, solvate or prodrug thereof.

[0011] The present invention also provides a method for treating a disease or disorder associated with Toll-like receptor 7, 8 or 9 activity, comprising administering to a mammal in need of such treatment at least one compound of formula (I) or salts, solvates and prodrugs thereof. The present invention also provides processes and intermediates for making compounds of formula (I), including salts, solvates and prodrugs thereof. The present invention also provides at least one compound of formula (I) or salts, solvates and prodrugs thereof for use in therapy.

[0012] The present invention also provides the use of at least one compound of formula (I) or salts, solvates and prodrugs thereof in the manufacture of a medicament for the prophylactic treatment of Toll-like receptor 7, 8 or 9 associated conditions, such as allergic diseases, autoimmune diseases, inflammatory diseases and proliferative diseases.

[0013] The compounds of formula (I) and compositions comprising the compounds of formula (I) may be used to treat, prevent or cure various Toll-like receptor 7, 8 or 9 associated conditions. Pharmaceutical compositions comprising these compounds are useful in treating, preventing or slowing the progression of diseases or disorders in a variety of therapeutic areas, such as allergic diseases, autoimmune diseases, inflammatory diseases and proliferative diseases. These and other features of the invention will be set forth in expanded form as the disclosure continues. DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

[0014] The first aspect of the present invention relates to a compound of formula (I): [ka] [In formula: G is (i) [ka] Is it; (ii) [ka] Is it; (iii) [ka] Is it; (iv) [ka] [ka] [ka] or a 9-membered heterocyclic ring selected from (v) [ka] A 10-membered heterocyclic ring selected from and; Each R1 is independently hydrogen, F, Cl, -CN, C 1-3 Alkyl, C 1-2 Fluoroalkyl, -OCH3, or -S(O)2(C 1-3 alkyl); Each R2 is independently halo, -CN, -OH, -NO2, C 1-4 Alkyl, C 1-2 Fluoroalkyl, C 1-2 Cyanoalkyl, C 1-3 Hydroxyalkyl, C 1-3 Aminoalkyl, -O(CH2) 1-2 OH, -(CH2) 0-4 O(C 1-4 Alkyl), C 1-3 Fluoroalkoxy, -O(CH2) 1-2 O.C.(O)(C 1-3 alkyl), -O(CH2) 1-2 NR x R x , -C(O)O(C 1-3 alkyl), -(CH2) 0-2 C(O)NR y R y , -C(O)NR x (C 1-5 Hydroxyalkyl), -C(O)NR x (C 2-6 Alkoxyalkyl), -C(O)NR x (C3-6 Cycloalkyl), -NR y R y , -NR y (C 1-3 Fluoroalkyl), -NR y (C 1-4 Hydroxyalkyl), -NR x CH2(phenyl), -NR x S(O)2(C 3-6 Cycloalkyl), -NR x C(O)(C 1-3 alkyl), -NR x CH2(C 3-6 Cycloalkyl), -(CH2) 0-2 S(O)2(C 1-3 alkyl), -(CH2) 0-2 (C 3-6 Cycloalkyl), -(CH2) 0-2 (phenyl), morpholinyl, dioxothiomorpholinyl, dimethylpyrazolyl, methylpiperidinyl, methylpiperazinyl, amino-oxadiazolyl, imidazolyl, pyrimidinyl, triazolyl, or -C(O)(thiazolyl); R 2a is C 1-6 Alkyl, C 1-3 Fluoroalkyl, C 1-6 Hydroxyalkyl, C 1-3 Aminoalkyl, -(CH2) 0-4 O(C 1-3 Alkyl), C 3-6 Cycloalkyl, -(CH2) 1-3 C(O)NR y R y , -CH2(C 3-6 cycloalkyl), -CH2(phenyl), tetrahydrofuranyl, tetrahydropyranyl, or phenyl; Each R 2b are independently hydrogen, halo, -CN, -NR x R x , C 1-6 Alkyl, C 1-3 Fluoroalkyl, C 1-3 Hydroxyalkyl, C 1-3 Fluoroalkoxy, -(CH2) 0-2 O(C1-3 alkyl), -(CH2) 0-3 C(O)NR x R x , -(CH2) 1-3 (C 3-6 Cycloalkyl), -C(O)O(C 1-3 alkyl), -C(O)NR x (C 1-3 alkyl), -CR x =CR x R x , or -CR x =CH(C 3-6 cycloalkyl); R 2c is R 2a or R 2b And; R 2d is R 2a or R 2b where R 2c and R 2d One of them is R 2a and R 2c and the other of R2 is R 2b and; A is -CR x R x R3, -(CH2) 1-2 NR x R3, or R3; R3 is C 3-6 cycloalkyl, azetidinyl, morpholinyl, piperazinyl, piperidinyl, or pyrrolidinyl, each of which is 0 to 2 R 3a Replaced with; Each R 3a is independently 1-6 Alkyl, C 1-6 Cyanoalkyl, C 1-6 Fluoroalkyl, C 1-6 Hydroxyalkyl, C 2-6 Alkoxyalkyl, -CH2C(O)NR y R y , -C(O)(CH2) 1-3 NR y R y , -NR y R y , -NR y (C1-3 Fluoroalkyl), -NR y (C 2-4 Alkoxyalkyl), -(CH2) 1-3 S(O)2(C 1-3 alkyl), -(CH2) 1-3 NR x S(O)2(C 1-3 alkyl), -NR x (CH2) 1-2 C(O)NR y R y , -NR x (CH2) 1-3 S(O)2(C 1-3 alkyl), -NR x R w , -NR x CH2R w , R w , -CH2R w , oxazaspiro[3.3]heptanyl, dioxothiazaspiro[3.3]heptanyl, oxazabicyclo[3.2.1]octanyl, oxazaspiro[3.4]octanyl, or oxazaspiro[3.5]nonanyl; R w is C 3-6 Cycloalkyl, azetidinyl, pyrrolidinyl, oxetanyl, tetrahydrofuranyl, tetrahydropyranyl, piperidinyl, morpholinyl, piperazinonyl, oxazepanyl, thiomorpholinyl, pyridinyl, pyrimidinyl, or triazolyl, each of which is 0 to 3 substituents (F, Cl, -OH, -CN, C 1-3 Alkyl, C 1-3 Hydroxyalkyl, C 1-3 Fluoroalkyl, C 1-3 alkoxy, -CH2OCH3, and -S(O)2CH3; Each R x are independently hydrogen or -CH3; Each R y are independently hydrogen or C 1-6 is alkyl; n is 0, 1, or 2; and p is 0, 1, or 2] or a salt thereof.

[0015] One embodiment is a compound of formula (I) or a salt thereof, wherein G (i) [ka] Is it; (ii) [ka] or (iii) [ka] A, R1, R2, R 2a , R 2b , R 2c , R 2d , n and p are as defined in the first aspect, or a salt thereof.

[0016] In one embodiment, G is [ka] [ka] [ka] and A, R1, R2, n, and p are as defined in the first aspect, or a salt thereof.

[0017] In one embodiment, G is [ka] and A, R1, R2, n, and p are as defined in the first aspect, or a salt thereof.

[0018] In one embodiment, G is: [ka] and A, R1, R2, n, and p are as defined in the first aspect, or a salt thereof.

[0019] One embodiment is a compound of formula (II): [ka] [In the formula, A, R1, R2, R 3a , n, and p are as defined in the first aspect. or a salt thereof. In this embodiment, A is cyclohexyl or piperidinyl, each of which contains 0-2 R 3a The present invention includes compounds in which the compound is substituted with

[0020] One embodiment is a compound of formula (III): [ka] [In the formula, A, R1, R2, R 3a , n, and p are as defined in the first aspect. or a salt thereof. In this embodiment, A is cyclohexyl or piperidinyl, each of which contains 0-2 R 3a The present invention includes compounds in which the compound is substituted with

[0021] One embodiment is a compound of formula (II) or a salt thereof, wherein each R is independently hydrogen, C 1-3 alkyl, or -CF; each R2 is independently hydrogen, -CH3, or -OCH3; A is cyclohexyl or piperidinyl, each of which contains 0 to 2 R 3a Each R 3a But independently, C 1-6 Alkyl, C1-2 Cyanoalkyl, C 1-4 Fluoroalkyl, C 2-4 Alkoxyalkyl, -(CH2) 1-3 S(O)2(C 1-3 alkyl), -CH2(C 3-6 Cycloalkyl), -CHR w , -CH2C(O)NR x R x , -NR y R y , -NR x (C 1-3 Fluoroalkyl), -NR x (C 2-4 Alkoxyalkyl), -NR x R w , -NR x CH2R w , R w , oxaazaspiro[3.3]heptanyl, dioxothiazaspiro[3.3]heptanyl, oxazabicyclo[3.2.1]octanyl, or oxazaspiro[3.5]nonanyl; R w But, C 3-6 cycloalkyl, azetidinyl, pyrrolidinyl, oxetanyl, tetrahydrofuranyl, tetrahydropyranyl, piperidinyl, piperazinonyl, oxazepanyl, thiomorpholinyl, pyridinyl, pyrimidinyl, or triazolyl, each of which is 0 to 2 substituents (F, -OH, C 1-3 each R is substituted with an alkyl group selected from -CF, -OCH, -CHOCH, and -S(O)CH; x is independently hydrogen or -CH; each R y are independently hydrogen or C 1-6 is alkyl; n is 0, 1, or 2; and p is 0, 1, or 2, or a salt thereof.

[0022] One embodiment is a compound of formula (I), an N-oxide, or a salt thereof, wherein each R is independently hydrogen, F, Cl, -CN, C 1-3 Alkyl, C 1-2A, R2, n, and p are as defined in the first aspect. In this embodiment, each R1 is independently hydrogen, C 1-3 Also included within this embodiment are compounds where each R1 is hydrogen, -CH3, -CH2CH3, or -CH(CH3)2.

[0023] One embodiment is a compound of formula (I), an N-oxide, or a salt thereof, wherein each R2 is independently F, Cl, -CN, C 1-4 Alkyl, C 1-2 Fluoroalkyl, C 1-2 Cyanoalkyl, C 1-3 Hydroxyalkyl, -O(CH2) 1-2 OH, -(CH2) 0-4 O(C 1-4 Alkyl), C 1-3 Fluoroalkoxy, -(CH2) 0-2 C(O)NR y R y , -C(O)NR x (C 3-6 Cycloalkyl), -NR y R y , -NR x S(O)2(C 3-6 Cycloalkyl), -NR x C(O)(C 1-3 alkyl), -NR x CH2(C 3-6 Cycloalkyl), -(CH2) 0-2 S(O)2(C 1-3 alkyl), or -(CH2) 0-2 (C 3-6 cycloalkyl); A, R, R x , R y The present invention provides a compound, N-oxide, or salt thereof, wherein R, n, and p are as defined in the first aspect. This embodiment includes compounds, N-oxides, or salts thereof, wherein each R is independently hydrogen, C 1-2Included in this embodiment are compounds where each R2 is independently hydrogen, -CH3, or -OCH3.

[0024] One embodiment is a compound, N-oxide, or salt thereof of formula (I), wherein R 2a But, C 1-4 Alkyl, C 1-2 Fluoroalkyl, C 1-4 Hydroxyalkyl, or -(CH2) 0-4 O(C 1-3 alkyl); each R 2b are independently hydrogen, F, Cl, -CN, -NR x R x , C 1-4 Alkyl, C 1-2 Fluoroalkyl, C 1-3 Hydroxyalkyl, or -(CH2) 0-2 O(C 1-2 alkyl); A, R, R x and n is as defined in the first aspect.

[0025] One embodiment is a compound of formula (I), an N-oxide, or a salt thereof, where A is -CR x R x R3, -CH2NR x R3, or R3; R1, R2, R3, R x , n, and p are as defined in the first aspect. x R x R3, or R3. This embodiment also includes compounds in which A is -CR x R x R3, -(CH2) 1-2 NR x R3, or R3.

[0026] One embodiment is a compound, N-oxide, or salt thereof of formula (I) where A is R3; R1, R2, R3, R 3a , n, and p are as defined in the first aspect. 5-6 cycloalkyl, piperazinyl, piperidinyl, or pyrrolidinyl, each of which is selected from 0 to 2 R 3a Also included in this embodiment are compounds where A is cyclohexyl or piperidinyl, each of which is substituted with 0-2 R 3a The present invention includes compounds in which the compound is substituted with

[0027] One embodiment is a compound, N-oxide, or salt thereof of Formula (I) where A is cyclohexyl or piperidinyl, each of which contains 0 to 2 R 3a R1, R2, R 3a , R x , R y The present invention provides a compound, N-oxide, or salt thereof, wherein each R 3a But independently, C 1-6 Alkyl, C 1-2 Cyanoalkyl, C 1-4 Fluoroalkyl, C 2-4 Alkoxyalkyl, -(CH2) 1-3 S(O)2(C 1-3 alkyl), -CH2(C 3-6 Cycloalkyl), -CHR w , -CH2C(O)NR x R x , -NR y R y , -NR x (C 1-3 Fluoroalkyl), -NR x (C 2-4 Alkoxyalkyl), -NR x R w , -NR x CH2R w , R w, oxaazaspiro[3.3]heptanyl, dioxothiazaspiro[3.3]heptanyl, oxazabicyclo[3.2.1]octanyl, or oxazaspiro[3.5]nonanyl; R w C 3-6 cycloalkyl, azetidinyl, pyrrolidinyl, oxetanyl, tetrahydrofuranyl, tetrahydropyranyl, piperidinyl, piperazinonyl, oxazepanyl, thiomorpholinyl, pyridinyl, pyrimidinyl, or triazolyl, each of which is 0 to 2 substituents (F, -OH, C 1-3 The compounds include those substituted with a substituted or unsubstituted alkyl group selected from the group consisting of -alkyl, -CF3, -OCH3, -CH2OCH3, and -S(O)2CH3.

[0028] One embodiment is a compound, N-oxide, or salt thereof of Formula (I) where A is cyclohexyl or piperidinyl, each of which contains 0 to 1 R 3a Each R 3a are independently -CH3, -CH2CH3, -CH2CH2CH3, -CH(CH3)2, -CH2CH(CH3)2, -CH2C(CH3)3, -CH(CH3)CH2CH3, -CH2CH2CH(CH3)2, -CH(CH 2CH3)2, -CH2CH(CH2CH3)2, -CH2CH2C(CH3)3, -CH2CN, -CH2CH2CF3, -CH2CH2CH2CF3, -CH2CH2OCH3, -CH2CH2S(O)2CH3, -CH2(C 3-5cycloalkyl), -CH2(pyridinyl), -CH2(methoxypyrimidinyl), -CH2(tetrahydrofuranyl), -CH2(tetrahydropyranyl), -CH2(methyltriazolyl), -CH2C(O)NH2, -CH2C(O)NH(CH3), -C(O)CH2N(CH3)2, -NH2, -NH(CH2CH3), -NH(CH2CH2CH3), -NH(CH(CH3)2), -NH(CH2CH( CH3)2), -NH(CH(CH3)CH2CH3), -NH(CH2C(CH3)3), -NH(CH2CH(CH2CH3)2), -NH(CH2CH2CF3), -NH(CH2CH2OCH3), - N(CH3)2, -N(CH3)(CH(CH3)2)), -N(CH3)(CH2CH2CF3), -N(CH2CH3)2, -N(CH2CH2CH3)2, -N(CH2CH(CH3)2)2, -NH(C 3-6 cycloalkyl), -NH(oxetanyl), -NH(tetrahydropyranyl), -NH(isopropylpiperidinyl), -N(CH3)(tetrahydropyranyl), -N(CH3)(cyclohexyl), -NH(CH2(cyclopropyl)), -NH(CH2(cyclohexyl)), -NH(CH2(methylsulfonylcyclopropyl)), -NH(CH2(tetrahydropyranyl)), -NH(CH2(methyltriazolyl)), fluoroazetidinyl, difluoroazetidinyl, methoxyazetidinyl, hydroxy, trifluoromethylazetidinyl, cyclobutyl, oxetanyl, tetra The present invention provides a compound, N-oxide, or salt thereof, wherein A is hydrofuranyl, pyrrolidinyl, difluoropyrrolidinyl, tetrahydropyranyl, thiomorpholinyl, fluoropiperidinyl, difluoropiperidinyl, methoxypiperidinyl, methoxymethylpiperidinyl, methylsulfonylpiperidinyl, piperazinonyl, oxazepanyl, oxazaspiro[3.3]heptanyl, dioxothiazaspiro[3.3]heptanyl, oxazabicyclo[3.2.1]octanyl, or oxazaspiro[3.5]nonanyl; R1, R2, n, and p are as defined in the first aspect. This embodiment includes compounds, N-oxides, or salts thereof, wherein A is 0 to 1 R 3aAlso provided in this embodiment is a compound, N-oxide, or salt thereof, wherein A is cyclohexyl substituted with 0-1 R 3a Also included are compounds which are piperidinyl substituted with:

[0029] One embodiment is a compound of formula (I), an N-oxide, or a salt thereof, wherein the compound is 5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-methyl-1-(1-methylpiperidin-4-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (1); 1-(1-isopropylpiperidin-4-yl)-6-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (2); 6-Methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-methylpiperidin-4-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one(3);5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-methylpiperidin-4-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one(4);1-(1-isopropylpiperidin-4-yl)-5-(8-methylpiperidin-4-yl) 1-(1-ethylpiperidin-4-yl)-6-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (5); 1-(1-ethylpiperidin-4-yl)-6-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (6); 6-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-propylpiperidin-4-yl)-1,3 -dihydro-2H-benzo[d]imidazol-2-one (7); 1-(1-ethylpiperidin-4-yl)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-methyl-1,3-dihydro-2H-benzo[d]imidazol-2-one (9); 1-(1-isopropylpiperidin-4-yl)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-methyl-1,3-dihydro-2H-benzo[d]imidazol-2-one (10);(S)-6-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-methylpiperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (11); (S)-1-(1-ethylpiperidin-3-yl)-6-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (12); (S)-1-(1-isopropylpiperidin-3-yl)-6-methyl- 5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (13);(S)-6-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-(oxetan-3-yl)piperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (14);(R)-6-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-methyl (R)-1-(1-ethylpiperidin-3-yl)-6-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (15); (R)-1-(1-ethylpiperidin-3-yl)-6-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (16); (R)-1-(1-isopropylpiperidin-3-yl)-6-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[ d]imidazol-2-one (17); (R)-6-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-(oxetan-3-yl)piperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (18); 1-((1s,4s)-4-(dimethylamino)cyclohexyl)-6-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (19);1-((1s,4s)-4-(diethylamino)cyclohexyl)-6-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (20);

[0030] 1-((1s,4s)-4-(ethylamino)cyclohexyl)-6-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (21); 1-((1s,4s)-4-(isopropylamino)cyclohexyl)-6-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (22); 1 -((1r,4r)-4-(dimethylamino)cyclohexyl)-6-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (23); 1-((1r,4r)-4-(ethylamino)cyclohexyl)-6-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (24); 1-(( 1r,4r)-4-(isopropylamino)cyclohexyl)-6-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (25);(R)-6-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-neopentylpiperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (26);(R)-6-methyl 1-((3R)-1-(sec-butyl)piperidin-3-yl)-6-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-(tetrahydro-2H-pyran-4-yl)piperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (27); 1-((3R)-1-(sec-butyl)piperidin-3-yl)-6-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (28);(R)-6-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-(3,3,3-trifluoropropyl)piperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (29); 6-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-((1s,4s)-4-((tetrahydro-2H-pyran-4-yl)amino)cyclohexyl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (30); 6-methyl 6-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-((1s,4s)-4-((3,3,3-trifluoropropyl)amino)cyclohexyl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (31);6-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-((1s,4s)-4-(neopentylamino)cyclohexyl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (32);6-methyl-1-((1s,4 s)-4-(((1-methyl-1H-1,2,4-triazol-3-yl)methyl)amino)cyclohexyl)-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (33); 1-((1s,4s)-4-(sec-butylamino)cyclohexyl)-6-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (34); (R)-6-methyl -1-(1-((1-methyl-1H-1,2,4-triazol-3-yl)methyl)piperidin-3-yl)-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (35); (S)-1-(1-((2-methoxypyrimidin-5-yl)methyl)piperidin-3-yl)-6-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (36);(R)-1-(1-(cyclopropylmethyl)piperidin-3-yl)-6-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (37); (R)-1-(1-isopentylpiperidin-3-yl)-6-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (38); (R )-6-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-(4,4,4-trifluorobutyl)piperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (39); (R)-1-(1-isobutylpiperidin-3-yl)-6-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (40);

[0031] (R)-6-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-((tetrahydro-2H-pyran-4-yl)methyl)piperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (41); (R)-6-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-propylpiperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (42 );6-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-((3R)-1-((tetrahydrofuran-3-yl)methyl)piperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (43);(R)-1-(1-(3,3-dimethylbutyl)piperidin-3-yl)-6-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol- 2-one (44); (R)-1-(1-(2-ethylbutyl)piperidin-3-yl)-6-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (45); (R)-6-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-(pyridin-3-ylmethyl)piperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (46);(R)-1-(1-(cyclopentylmethyl)piperidin-3-yl)-6-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (47);1-((1s,4s)-4-(dimethylamino)cyclohexyl)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-methyl-1,3-dihydro-2H-benzo[d]imidazol-2-one (48);5-(8-Methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-methyl-1-((1s,4s)-4-((tetrahydro-2H-pyran-4-yl)amino)cyclohexyl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (49); 1-((1s,4s)-4-(isopropylamino)cyclohexyl)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-methyl-1,3-dihydro-2H-benzo[d]imidazol-2-one Benzo[d]imidazol-2-one (50);(R)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-methyl-1-(1-methylpiperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (51);(R)-1-(1-ethylpiperidin-3-yl)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-methyl-1,3-dihydro-2H-benzo[d]imidazol- 2-one (52); (R)-1-(1-isopropylpiperidin-3-yl)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-methyl-1,3-dihydro-2H-benzo[d]imidazol-2-one (53); (R)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-methyl-1-(1-propylpiperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (54) ;(R)-1-(1-(cyclopropylmethyl)piperidin-3-yl)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-methyl-1,3-dihydro-2H-benzo[d]imidazol-2-one (55);(R)-1-(1-isobutylpiperidin-3-yl)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-methyl-1,3-dihydro-2H-benzo[d]imidazol-2-one (56);(R)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-methyl-1-(1-((tetrahydro-2H-pyran-4-yl)methyl)piperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (57); 1-((1s,4s)-4-(cyclobutylamino)cyclohexyl)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-methyl-1,3-dihydro-2H-benzo[d]imidazol-2-one (58) );5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-methyl-1-((1s,4s)-4-(oxetan-3-ylamino)cyclohexyl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (59);1-((1s,4s)-4-((cyclopropylmethyl)amino)cyclohexyl)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-methyl-1,3-dihydro-2H-benzo[d]imidazol-2-one (60);

[0032] 1-((1s,4s)-4-(isobutylamino)cyclohexyl)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-methyl-1,3-dihydro-2H-benzo[d]imidazol-2-one (61); 1-((1s,4s)-4-(cyclohexylamino)cyclohexyl)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-methyl-1,3-dihydro-2H-benzo[d]imidazol-2-one (62); 1 -((1s,4s)-4-(ethylamino)cyclohexyl)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-methyl-1,3-dihydro-2H-benzo[d]imidazol-2-one (63); 5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-methyl-1-((1s,4s)-4-(propylamino)cyclohexyl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (64); 1-((1s,4 s)-4-(cyclopentylamino)cyclohexyl)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-methyl-1,3-dihydro-2H-benzo[d]imidazol-2-one (65); 1-((1s,4s)-4-((cyclohexylmethyl)amino)cyclohexyl)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-methyl-1,3-dihydro-2H-benzo[d]imidazol-2-one (66); (R -5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-methyl-1-(1-(pentan-3-yl)piperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (67); (R)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-methyl-1-(1-(3,3,3-trifluoropropyl)piperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (68);(R)-1-(1-cyclobutylpiperidin-3-yl)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-methyl-1,3-dihydro-2H-benzo[d]imidazol-2-one (69); (R)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-methyl-1-(1-(tetrahydro-2H-pyran-4-yl)piperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (70); (R)-5-(8 -Methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-methyl-1-(1-neopentylpiperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (71);(R)-5-(8-Methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-methyl-1-(1-(oxetan-3-yl)piperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (72);(R)-1-(1-(2-ethylbutyl)piperidine- 3-yl)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-methyl-1,3-dihydro-2H-benzo[d]imidazol-2-one (73);5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-methylpiperidin-4-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (74);1-(1-(2-ethylbutyl)piperidin-4-yl)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)- 5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-propylpiperidin-4-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (76); 1-(1-isopropylpiperidin-4-yl)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (77);5-(8-Methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-((tetrahydro-2H-pyran-4-yl)methyl)piperidin-4-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (78); 1-(1-(cyclopropylmethyl)piperidin-4-yl)-5-(8-methoxy-[1,2,4 ]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (79);5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-(oxetan-3-yl)piperidin-4-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (80);

[0033] 5-(8-Methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-(tetrahydrofuran-3-yl)piperidin-4-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (81); 5-(8-Methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-((tetrahydrofuran-3-yl)methyl)piperidin-4-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (82); 1-(1-Cyclobutyric Acid 1-((1s,4s)-4-(isopropyl(methyl)amino)cyclohexyl)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-methyl-1,3-dihydro-2H-benzo[d]imidazol-2-one (83); 1-((1s,4s)-4-(isopropyl(methyl)amino)cyclohexyl)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-methyl-1,3-dihydro-2H-benzo[d]imidazol-2-one (84); 5-(8-methoxy-[1,2,4]triazolo[ 1,5-a]pyridin-6-yl)-6-methyl-1-((1s,4s)-4-(methyl(tetrahydro-2H-pyran-4-yl)amino)cyclohexyl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (85); 2-(4-(5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-methyl-2-oxo-2,3-dihydro-1H-benzo[d]imidazol-1-yl)piperidin-1-yl)-N,N-dimethylacetamide (86); 2- (4-(5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-methyl-2-oxo-2,3-dihydro-1H-benzo[d]imidazol-1-yl)piperidin-1-yl)-N-methylacetamide (87); N-methyl-2-(4-(6-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-2-oxo-2,3-dihydro-1H-benzo[d]imidazol-1-yl)piperidin-1-yl)acetamide (88);N,N-Dimethyl-2-(4-(6-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-2-oxo-2,3-dihydro-1H-benzo[d]imidazol-1-yl)piperidin-1-yl)acetamide (89);N,N-Dimethyl-2-(4-(5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-2-oxo-2,3-dihydro-1H-benzo[d]imidazol-1-yl)piperidin-1-yl)acetamide (90);N,N -Dimethyl-2-(4-(6-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-2-oxo-2,3-dihydro-1H-benzo[d]imidazol-1-yl)piperidin-1-yl)acetamide (91); (S)-2-(3-(6-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-2-oxo-2,3-dihydro-1H-benzo[d]imidazol-1-yl)piperidin-1-yl)acetamide (92); (S)-N ,N-Dimethyl-2-(3-(6-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-2-oxo-2,3-dihydro-1H-benzo[d]imidazol-1-yl)piperidin-1-yl)acetamide (93);(R)-2-(3-(6-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-2-oxo-2,3-dihydro-1H-benzo[d]imidazol-1-yl)piperidin-1-yl)acetamide (94);(R) -N,N-dimethyl-2-(3-(6-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-2-oxo-2,3-dihydro-1H-benzo[d]imidazol-1-yl)piperidin-1-yl)acetamide (95); (R)-2-(3-(6-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-2-oxo-2,3-dihydro-1H-benzo[d]imidazol-1-yl)piperidin-1-yl)acetonitrile (96);(R)-1-(1-(2-methoxyethyl)piperidin-3-yl)-6-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (97); (R)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-(2-methoxyethyl)piperidin-3-yl)-6-methyl-1,3-dihydro-2H-benzo[d]imidazol-2-one (98); (R)-2 -(3-(5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-methyl-2-oxo-2,3-dihydro-1H-benzo[d]imidazol-1-yl)piperidin-1-yl)-N,N-dimethylacetamide (99); 1-(1-(2-(dimethylamino)acetyl)piperidin-4-yl)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-methyl-1H-benzo[d]imidazol-2(3H)-one (100);

[0034] 1-(1-(dimethylglycyl)piperidin-4-yl)-6-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (101); 1-(1-(dimethylglycyl)piperidin-4-yl)-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (102); (S)-1-(1-(dimethylglycyl)piperidin-3-yl)-6 -methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (103); (R)-1-(1-(dimethylglycyl)piperidin-3-yl)-6-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (104); 1-(1-(dimethylglycyl)piperidin-3-yl)-5-(8-methoxy-[1,2,4]triazolo[ 1,5-a]pyridin-6-yl)-6-methyl-1,3-dihydro-2H-benzo[d]imidazol-2-one (105);7-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-methylpiperidin-4-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (106);1-(1-isopropylpiperidin-4-yl)-7-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one 1-(1-ethylpiperidin-4-yl)-7-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (108); N,N-dimethyl-2-(4-(7-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-2-oxo-2,3-dihydro-1H-benzo[d]imidazol-1-yl)piperidin-1-yl)acetamide (109);(R)-1-(1-ethylpiperidin-3-yl)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-(trifluoromethyl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (110); (R)-1-(1-isopropylpiperidin-3-yl)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-(trifluoromethyl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (111); (R)-5-(8 -Methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-((tetrahydro-2H-pyran-4-yl)methyl)piperidin-3-yl)-6-(trifluoromethyl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (112); (R)-5-(8-Methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-(1-(oxetan-3-yl)piperidin-3-yl)-6-(trifluoromethyl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (112); (R)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-methylpiperidin-3-yl)-6-(trifluoromethyl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (114); (R)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-propylpiperidin-3-yl)-6-(trifluoromethyl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (115) );(R)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-neopentylpiperidin-3-yl)-6-(trifluoromethyl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (116);(R)-1-(1-(2-ethylbutyl)piperidin-3-yl)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-(trifluoromethyl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (117);(R)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-(2-methoxyethyl)piperidin-3-yl)-6-(trifluoromethyl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (118); (S)-6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)- (S)-6-Isopropyl-1-(1-isopropylpiperidin-3-yl)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (120);

[0035] (S)-6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-propylpiperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (121); (S)-1-(1-cyclobutylpiperidin-3-yl)-6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (122); (S)-6-isopropyl-5-(8- Methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-(oxetan-3-yl)piperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (123);(S)-6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-(tetrahydro-2H-pyran-4-yl)piperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (124);(S)-6-isopropyl-5 -(8-Methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-((tetrahydro-2H-pyran-4-yl)methyl)piperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (125); 6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-((3S)-1-((tetrahydrofuran-3-yl)methyl)piperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one ( 126);(S)-1-(1-(cyclopropylmethyl)piperidin-3-yl)-6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (127);(S)-1-(1-(cyclopropylmethyl)piperidin-3-yl)-6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (128);(S)-1-(1-isobutylpiperidin-3-yl)-6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (129); (S)-1-(1-(2-ethylbutyl)piperidin-3-yl)-6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (130) ;(S)-1-(1-isopentylpiperidin-3-yl)-6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (131);(S)-1-(1-isopentylpiperidin-3-yl)-6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (132);( S)-1-(1-(cyclobutylmethyl)piperidin-3-yl)-6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (133); (R)-6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-propylpiperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (134); (R)-6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-(oxetan-3-yl)piperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (135); (R)-6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-methylpiperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (136);(R)-6-isopropyl-1-(1-isopropylpiperidin-3-yl)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (137); (R)-1-(1-ethylpiperidin-3-yl)-6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (138); (R)-6-isopropyl- 5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-((tetrahydro-2H-pyran-4-yl)methyl)piperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (139); (R)-1-(1-(cyclobutylmethyl)piperidin-3-yl)-6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (140);

[0036] (R)-1-(1-isobutylpiperidin-3-yl)-6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (141); (R)-1-(1-(cyclopropylmethyl)piperidin-3-yl)-6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (142); (R )-6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-(tetrahydro-2H-pyran-4-yl)piperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (143); (R)-1-(1-ethylpiperidin-3-yl)-6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (144 );(R)-5-(7,8-dimethyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-isopropyl-1-(1-isopropylpiperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (145);(R)-5-(7,8-dimethyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-isopropyl-1-(1-(oxetan-3-yl)piperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one ( 146);(R)-5-(7,8-dimethyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-isopropyl-1-(1-methylpiperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (147);(R)-1-(1-(2-ethylbutyl)piperidin-3-yl)-6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (148);(R)-5-(7,8-dimethyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-isopropyl-1-(1-((tetrahydro-2H-pyran-4-yl)methyl)piperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (149); (R)-5-(7,8-dimethyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-isopropyl-1-(1-propylpiperidin-3-yl)-1,3-dihydro-2H-benzo[d ]imidazol-2-one (150);(R)-5-(7,8-dimethyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-(2-ethylbutyl)piperidin-3-yl)-6-isopropyl-1,3-dihydro-2H-benzo[d]imidazol-2-one (151);(R)-5-(7,8-dimethyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-isopropyl-1-(1-neopentylpiperidin-3-yl)-1,3-dihydro-2H- Benz[d]imidazol-2-one (152);(R)-6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-neopentylpiperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (153);6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-methylpiperidin-4-yl)-1,3-dihydro-2H-benzo[d]imidazo 6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-propylpiperidin-4-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (155); 1-(1-cyclobutylpiperidin-4-yl)-6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (156);6-Isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-(oxetan-3-yl)piperidin-4-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (157); 6-Isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-(tetrahydro-2H-pyran-4-yl)piperidin-4-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (158); 6-Isopropyl 6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-((tetrahydro-2H-pyran-4-yl)methyl)piperidin-4-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (159); 6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-((tetrahydrofuran-3-yl)methyl)piperidin-4-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (160);

[0037] 1-(1-(cyclopropylmethyl)piperidin-4-yl)-6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (161); 6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-(tetrahydrofuran-3-yl)piperidin-4-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (16 2);6-isopropyl-1-(1-isopropylpiperidin-4-yl)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (163);1-(1-isobutylpiperidin-4-yl)-6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (164);1-(1-(2-ethyl Butyl)piperidin-4-yl)-6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (165);6-ethyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-((1s,4s)-4-((tetrahydro-2H-pyran-4-yl)amino)cyclohexyl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (166) 6-Ethyl-1-((1s,4s)-4-(isopropylamino)cyclohexyl)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (167); 1-((1s,4s)-4-(dipropylamino)cyclohexyl)-6-ethyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (168);1-((1s,4s)-4-(diethylamino)cyclohexyl)-6-ethyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (169); 6-ethyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-((1s,4s)-4-(oxetan-3-ylamino)cyclohexyl)-1,3-dihydro-2H-benzo[d]imidazol-2-one ( 170;(R)-6-ethyl-1-(1-ethylpiperidin-3-yl)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (171);(R)-6-ethyl-1-(1-isopropylpiperidin-3-yl)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (172);(R)-6-ethyl (R)-6-ethyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-(oxetan-3-yl)piperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (173); (R)-6-ethyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-methylpiperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (174); (R)-6-ethyl-5-( 8-Methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-((tetrahydro-2H-pyran-4-yl)methyl)piperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (175); 1-((3R)-1-(sec-butyl)piperidin-3-yl)-6-ethyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (176);(R)-6-ethyl-1-(1-isobutylpiperidin-3-yl)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (177); (R)-6-ethyl-1-(1-(2-ethylbutyl)piperidin-3-yl)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (17 8);(R)-6-ethyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-propylpiperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (179);(R)-6-ethyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-neopentylpiperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (180);

[0038] (R)-1-(1-(cyclobutylmethyl)piperidin-3-yl)-6-ethyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (181); (R)-1-(1-(cyclopropylmethyl)piperidin-3-yl)-6-ethyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (182); (R)-6-ethyl-5-( 8-Methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-(3,3,3-trifluoropropyl)piperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (183);(R)-6-ethyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-(tetrahydro-2H-pyran-4-yl)piperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (184);5-(7,8-dimethyl -[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-((1s,4s)-4-(dimethylamino)cyclohexyl)-6-isopropyl-1,3-dihydro-2H-benzo[d]imidazol-2-one (185);5-(7,8-dimethyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-isopropyl-1-((1s,4s)-4-(isopropylamino)cyclohexyl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (186);5-(7,8-dimethyl-[1, 2,4]triazolo[1,5-a]pyridin-6-yl)-6-isopropyl-1-((1s,4s)-4-((tetrahydro-2H-pyran-4-yl)amino)cyclohexyl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (187); 5-(7,8-dimethyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-isopropyl-1-((1s,4s)-4-(oxetan-3-ylamino)cyclohexyl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (188);5-(7,8-dimethyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-((1s,4s)-4-(ethylamino)cyclohexyl)-6-isopropyl-1,3-dihydro-2H-benzo[d]imidazol-2-one (189); 5-(7,8-dimethyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-isopropyl-1-((1s,4s)-4-(neopentylamino)cyclohexyl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (190); 1-((1s, 4s)-4-(dimethylamino)cyclohexyl)-6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (191);6-isopropyl-1-((1s,4s)-4-(isopropylamino)cyclohexyl)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (192);6-isopropyl-5-(8-methoxy -[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-((1s,4s)-4-((tetrahydro-2H-pyran-4-yl)amino)cyclohexyl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (193);1-((1s,4s)-4-((2-ethylbutyl)amino)cyclohexyl)-6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (194);6-isopropyl -5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-((1s,4s)-4-(propylamino)cyclohexyl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (195); 6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-((1s,4s)-4-(((tetrahydro-2H-pyran-4-yl)methyl)amino)cyclohexyl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (196);6-Isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-((1s,4s)-4-(neopentylamino)cyclohexyl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (197); 5-(7,8-dimethyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-((1s,4s)-4-((2-ethylbutyl)amino)cyclohexyl)-6-isopropyl-1,3-dihydro-2H-benzo[d]imidazol-2-one (198); 5-(7,8-di Methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-((1s,4s)-4-(dipropylamino)cyclohexyl)-6-isopropyl-1,3-dihydro-2H-benzo[d]imidazol-2-one (199); 5-(7,8-dimethyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-isopropyl-1-((1s,4s)-4-(((tetrahydro-2H-pyran-4-yl)methyl)amino)cyclohexyl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (200);

[0039] 6-Isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-((1r,4r)-4-(oxetan-3-ylamino)cyclohexyl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (201); 1-((1r,4r)-4-(dimethylamino)cyclohexyl)-6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (202); 6-Isopropyl isopropyl-1-((1r,4r)-4-(isopropylamino)cyclohexyl)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (203); 1-((1r,4r)-4-(isobutylamino)cyclohexyl)-6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (204); 1-((1r,4r )-4-(diisobutylamino)cyclohexyl)-6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (205);1-((1r,4r)-4-(bis(cyclopropylmethyl)amino)cyclohexyl)-6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (206);6-isopropyl Pyr-1-((1r,4r)-4-((1-isopropylpiperidin-4-yl)amino)cyclohexyl)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (207); (R)-1-(1-(3,3-dimethylbutyl)piperidin-3-yl)-6-ethyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (208);(R)-1-(1-(cyclopentylmethyl)piperidin-3-yl)-6-ethyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (209); (R)-1-(1-(3,3-dimethylbutyl)piperidin-3-yl)-6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (210); (R)-1-(1-( Cyclopentylmethyl)piperidin-3-yl)-6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (211); 6-ethyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-((3R)-1-(tetrahydrofuran-3-yl)piperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (212); 6-ethyl-5-(8-methoxy-[ 1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-((3R)-1-(tetrahydrofuran-3-yl)piperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (213);6-ethyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-((3R)-1-(tetrahydro-2H-pyran-3-yl)piperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (214-215);6-isopropyl-5-(8 -Methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-((3R)-1-(tetrahydrofuran-3-yl)piperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (216-217); 6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-((3R)-1-(tetrahydro-2H-pyran-3-yl)piperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (218-219);(S)-2-(3-(6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-2-oxo-2,3-dihydro-1H-benzo[d]imidazol-1-yl)piperidin-1-yl)acetamide (220);

[0040] (S)-6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-(2-methoxyethyl)piperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (221); (S)-6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-(2-(methylsulfonyl)ethyl)piperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one 6-Isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-(2-methoxyethyl)piperidin-4-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (223); 6-Isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-(2-(methylsulfonyl)ethyl)piperidin-4-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (224);(R)-6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-(2-methoxyethyl)piperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (225);(R)-6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-(2-methoxyethyl)piperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (R)-6-ethyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-(2-methoxyethyl)piperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (227); (R)-1-(1-(dimethylglycyl)piperidin-3-yl)-6-ethyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (228);1-(4-(4,4-difluoropiperidin-1-yl)cyclohexyl)-6-isopropyl-5-(8-methoxy-7-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (229-230); 6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(4-(pyrrolidin-1-yl)cyclohexyl)-1,3-dihydro -2H-benzo[d]imidazol-2-one (231); 6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(4-(pyrrolidin-1-yl)cyclohexyl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (232); 6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(4-(3-oxopiperazin-1-yl)cyclohexyl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (233); xyl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (233-234);1-(4-(7-oxa-2-azaspiro[3.5]nonan-2-yl)cyclohexyl)-6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (235-236);6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (235-236). 1-(4-(2-oxa-7-azaspiro[3.5]non-7-yl)cyclohexyl)-6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (239-240);

[0041] 1-(4-(3-hydroxy-3-(trifluoromethyl)azetidin-1-yl)cyclohexyl)-6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (241-242); 6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(4-(3-oxopiperazin-1-yl)cyclohexyl)-1,3-dihydro-2H -benzo[d]imidazol-2-one (243); 1-(4-(2,2-dioxido-2-thia-6-azaspiro[3.3]heptan-6-yl)cyclohexyl)-6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (244-245); 1-(4-(4,4-difluoropiperidin-1-yl)cyclohexyl)-6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)- Azolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (246-247); 6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(4-(methyl(3,3,3-trifluoropropyl)amino)cyclohexyl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (248-249); 6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(4-(methyl(3,3,3-trifluoropropyl)amino)cyclohexyl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (248-249); pyridin-6-yl)-1-(4-thiomorpholinocyclohexyl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (250-251); 1-(4-(3-oxa-8-azabicyclo[3.2.1]octan-8-yl)cyclohexyl)-6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (252-253); 1-(4-(2-oxa-6-azaspiro[3.3]heptan-6-yl)cyclohexyl)-6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (254); 6-isopropyl-5-(8-methoxy-7-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(4-((2-methoxyethyl)amino)cyclo 6-isopropyl-5-(8-methoxy-7-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(4-(((1-(methylsulfonyl)cyclopropyl)methyl)amino)cyclohexyl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (259-260);.

[0042] 1-(4-(1,4-oxazepan-4-yl)cyclohexyl)-6-isopropyl-5-(8-methoxy-7-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (261-262); 1-(4-(3-fluoroazetidin-1-yl)cyclohexyl)-6-isopropyl-5-(8-methoxy-7-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (263-264); 6-isopropyl-5-(8-methoxy 1-(4-(2-oxa-7-azaspiro[3.5]nonan-7-yl)cyclohexyl)-6-isopropyl-5-(8-methoxy-7-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (265-266); 1-(4-(2-oxa-7-azaspiro[3.5]nonan-7-yl)cyclohexyl)-6-isopropyl-5-(8-methoxy-7-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (267-268); 1-(4-(2-oxa-6-azaspiro[3.3]Heptan-6-yl)cyclohexyl)-6-isopropyl-5-(8-methoxy-7-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (269-270); 1-(4-(1,4-oxazepan-4-yl)cyclohexyl)-5-(7,8-dimethyl-[1,2,4]triazolo[1,5-a]pyridin- 6-yl)-6-isopropyl-1,3-dihydro-2H-benzo[d]imidazol-2-one (271-272); 5-(7,8-dimethyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(4-(3-fluoropiperidin-1-yl)cyclohexyl)-6-isopropyl-1,3-dihydro-2H-benzo[d]imidazol-2-one (273-274); 1-(4-( 4,4-difluoropiperidin-1-yl)cyclohexyl)-5-(7,8-dimethyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-isopropyl-1,3-dihydro-2H-benzo[d]imidazol-2-one (275-276); 5-(7,8-dimethyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-isopropyl-1-(4-(3-methoxyphenyl) 5-(7,8-dimethyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(4-(3-fluoroazetidin-1-yl)cyclohexyl)-6-isopropyl-1,3-dihydro-2H-benzo[d]imidazol-2-one (279-280);.

[0043] 1-(4-(2-oxa-6-azaspiro[3.3]heptan-6-yl)cyclohexyl)-5-(7,8-dimethyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-isopropyl-1,3-dihydro-2H-benzo[d]imidazol-2-one (281); 1-(4-(2-oxa-7-azaspiro[3.5]nonan-7-yl)cyclohexyl)-5-(7,8-dimethyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-isopropyl- 1,3-Dihydro-2H-benzo[d]imidazol-2-one (282-283);6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(4-(3-methoxypyrrolidin-1-yl)cyclohexyl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (284-285);(S)-1-(4-(3-fluoropyrrolidin-1-yl)cyclohexyl)-6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl) azolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (286-287); 6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(4-(3-(methylsulfonyl)pyrrolidin-1-yl)cyclohexyl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (288-289); (R)-6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1 ,5-a]pyridin-6-yl)-1-(4-(3-(methoxymethyl)pyrrolidin-1-yl)cyclohexyl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (290-291); 1-(4-((3S,4R)-3,4-difluoropyrrolidin-1-yl)cyclohexyl)-6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (292-293);1-(4-(3,3-difluoropyrrolidin-1-yl)cyclohexyl)-6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (294-295); 1-(4-(3,3-difluoroazetidin-1-yl)cyclohexyl)-6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)- 1-(4-(2-oxa-6-azaspiro[3.3]heptan-6-yl)cyclohexyl)-5-(7,8-dimethyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-isopropyl-1,3-dihydro-2H-benzo[d]imidazol-2-one (297);

[0044] 5-(8-Methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-methyl-1-(piperidin-4-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (1E);6-Methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(piperidin-4-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (1EA);5-(8-Methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(piperidin-4-yl )-1,3-dihydro-2H-benzo[d]imidazol-2-one (1EB);6-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(piperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (1EC);(R)-6-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(piperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (1ED);1-((1r,4r)-4 -aminocyclohexyl)-6-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (1EF); 1-((1s,4s)-4-aminocyclohexyl)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-methyl-1,3-dihydro-2H-benzo[d]imidazol-2-one (1EG); (R)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl) -6-methyl-1-(piperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (1EH); 5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(piperidin-4-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (1EG); 7-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(piperidin-4-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (106F);(S)-6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(piperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (110F); (R)-6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(piperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (119F); 6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(piperidin-4-yl)-1 (R)-6-ethyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(piperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (119FA); (R)-6-ethyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(piperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (119FB); or (R)-5-(7,8-dimethyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-isopropyl-1-(piperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (119FC).

[0045] The present invention may be embodied in other specific forms without departing from its spirit or essential attributes. The present invention includes all combinations of the aspects and / or embodiments of the invention described herein. It is understood that any and all embodiments of the present invention can be taken in combination with any other embodiment to describe further embodiments. It should also be understood that each individual element of an embodiment shall be combined with any and all other elements from any embodiment to describe further embodiments.

[0046] definition The features and advantages of the present invention may be more readily understood by those skilled in the art upon reading the following detailed description. It should be understood that, for clarity of reason, certain features of the present invention that are described in the context of separate embodiments may also be combined to form a single embodiment. Conversely, various features of the present invention that are described in the context of a single embodiment may also be combined to form subcombinations thereof for clarity of reason. The embodiments described herein as typical or preferred examples are intended to be illustrative and not limiting of the invention.

[0047] Unless otherwise stated herein, references made in the singular may also include the plural, for example, "a" and "an" may refer to either one or one or more. As used herein, the term "compound" refers to at least one compound. For example, a compound of formula (I) includes a compound of formula (I), and two or more compounds of formula (I).

[0048] Unless otherwise specified, any heteroatom with unsatisfied valences is intended to have sufficient hydrogen atoms to satisfy the valences. The definitions set forth herein take precedence over definitions set forth in any patents, patent applications, and / or publications, which are incorporated herein by reference.

[0049] Listed below are definitions of various terms used to describe this invention. These definitions apply to those terms as they are used throughout the specification (except where they are limited in specific instances) either individually or as part of a larger group. Throughout the specification, groups and substituents thereof may be chosen by one skilled in the art to provide stable moieties and compounds.

[0050] According to the convention in the field, the symbols: [ka] is used in structural formulas herein to indicate the bond that is the point of attachment of a moiety or substituent to a core or backbone structure.

[0051] The terms “halo” and “halogen” as used herein refer to F, Cl, Br, and I. The term "cyano" refers to the group --CN. The term "amino" refers to the group -NH2. The term "oxo" refers to the group =O.

[0052] The term "alkyl" as used herein refers to both branched and straight chain saturated aliphatic hydrocarbon groups containing, for example, 1 to 12 carbon atoms, 1 to 6 carbon atoms, and 1 to 4 carbon atoms. Examples of alkyl groups include, but are not limited to, methyl (Me), ethyl (Et), propyl (e.g., n-propyl and i-propyl), butyl (e.g., n-butyl, i-butyl, sec-butyl, and t-butyl), and pentyl (e.g., n-pentyl, isopentyl, neopentyl), n-hexyl, 2-methylpentyl, 2-ethylbutyl, 3-methylpentyl, and 4-methylpentyl. When a number appears in a subscript after the symbol "C," the subscript more specifically defines the number of carbon atoms that a particular group may contain. For example, "C 1-6 "Alkyl" means straight and branched chain alkyl groups having from 1 to 6 carbon atoms.

[0053] As used herein, the term "fluoroalkyl" is intended to include both branched and straight-chain saturated aliphatic hydrocarbon groups substituted with one or more fluorine atoms. For example, "C 1-4 "Fluoroalkyl" is intended to include C1, C2, C3, and C4 alkyl groups substituted with one or more fluorine atoms. Representative examples of fluoroalkyl groups include, but are not limited to, -CF3 and -CH2CF3.

[0054] The term "cyanoalkyl" includes both branched and straight chain saturated alkyl groups substituted with one or more cyano groups. For example, "cyanoalkyl" includes -CHCN, -CHCHCN, and -C 1-4 Cyanoalkyl is included. The term "aminoalkyl" includes both branched and straight chain saturated alkyl groups substituted with one or more amine groups. For example, "aminoalkyl" includes -CH2NH2, -CH2CH2NH2, and -C 1-4 Aminoalkyl is included.

[0055] The term "hydroxyalkyl" includes both branched and straight-chain saturated alkyl groups substituted with one or more hydroxyl groups. For example, "hydroxyalkyl" includes -CHOH, -CHCHOH, and -CH 1-4 Includes hydroxyalkyl. The term "cycloalkyl" as used herein refers to a group derived from a non-aromatic monocyclic or polycyclic hydrocarbon molecule by removing one hydrogen atom from a saturated ring carbon atom. Representative examples of cycloalkyl groups include, but are not limited to, cyclopropyl, cyclopentyl, and cyclohexyl. When a number appears in a subscript after the symbol "C", the subscript more specifically defines the number of carbon atoms that a particular cycloalkyl group may contain. For example, "C3-C6 cycloalkyl" refers to a cycloalkyl group having 3 to 6 carbon atoms.

[0056] The term "alkoxy," as used herein, refers to an alkyl group attached to the parent molecular moiety through an oxygen atom, such as a methoxy group (-OCH). 1-3 "Alkoxy" means an alkoxy group of 1 to 3 carbon atoms. The terms "fluoroalkoxy" and "-O(fluoroalkyl)" refer to a fluoroalkyl group as defined above attached via an oxygen linking group (-O-). For example, 1-4 "Fluoroalkoxy" is intended to include C1, C2, C3, and C4 fluoroalkoxy groups.

[0057] The term "alkoxyalkyl," as used herein, refers to an alkoxy group attached to an alkyl group attached to the parent molecular moiety through its oxygen atom, such as a methoxymethyl group (-CH2OCH3). For example, 2-4 "Alkoxyalkyl" means an alkoxyalkyl group having 2 to 4 carbon atoms, such as -CH2OCH3, -CH2CH2OCH3, -CH2OCH2CH3, and -CH2CH2OCH2CH3.

[0058] The term "pharmacologically acceptable" is used herein to refer to those compounds, materials, compositions and / or dosage forms which, within the scope of sound medical judgment, are suitable for use in contact with the tissues of human beings and animals without undue toxicity, irritation, allergic response or other problem or complication, and are commensurate with a reasonable benefit / risk ratio.

[0059] Compounds of formula (I) may form salts, which are also within the scope of the present invention. Unless otherwise specified, reference to a compound of the present invention is understood to include reference to one or more of its salts. The term "salts" refers to acidic and / or basic salts formed with inorganic and organic acids and bases. In addition, the term "salts" may include zwitterions (internal salts), for example, when a compound of formula (I) contains both a basic moiety, such as an amine or a pyridine or imidazole ring, and an acidic moiety, such as a carboxylic acid. Pharmaceutically acceptable (i.e., non-toxic, physiologically acceptable) salts, such as, for example, acceptable metal and amine salts, in which the cation does not contribute significantly to the toxicity or biological activity of the salt, are preferred. However, other salts may also be useful, for example, in isolation or purification steps that may be utilized during preparation, and thus are considered to be within the scope of the present invention. Salts of compounds of formula (I) can be formed, for example, by reacting a compound of formula (I) with an amount, such as an equivalent amount, of an acid or base in a solvent, such as a medium in which the salt precipitates, or in an aqueous medium, followed by lyophilization.

[0060] Exemplary acid addition salts include acetates (such as salts formed with acetic acid or trihaloacetic acids, e.g., trifluoroacetic acid), adipates, alginates, ascorbates, aspartates, benzoates, benzenesulfonates, bisulfates, borates, butyrates, citrates, camphorates, camphorsulfonates, cyclopentanepropionates, digluconates, dodecyl sulfates, ethanesulfonates, fumarates, glucoheptanoates, glycerophosphates, hemisulfates, heptanoates, hexanoates, hydrochlorides (formed with hydrochloric acid), hydrobromides (formed with hydrogen bromide), iodides, and the like. These include hydrochloride, maleate (formed with maleic acid), 2-hydroxyethanesulfonate, lactate, methanesulfonate (formed with methanesulfonic acid), 2-naphthalenesulfonate, nicotinate, nitrate, oxalate, pectinate, persulfate, 3-phenylpropionate, phosphate, picrate, pivalate, propionate, salicylate, succinate, sulfate (such as formed with sulfuric acid), sulfonate (such as those described herein), tartrate, thiocyanate, toluenesulfonate such as tosylate, undecanoate, and the like.

[0061] Exemplary base salts include alkali metal salts, such as ammonium, sodium, lithium and potassium salts; alkaline earth metal salts, such as calcium and magnesium salts; barium, zinc, and aluminum salts; salts with organic bases (e.g., organic amines), such as trialkyls, such as triethylamine, procaine, dibenzylamine, N-benzyl-β-phenethylamine, 1-ephenamine, N,N′-dibenzylethylene-diamine, dehydroabietylamine, N-ethylpiperidine, benzylamine, dicyclohexylamine or similar pharma- ceutically acceptable amines, and salts with amino acids, such as arginine, lysine, and the like. Basic nitrogen-containing groups may be quaternized with agents such as lower alkyl halides (e.g., methyl, ethyl, propyl, and butyl chlorides, bromides and iodides), dialkyl sulfates (e.g., dimethyl, diethyl, dibutyl, and diamyl sulfate), long chain halides (e.g., decyl, lauryl, myristyl and stearyl chloride, bromide and iodide), aralkyl halides (e.g., benzyl and phenethyl bromide), etc. Preferred salts include monohydrochlorides, hydrogen sulfates, methanesulfonates, phosphates or nitrates.

[0062] The compound of formula (I) may be provided as an amorphous solid or a crystalline solid. A freeze-drying procedure may be utilized to provide the compound of formula (I) as an amorphous solid. It should further be recognized that solvates (e.g., hydrates) of the compounds of formula (I) are also within the scope of the present invention. The term "solvate" refers to a physical association of a compound of formula (I) with one or more solvent molecules, whether organic or inorganic. This physical association includes hydrogen bonding. In some cases, for example, when one or more solvent molecules are incorporated into the crystal lattice of a crystalline solid, the solvate will be capable of isolation. A "solvate" consists of both a solution phase and a separable solvate phase. Exemplary solvates include hydrates, ethanolates, methanolates, isopropanolates, acetonitrile solvates, and ethyl acetate solvates. Methods of solvation are known in the art.

[0063] Various forms of prodrugs are well known in the art and are described in the following documents: a)The Practice of Medicinal Chemistry, Camille G. Wermuth et al., Ch 31, (Academic Press, 1996); b) Design of Prodrugs, edited by H. Bundgaard, (Elsevier, 1985); c) A Textbook of Drug Design and Development, edited by P. Krogsgaard-Larson and H. Bundgaard, Ch 5, pgs 113-191 (Harwood Academic Publishers, 1991); and d)Hydrolysis in Drug and Prodrug Metabolism, Bernard Testa and Joachim M. Mayer, (Wiley-VCH, 2003)

[0064] The manufacture of prodrugs is well known in the art and is described, for example, in King, FD (ed.), Medicinal Chemistry: Principles and Practice, The Royal Society of Chemistry, Cambridge, UK (1994); Testa, B. et al., Hydrolysis in Drug and Prodrug Metabolism. Chemistry, Biochemistry and Enzymology, VCHA and Wiley-VCH, Zurich, Switzerland (2003); Wermuth, CG (ed.), The Practice of Medicinal Chemistry, Academic Press, San Diego, CA (1999); Rautio, J. et al., Nature Review Drug Discovery, 17, 559-587 (2018).

[0065] Additionally, following its preparation, the compound of formula (I) may be isolated and purified to obtain a composition containing 99% by weight or more of the compound of formula (I) ("substantially pure"), which is then used or formulated as described herein. Such "substantially pure" compounds of formula (I) are also considered herein to be part of the invention.

[0066] "Stable compound" and "stable structure" are intended to refer to a compound that is sufficiently robust to survive isolation to a useful degree of purity from a reaction mixture and formulation into an efficacious therapeutic agent. The present invention embodies stable compounds. A "therapeutically effective amount" is intended to encompass an amount of a compound of the invention alone, or in combination with the claimed compounds, or an amount of a compound of the invention in combination with other active ingredients effective to act as an inhibitor of TLR7 / 8 / 9, or to treat or prevent autoimmune and / or inflammatory conditions, such as SLE, IBD, multiple sclerosis (MS), Sjogren's syndrome, and rheumatoid arthritis.

[0067] The term "treating" or "treatment" as used herein extends to the treatment of a condition in a mammal, particularly a human, and includes (a) preventing the onset of the condition in a mammal, particularly where such mammal is susceptible to, but has not yet been diagnosed as having, the condition; (b) inhibiting the condition, i.e., arresting its onset; and / or (c) alleviating the condition, i.e., causing regression of the condition.

[0068] The compounds of the present invention are intended to include all isotopes of atoms present in the compounds. Isotopes include those atoms having the same atomic number but different mass numbers. By way of general example and without limitation, isotopes of hydrogen include deuterium (D) and tritium (T). Isotopes of carbon include 13 C and 14C. Isotopically labeled compounds of the invention can generally be prepared by common techniques known to those of skill in the art, or by methods analogous to those described herein, substituting appropriately isotopically labeled reagents for unlabeled reagents otherwise used. For example, methyl (-CH3) also encompasses deuterated methyl groups, such as -CD3.

[0069] usefulness The human immune system evolved to defend the body against microbes, viruses and parasites that can cause infection, disease or death. Complex control mechanisms ensure that the various cellular components of the immune system target foreign substances or organisms while not causing permanent or significant damage to the individual. Although the initiating events are not fully understood at present, in autoimmune pathologies, the immune system directs its inflammatory response towards target organs in the affected individual. Different autoimmune diseases are typically characterized by the predominant or initially affected target organ or tissue, such as the joints in the case of rheumatoid arthritis, the thyroid in the case of Hashimoto's thyroiditis, the central nervous system in the case of multiple sclerosis, the pancreas in the case of type I diabetes, and the intestine in the case of inflammatory bowel disease.

[0070] The compounds of the present invention inhibit signaling through Toll-like receptors 7, 8, or 9 (TLR7, TLR8, TLR9) or combinations thereof. Thus, the compounds of formula (I) have utility in treating conditions associated with inhibition of signaling through one or more of TLR7, TLR8, or TLR9. Such conditions include TLR7, TLR8, or TLR9 receptor-associated diseases in which cytokine levels are regulated as a result of intracellular signaling.

[0071] As used herein, the term "treat" or "treatment" includes the treatment of a condition in a mammal, particularly a human, and includes (a) preventing or delaying the onset of the condition in a mammal, particularly when the mammal is susceptible to the disease but has not yet been diagnosed as suffering from the disease; (b) inhibiting the condition, i.e., arresting its progression; and / or (c) achieving a complete or partial alleviation of the symptoms or condition, and / or palliating, ameliorating, reducing or curing the disease or disorder and / or its symptoms.

[0072] In view of their activity as selective inhibitors of TLR7, TLR8 or TLR9, the compounds of formula (I) are also useful in treating TLR7, TLR8 or TLR91 family receptor associated diseases, respectively, but are not limited to inflammatory diseases such as Crohn's disease, ulcerative colitis, asthma, graft-versus-host disease, allograft rejection, chronic obstructive pulmonary disease; autoimmune diseases such as Graves' disease, rheumatoid arthritis, systemic lupus erythematosus, lupus nephritis, cutaneous lupus, psoriasis; autoimmune diseases including cryopyrin-associated periodic syndromes (CAPS), TNF receptor-associated periodic syndromes (TRAPS), familial Mediterranean fever (FMF), adult-onset Still's disease, systemic juvenile idiopathic arthritis, gout, gouty arthritis. These compounds are useful for treating autoinflammatory diseases; metabolic diseases including type 2 diabetes, atherosclerosis, myocardial infarction; destructive bone disorders such as bone resorption diseases, osteoarthritis, osteoporosis, multiple myeloma-related bone disorder; proliferative disorders such as acute myeloid leukemia, chronic myeloid leukemia; angiogenic disorders including solid tumors, ocular neovascularization, and infantile hemangiomas; infectious diseases such as sepsis, septic shock, and bacterial dysentery; neurodegenerative diseases such as Alzheimer's disease, Parkinson's disease, cerebral ischemia, or neurodegenerative diseases caused by traumatic injury, neoplastic and viral diseases such as metastatic melanoma, Kaposi's sarcoma, multiple myeloma, and HIV infection, and CMV retinitis, AIDS.

[0073] More specifically, specific conditions or diseases that may be treated with the compounds of the present invention include, but are not limited to, pancreatitis (acute or chronic), asthma, allergies, adult respiratory distress syndrome, chronic obstructive pulmonary disease, glomerulonephritis, rheumatoid arthritis, systemic lupus erythematosus, scleroderma, chronic thyroiditis, Graves' disease, autoimmune gastritis, diabetes, autoimmune hemolytic anemia, autoimmune neutropenia, thrombocytopenia, atopic dermatitis, chronic active hepatitis, myasthenia gravis, multiple sclerosis, inflammatory bowel disease, ulcerative colitis, and the like. Enteritis, Crohn's disease, psoriasis, graft-versus-host disease, endotoxin-induced inflammatory responses, tuberculosis, atherosclerosis, muscle degeneration, cachexia, psoriatic arthritis, Reiter's syndrome, gout, traumatic arthritis, rubella arthritis, acute synovitis, pancreatic beta-cell disease; diseases characterized by massive neutrophil infiltration; rheumatoid spondylitis, gouty arthritis and other arthritic conditions, cerebral malaria, chronic pulmonary inflammatory diseases, silicosis, pulmonary sarcoidosis, bone resorption diseases, allograft rejection, fever due to infection, and myalgia, cachexia secondary to infection, keloid formation, scar tissue formation, ulcerative colitis, heartburn, influenza, osteoporosis, osteoarthritis, acute myeloid leukemia, chronic myeloid leukemia, metastatic melanoma, Kaposi's sarcoma, multiple myeloma, sepsis, septic shock and shigellosis; Alzheimer's disease, Parkinson's disease, neurodegenerative diseases caused by cerebral ischemia or traumatic injury; angiogenic disorders including solid tumors, ocular neovascularization and infantile hemangiomas; acute hepatitis infection (hepatitis A, hepatitis B, and hepatitis C), HIV infection and CMV retinitis, AIDS, ARC or viral diseases including malignancies and herpes; stroke, myocardial ischemia, ischemia in apoptotic heart attacks, organ hypoxia, vascular hyperplasia, cardiac and renal reperfusion injury, thrombosis, cardiac hypertrophy, thrombin-induced platelet aggregation, endotoxemia, and / or toxic shock syndrome, conditions associated with prostaglandin endoperoxidase synthase-2, and pemphigus vulgaris. This embodiment includes a method of treatment where the condition is selected from lupus, including lupus nephritis and systemic lupus erythematosus (SLE), Crohn's disease, ulcerative colitis, allograft rejection, rheumatoid arthritis, psoriasis, ankylosing spondylitis, psoriatic arthritis, and pemphigus vulgaris.Also included are methods of treatment in which the condition is selected from ischemia-reperfusion injury, including cerebral ischemia-reperfusion injury caused by stroke, and cardiac ischemia-reperfusion injury caused by myocardial infarction. Another method of treatment is one in which the condition is multiple myeloma.

[0074] In one embodiment, the compounds of formula (I) are useful for treating cancer, including Waldenstrom's Macroglobulinemia (WM), diffuse large B-cell lymphoma (DLBCL), chronic lymphocytic leukemia (CLL), cutaneous diffuse large B-cell lymphoma, and primary CNS lymphoma.

[0075] In addition, the TLR7, TLR8, or TLR9 inhibitors of the present invention inhibit the expression of inducible pro-inflammatory proteins, such as prostaglandin endoperoxide synthase-2 (PGHS-2) (also called cyclooxygenase-2 (COX-2)), IL-1, IL-6, IL-18, chemokines, etc. Thus, further TLR7 / 8 / 9-associated conditions include edema, analgesia, fever, and pain, such as neuromuscular pain, headache, cancer-induced pain, dental pain, and arthritis pain. The compounds of the present invention may also be used to treat veterinary viral infections, such as lentivirus infections (including, but not limited to, equine infectious anemia virus infections); or retrovirus infections (including feline immunodeficiency virus, bovine immunodeficiency virus, and canine immunodeficiency virus infections).

[0076] Thus, the present invention provides a method of treating such conditions, comprising administering to a subject in need thereof a therapeutically effective amount of at least one compound of formula (I) or a salt thereof. "Therapeutically effective amount" is intended to encompass an amount of a compound of the present invention that is effective, when administered alone or in combination, to inhibit an autoimmune disease or chronic inflammatory disease. Methods for treating TLR7, TLR8, or TLR9-associated conditions may involve administering the compounds of formula (I) alone or in combination with each other and / or other suitable therapeutic agents useful in treating such conditions. Thus, a "therapeutically effective amount" is also intended to encompass an amount of a combination of the claimed compounds that is effective to inhibit TLR7, TLR8, or TLR9 and / or treat a disease associated with TLR7, TLR8, or TLR9.

[0077] Examples of such other therapeutic agents include corticosteroids, rolipram, calphostin, cytokine suppressive anti-inflammatory drugs (CSAIDs), interleukin-10, glucocorticoids, salicylates, carbon monoxide, and other immunosuppressants; nuclear translocation inhibitors such as deoxyspergualin (DSG); nonsteroidal anti-inflammatory drugs (NSAIDs) such as ibuprofen, celecoxib and rofecoxib; antiviral agents such as abacavir; antiproliferative agents such as methotrexate, leflunomide, FK506 (tacrolimus, PROGRAF®); antimalarials such as hydroxychloroquine; cytotoxic agents such as azathiprine and cyclophosphamide; TNF-α inhibitors such as tenidap, anti-TNF antibodies or soluble TNF receptors, and rapamycin (sirolimus or RAPAMUNE®) or derivatives thereof.

[0078] The above-mentioned other therapeutic agents, when utilized in combination with the compounds of the present invention, may be used, for example, in amounts set forth in the Physicians' Desk Reference (PDR) or as otherwise determined by one of skill in the art. In the methods of the present invention, such other therapeutic agents may be administered prior to, simultaneously with, or after administration of the compounds of the present invention. The present invention also provides pharmaceutical compositions capable of treating TLR7 / 8 / 9 receptor-associated conditions, including the IL-1 family receptor-mediated diseases described above.

[0079] The compositions of the present invention may contain other therapeutic agents as described above and may be formulated, for example, by utilizing conventional solid or liquid vehicles or diluents, as well as pharmaceutical additives (e.g., excipients, binders, preservatives, stabilizers, flavorings, etc.) of a type appropriate for the desired method of administration, according to methods such as techniques well known in the art of formulation.

[0080] Accordingly, the present invention further includes compositions comprising one or more compounds of formula (I) and a pharma- ceutically acceptable carrier. "Pharmaceutically acceptable carrier" refers to a medium generally accepted in the art for delivering biologically active agents to animals, particularly mammals. Pharmaceutically acceptable carriers are formulated according to a number of factors well within the scope of one skilled in the art. These factors include, but are not limited to, the type and characteristics of the active agent being formulated; the subject to which the composition containing the agent is to be administered; the intended route of administration of the composition; and the targeted therapeutic indication. Pharmaceutically acceptable carriers include both aqueous and non-aqueous liquid media, as well as a variety of solid and semi-solid dosage forms. Such carriers can include many different ingredients and additives in addition to the active agent, and such additional ingredients are included in the formulation for a variety of reasons, such as stabilization of the active agent, binders, etc., as is well known to those skilled in the art. Descriptions of suitable pharmacopoeia acceptable carriers, and factors involved in their selection, can be found in a variety of readily available sources, such as, for example, Remington's Pharmaceutical Sciences, 17th Edition (1985), the contents of which are incorporated herein by reference.

[0081] The compounds of formula (I) may be administered by any means appropriate to the condition to be treated, which may depend on the need for site-specific treatment and on the amount of compound of formula (I) to be delivered. Also included within the scope of the present invention is a series of pharmaceutical compositions comprising a compound of formula (I) and one or more non-toxic pharma- ceutically acceptable carriers and / or diluents and / or adjuvants (collectively referred to herein as "carrier" materials), and optionally other active ingredients. The compound of formula (I) may be administered by any suitable route, preferably in the form of a pharmaceutical composition adapted for such route, in a dose effective for the intended treatment. The compounds and compositions of the present invention may be administered, for example, orally, transmucosally, or parenterally, including intravascularly, intravenously, intraperitoneally, subcutaneously, intramuscularly, and intrasternally, in dosage unit formulations containing conventional pharma- cetically acceptable carriers, adjuvants, and vehicles. For example, the pharmaceutical carrier may contain a mixture of mannitol or lactose and microcrystalline cellulose. The mixture may contain additional components such as lubricants, disintegrants such as magnesium stearate, crospovidone, and the like. The carrier mixture may be filled into gelatin capsules or compressed into tablets. For example, the pharmaceutical composition may be administered as an oral dosage form or as an injection.

[0082] For oral administration, the pharmaceutical composition may be in the form of, for example, a tablet, capsule, liquid capsule, suspension or liquid. The pharmaceutical composition is preferably prepared in the form of a dosage unit containing a specific amount of the active ingredient. For example, the pharmaceutical composition may be provided as a tablet or capsule containing an amount of the active ingredient ranging from about 0.1 to 1000 mg, preferably about 0.25 to 250 mg, more preferably about 0.5 to 100 mg. The daily dose suitable for a human or other mammal may vary widely depending on the condition of the patient and other factors, but can be determined using routine methods.

[0083] Any pharmaceutical composition contemplated herein can be delivered orally, for example, via any acceptable and suitable oral formulation. Exemplary oral formulations include, but are not limited to, tablets, troches, lozenges, aqueous and oily suspensions, dispersible powders or granules, emulsions, hard and soft capsules, liquid capsules, syrups and elixirs. Pharmaceutical compositions intended for oral administration can be prepared according to any method known in the art for preparing pharmaceutical compositions for oral administration. In order to provide a pharma-ceutically acceptable formulation, the pharmaceutical composition of the present invention can contain at least one agent selected from sweeteners, flavoring agents, coloring agents, analgesics, antioxidants and preservatives.

[0084] Tablets can be prepared, for example, by mixing at least one compound of formula (I) with at least one non-toxic pharma- ceutically acceptable excipient suitable for tablet manufacture. Exemplary excipients include, but are not limited to, inert diluents such as, for example, calcium carbonate, sodium carbonate, lactose, calcium phosphate, and sodium phosphate; granulating and disintegrating agents such as, for example, microcrystalline cellulose, sodium croscarmellose, corn starch, and alginic acid; binding agents such as, for example, starch, gelatin, polyvinylpyrrolidone, and acacia; and lubricants such as, for example, magnesium stearate, stearic acid, and talc. In addition, tablets can be either uncoated or coated by known techniques to either mask the unpleasant taste of unpleasant-tasting drugs, delay disintegration, and delay the absorption of active ingredients in the digestive tract, thereby prolonging the action of the active ingredients. Exemplary water-soluble taste-masking substances include, but are not limited to, hydroxypropylmethylcellulose and hydroxypropylcellulose. Exemplary time delay materials include, but are not limited to, ethyl cellulose and cellulose acetate butyrate.

[0085] Hard gelatin capsules may be prepared, for example, by mixing at least one compound of Formula (I) with at least one inert solid diluent, such as, for example, calcium carbonate; calcium phosphate; and kaolin. Soft gelatin capsules can be prepared, for example, by mixing at least one compound of formula (I) with at least one water-soluble carrier, such as, for example, polyethylene glycol; at least one oil medium, such as, for example, peanut oil, liquid paraffin, and olive oil.

[0086] Aqueous suspensions can be prepared, for example, by mixing at least one compound of formula (I) with at least one excipient suitable for preparing aqueous suspensions.Exemplary excipients suitable for preparing aqueous suspensions include, but are not limited to, suspending agents, such as sodium carboxymethylcellulose, methylcellulose, hydroxypropylmethylcellulose, sodium alginate, alginic acid, polyvinylpyrrolidone, gum tragacanth, and gum acacia; dispersing or wetting agents, such as naturally occurring phosphatides, such as lecithin; condensation products of alkylene oxides and fatty acids, such as polyoxyethylene stearate; condensation products of ethylene oxides and long-chain aliphatic alcohols, such as heptadecaethylene-oxycetanol; condensation products of ethylene oxides and partial esters derived from fatty acids and hexitols, such as polyoxyethylene sorbitol monooleate; and condensation products of ethylene oxides and partial esters derived from fatty acids and hexitol anhydrides, such as polyethylene sorbitan monooleate. The aqueous suspensions may also contain, by way of example only, at least one preservative, such as ethyl and n-propyl p-hydroxybenzoate; at least one coloring agent; at least one flavoring agent; and / or at least one sweetening agent (including, but not limited to, for example, sucrose, saccharin and aspartame).

[0087] Oily suspensions can be prepared by suspending at least one compound of formula (I) in any of the following: vegetable oils, such as peanut oil; olive oil; sesame oil; and coconut oil; or mineral oils, such as liquid paraffin.Oily suspensions can also contain at least one thickening agent, such as beeswax; hard paraffin; and cetyl alcohol.To provide acceptable oily suspensions, at least one sweetener and / or at least one flavoring agent, as described above, can be added to the oily suspension.Oily suspensions can further contain at least one preservative, including, but not limited to, antioxidants, such as butylated hydroxyanisole and alpha-tocopherol.

[0088] Dispersible powder or granule can be prepared, for example, by mixing at least one compound represented by formula (I) with at least one dispersing agent and / or wetting agent; with at least one suspending agent; and / or with at least one preservative. Suitable dispersing agents, wetting agents and suspending agents are as described above. Exemplary preservatives include, but are not limited to, for example, antioxidants, e.g., ascorbic acid. In addition, dispersible powder or granule can also contain at least one excipient (including, but are not limited to, for example, sweeteners; flavoring agents; and coloring agents).

[0089] The emulsion of at least one compound of formula (I) may be prepared, for example, as an oil-in-water emulsion. The oil phase of the emulsion containing the compound of formula (I) may be composed of known ingredients in a known manner. The oil phase may be provided, for example, but not limited to, vegetable oils, such as olive oil and peanut oil; mineral oils, such as liquid paraffin; and mixtures thereof. The phase may contain only an emulsifier, but may also contain a mixture of at least one emulsifier with a fat or oil, or both a fat and an oil. Suitable emulsifiers include, but are not limited to, naturally occurring phosphatides, such as soybean lecithin; esters or partial esters derived from fatty acids, such as sorbitan monooleate, and hexitol anhydrides; and condensation products of partial esters, such as polyoxyethylene sorbitan monooleate, and ethylene oxide. The hydrophilic emulsifier is preferably formulated together with a lipophilic emulsifier, which acts as a stabilizer. It is also preferred to formulate both oils and fats. The emulsifier, with or without stabilizers, forms the so-called emulsifying wax, which, together with fats and oils, forms the so-called emulsifying ointment base, which forms the oily dispersed phase of cream formulations. The emulsion may also contain sweeteners, flavorings, preservatives and / or antioxidants. Emulsifiers and emulsion stabilizers suitable for use in the formulations of the present invention include Tween 60, Span 80, cetostearyl alcohol, myristyl alcohol, glyceryl monostearate, sodium lauryl sulfate, glyceryl distearate, alone or together with waxes, or other materials well known in the art.

[0090] The compound of formula (I) can also be delivered, for example, intravenously, subcutaneously, and / or intramuscularly, via any medicamentously acceptable and suitable injectable form.Exemplary injectable forms include, but are not limited to, for example, sterile aqueous solutions, including acceptable vehicles and solvents such as water, Ringer's solution and sodium chloride isotonic solution; sterile oil-in-water microemulsions; and aqueous or oily suspensions.

[0091] Preparations for parenteral administration may be in the form of aqueous or non-aqueous isotonic sterile injection solutions or suspensions. These solutions and suspensions may be prepared from sterile powders or granules using one or more carriers or diluents mentioned for use in preparations for oral administration, or by using other suitable dispersing or wetting agents and suspending agents. The compounds may be dissolved in water, polyethylene glycol, propylene glycol, ethanol, corn oil, cottonseed oil, peanut oil, sesame oil, benzyl alcohol, sodium chloride solution, tragacanth gum and / or various buffers. Other adjuvants and methods of administration are well and widely known in the pharmaceutical field. The active ingredient may also be administered by injection as a composition containing a suitable carrier (including saline, dextrose or water) or containing a cyclodextrin (i.e., Captisol), a cosolvent solubilizer (i.e., propylene glycol) or a micelle solubilizer (i.e., Tween 80).

[0092] Sterile injectable preparations may also be sterile injectable solutions or suspensions in non-toxic parenterally acceptable diluents or solvents, such as solutions in 1,3-butanediol. Among the acceptable vehicles and solvents, usable vehicles and solvents are water, Ringer's solution and isotonic sodium chloride solution. In addition, sterile fixed oils are commonly used as solvents or suspending media. For this purpose, any sterile fixed oil may be used, including synthetic mono- or diglycerides. In addition, fatty acids such as oleic acid find use in the preparation of injectables.

[0093] Sterile injectable oil-in-water microemulsions can be prepared, for example, by 1) dissolving at least one compound of formula (I) in an oil phase, such as a mixture of soybean oil and lecithin; 2) combining the oil phase containing the compound of formula (I) with a mixture of water and glycerol; and 3) processing the combination to form a microemulsion.

[0094] Sterile aqueous or oily suspensions can be prepared according to methods known in the art. For example, sterile aqueous solutions or suspensions can be prepared using non-toxic parenterally acceptable diluents or solvents, such as 1,3-butanediol; sterile oily suspensions can be prepared using sterile, non-toxic acceptable solvents or suspending media, such as sterile fixed oils, e.g., synthetic mono- or diglycerides; and fatty acids, such as oleic acid.

[0095] Pharmaceutically acceptable carriers, adjuvants and vehicles that can be used in the pharmaceutical compositions of the present invention include, but are not limited to, ion exchangers, alumina, aluminum stearate, lecithin, self-emulsifying drug delivery systems (SEDDS) such as d-alpha-tocopherol polyethylene glycol 1000 succinate, surfactants used in pharmaceutical dosage forms such as Tween, polyethoxylated castor oil such as CREMOPHOR® surfactants (BASF), or other similar polymeric delivery matrices, serum proteins such as human serum albumin, buffer substances such as phosphates, glycine, sorbic acid, potassium sorbate, partial glyceride mixtures of saturated vegetable fatty acids, water, salts or electrolytes such as protamine sulfate, disodium hydrogen phosphate, potassium hydrogen phosphate, sodium chloride, zinc salts, colloidal silica, magnesium trisilicate, polyvinylpyrrolidone, cellulosic materials, polyethylene glycol, sodium carboxymethylcellulose, polyacrylates, waxes, polyethylene-polyoxypropylene-block polymers, polyethylene glycol and wool fat. Cyclodextrins, such as alpha-, beta-, and gamma-cyclodextrin, or chemically modified derivatives, such as hydroxyalkylcyclodextrins, including 2- and 3-hydroxypropyl-cyclodextrin, or other solubilizing derivatives, may also be advantageously used to facilitate delivery of the compounds in the formulations described herein.

[0096] The pharma- ceutical active compounds of the present invention can be processed according to conventional operations in the field of pharmacy to produce medicaments for administration to patients, including humans and other mammals. The pharmaceutical compositions may be subjected to common pharmaceutical practices, such as sterilization, and / or may contain conventional adjuvants, such as preservatives, stabilizers, wetting agents, emulsifiers, buffers, and the like. Tablets and pills may additionally be prepared with enteric coatings. Such compositions may also contain adjuvants, such as wetting agents, sweeteners, flavoring agents, and fragrances.

[0097] The amount of compound and dosing regimen administered to treat a condition with the compounds and / or compositions of the present invention will depend on a variety of factors, including the age, weight, sex, medical condition, type of disease, severity of disease, route and frequency of administration, and the particular compound utilized. Thus, dosing regimens may vary widely, but can be routinely determined using standard methods. A daily dose of about 0.001-100 mg / kg body weight, preferably between about 0.0025 and about 50 mg / kg body weight, and most preferably about 0.005-10 mg / kg body weight, is suitable. The daily dose may be administered in one to four doses per day. Other dosing regimens include cycles of administration once a week and once every two days.

[0098] For therapeutic use, the active compound of the present invention is usually combined with one or more adjuvants suitable for the suggested administration route.When administered orally, the compound can be mixed with lactose, sucrose, starch powder, cellulose esters of alkanoic acid, cellulose alkyl esters, talc, stearic acid, magnesium stearate, magnesium oxide, sodium and calcium salts of phosphate and sulfate, gelatin, gum acacia, sodium alginate, polyvinylpyrrolidone, and / or polyvinyl alcohol, and then tableted or encapsulated for convenient administration.Such capsules or tablets can contain release control agents, as can be provided by dispersing the active compound in hydroxypropylmethylcellulose.

[0099] The pharmaceutical compositions of the present invention comprise at least one compound of formula (I) and, optionally, an additive selected from any pharma- ceutically acceptable carrier, adjuvant, and vehicle. Alternatively, the compositions of the present invention comprise a compound of formula (I) or a prodrug thereof as described herein, and a pharma- ceutically acceptable carrier, adjuvant, or vehicle.

[0100] The present invention also encompasses an article of manufacture. As used herein, an article of manufacture includes, but is not limited to, a kit and a package. The article of manufacture of the present invention includes (a) a first container, (b) a pharmaceutical composition contained in the first container, wherein the composition comprises a first therapeutic agent comprising a compound of the present invention or a pharma- ceutically acceptable salt form thereof, and (c) a package insert stating that the pharmaceutical composition can be used to treat inflammatory disorders and / or autoimmune diseases (as defined above). In another embodiment, the package insert states that the pharmaceutical composition can be used in combination with a second therapeutic agent (as defined above) for treating inflammatory disorders and / or autoimmune diseases. The article of manufacture may further include (d) a second container, wherein components (a) and (b) are contained in the second container, and component (c) is located within or outside the second container. Being contained in the first and second containers means that each container holds the item within its area.

[0101] A first container is a container used to hold a pharmaceutical composition. This container is for manufacturing, storage, shipping, and / or individual / bulk sale. A first container is intended to include a bottle, jar, vial, flask, syringe, tube (e.g., for a cream formulation), or any other container used in manufacturing, holding, storing, or distributing a pharmaceutical formulation.

[0102] The second container is used to hold the first container and, optionally, the package insert. Examples of the second container include, but are not limited to, boxes (e.g., cardboard or plastic), wooden boxes, cartons, bags (e.g., paper or plastic bags), pouches, and sacks. The package insert can be physically attached to the outside of the first container by tape, glue, staples, or other attachment methods, or can be placed in the second container without any means of physical attachment to the first container. Alternatively, the package insert is placed outside the second container. When placed outside the second container, the package insert is preferably physically attached by tape, glue, staples, or other attachment methods. Alternatively, the package insert can be in close proximity to or in contact with the outside of the second container without being physically attached.

[0103] The package insert is a label, tag, marker, etc., that contains information related to the pharmaceutical composition contained in the first container. The information contained therein will usually be determined by the regulatory agency (e.g., the United States Food and Drug Administration) that governs the area in which the product is sold. In one embodiment, the package insert specifically describes the indication that the pharmaceutical composition is approved. The package insert can be made of any material that allows people to read the information contained therein or thereon. For example, the package insert is a printable material (e.g., paper, plastic, cardboard, wheel, paper or plastic sticker) on which the desired information is formed (e.g., printed or attached).

[0104] Manufacturing method The compounds of the present invention can be prepared in many ways well known to those skilled in the art of organic synthesis. The compounds of the present invention can be synthesized using the methods described below, together with synthetic methods known in the art of synthetic organic chemistry, or variations thereof as would be understood by those skilled in the art. Preferred methods include, but are not limited to, the methods described below. All references cited herein are incorporated herein in their entirety by reference.

[0105] The compounds of the present invention may be prepared using the reactions and techniques described in this section. The reactions are carried out in solvents suitable for the reagents and materials employed, and the reactions are suitable for making modifications. It should also be understood that in the following description of synthetic methods, all reaction conditions proposed (including the choice of solvent, reaction environment, reaction temperature, duration of the experiment, and work-up procedures) are selected to be standard conditions for the reaction, which would be readily recognized by one skilled in the art. Those skilled in the art of organic synthesis will understand that the functionality on the various parts of the molecule must be compatible with the proposed reagents and reactions. Such limitations on the substituents compatible with the reaction conditions will be obvious to those skilled in the art, and in the case of limitations, alternative methods must be used. This will sometimes require a judgment to modify the order of synthetic steps or to select one particular process scheme over another to obtain the desired compounds of the present invention. It will also be understood that another major consideration in planning any synthetic route in this field is the careful selection of the protecting groups used to protect the reactive functionalities present in the compounds described in the present invention. An authoritative manual describing many options for those of skill in the art is Greene and Wuts (Protective Groups In Organic Synthesis, Third Edition, Wiley and Sons, 1999).

[0106] Working Example The preparation of the compounds of formula (I) and intermediates used in the preparation of the compounds of formula (I) can be carried out using the procedures described in the following examples and related procedures. The methods and conditions used in these examples, and the actual compounds prepared in these examples, are not intended to be limiting, but rather to illustrate how the compounds of formula (I) can be prepared. The starting materials and reagents used in these examples, if not prepared by the procedures described herein, are generally either commercially available, reported in the chemical literature, or can be prepared using procedures described in the chemical literature.

[0107] Abbreviation [Table 1] [Table 2]

[0108] Analytical LCMS / HPLC conditions: (A) Column: Acquity UPLC BEH C18, 3.0x50 mm, 1.7 μm particles; Mobile phase A: 5:95 acetonitrile:water + 5 mM ammonium acetate; Mobile phase B: 95:5 acetonitrile:water + 5 mM ammonium acetate; Method: %B:O min-20%: 1.1 min-90%: 1.7 min-90%; Flow: 0.7 mL / min (B) Kinetex XB-C18 (75x3mm) 2.6 micron; Solvent A: 10 mM ammonium formate in water:acetonitrile (98:2); Mobile phase B: 10 mM ammonium formate in water:acetonitrile (02:98); Temperature: 50°C; Gradient: 0-100% B over 3 min; Flow rate: 1.1 mL / min; Detection: UV (220 nm). (C) Waters XBridge BEH C18 XP (50x2.1mm) 2.5μm; Mobile phase A: 5:95 acetonitrile:water + 10mM NH4OAc; Mobile phase B: 95:5 acetonitrile:water + 10mM NH4OAc; Temperature: 50°C; Gradient: 0-100% B over 3 min; Flow: 1.1mL / min (D) Waters Xbridge BEH C18 XP (50x2.1mm) 2.5μm; Mobile phase A: 5:95 acetonitrile:water + 0.1% TFA; Mobile phase B: 95:5 acetonitrile:water + 0.1% TFA; Temperature: 50°C; Gradient: 0-100% B over 3 min; Flow: 1.1mL / min (E) Ascentis Express C18 (50x2.1mm), 2.7μm; Mobile phase A: 5:95 acetonitrile:water + 10mM NH4OAc; Mobile phase B: 95:5 acetonitrile:water + 10mM NH4OAc; Temperature: 50°C; Gradient: 0-100% B over 3 min; Flow: 1.1mL / min (F) Azusentis Express C18 (50x2.1mm), 2.7μm; Mobile phase A: 5:95 acetonitrile:water + 0.1% TFA; Mobile phase B: 95:5 acetonitrile:water + 0.1% TFA; Temperature: 50°C; Gradient: 0-100% B over 3 min; Flow: 1.1mL / min (G) Column: Waters Acquity UPLC BEH C18 (2.1x50mm), 1.7 micron; Solvent A = 100% water + 0.05% TFA; Solvent B = 100% acetonitrile + 0.05% TFA; Gradient = 2-98% B over 1 min, then hold at 98% B for 0.5 min; Flow rate: 0.8 mL / min; Detection: UV (220 nm). (H) Column: ZORBAX SB AQ (4.6x50) mm, 3.5 micron, Solvent A: Acetonitrile (98:2); Mobile phase B: 10 mM ammonium formate in water: Acetonitrile (2:98); Temperature: 50°C; Gradient: 0-100% B over 3 min; Flow rate: 1.1 mL / min; Detection: UV (220 nm). (I) Kinetex XB-C18 (75x3mm) 2.6 micron; Solvent A: 0.1% TFA in water:acetonitrile (98:2); Mobile phase B: 10 mM ammonium formate in water:acetonitrile (2:98); Temperature: 50°C; Gradient: 0-100% B over 3 min; Flow rate: 1.1 mL / min; Detection: UV (220 nm).

[0109] Preparative purification conditions Method AA: Waters Xbridge C18, 19x150mm, 5μm particles; Mobile phase A: 10mM ammonium acetate; Mobile phase B: methanol; Gradient: 10-45% B over 20 min, then hold at 100% B for 5 min; Flow: 20mL / min Method AB: Waters Xbridge C18, 19x150mm, 5μm particles; Mobile phase A: 0.1% trifluoroacetic acid; Mobile phase B: acetonitrile; Gradient: 5-25% B over 25 min, then hold at 100% B for 5 min; Flow: 15mL / min

[0110] Example 1 5-(8-Methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-methyl-1-(1-methylpiperidin-4-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one [ka]

[0111] Intermediate 1A: tert-Butyl 4-((4-bromo-5-methyl-2-nitrophenyl)amino)piperidine-1-carboxylate [ka]

[0112] To a mixture of 1-bromo-4-fluoro-2-methyl-5-nitrobenzene (0.500 g, 2.137 mmol) and tert-butyl 4-aminopiperidine-1-carboxylate (0.513 g, 2.56 mmol) in DMF (10.0 mL) was added K2CO3 (0.591 g, 4.27 mmol). The mixture was stirred at 90° C. for 3 h. The reaction mixture was diluted with water (20 mL) and the precipitated solid was filtered, washed with water (2×10 mL) and dried under vacuum to give tert-butyl 4-((4-bromo-5-methyl-2-nitrophenyl)amino)piperidine-1-carboxylate (0.824 g, 1.989 mmol, 93% yield) as a yellow solid. LCMS retention time: 1.71 min [A], MS (ES): m / z=360.4 [M+2H-tBu]

[0113] The following intermediates were prepared following the procedure used to prepare intermediate 1A. Table 1 [Table 3]

[0114] Intermediate 1B: tert-butyl 4-((4-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-5-methyl-2-nitrophenyl)amino)piperidine-1-carboxylate [ka]

[0115] A mixture of tert-butyl 4-((4-bromo-5-methyl-2-nitrophenyl)amino)piperidine-1-carboxylate (0.400g, 0.965mmol), 8-methoxy-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-[1,2,4]triazolo[1,5-a]pyridine (0.398g, 1.448mmol) and potassium phosphate tribasic (0.615g, 2.90mmol) in dioxane (15.0mL) and water (5.0mL) was degassed for 10 minutes, and then PdCl2(dppf)-CH2Cl2 adduct (0.079g, 0.097mmol) was added. The solution was degassed again for 2 minutes, and the mixture was stirred at 90°C for 2 hours. The reaction mixture was allowed to reach room temperature and diluted with DCM (20 mL) and water (10 mL), both layers were separated, the aqueous layer was extracted with 10% MeOH in DCM (2x30 mL), the organic extracts were combined, dried (Na2SO4) and concentrated to give the crude compound. The crude was purified by ISCO using a 24 g silica column, the compound was eluted with EA, fractions were collected and concentrated to give tert-butyl 4-((4-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-5-methyl-2-nitrophenyl)amino)piperidine-1-carboxylate (0.423 g, 0.877 mmol, 91% yield) as an off-white solid. LCMS retention time: 1.35 min [A], MS (ES): m / z=483.6 [M+H]

[0116] The following intermediates were prepared following the procedure used to prepare Intermediate 1B. Table 2 [Table 4] [Table 5]

[0117] Intermediate 1C: tert-butyl 4-((2-amino-4-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-5-methylphenyl)amino)piperidine-1-carboxylate [ka]

[0118] To a solution of tert-butyl 4-((4-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-5-methyl-2-nitrophenyl)amino)piperidine-1-carboxylate (0.420 g, 0.870 mmol) in MeOH (9.00 mL) was added Pd / C (0.093 g, 0.870 mmol) at room temperature. The mixture was stirred at the same temperature under a hydrogen bladder for 3 h. The reaction product was filtered through Celite, washed with MeOH, and the filtrate was concentrated and dried under vacuum to give tert-butyl 4-((2-amino-4-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-5-methylphenyl)amino)piperidine-1-carboxylate (0.384 g, 0.849 mmol, 97% yield) as an off-white solid. LCMS retention time: 1.17 min [A], MS (ES): m / z = 453.6 [M + H]

[0119] Intermediate 1D: tert-Butyl 4-(5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-methyl-2-oxo-2,3-dihydro-1H-benzo[d]imidazol-1-yl)piperidine-1-carboxylate [ka]

[0120] To a solution of tert-butyl 4-((2-amino-4-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-5-methylphenyl)amino)piperidine-1-carboxylate (0.313 g, 0.692 mmol) in acetonitrile (15.00 mL), CDI (0.168 g, 1.037 mmol) was added at room temperature. The mixture was stirred at the same temperature for 16 hours. The reaction was concentrated to give the crude compound, which was purified by ISCO using a 12 g silica column, the compound was eluted with EA, and the fractions were collected and concentrated to give tert-butyl 4-(5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-methyl-2-oxo-2,3-dihydro-1H-benzo[d]imidazol-1-yl)piperidine-1-carboxylate (0.303 g, 0.633 mmol, 92% yield) as a white solid. LCMS retention time: 1.07 min [A], MS (ES): m / z=479.5 [M+H]

[0121] Intermediate 1E: 5-(8-Methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-methyl-1-(piperidin-4-yl)-1H-benzo[d]imidazol-2(3H)-one·TFA [ka]

[0122] To a solution of tert-butyl 4-(5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-methyl-2-oxo-2,3-dihydro-1H-benzo[d]imidazol-1-yl)piperidine-1-carboxylate (0.350 g, 0.731 mmol) in DCM (10.0 mL) was added TFA (1.00 mL) at 0° C. The mixture was stirred at the same temperature for 1 h. The volatiles were removed by flushing with nitrogen gas and dried under vacuum to give the crude compound. The crude material was triturated with diethyl ether (2x10 mL) and then dried under vacuum to give 5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-methyl-1-(piperidin-4-yl)-1H-benzo[d]imidazol-2(3H)-one·TFA (0.330 g, 0.671 mmol, 92% yield) as a white solid. LCMS retention time: 0.49 [A], MS (ES): m / z = 379.6 [M+H]; 1 H NMR (400MHz, methanol-d4) δ ppm 8.38(s,1H), 8.32(s,1H), 7.28(s,1H), 7.06-7.03(m,2H), 4.07(s,3H), 3.60-3.55(m,2H) , 3.36-3.34(m,1H), 3.24-3.16(m,2H), 2.77-2.68(m,2H), 2.37(s,3H), 2.10-2.02(m,2H)

[0123] The following intermediates were prepared following the procedure used to prepare intermediate 1E. Table 3 [Table 6] [Table 7] [Table 8]

[0124] Example 1: 5-(8-Methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-methyl-1-(1-methylpiperidin-4-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one To a solution of 5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-methyl-1-(piperidin-4-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (0.024 g, 0.063 mmol) in MeOH (2.00 mL), formaldehyde / water (0.2 mL, 2.178 mmol) was added. The reaction mixture was stirred for 5 minutes, acetic acid (0.1 mL, 1.747 mmol) was added, and the reaction mixture was stirred at room temperature for 6 hours. Sodium cyanoborohydride (0.012 g, 0.190 mmol) was then added, and the reaction mixture was stirred for another 16 hours. The reaction product was purified by preparative LCMS using method AA and the product containing fractions were combined and dried using a Genevac centrifugal concentrator to give 5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-methyl-1-(1-methylpiperidin-4-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (0.0031 g, 7.82 μmol, 12.33% yield) as a pale solid. LCMS RT=0.806 min [E], MS(ES): m / z=393.2 [M+H]; 1 H NMR (400MHz, methanol-d4) δ ppm 8.40(s,1H), 8.34(s,1H), 7.38(s,1H), 7.06(s,2H), 4.42(s,1H), 4.09(s,3H), 3.23( d,J=11.0Hz,2H), 2.70-2.60(m,2H), 2.53(s,5H), 2.38(s,3H), 1.90(d,J=13.9Hz,2H)

[0125] The following examples were prepared following the general procedure used to prepare Example 1. Table 4 [Table 9] [Table 10]

Table 11

Table 12

Table 13

Table 14

[0126]

Table 15

Table 16

Table 17

Table 18

Table 19

[0127]

Table 20

Table 21

Table 22

Table 23

Table 24

Table 25

[0128] [Table 26] [Table 27] [Table 28]

[0129] Example 84 1-((1s,4s)-4-(isopropyl(methyl)amino)cyclohexyl)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-methyl-1,3-dihydro-2H-benzo[d]imidazol-2-one [ka]

[0130] To a stirred solution of 1-((1s,4s)-4-(isopropylamino)cyclohexyl)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-methyl-1,3-dihydro-2H-benzo[d]imidazol-2-one (50 mg, 0.115 mmol) in THF (1 mL) and DMF (1 mL) was added formaldehyde (3.45 mg, 0.115 mmol) and acetic acid (6.59 μL, 0.115 mmol). The reaction mixture was stirred at room temperature for 16 h, and then NaCNBH3 (7.23 mg, 0.115 mmol) was added. The reaction mixture was stirred for another 2 h. The reaction product was purified by preparative LCMS using method AA to give 1-((1s,4s)-4-(isopropyl(methyl)amino)cyclohexyl)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-methyl-1,3-dihydro-2H-benzo[d]imidazol-2-one (3.1 mg) as an off-white solid. LCMS retention time: 1.025 min [A], MS (ES): m / z = 449.3 [M+H]; 1H NMR (400MHz, DMSO-d6) δ 10.83(s,1H), 8.50(d,J=1.2Hz,1H), 8.45(s,1H), 7.26(s,1H), 7.06(d,J=1. 2Hz,1H), 6.94(s,1H), 4.39-4.30(m,1H), 4.06-3.96(m,3H), 3.28-3.24(m,1 H), 2.47-2.34(m,2H), 2.28(s,3H), 2.14(s,3H), 2.09(d,J=13.4Hz,2H), 1.9 0(s,1H), 1.52(t,J=13.6Hz,2H), 1.42(d,J=8.3Hz,2H), 1.04(d,J=6.4Hz,6H)

[0131] Example 85 5-(8-Methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-methyl-1-((1s,4s)-4-(methyl(tetrahydro-2H-pyran-4-yl)amino)cyclohexyl)-1,3-dihydro-2H-benzo[d]imidazol-2-one [ka]

[0132] 5-(8-Methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-methyl-1-((1s,4s)-4-(methyl(tetrahydro-2H-pyran-4-yl)amino)cyclohexyl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (6 mg) was prepared according to the general procedure described in Example 84 using 5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-methyl-1-((1s,4s)-4-((tetrahydro-2H-pyran-4-yl)amino)cyclohexyl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (30 mg, 0.063 mmol) as the starting intermediate to give the title compound as a white solid. LCMS retention time: 1.10 min [A], MS(ES): m / z = 491.3 [M+H]; 1H NMR (400MHz, DMSO-d6) δ 10.88(s,1H), 9.05(brs,1H), 8.57-8.38(m,2H), 8.29(brs,1H), 7.34-7.19(m,1H), 7.14(s,1H), 7.0 6-6.96(m,1H), 6.94(s,1H), 4.37(brs,1H), 4.10-3.89(m,4H), 3.69(brs,1H), 3.63(brs,1H), 3.52-3 .39(m,2H), 2.94(dd,J=12.5, 6.8Hz,1H), 2.78(d,J=4.9Hz,2H), 2.45-2.15(m,6H), 2.10-1.99(m,1H ), 1.93(d,J=10.0Hz,2H), 1.84(d,J=12.2Hz,2H), 1.69(dd,J=12.5,4.4Hz,1H), 1.17(t,J=7.3Hz,1H)

[0133] Example 86 2-(4-(5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-methyl-2-oxo-2,3-dihydro-1H-benzo[d]imidazol-1-yl)piperidin-1-yl)-N,N-dimethylacetamide [ka]

[0134] To a solution of 5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-methyl-1-(piperidin-4-yl)-1H-benzo[d]imidazol-2(3H)-one·TFA (0.030 g, 0.061 mmol) and 2-chloro-N,N-dimethylacetamide (0.015 g, 0.122 mmol) in a solvent mixture of THF (1.00 mL) and DMF (0.50 mL), TEA (0.1 mL, 0.717 mmol) was added at room temperature. The reaction mixture was stirred at the same temperature for 16 hours. The reaction product was purified by preparative LCMS using method AA and the product containing fractions were combined and dried using a Genevac centrifugal concentrator to give 2-(4-(5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-methyl-2-oxo-2,3-dihydro-1H-benzo[d]imidazol-1-yl)piperidin-1-yl)-N,N-dimethylacetamide (0.0058 g, 0.012 mmol, 20% yield) as a pale solid. LCMS retention time: 0.983 min [E], MS (ES): m / z = 464.3 [M+H]; 1 H NMR (400MHz, methanol-d4) δ ppm 8.40(s,1H), 8.35(d,J=1.5Hz,1H), 7.49(s,1H), 7.12-7.01(m,2H), 4. 91(s,2H), 4.47-4.29(m,1H), 4.09(s,3H), 3.44(s,2H), 3.39-3.35(m, 1H), 3.23(d,J=11.5Hz,2H), 3.17-3.11(m,3H), 3.07-2.91(m,3H), 2.7 8-2.58(m,2H), 2.53-2.41(m,2H), 2.39(s,3H), 1.81(d,J=10.0Hz,2H)

[0135] The following example was prepared according to the procedure used to prepare Example 86. Table 5 [Table 29] [Table 30] [Table 31] [Table 32]

[0136] Example 100 1-(1-(2-(dimethylamino)acetyl)piperidin-4-yl)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-methyl-1H-benzo[d]imidazol-2(3H)-one [ka]

[0137] To a solution of 5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-methyl-1-(piperidin-4-yl)-1H-benzo[d]imidazol-2(3H)-one·TFA (0.030 g, 0.061 mmol) and 2-(dimethylamino)acetic acid (0.013 g, 0.122 mmol) in DMF (1.00 mL), TEA (0.1 mL, 0.717 mmol) and HATU (0.023 g, 0.061 mmol) were added at room temperature. The mixture was stirred at the same temperature for 16 hours. The reaction product was purified by preparative LCMS using method AB and the product containing fractions were combined and dried using a Genevac centrifugal concentrator to give 1-(1-(2-(dimethylamino)acetyl)piperidin-4-yl)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-methyl-1H-benzo[d]imidazol-2(3H)-one (0.0077 g, 0.017 mmol, 27% yield) as a pale solid. LCMS retention time: 0.759 min [F], MS (ES): m / z = 464.3 [M+H]; 1H NMR (400MHz, methanol-d4) δ ppm 8.40(s,1H), 8.34(d,J=1.5Hz,1H), 7.25(s,1H), 7.13-7.00(m,2H), 4.7 7(d,J=13.6Hz,1H), 4.56-4.50(m,1H), 4.16(d,J=14.1Hz,1H), 4.09(s,3 H), 3.70(d,J=14.6Hz,1H), 3.57(d,J=15.1Hz,1H), 3.32-3.23(m,1H), 2. 95-2.76(m,1H), 2.59-2.49(m,7H), 2.47-2.29(m,4H), 2.01-1.85(m,3H)

[0138] The following examples were prepared according to the procedure used to prepare Example 100. Table 6 [Table 33] [Table 34]

[0139] Example 106 7-Methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-methylpiperidin-4-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one [ka]

[0140] Intermediate 106A: tert-butyl 4-((2-methyl-6-nitrophenyl)amino)piperidine-1-carboxylate [ka]

[0141] To a mixture of 2-fluoro-1-methyl-3-nitrobenzene (0.360 g, 2.321 mmol) and tert-butyl 4-aminopiperidine-1-carboxylate (0.558 g, 2.78 mmol) in DMF (10.0 mL), K2CO3 (0.641 g, 4.64 mmol) was added. The mixture was stirred at 90° C. for 3 hours. The reaction mixture was diluted with water (20 mL), extracted with EtOAc (2×40 mL), the extracts were combined, washed with brine (10 mL), and dried under vacuum to obtain crude compound. The crude material was purified by ISCO using a 24 g silica column, the compound was eluted with 20% EA in hexane, and the fractions were collected and concentrated to obtain tert-butyl 4-((2-methyl-6-nitrophenyl)amino)piperidine-1-carboxylate (0.540 g, 1.610 mmol, 69% yield) as a yellow oil. LCMS retention time: 1.52 minutes [A], MS (ES): m / z=280.2 [M+2H-tBu]

[0142] Intermediate 106B: tert-butyl 4-((4-bromo-2-methyl-6-nitrophenyl)amino)piperidine-1-carboxylate [ka]

[0143] To a solution of tert-butyl 4-((2-methyl-6-nitrophenyl)amino)piperidine-1-carboxylate (0.450 g, 1.342 mmol) in acetonitrile (30.00 mL) was added NBS (0.263 g, 1.476 mmol) at 0° C. The mixture was stirred at room temperature for 16 h. The reaction product was diluted with EtOAc, washed with water, dried (Na2SO4), and concentrated to give crude compound. The crude material was purified by ISCO using a 24 g silica column, the compound was eluted with 12% EA in hexanes, and the fractions were collected and concentrated to give tert-butyl 4-((4-bromo-2-methyl-6-nitrophenyl)amino)piperidine-1-carboxylate (0.540 g, 1.303 mmol, 97% yield) as a yellow solid. LCMS retention time: 1.75 min [A], MS(ES): m / z=358.4 [M-tBu]

[0144] Intermediate 106C: tert-butyl 4-((2-methyl-4-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-nitrophenyl)amino)piperidine-1-carboxylate [ka]

[0145] A mixture of tert-butyl 4-((4-bromo-2-methyl-6-nitrophenyl)amino)piperidine-1-carboxylate (0.280 g, 0.676 mmol), 8-methyl-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-[1,2,4]triazolo[1,5-a]pyridine (0.263 g, 1.014 mmol) and potassium phosphate tribasic (0.430 g, 2.028 mmol) in dioxane (15.0 mL) and water (5.0 mL) was degassed for 10 minutes. Then, PdCl2(dppf)-CH2Cl2 adduct (0.055 g, 0.068 mmol) was added, the mixture was degassed for 2 minutes, and the mixture was stirred at 90 ° C for 2 hours. The reaction mixture was diluted with DCM (20 mL) and water (10 mL), the two layers were separated, the aqueous layer was extracted with 10% MeOH in DCM (2x30 mL), the organic extracts were combined, dried (Na2SO4) and concentrated to give the crude compound. The crude material was purified by ISCO using a 12 g silica column, the compound was eluted with EA, the fractions were collected and concentrated to give tert-butyl 4-((2-methyl-4-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-nitrophenyl)amino)piperidine-1-carboxylate (250 mg, 0.536 mmol, 79% yield) as an off-white solid. LCMS retention time: 1.50 min [A], MS (ES): m / z=465.4 [MH]

[0146] Intermediate 106D: tert-butyl 4-((2-amino-6-methyl-4-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)phenyl)amino)piperidine-1-carboxylate [ka]

[0147] To a solution of tert-butyl 4-((2-methyl-4-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-nitrophenyl)amino)piperidine-1-carboxylate (0.250 g, 0.536 mmol) in MeOH (10.00 mL) was added Pd-C (0.057 g, 0.536 mmol) at room temperature. The mixture was stirred at the same temperature under a hydrogen bladder for 16 h. The reaction product was filtered through Celite, washed with methanol, and the filtrate was collected, concentrated, and dried under vacuum to give tert-butyl 4-((2-amino-6-methyl-4-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)phenyl)amino)piperidine-1-carboxylate (210 mg, 0.481 mmol, 90% yield) as a fluffy solid. LCMS retention time: 1.26 min [A], MS (ES): m / z = 437.4 [M+H]

[0148] Intermediate 106E: tert-butyl 4-(7-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-2-oxo-2,3-dihydro-1H-benzo[d]imidazol-1-yl)piperidine-1-carboxylate [ka]

[0149] To a solution of tert-butyl 4-((2-amino-6-methyl-4-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)phenyl)amino)piperidine-1-carboxylate (0.210 g, 0.481 mmol) in acetonitrile (15.00 mL) was added CDI (0.117 g, 0.722 mmol) at room temperature. The mixture was stirred at the same temperature for 16 hours. The reaction product was concentrated to obtain crude compound. The crude material was purified by ISCO using a 24 g silica column, the compound was eluted with neat EA, and fractions were collected and concentrated to give tert-butyl 4-(7-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-2-oxo-2,3-dihydro-1H-benzo[d]imidazol-1-yl)piperidine-1-carboxylate (150 mg, 0.324 mmol, 67% yield) as a white solid. LCMS retention time: 1.16 min [A], MS (ES): m / z=463.3 [M+H]

[0150] Intermediate 106F: 7-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(piperidin-4-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one [ka]

[0151] To a solution of tert-butyl 4-(7-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-2-oxo-2,3-dihydro-1H-benzo[d]imidazol-1-yl)piperidine-1-carboxylate (0.150 g, 0.324 mmol) in DCM (5.0 mL) was added TFA (0.50 mL) at 0° C. The mixture was stirred at the same temperature for 1 h. Volatiles were removed by blowing nitrogen gas. The mixture was dried under vacuum to give crude compound. The crude material was triturated with diethyl ether (2x10 mL) and then dried under vacuum to give 7-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(piperidin-4-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one·TFA (0.126 g, 0.265 mmol, 82% yield) as an off-white solid. LCMS retention time: 1.350 min [E], MS (ES): m / z = 363.2 [M+H]; 1 H NMR (400MHz, methanol-d4) δ ppm 8.84(s,1H), 8.43(s,1H), 7.80(s,1H), 7.26(d,J=3.7Hz,2H), 3.59(d,J=12.7Hz,2H), 3.2 9-3.20(m,2H), 3.10-2.98(m,2H), 2.76(s,3H), 2.72-2.63(m,3H), 2.19(d,J=12.0Hz,2H)

[0152] Example 106: 7-Methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-methylpiperidin-4-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one To a solution of 7-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(piperidin-4-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one·TFA (24 mg, 0.050 mmol) in MeOH (1.5 mL) was added formaldehyde (0.2 mL, 2.178 mmol) and acetic acid (0.2 mL, 3.49 mmol) in water at room temperature. The reaction mixture was stirred for 5 h, then sodium cyanoborohydride (15.83 mg, 0.252 mmol) was added and the reaction mixture was stirred for another 16 h. The reaction product was subjected to preparative LCMS and purified using method AA, the product containing fractions were combined and dried using a Genevac centrifugal concentrator to give 7-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-methylpiperidin-4-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (4.6 mg, 0.012 mmol, 23% yield) as a pale solid. LCMS retention time: 0.840 min [F], MS (ES): m / z = 377.2 [MH]; 1 H NMR (400MHz, methanol-d4) δ ppm 8.83(s,1H), 8.42(s,1H), 7.80(s,1H), 7.23(d,J=5.6Hz,2H), 4.67-4.53(m,1H), 3.20(d,J=11. 7Hz,2H), 3.03-2.87(m,2H), 2.70(s,3H), 2.72(s,3H), 2.56-2.33(m,5H), 1.96(d,J=10.8Hz,2H)

[0153] The following examples were prepared according to the procedure used to prepare Example 106. Table 7 [Table 35]

[0154] Example 109 N,N-Dimethyl-2-(4-(7-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-2-oxo-2,3-dihydro-1H-benzo[d]imidazol-1-yl)piperidin-1-yl)acetamide [ka]

[0155] To a solution of 7-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(piperidin-4-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one·TFA (24 mg, 0.050 mmol) in a solvent mixture of THF (1.0 mL) and DMF (0.5 mL), 2-chloro-N,N-dimethylacetamide (30.6 mg, 0.252 mmol) and TEA (0.2 mL, 1.435 mmol) were added at room temperature. The reaction mixture was stirred at the same temperature for 16 h. The reaction product was subjected to preparative LCMS and purified using method AA, the product containing fractions were combined and dried using a Genevac centrifugal concentrator to give 1-(1-isopropylpiperidin-4-yl)-7-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (5.2 mg, 0.012 mmol, 24% yield) as a pale solid. LCMS retention time 1.184 min [E], MS (ES): m / z = 448.3 [M+H]; 1 H NMR (400MHz, methanol-d4) δ ppm 8.83(s,1H), 8.42(s,1H), 7.80(s,1H), 7.23(d,J=5.6Hz,2H), 4.62-4.52(m,1H ), 3.45(brs,2H), 3.27-3.10(m,5H), 3.04-2.89(m,5H), 2.87(brs,1H), 2.77-2 63(m,6H), 2.48(d,J=10.8Hz,3H), 1.91(d,J=11.2Hz,2H)

[0156] Example 110 (R)-1-(1-ethylpiperidin-3-yl)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-(trifluoromethyl)-1,3-dihydro-2H-benzo[d]imidazol-2-one [ka]

[0157] Intermediate 110A: tert-butyl (R)-3-((2-nitro-5-(trifluoromethyl)phenyl)amino)piperidine-1-carboxylate [ka] To a solution of 2-chloro-1-nitro-4-(trifluoromethyl)benzene (300 mg, 1.330 mmol) in toluene (20 mL) was added cesium carbonate (1300 mg, 3.99 mmol) and BINAP (83 mg, 0.133 mmol). The solution was degassed with nitrogen for 10 min, then palladium(II) acetate (14.93 mg, 0.067 mmol) was added and the mixture was stirred at 110° C. for 16 h. The reaction mixture was diluted with ethyl acetate (50 mL), washed with water (2×30 mL), brine (10 mL), dried over sodium sulfate and concentrated to give the product. The crude material was purified by ISCO using a 24 g silica column, the compound was eluted with 45% ethyl acetate in petroleum ether, and fractions were collected and concentrated to give tert-butyl (R)-3-((2-nitro-5-(trifluoromethyl)phenyl)amino)piperidine-1-carboxylate (500 mg, 0.706 mmol, 53% yield) as a pale solid. LCMS retention time: 3.685 min [B], MS (E - ) m / z: 334[M-tBu+H]

[0158] Intermediate 110B: tert-butyl (R)-3-((4-bromo-2-nitro-5-(trifluoromethyl)phenyl)amino)piperidine-1-carboxylate [ka]

[0159] tert-Butyl (R)-3-((4-bromo-2-nitro-5-(trifluoromethyl)phenyl)amino)piperidine-1-carboxylate (2 g, 4.52 mmol, 82% yield) was prepared following the general procedure described in Intermediate 104B using tert-butyl (R)-3-((2-nitro-5-(trifluoromethyl)phenyl)amino)piperidine-1-carboxylate (700 mg, 1.798 mmol) as the starting intermediate to give the title compound as a yellow solid. LCMS retention time: 4.131 min [B], MS (E - ) m / z: 466.0[M-2H]

[0160] Intermediate 110C: tert-butyl (R)-3-((4-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-2-nitro-5-(trifluoromethyl)phenyl)amino)piperidine-1-carboxylate [ka]

[0161] tert-Butyl (R)-3-((4-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-2-nitro-5-(trifluoromethyl)phenyl)amino)piperidine-1-carboxylate (800 mg, 0.790 mmol, 46% yield) was prepared following the general procedure described in Intermediate 1B using tert-butyl (R)-3-((4-bromo-2-nitro-5-(trifluoromethyl)phenyl)amino)piperidine-1-carboxylate (800 mg, 1.708 mmol) and 8-methoxy-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-[1,2,4]triazolo[1,5-a]pyridine (564 mg, 2.050 mmol) as starting intermediates to afford the title compound as a pale yellow solid. LCMS retention time: 3.274 min [B], MS(E -) m / z: 537.0[M+H]

[0162] Intermediate 110D: tert-butyl (R)-3-((2-amino-4-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-5-(trifluoromethyl)phenyl)amino)piperidine-1-carboxylate [ka]

[0163] A solution of tert-butyl (R)-3-((4-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-2-nitro-5-(trifluoromethyl)phenyl)amino)piperidine-1-carboxylate (700 mg, 1.305 mmol) in methanol (20 mL) was purged with nitrogen, then Pd / C (250 mg, 2.349 mmol) was added and the solution was purged again with nitrogen. The reaction mixture was stirred at room temperature under a hydrogen bladder for 8 h. The reaction mixture was filtered through a bed of Celite, washed with methanol, and the filtrate was collected and concentrated to give tert-butyl (R)-3-((2-amino-4-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-5-(trifluoromethyl)phenyl)amino)piperidine-1-carboxylate (506 mg, 0.849 mmol, 65% yield) as an orange solid. LCMS retention time: 0.67 min [A], MS (E - ) m / z: 507.4[M+H]

[0164] Intermediate 110E: tert-butyl (R)-3-(5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-2-oxo-6-(trifluoromethyl)-2,3-dihydro-1H-benzo[d]imidazol-1-yl)piperidine-1-carboxylate [ka]

[0165] To a solution of tert-butyl (R)-3-((2-amino-4-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-5-(trifluoromethyl)phenyl)amino)piperidine-1-carboxylate (600 mg, 1.185 mmol) in ACN (60 mL) was added CDI (576 mg, 3.55 mmol) at room temperature. The reaction mixture was stirred at the same temperature for 12 hours. The reaction was concentrated and the resulting residue was subjected to ISCO purification using a 40 g silica column, the compound was eluted with 10% methanol in CHCl3, and the fractions were collected and concentrated to give tert-butyl (R)-3-(5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-2-oxo-6-(trifluoromethyl)-2,3-dihydro-1H-benzo[d]imidazol-1-yl)piperidine-1-carboxylate (500 mg, 0.685 mmol, 58% yield) as an off-white solid. LCMS retention time: 2.691 min [B], MS (E - ) m / z: 533.1[MH]

[0166] Intermediate 110F: (R)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(piperidin-3-yl)-6-(trifluoromethyl-1,3-dihydro-2H-benzo[d]imidazol-2-one [ka]

[0167] To a solution of tert-butyl (R)-3-(5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-2-oxo-6-(trifluoromethyl)-2,3-dihydro-1H-benzo[d]imidazol-1-yl)piperidine-1-carboxylate (300 mg, 0.563 mmol) in DCM (2 mL) was added TFA (1 mL, 12.98 mmol) at room temperature. The reaction mixture was stirred at the same temperature for 1 h. The reaction product was purged with nitrogen until the TFA was removed and dried under vacuum to give (R)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(piperidin-3-yl)-6-(trifluoromethyl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (180 mg, 0.387 mmol, 69% yield) as an off-white solid. LCMS retention time: 0.972 min [C], MS (E - ) m / z: 433.1[M+H]; 1 H NMR (400MHz, DMSO-d6) δ 8.54(d,J=1.0Hz,1H), 8.50(s,1H), 7.68(s,1H), 7.12(s,1H), 7.05(s,1H), 4.38-4.29(m,1H), 3.98(s,3H), 3 .24(brs,2H), 3.04-2.95(m,2H), 2.66-2.55(m,1H), 2.36-2.29(m,1H), 1.96-1.73(m,3H), 1.69-1.56(m,1H)

[0168] Example 110: (R)-1-(1-ethylpiperidin-3-yl)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-(trifluoromethyl)-1,3-dihydro-2H-benzo[d]imidazol-2-one To a solution of (R)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(piperidin-3-yl)-6-(trifluoromethyl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (20 mg, 0.046 mmol) in methanol (2 mL) was added acetic acid (0.1 mL, 1.747 mmol), acetaldehyde (6.11 mg, 0.139 mmol). The reaction mixture was stirred at ambient temperature for 30 minutes, then sodium cyanoborohydride (14.53 mg, 0.231 mmol) was added and the reaction mixture was further stirred at the same temperature for 3 hours. The reaction product was concentrated and the residue was diluted with water (3 mL), extracted with ethyl acetate (3x10 mL), dried over sodium sulfate, filtered and concentrated to give the crude compound. The crude sample was subjected to preparative LCMS and purified using Method AA, and the product-containing fractions were combined and dried via centrifugal concentration to give (R)-1-(1-ethylpiperidin-3-yl)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-(trifluoromethyl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (15.8 mg, 0.032 mmol, 68% yield). LCMS retention time: 1.271 min [E], MS (E - ) m / z: 461.3[M+H]; 1 H NMR (400MHz, DMSO-d6) δ 11.68-11.56(m,1H), 8.54(d,J=1.0Hz,1H), 8.51-8.45(m,1H), 7.73(s,1H), 7.19-7.10(m,1H), 7.03(s,1H) , 4.61-4.44(m,1H), 3.99(s,3H), 3.21-2.81(m,3H), 2.31-2.18(m,1H), 2.00-1.67(m,3H), 1.32-1.04(m,3H)

[0169] The following examples were prepared according to the procedure used to prepare Example 110. Table 8 [Table 36] [Table 37]

[0170] Example 118 (R)-5-(8-Methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-(2-methoxyethyl)piperidin-3-yl)-6-(trifluoromethyl)-1,3-dihydro-2H-benzo[d]imidazol-2-one [ka]

[0171] To a stirred solution of (R)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(piperidin-3-yl)-6-(trifluoromethyl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (50 mg, 0.116 mmol) in a mixture of THF (1.5 mL) and DMF (0.5 mL) solvents, 1-bromo-2-methoxyethane (48.2 mg, 0.347 mmol) and triethylamine (0.081 mL, 0.578 mmol) were added at room temperature. The reaction mixture was stirred at the same temperature for 16 hours. The reaction product was subjected to preparative LCMS and purified using Method AB, the product-containing fractions were combined and dried via centrifugal concentration to give (R)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-(2-methoxyethyl)piperidin-3-yl)-6-(trifluoromethyl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (10.7 mg, 0.022 mmol, 19% yield). LCMS retention time: 1.380 min [E], MS (E - ) m / z: 461.3[M+H]; 1H NMR (400MHz, DMSO-d6) δ 11.60-11.47(m,1H), 8.54(s,1H), 8.50(s,1H), 7.72(s,1H), 7.12(s,1H), 7.05(s,1H), 4.50-4.33(m,1H), 3.98(s,3H), 3.48( brd,J=4.4Hz,2H), 3.24(s,3H), 3.09-2.70(m,4H), 2.65-2.54(m,1H), 2.28-2.02(m,2H), 1.88-1.75(m,2H), 1.74-1.59(m,1H)

[0172] Example 119 (S)-6-Isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-methylpiperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one [ka]

[0173] Intermediate 119A: 2-fluoro-1-nitro-4-(prop-1-en-2-yl)benzene [ka]

[0174] To a mixture of 4-bromo-2-fluoro-1-nitrobenzene (5 g, 22.73 mmol) in THF (100 mL) and water (25.00 mL), 4,4,5,5-tetramethyl-2-(prop-1-en-2-yl)-1,3,2-dioxaborolane (7.64 g, 45.5 mmol) and potassium phosphate (14.47 g, 68.2 mmol) were added. The solution was degassed with argon for 10 minutes, PdCl2(dppf)-CH2Cl2 adduct (1.856 g, 2.273 mmol) was added, and the reaction mixture was heated at 70° C. for 12 hours. The reaction mixture was diluted with ethyl acetate (150 mL), washed with water (2×100 mL), brine (100 mL), dried over sodium sulfate, and concentrated to give the crude product. The crude material was purified by Combiflash using a 80 g silica column, the compound was eluted with 20% ethyl acetate in petroleum ether, fractions were collected and concentrated to give 2-fluoro-1-nitro-4-(prop-1-en-2-yl)benzene (4 g, 22.08 mmol, 97% yield) as a pale yellow solid. 1 H NMR (400MHz, DMSO-d6) δ ppm 8.13(t,J=8.4Hz,1H), 7.71(dd,J=2.0, 13.2Hz,1H), 7.62-7.45(m,1H), 5.83-5.67(m,1H), 5.42-5.37(m,1H), 2.15(dd,J=0.7, 1.5Hz,3H)

[0175] The following intermediates were prepared following the procedure used to prepare intermediate 119A. Table 9 [Table 38]

[0176] Intermediate 119B: 2-Fluoro-4-isopropyl-1-nitrobenzene [ka]

[0177] A solution of 2-fluoro-1-nitro-4-(prop-1-en-2-yl)benzene (4.4 g, 24.29 mmol) in dioxane (500 mL) was purged with nitrogen, Pd / C (1.551 g, 14.57 mmol) was added, and the mixture was purged with N2 three times. The slurry was stirred under a hydrogen bladder at room temperature for 12 hours. The slurry was filtered through Celite, and the filtrate was collected and concentrated to give 2-fluoro-4-isopropyl-1-nitrobenzene (2.2 g, 12.01 mmol, 45% yield) as a pale yellow solid. 1 H NMR (300MHz, DMSO-d6) δ ppm 8.09(t,J=8.3Hz,1H), 7.51(dd,J=1.5, 13.0Hz,1H), 7.39-7.23(m,1H), 3.04(td,J=6.8, 13.8Hz,1H), 1.23(d,J=6.9Hz,7H)

[0178] Intermediate 119C: tert-Butyl (S)-3-((5-isopropyl-2-nitrophenyl)amino)piperidine-1-carboxylate [ka]

[0179] To a solution of 2-fluoro-4-isopropyl-1-nitrobenzene (1.1 g, 6.00 mmol) in DMF (10 mL) was added (S)-1-Boc-3-aminopiperidine (2.405 g, 12.01 mmol), and K2CO3 (2.490 g, 18.01 mmol). The reaction mixture was stirred at 100 °C for 3 h. The reaction product was concentrated and the resulting residue was dissolved in ice-cold water, and the precipitated white solid was filtered and dried under vacuum to give tert-butyl (S)-3-((5-isopropyl-2-nitrophenyl)amino)piperidine-1-carboxylate (1.5 g, 4.13 mmol, 68% yield) as a pale yellow solid. LCMS retention time: 3.96 min [D], MS (E - ) m / z: 307[M-tBu+H]

[0180] The following intermediates were prepared following the procedure used to prepare intermediate 119C. Table 10 [Table 39] [Table 40]

[0181] Intermediate 119D: tert-Butyl (S)-3-((4-bromo-5-isopropyl-2-nitrophenyl)amino)piperidine-1-carboxylate [ka]

[0182] To a solution of tert-butyl (S)-3-((5-isopropyl-2-nitrophenyl)amino)piperidine-1-carboxylate (2 g, 5.50 mmol) in ACN (30 mL) was added NBS (0.979 g, 5.50 mmol) dissolved in ACN (30 mL) at room temperature. The reaction mixture was stirred for 12 hours. The reaction product was quenched with water (50 ml), extracted with ethyl acetate (3x50 mL), dried over sodium sulfate, filtered and concentrated to give the crude product. The crude material was purified on a CombiFlash using a 40 g silica column, the compound was eluted with 8% EtOAc in petroleum ether, fractions were collected and concentrated to give tert-butyl (S)-3-((4-bromo-5-isopropyl-2-nitrophenyl)amino)piperidine-1-carboxylate (2 g, 4.52 mmol, 82% yield) as a yellow solid. LCMS retention time: 4.45 min [D], MS (E - ) m / z: 388[M-tBu+H]

[0183] Intermediate 119E: tert-butyl (S)-3-((5-isopropyl-4-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-2-nitrophenyl)amino)piperidine-1-carboxylate [ka]

[0184] tert-Butyl (S)-3-((5-isopropyl-4-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-2-nitrophenyl)amino)piperidine-1-carboxylate (2 g, 3.92 mmol, 87% yield) was prepared following the general procedure described for Intermediate 1B using tert-butyl (S)-3-((4-bromo-5-isopropyl-2-nitrophenyl)amino)piperidine-1-carboxylate (2 g, 4.52 mmol) and 8-methoxy-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-[1,2,4]triazolo[1,5-a]pyridine (1.493 g, 5.43 mmol) as starting intermediates to give the title compound as a pale yellow solid. LCMS retention time: 3.49 min [D], MS (E - ) m / z: 511.1[M+H]

[0185] The following intermediates were prepared following the procedure used to prepare intermediate 119E. Table 11 [Table 41] [Table 42]

[0186] Intermediate 119F: tert-butyl (S)-3-((2-amino-5-isopropyl-4-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)phenyl)amino)piperidine-1-carboxylate [ka]

[0187] tert-Butyl (S)-3-((2-amino-5-isopropyl-4-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)phenyl)amino)piperidine-1-carboxylate (1.1 g, 2.28 mmol, 97% yield) was prepared following the general procedure described in Intermediate 1C using tert-butyl (S)-3-((5-isopropyl-4-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-2-nitrophenyl)amino)piperidine-1-carboxylate (1.2 g, 2.350 mmol) as the starting intermediate to give the title compound as a pale yellow solid. LCMS retention time: 2.9 min [D], MS (E - ) m / z: 481.2[M+H]

[0188] Intermediate 119G: tert-butyl (S)-3-(6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-2-oxo-2,3-dihydro-1H-benzo[d]imidazol-1-yl)piperidine-1-carboxylate [ka]

[0189] tert-Butyl (S)-3-(6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-2-oxo-2,3-dihydro-1H-benzo[d]imidazol-1-yl)piperidine-1-carboxylate (1.1 g, 2.17 mmol, 87% yield) was prepared following the general procedure described in Intermediate 1D using tert-butyl (S)-3-((2-amino-5-isopropyl-4-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)phenyl)amino)piperidine-1-carboxylate (1.2 g, 2.497 mmol) as the starting intermediate to give the title compound as an off-white solid. LCMS retention time: 2.72 min [D], MS (E - ) m / z: 505.2[MH]

[0190] Intermediate 119H: (S)-6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(piperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one [ka]

[0191] (S)-6-Isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(piperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (0.8 g, 1.94 mmol, 90% yield) was prepared following the general procedure described in Intermediate 1E using tert-butyl (S)-3-(6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-2-oxo-2,3-dihydro-1H-benzo[d]imidazol-1-yl)piperidine-1-carboxylate (1.1 g, 2.171 mmol) as the starting intermediate to give the title compound as a gummy solid. LCMS retention time: 1.56 min [D], MS (E - ) m / z: 407.2[M+H]

[0192] The following intermediates were prepared following the procedure used to prepare intermediate 119H. Table 12 [Table 43]

[0193] Example 119: (S)-6-Isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-methylpiperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (S)-6-Isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-methylpiperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (3.7 mg, 8.71 μmol, 7%) was prepared according to the general procedure described in Example 1 using (S)-6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(piperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (50 mg, 0.123 mmol) as the starting intermediate to give the title compound as a white solid. LCMS retention time: 1.33 min [E], MS (E - ) m / z: 421.2[M+H]; 1 H NMR (400MHz, DMSO-d6) δ ppm 10.88(s,1H), 8.46(s,2H), 7.27(s,1H), 6.98(s,1H), 6.85(s,1H), 4.56( s,1H), 4.42-4.31(m,1H), 3.97-3.96(m,1H), 3.99(s,2H), 3.03-2.92(m,1 H), 2.84-2.75(m,2H), 2.65-2.57(m,1H), 2.26(s,3H), 2.21-2.12(m,1H) , 2.03-1.93(m,1H), 1.92(s,1H), 1.83-1.72(m,2H), 1.20(d,J=6.6Hz,6H)

[0194] The following examples were prepared following the general procedure used to prepare Example 119. Table 13 [Table 44] [Table 45] [Table 46] [Table 47] [Table 48]

Table 49

Table 50

Table 51

Table 52

Table 53

Table 54

Table 55

Table 56

Table 57

Table 58

Table 59

Table 60

Table 61

Table 62

Table 63

Table 64

Table 65

[0195] Example 220 (S)-2-(3-(6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-2-oxo-2,3-dihydro-1H-benzo[d]imidazol-1-yl)piperidin-1-yl)acetamide [ka]

[0196] To a solution of (S)-6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(piperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (50 mg, 0.123 mmol) in THF (2 mL) and DMF (2 mL), TEA (0.08 mL, 0.61 mmol) and 2-bromoacetamide (50.9 mg, 0.369 mmol) were added at room temperature.The reaction mixture was then stirred at 50° C. for 12 hours. The reaction was concentrated, the residue dissolved in methanol, a sample submitted for preparative LCMS and purified using Method AB, and the product containing fractions combined and dried using a Genevac centrifugal concentrator to give (S)-2-(3-(6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-2-oxo-2,3-dihydro-1H-benzo[d]imidazol-1-yl)piperidin-1-yl)acetamide (2.9 mg, 6.26 μmol, 5%) as a pale yellow solid. LCMS retention time: 1.22 min [C], MS (E - ) m / z: 464.2[M+H]; 1 H NMR (400MHz, DMSO-d6) δ ppm 10.87(s,1H), 8.46(s,2H), 7.32(brd,J=2.2Hz,1H), 7.26(s,1H), 7.13(brd,J=1.2Hz,1H), 6.98(s,1H), 6.85(s,1H), 4.50- 4.39(m,1H), 3.99(s,3H), 3.04-2.92(m,3H), 2.89-2.79(m,3H), 2.26-2.13(m,2H), 1.85-1.70(m,3H), 1.20(d,J=6.8Hz,6H)

[0197] The following examples were prepared according to the procedures used to prepare Example 220. Table 14 [Table 72] [Table 73]

[0198] Example 228 (R)-1-(1-(dimethylglycyl)piperidin-3-yl)-6-ethyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one [ka] (R)-1-(1-(dimethylglycyl)piperidin-3-yl)-6-ethyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (9.1 mg, 0.019 mmol, 50% yield) was prepared following the general procedure described in Example 100 using (R)-6-ethyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(piperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (15 mg, 0.038 mmol) as the starting intermediate to afford the title compound as an off-white solid. LCMS retention time: 0.784 min [F], MS(ES): m / z = 478.3 [M+H]; 1 H NMR (400MHz, DMSO-d6) δ ppm 10.94(d,J=10.8Hz,1H), 8.49(d,J=2.9Hz,1H), 8.46(s,1H), 7.34(s,1H), 7.27(s,1H) ), 7.01(d,J=8.6Hz,1H), 6.90(s,1H), 4.43(brs,1H), 4.26(brs,1H), 4.15(brs,2H), 4 .00(s,2H), 3.91(s,1H), 3.74(t,J=11.6Hz,1H), 2.62(q,J=7.0Hz,2H), 2.38-2.29(m, 3H), 2.27(brs,2H), 1.96-1.77(m,3H), 1.65(brs,1H), 1.48(s,1H), 1.15-1.02(m,3H)

[0199] Examples 229 and 230 1-(4-(4,4-difluoropiperidin-1-yl)cyclohexyl)-6-isopropyl-5-(8-methoxy-7-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one [ka]

[0200] Intermediate 229A: N-(5-methyl-2-nitrophenyl)-1,4-dioxaspiro[4.5]decan-8-amine: [ka]

[0201] K2CO3 (2.72 g, 19.65 mmol) and 1,4-dioxaspiro[4.5]decane-8-amine (1.236 g, 7.86 mmol) were added to a solution of 2-fluoro-4-isopropyl-1-nitrobenzene (1.2 g, 6.55 mmol) in DMF (20.0 mL). The mixture was stirred at 110° C. for 14 hours. The reaction mixture was diluted with ethyl acetate, filtered, washed with excess ethyl acetate, the filtrate was collected and concentrated, dried over sodium sulfate, and concentrated to give the crude compound. The crude material was purified by ISCO using a 40 g silica column, the compound was eluted with 25-35% ethyl acetate in petroleum ether, the fractions were collected and concentrated to give N-(5-isopropyl-2-nitrophenyl)-1,4-dioxaspiro[4.5]decane-8-amine (1.2 g, 3.75 mmol, 57% yield) as a pale yellow solid. LCMS retention time: 2.19 min [A], MS (ES): m / z = 321.1 [M+H]

[0202] Intermediate 229B: N-(4-bromo-5-methyl-2-nitrophenyl)-1,4-dioxaspiro[4.5]decane-8-amine [ka]

[0203] NBS (0.667 g, 3.75 mmol) was added to a solution of N-(5-isopropyl-2-nitrophenyl)-1,4-dioxaspiro[4.5]decane-8-amine (1.2 g, 3.75 mmol) in ACN (20.0 mL) at room temperature. The mixture was stirred at the same temperature for 1 h. The reaction mixture was diluted with ethyl acetate, filtered, washed with excess ethyl acetate, the organic layers were combined, washed with water, brine, dried over sodium sulfate, and concentrated to give the crude compound. The crude material was purified by ISCO using a 40 g silica column, the compound was eluted with 25-35% ethyl acetate in petroleum ether, the fractions were collected and concentrated to give N-(4-bromo-5-isopropyl-2-nitrophenyl)-1,4-dioxaspiro[4.5]decane-8-amine (1.1 g, 2.75 mmol, 73% yield) as a light brown solid. LCMS retention time: 3.074 minutes [B], MS(ES): m / z=399.1 [M+H]

[0204] Intermediate 229C: N-(5-isopropyl-4-(8-methoxy-7-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-2-nitrophenyl)-1,4-dioxaspiro[4.5]decan-8-amine [ka]

[0205] N-(5-isopropyl-4-(8-methoxy-7-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-2-nitrophenyl)-1,4-dioxaspiro[4.5]decane-8-amine (1.2 g, 2.492 mmol, 90% yield) was prepared following the general procedure described in Intermediate 1B using N-(4-bromo-5-isopropyl-2-nitrophenyl)-1,4-dioxaspiro[4.5]decane-8-amine (1.1 g, 2.75 mmol) and 8-methoxy-7-methyl-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-[1,2,4]triazolo[1,5-a]pyridine (1.036 g, 3.58 mmol) as starting intermediates to give the title compound as a pale yellow solid. LCMS retention time: 1.98 min [A], MS (ES): m / z = 482.3 [M+H]

[0206] The following intermediates were prepared following the procedure used to prepare intermediate 229C. Table 15 [Table 74]

[0207] Intermediate 229D: 5-isopropyl-4-(8-methoxy-7-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-N1-(1,4-dioxaspiro[4.5]decan-8-yl)benzene-1,2-diamine [ka]

[0208] To a solution of N-(5-isopropyl-4-(8-methoxy-7-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-2-nitrophenyl)-1,4-dioxaspiro[4.5]decane-8-amine (1.2 g, 2.492 mmol) in MeOH (30.0 mL) was added Pd / C (0.530 g, 4.98 mmol) at room temperature. The reaction mixture was stirred under a hydrogen bladder at the same temperature for 12 h. The reaction mixture was filtered through Celite, washed with excess methanol and THF, and the filtrate was collected, concentrated and dried under vacuum to give 5-isopropyl-4-(8-methoxy-7-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-N1-(1,4-dioxaspiro[4.5]decan-8-yl)benzene-1,2-diamine (950 mg, 2.104 mmol, 84% yield) as an off-white solid. LCMS retention time: 1.60 min [A], MS (ES): m / z = 452.3 [M+H].

[0209] Intermediate 229E: 6-isopropyl-5-(8-methoxy-7-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1,4-dioxaspiro[4.5]decan-8-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one [ka]

[0210] To a solution of 5-isopropyl-4-(8-methoxy-7-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-N1-(1,4-dioxaspiro[4.5]decan-8-yl)benzene-1,2-diamine (950 mg, 2.104 mmol) in ACN (30.0 mL), CDI (853 mg, 5.26 mmol) was added at room temperature and stirred at the same temperature for 12 hours. The reaction product was concentrated and dried under high vacuum to obtain a crude material. The crude material was purified by ISCO using a 40 g silica column, the compound was eluted with 8-10% methanol in chloroform, fractions were collected and concentrated to give 6-isopropyl-5-(8-methoxy-7-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1,4-dioxaspiro[4.5]decan-8-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (800 mg, 1.675 mmol, 80% yield) as a white solid. LCMS retention time: 1.45 min [A], MS (ES): m / z=476.2 [MH]

[0211] Intermediate 229F: 6-isopropyl-5-(8-methoxy-7-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(4-oxocyclohexyl)-1,3-dihydro-2H-benzo[d]imidazol-2-one [ka]

[0212] To a solution of 6-isopropyl-5-(8-methoxy-7-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1,4-dioxaspiro[4.5]decan-8-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (650 mg, 1.361 mmol) in DCM (10.0 mL) was added TFA (2.62 mL, 34.0 mmol) at 0° C. The reaction mixture was stirred at room temperature for 6 h. The reaction product was purged with nitrogen and then dried under vacuum to give 6-isopropyl-5-(8-methoxy-7-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(4-oxocyclohexyl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (550 mg, 1.269 mmol, 93% yield) as an off-white solid. LCMS retention time: 1.24 min [A], MS (ES): m / z = 434.3 [M+H].

[0213] Examples 229 and 230: 1-(4-(4,4-difluoropiperidin-1-yl)cyclohexyl)-6-isopropyl-5-(8-methoxy-7-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one To a solution of 6-isopropyl-5-(8-methoxy-7-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(4-oxocyclohexyl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (80.0 mg, 0.185 mmol), 4,4-difluoropiperidine (67.1 mg, 0.554 mmol) and acetic acid (1.056 μL, 0.018 mmol) in DMF (1.0 mL) was added THF (1.5 mL). The reaction mixture was stirred at room temperature for 8 hours, then sodium cyanoborohydride (23.19 mg, 0.369 mmol) was added at 0° C. and the reaction mixture was stirred at room temperature for 16 hours. The reaction mixture was concentrated and subjected to preparative LCMS and purified using Method AA to separate both isomers, the fractions containing the product were combined and dried via centrifugal concentration to separate the isomers.

[0214] Example 229: Obtained 3.1 mg as an off-white solid. LCMS retention time: 1.94 min [E], MS (ES): m / z = 539.3 [M+H]; 1 H NMR (400MHz, DMSO-d6) δ ppm 10.81(s,1H), 8.52(s,1H), 8.45(s,1H), 7.25(s,1H), 6.71(s,1H), 4.27(s,3H), 4.21(brs,1H), 2.81-2.62(m,5H), 2.56(s,1 H), 2.32-2.21(m,2H), 2.05-1.85(m,10H), 1.84-1.75(m,2H), 1.61-1.46(m,2H), 1.21(d,J=7.1Hz,3H), 1.07(d,J=6.6Hz,3H) Example 230: Obtained 5 mg as an off-white solid. LCMS retention time: 2.13 min [E], MS (ES): m / z = 539.3 [M+H]; 1 H NMR (400MHz, DMSO-d6) δ ppm 10.85(s,1H), 9.37-9.24(m,1H), 8.52(brs,1H), 8.46(s,1H), 7.28-6.94(m,2 H), 6.73(s,1H), 4.43-4.34(m,1H), 4.27(s,3H), 3.73(brs,2H), 3.24(brdd,J =3.1, 4.8Hz,1H), 2.98-2.90(m,1H), 2.59(brd,J=7.3Hz,1H), 2.44-2.22(m,7 H), 2.00-1.90(m,4H), 1.89-1.73(m,1H), 1.30-1.13(m,5H), 1.09-1.02(m,3H)

[0215] The following examples were prepared according to the procedures used to prepare Examples 229 and 230. Table 16 [Table 75] [Table 76] [Table 77]

Table 78

Table 79

Table 80

Table 81

Table 82

Table 83

Table 84

Table 85

Table 86

Table 87

Table 88

Table 89

Table 90

Table 91

Table 92

Table 93

Table 94

Table 95

[0216] Further examples shown in the table below are described above in the preparation of intermediates. Table 17 [Table 97] [Table 98] [Table 99] [Table 100]

[0217] Biological assays The pharmacological properties of the compounds of the invention can be confirmed by several biological assays. The biological assays exemplified below have been carried out with the compounds of the invention.

[0218] TLR7 / 8 / 9 Inhibitory Receptor Assay HEK-Blue®-cells (Invivogen), overexpressing human TLR7, TLR8 or TLR9 receptors, using an inducible SEAP (secreted embryonic alkaline phosphatase) reporter gene under the control of IFN-β minimal promoter fusion to five NF-κB and AP-1 binding sites, were used to screen inhibitors of these receptors. Briefly, cells were seeded in Greiner 384-well plates (15000 cells / well for TIR7, 20,000 cells for TIR8, and 25,000 cells for TLR9) and then treated with test compounds in DMSO to obtain a final dose response in the concentration range of 0.05 nM-50 μM. After 30 minutes of compound pretreatment at room temperature, cells are then stimulated with TLR7 ligand (gardiquimod at a final concentration of 7.5 μM), TLR8 ligand (R848 at a final concentration of 15.9 μM) or TLR9 ligand (ODN2006 at a final concentration of 5 nM) to activate NF-κB and AP-1, which induces the production of SEAP. After 22 hours of incubation at 37° C. and 5% CO2, SEAP levels are measured by adding cell culture medium with HEK-Blue® detection reagent (Invivogen) to detect SEAP according to the manufacturer's specifications. Percentage of inhibition is determined as the percent reduction in HEK-Blue signal present in wells treated with agonist + DMSO alone compared to wells treated with known inhibitors.

[0219] Table 18 TLR7 / 8 / 9 Receptor Assay Data (NT=not tested) [Table 101] [Table 102] [Table 103] [Table 104]

Table 105

Table 106

Table 107

Table 108

Claims

1. Formula (II): 【Chemistry 1】 [In the formula: Each R １ are independently hydrogen, C １－３ Alkyl, or -CF ３ and Each R ２ are independently hydrogen, -CH ３ , or -OCH ３ and A is cyclohexyl or piperidinyl, each of which is 0 to 1 R ３ａ is replaced by; Each R ３ａ are independently -CH ３ , -CH ２ CH ３ , -CH ２ CH ２ CH ３ , -CH(CH ３ ) ２ , -CH ２ CH (CH ３ ) ２ , -CH ２ C (CH ３ ) ３ , -CH(CH ３ ) CH ２ CH ３ , -CH ２ CH ２ CH (CH ３ ) ２ , -CH(CH ２ CH ３ ) ２ , -CH ２ CH (CH ２ CH ３ ) ２ , -CH ２ CH ２ C (CH ３ ) ３ , -CH ２ CN, -CH ２ CH ２ CF ３ , -CH ２ CH ２ CH ２ CF ３ , -CH ２ CH ２ OCH ３ , -CH ２ CH ２ S (O) ２ CH ３ , -CH ２ (C ３－５ Cycloalkyl), -CH ２ (pyridinyl), -CH ２ (methoxypyrimidinyl), -CH ２ (tetrahydrofuranyl), -CH ２ (tetrahydropyranyl), -CH ２ (methyltriazolyl), -CH ２ C(O)NH ２ , -CH ２ C(O)NH(CH ３ ), -C(O)CH ２ N (CH ３ ) ２ , -NH ２ , -NH(CH ２ CH ３ ), -NH(CH ２ CH ２ CH ３ ), -NH(CH(CH ３ ) ２ ), -NH(CH ２ CH (CH ３ ) ２ ), -NH(CH(CH ３ ) CH ２ CH ３ ), -NH(CH ２ C (CH ３ ) ３ ), -NH(CH ２ CH (CH ２ CH ３ ) ２ ), -NH(CH ２ CH ２ CF ３ ), -NH(CH ２ CH ２ OCH ３ ), -N(CH ３ ) ２ , -N(CH ３ ) (CH (CH ３ ) ２ )), -N(CH ３ ) (CH ２ CH ２ CF ３ ), -N(CH ２ CH ３ ) ２ , -N(CH ２ CH ２ CH ３ ) ２ , -N(CH ２ CH (CH ３ ) ２ ) ２ , -NH(C ３－６ Cycloalkyl), -NH(oxetanyl), -NH(tetrahydropyranyl), -NH(isopropylpiperidinyl), -N(CH ３ ) (tetrahydropyranyl), -N(CH ３ ) (cyclohexyl), -NH(CH ２ (cyclopropyl)), -NH(CH ２ (cyclohexyl)), -NH(CH ２ (methylsulfonylcyclopropyl)), —NH(CH ２ (tetrahydropyranyl)), -NH(CH ２ (methyltriazolyl)), fluoroazetidinyl, difluoroazetidinyl, methoxyazetidinyl, hydroxy, trifluoromethylazetidinyl, cyclobutyl, oxetanyl, tetrahydrofuranyl, pyrrolidinyl, difluoropyrrolidinyl, tetrahydropyranyl, thiomorpholinyl, fluoropiperidinyl, difluoropiperidinyl, methoxypiperidinyl, methoxymethylpiperidinyl, methylsulfonylpiperidinyl, piperazinonyl, oxazepanyl, oxazaspiro[3.3]heptanyl, dioxothiazaspiro[3.3]heptanyl, oxazabicyclo[3.2.1]octanyl, or oxazaspiro[3.5]nonanyl; n is 0, 1, or 2; and p is 0, 1, or 2. or a pharma- ceutically acceptable salt thereof.

2. Formula (III): 【Chemistry 2】 [In the formula: Each R １ are independently hydrogen, C １－３ Alkyl, or -CF ３ and Each R ２ are independently hydrogen, -CH ３ , or -OCH ３ and A is cyclohexyl or piperidinyl, each of which is 0 to 1 R ３ａ is replaced by; and Each R ３ａ are independently -CH ３ , -CH ２ CH ３ , -CH ２ CH ２ CH ３ , -CH(CH ３ ) ２ , -CH ２ CH (CH ３ ) ２ , -CH ２ C (CH ３ ) ３ , -CH(CH ３ ) CH ２ CH ３ , -CH ２ CH ２ CH (CH ３ ) ２ , -CH(CH ２ CH ３ ) ２ , -CH ２ CH (CH ２ CH ３ ) ２ , -CH ２ CH ２ C (CH ３ ) ３ , -CH ２ CN, -CH ２ CH ２ CF ３ , -CH ２ CH ２ CH ２ CF ３ , -CH ２ CH ２ OCH ３ , -CH ２ CH ２ S (O) ２ CH ３ , -CH ２ (C ３－５ Cycloalkyl), -CH ２ (pyridinyl), -CH ２ (methoxypyrimidinyl), -CH ２ (tetrahydrofuranyl), -CH ２ (tetrahydropyranyl), -CH ２ (methyltriazolyl), -CH ２ C(O)NH ２ , -CH ２ C(O)NH(CH ３ ), -C(O)CH ２ N (CH ３ ) ２ , -NH ２ , -NH(CH ２ CH ３ ), -NH(CH ２ CH ２ CH ３ ), -NH(CH(CH ３ ) ２ ), -NH(CH ２ CH (CH ３ ) ２ ), -NH(CH(CH ３ ) CH ２ CH ３ ), -NH(CH ２ C (CH ３ ) ３ ), -NH(CH ２ CH (CH ２ CH ３ ) ２ ), -NH(CH ２ CH ２ CF ３ ), -NH(CH ２ CH ２ OCH ３ ), -N(CH ３ ) ２ , -N(CH ３ ) (CH (CH ３ ) ２ )), -N(CH ３ ) (CH ２ CH ２ CF ３ ), -N(CH ２ CH ３ ) ２ , -N(CH ２ CH ２ CH ３ ) ２ , -N(CH ２ CH (CH ３ ) ２ ) ２ , -NH(C ３－６ Cycloalkyl), -NH(oxetanyl), -NH(tetrahydropyranyl), -NH(isopropylpiperidinyl), -N(CH ３ ) (tetrahydropyranyl), -N(CH ３ ) (cyclohexyl), -NH(CH ２ (cyclopropyl)), -NH(CH ２ (cyclohexyl)), -NH(CH ２ (methylsulfonylcyclopropyl)), —NH(CH ２ (tetrahydropyranyl)), -NH(CH ２ (methyltriazolyl)), fluoroazetidinyl, difluoroazetidinyl, methoxyazetidinyl, hydroxy, trifluoromethylazetidinyl, cyclobutyl, oxetanyl, tetrahydrofuranyl, pyrrolidinyl, difluoropyrrolidinyl, tetrahydropyranyl, thiomorpholinyl, fluoropiperidinyl, difluoropiperidinyl, methoxypiperidinyl, methoxymethylpiperidinyl, methylsulfonylpiperidinyl, piperazinonyl, oxazepanyl, oxazaspiro[3.3]heptanyl, dioxothiazaspiro[3.3]heptanyl, oxazabicyclo[3.2.1]octanyl, or oxazaspiro[3.5]nonanyl.

2. The compound of claim 1, which is a compound represented by the formula: or a pharma- ceutically acceptable salt thereof.

3. R with 0 to 1 A ３ａ 3. The compound of claim 1 or 2, wherein R is 1 or 2; or a pharma- ceutically acceptable salt thereof.

4. R with 0 to 1 A ３ａ 3. The compound of claim 1 or 2, wherein the compound is piperidinyl substituted with: or a pharma- ceutically acceptable salt thereof.

5. 5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-methyl-1-(1-methylpiperidin-4-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (1); 1-(1-isopropylpiperidin-4-yl)-6-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (2); 6-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1 -(1-methylpiperidin-4-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (3); 5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-methylpiperidin-4-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (4); 1-(1-isopropylpiperidin-4-yl)-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (5); 1-(1-ethyl piperidin-4-yl)-6-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (6); 6-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-propylpiperidin-4-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (7); 1-(1-ethylpiperidin-4-yl)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl )-6-methyl-1,3-dihydro-2H-benzo[d]imidazol-2-one (9); 1-(1-isopropylpiperidin-4-yl)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-methyl-1,3-dihydro-2H-benzo[d]imidazol-2-one (10); (S)-6-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-methylpiperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (11);(S)-1-(1-ethylpiperidin-3-yl)-6-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (12); (S)-1-(1-isopropylpiperidin-3-yl)-6-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (13); (S)-6-methyl-5-(8-methyl-[1,2,4]triazolo[ 1,5-a]pyridin-6-yl)-1-(1-(oxetan-3-yl)piperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (14); (R)-6-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-methylpiperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (15); (R)-1-(1-ethylpiperidin-3-yl)-6-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a] (R)-1-(1-isopropylpiperidin-3-yl)-6-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (17); (R)-6-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-(oxetan-3-yl)piperidin-3-yl)-1,3-dihydro-2H- Benz[d]imidazol-2-one (18); 1-((1s,4s)-4-(dimethylamino)cyclohexyl)-6-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (19); 1-((1s,4s)-4-(diethylamino)cyclohexyl)-6-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (20);1-((1s,4s)-4-(ethylamino)cyclohexyl)-6-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (21); 1-((1s,4s)-4-(isopropylamino)cyclohexyl)-6-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (22); 1 -((1r,4r)-4-(dimethylamino)cyclohexyl)-6-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (23); 1-((1r,4r)-4-(ethylamino)cyclohexyl)-6-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (24); 1-(( 1r,4r)-4-(isopropylamino)cyclohexyl)-6-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (25); (R)-6-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-neopentylpiperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (26); (R)-6-methyl 1-((3R)-1-(sec-butyl)piperidin-3-yl)-6-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-(tetrahydro-2H-pyran-4-yl)piperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (27); 1-((3R)-1-(sec-butyl)piperidin-3-yl)-6-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (28);(R)-6-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-(3,3,3-trifluoropropyl)piperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (29); 6-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-((1s,4s)-4-((tetrahydro-2H-pyran-4-yl)amino)cyclohexyl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (30); 6-methyl- 6-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-((1s,4s)-4-((3,3,3-trifluoropropyl)amino)cyclohexyl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (31); 6-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-((1s,4s)-4-(neopentylamino)cyclohexyl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (32); 6-methyl-1-((1s,4 s)-4-(((1-methyl-1H-1,2,4-triazol-3-yl)methyl)amino)cyclohexyl)-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (33); 1-((1s,4s)-4-(sec-butylamino)cyclohexyl)-6-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (34); (R)-6-methyl -1-(1-((1-methyl-1H-1,2,4-triazol-3-yl)methyl)piperidin-3-yl)-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (35); (S)-1-(1-((2-methoxypyrimidin-5-yl)methyl)piperidin-3-yl)-6-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (36);(R)-1-(1-(cyclopropylmethyl)piperidin-3-yl)-6-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (37); (R)-1-(1-isopentylpiperidin-3-yl)-6-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (38); (R)-6-methyl (R)-1-(1-isobutylpiperidin-3-yl)-6-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-(4,4,4-trifluorobutyl)piperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (39); (R)-1-(1-isobutylpiperidin-3-yl)-6-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (40); (R)-6-methyl-5- (8-Methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-((tetrahydro-2H-pyran-4-yl)methyl)piperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (41); (R)-6-Methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-propylpiperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (42); 6-Methyl-5-( 8-Methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-((3R)-1-((tetrahydrofuran-3-yl)methyl)piperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (43); (R)-1-(1-(3,3-dimethylbutyl)piperidin-3-yl)-6-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (44);(R)-1-(1-(2-ethylbutyl)piperidin-3-yl)-6-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (45); (R)-6-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-(pyridin-3-ylmethyl)piperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (46); (R)-1-(1-(cyclopentylmethyl)piperidin-3-yl) 1-((1s,4s)-4-(dimethylamino)cyclohexyl)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-methyl-1,3-dihydro-2H-benzo[d]imidazol-2-one (47); 1-((1s,4s)-4-(dimethylamino)cyclohexyl)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-methyl-1,3-dihydro-2H-benzo[d]imidazol-2-one (48); 5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-methyl-1-; ((1s,4s)-4-((tetrahydro-2H-pyran-4-yl)amino)cyclohexyl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (49); 1-((1s,4s)-4-(isopropylamino)cyclohexyl)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-methyl-1,3-dihydro-2H-benzo[d]imidazol-2-one (50); (R)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-methyl (R)-1-(1-ethylpiperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (51); (R)-1-(1-ethylpiperidin-3-yl)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-methyl-1,3-dihydro-2H-benzo[d]imidazol-2-one (52); (R)-1-(1-isopropylpiperidin-3-yl)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-methyl-1,3-di Hydro-2H-benzo[d]imidazol-2-one (53); (R)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-methyl-1-(1-propylpiperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (54); (R)-1-(1-(cyclopropylmethyl)piperidin-3-yl)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-methyl-1,3-dihydro-2H-benzo[d]imidazol-2-one (55); -one (55); (R)-1-(1-isobutylpiperidin-3-yl)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-methyl-1,3-dihydro-2H-benzo[d]imidazol-2-one (56); (R)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-methyl-1-(1-((tetrahydro-2H-pyran-4-yl)methyl)piperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (57);1-((1s,4s)-4-(cyclobutylamino)cyclohexyl)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-methyl-1,3-dihydro-2H-benzo[d]imidazol-2-one (58); 5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-methyl-1-((1s,4s)-4-(oxetan-3-ylamino)cyclohexyl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (5 9); 1-((1s,4s)-4-((cyclopropylmethyl)amino)cyclohexyl)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-methyl-1,3-dihydro-2H-benzo[d]imidazol-2-one (60); 1-((1s,4s)-4-(isobutylamino)cyclohexyl)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-methyl-1,3-dihydro-2H-benzo[d]imidazol-2-one 1-((1s,4s)-4-(cyclohexylamino)cyclohexyl)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-methyl-1,3-dihydro-2H-benzo[d]imidazol-2-one (62); 1-((1s,4s)-4-(ethylamino)cyclohexyl)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-methyl-1,3-dihydro-2H-benzo[d]imidazol-2-one (63); 3); 5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-methyl-1-((1s,4s)-4-(propylamino)cyclohexyl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (64); 1-((1s,4s)-4-(cyclopentylamino)cyclohexyl)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-methyl-1,3-dihydro-2H-benzo[d]imidazol-2-one (65);1-((1s,4s)-4-((cyclohexylmethyl)amino)cyclohexyl)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-methyl-1,3-dihydro-2H-benzo[d]imidazol-2-one (66); (R)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-methyl-1-(1-(pentan-3-yl)piperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one ( 67); (R)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-methyl-1-(1-(3,3,3-trifluoropropyl)piperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (68); (R)-1-(1-cyclobutylpiperidin-3-yl)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-methyl-1,3-dihydro-2H-benzo[d]imidazol-2-one (6 9); (R)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-methyl-1-(1-(tetrahydro-2H-pyran-4-yl)piperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (70); (R)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-methyl-1-(1-neopentylpiperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one ( 71); (R)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-methyl-1-(1-(oxetan-3-yl)piperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (72); (R)-1-(1-(2-ethylbutyl)piperidin-3-yl)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-methyl-1,3-dihydro-2H-benzo[d]imidazol-2-one (73);5-(8-Methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-methylpiperidin-4-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (74); 1-(1-(2-ethylbutyl)piperidin-4-yl)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (75); 5-(8-Methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (76); 1-(1-propylpiperidin-4-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (76); 1-(1-isopropylpiperidin-4-yl)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (77); 5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-((tetrahydro-2H-pyran-4-yl)methyl)piperidine-4 1-(1-(cyclopropylmethyl)piperidin-4-yl)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (78); 1-(1-(cyclopropylmethyl)piperidin-4-yl)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (79); 5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-(oxetan-3-yl)piperidin-4-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one 5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-(tetrahydrofuran-3-yl)piperidin-4-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (81); 5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-((tetrahydrofuran-3-yl)methyl)piperidin-4-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (82);1-(1-cyclobutylpiperidin-4-yl)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (83); 1-((1s,4s)-4-(isopropyl(methyl)amino)cyclohexyl)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-methyl-1,3-dihydro-2H-benzo[d]imidazol-2-one (84); 5-(8-methoxy-[1,2,4 ]triazolo[1,5-a]pyridin-6-yl)-6-methyl-1-((1s,4s)-4-(methyl(tetrahydro-2H-pyran-4-yl)amino)cyclohexyl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (85); 2-(4-(5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-methyl-2-oxo-2,3-dihydro-1H-benzo[d]imidazol-1-yl)piperidin-1-yl)-N,N-dimethylacetamide (86) ), 2-(4-(5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-methyl-2-oxo-2,3-dihydro-1H-benzo[d]imidazol-1-yl)piperidin-1-yl)-N-methylacetamide (87); N-methyl-2-(4-(6-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-2-oxo-2,3-dihydro-1H-benzo[d]imidazol-1-yl)piperidin-1-yl)acetamide (88) ); N,N-dimethyl-2-(4-(6-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-2-oxo-2,3-dihydro-1H-benzo[d]imidazol-1-yl)piperidin-1-yl)acetamide (89); N,N-dimethyl-2-(4-(5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-2-oxo-2,3-dihydro-1H-benzo[d]imidazol-1-yl)piperidin-1-yl)acetamide (90);N,N-dimethyl-2-(4-(6-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-2-oxo-2,3-dihydro-1H-benzo[d]imidazol-1-yl)piperidin-1-yl)acetamide (91); (S)-2-(3-(6-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-2-oxo-2,3-dihydro-1H-benzo[d]imidazol-1-yl)piperidin-1-yl)acetamide (92); (S)-N,N-dimethyl-2-(3-(6-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-2-oxo-2,3-dihydro-1H-benzo[d]imidazol-1-yl)piperidin-1-yl)acetamide (93); (R)-N,N-dimethyl-2-(3-(6-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-2-oxo-2,3-dihydro-1H-benzo[d]imidazol-1-yl)piperidin-1-yl)acetamide (94); (R)-N,N-dimethyl-2-(3-(6-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-2-oxo-2,3-dihydro-1H-benzo[d]imidazol-1-yl)piperidin-1-yl)acetamide (95); (R)-2-(; 3-(6-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-2-oxo-2,3-dihydro-1H-benzo[d]imidazol-1-yl)piperidin-1-yl)acetonitrile (96); (R)-1-(1-(2-methoxyethyl)piperidin-3-yl)-6-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (97); (R)-5-(8-methoxy-[1,2,4]triazolo[1,5 (R)-2-(3-(5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-methyl-2-oxo-2,3-dihydro-1H-benzo[d]imidazol-1-yl)piperidin-1-yl)-N,N-dimethylacetamide (99); 1-(1-(2-(dimethylamino)acetyl)piperidin-4-yl)-5-(8-methoxy -[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-methyl-1H-benzo[d]imidazol-2(3H)-one (100); 1-(1-(dimethylglycyl)piperidin-4-yl)-6-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (101); 1-(1-(dimethylglycyl)piperidin-4-yl)-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro -2H-benzo[d]imidazol-2-one (102); (S)-1-(1-(dimethylglycyl)piperidin-3-yl)-6-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (103); (R)-1-(1-(dimethylglycyl)piperidin-3-yl)-6-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (104);1-(1-(dimethylglycyl)piperidin-3-yl)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-methyl-1,3-dihydro-2H-benzo[d]imidazol-2-one (105); 7-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-methylpiperidin-4-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (106); 1-(1-isopropylpiperidinyl) N,N-dimethyl-2-(4-(7-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (107); 1-(1-ethylpiperidin-4-yl)-7-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (108); ]triazolo[1,5-a]pyridin-6-yl)-2-oxo-2,3-dihydro-1H-benzo[d]imidazol-1-yl)piperidin-1-yl)acetamide (109); (R)-1-(1-ethylpiperidin-3-yl)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-(trifluoromethyl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (110); (R)-1-(1-isopropylpiperidin-3-yl)- 5-(8-Methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-(trifluoromethyl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (111); (R)-5-(8-Methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-((tetrahydro-2H-pyran-4-yl)methyl)piperidin-3-yl)-6-(trifluoromethyl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (112);(R)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-(oxetan-3-yl)piperidin-3-yl)-6-(trifluoromethyl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (113); (R)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-methylpiperidin-3-yl)-6-(trifluoromethyl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (1 14); (R)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-propylpiperidin-3-yl)-6-(trifluoromethyl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (115); (R)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-neopentylpiperidin-3-yl)-6-(trifluoromethyl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (11 6); (R)-1-(1-(2-ethylbutyl)piperidin-3-yl)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-(trifluoromethyl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (117); (R)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-(2-methoxyethyl)piperidin-3-yl)-6-(trifluoromethyl)-1,3-dihydro-2H-benzo[d]imidazo (S)-6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-methylpiperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (119); (S)-6-isopropyl-1-(1-isopropylpiperidin-3-yl)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (120);(S)-6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-propylpiperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (121); (S)-1-(1-cyclobutylpiperidin-3-yl)-6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (122); (S)-6-isopropyl-5-( 8-Methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-(oxetan-3-yl)piperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (123); (S)-6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-(tetrahydro-2H-pyran-4-yl)piperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (124); (S)-6-isopropyl 6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-((3S)-1-((tetrahydrofuran-3-yl)methyl)piperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (125); 2-one (126); (S)-1-(1-(cyclopropylmethyl)piperidin-3-yl)-6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (127); (S)-1-(1-isobutylpiperidin-3-yl)-6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (129);(S)-1-(1-(2-ethylbutyl)piperidin-3-yl)-6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (130); (S)-1-(1-isopentylpiperidin-3-yl)-6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (131) ); (S)-1-(1-isopentylpiperidin-3-yl)-6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (132); (S)-1-(1-(cyclobutylmethyl)piperidin-3-yl)-6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (1 33); (R)-6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-propylpiperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (134); (R)-6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-(oxetan-3-yl)piperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (135); (R)-6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-methylpiperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (136); (R)-6-isopropyl-1-(1-isopropylpiperidin-3-yl)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (137);(R)-1-(1-ethylpiperidin-3-yl)-6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (138); (R)-6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-((tetrahydro-2H-pyran-4-yl)methyl)piperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (139); (R)-1-(1-(cyclobutylmethyl)piperidin-3-yl)-6-isopropyl- 5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (140); (R)-1-(1-isobutylpiperidin-3-yl)-6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (141); (R)-1-(1-(cyclopropylmethyl)piperidin-3-yl)-6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H; -benzo[d]imidazol-2-one (142); (R)-6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-(tetrahydro-2H-pyran-4-yl)piperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (143); (R)-5-(7,8-dimethyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-isopropyl-1-(1-isopropylpiperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (143). benzo[d]imidazol-2-one (145); (R)-5-(7,8-dimethyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-isopropyl-1-(1-(oxetan-3-yl)piperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (146); (R)-5-(7,8-dimethyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-isopropyl-1-(1-methylpiperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (147); (R)-1-(1-(2-ethylbutyl)piperidin-3-yl)-6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (148); (R)-5-(7,8-dimethyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-isopropyl-1-(1-((tetrahydro-2H-pyran-4-yl)methyl)piperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (149); zole-2-one (149); (R)-5-(7,8-dimethyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-isopropyl-1-(1-propylpiperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (150); (R)-5-(7,8-dimethyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-(2-ethylbutyl)piperidin-3-yl)-6-isopropyl-1,3-dihydro-2H-benzo[d]imidazol-2-one (151);(R)-5-(7,8-dimethyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-isopropyl-1-(1-neopentylpiperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (152); (R)-6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-neopentylpiperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (153); 6 -isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-methylpiperidin-4-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (154); 6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-propylpiperidin-4-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (155); 1-(1-cyclobutylpiperidine- 4-yl)-6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (156); 6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-(oxetan-3-yl)piperidin-4-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (157); 6-isopropyl-5-(8-methoxy-[1, 2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-(tetrahydro-2H-pyran-4-yl)piperidin-4-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (158); 6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-((tetrahydro-2H-pyran-4-yl)methyl)piperidin-4-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (159);6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-((tetrahydrofuran-3-yl)methyl)piperidin-4-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (160); 1-(1-(cyclopropylmethyl)piperidin-4-yl)-6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (161); 6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-(tetrahydrofuran-3-yl)piperidin-4-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (162); 6-isopropyl-1-(1-isopropylpiperidin-4-yl)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (163); 1-(1-isobutylpiperidin-4-yl)-6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (164); 1-(1-(2-ethylbutyl)piperidin-4-yl)-6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (165); 6-ethyl-5-(8-methyl- 6-Ethyl-1-((1s,4s)-4-(isopropylamino)cyclohexyl)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (167);1-((1s,4s)-4-(dipropylamino)cyclohexyl)-6-ethyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (168); 1-((1s,4s)-4-(diethylamino)cyclohexyl)-6-ethyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (169); 6-Ethyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-((1s,4s)-4-(oxetan-3-ylamino)cyclohexyl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (170); (R)-6-Ethyl-1-(1-ethylpiperidin-3-yl)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (171); (R) -6-ethyl-1-(1-isopropylpiperidin-3-yl)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (172); (R)-6-ethyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-(oxetan-3-yl)piperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (173); (R)-6- Ethyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-methylpiperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (174); (R)-6-ethyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-((tetrahydro-2H-pyran-4-yl)methyl)piperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (175);1-((3R)-1-(sec-butyl)piperidin-3-yl)-6-ethyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (176); (R)-6-ethyl-1-(1-isobutylpiperidin-3-yl)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (177); (R)- 6-Ethyl-1-(1-(2-ethylbutyl)piperidin-3-yl)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (178); (R)-6-Ethyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-propylpiperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (179); (R)-6-Ethyl -5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-neopentylpiperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (180); (R)-1-(1-(cyclobutylmethyl)piperidin-3-yl)-6-ethyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (181); (R)-1-(1-(cyclobutylmethyl)piperidin-3-yl)-6-ethyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (182); (R)-6-ethyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (182); (R)-6-ethyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-(3,3,3-trifluoropropyl)piperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (183);(R)-6-ethyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-(tetrahydro-2H-pyran-4-yl)piperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (184); 5-(7,8-dimethyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl) 5-(7,8-dimethyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-isopropyl-1-((1s,4s)-4-(isopropylamino)cyclohexyl)- 1,3-Dihydro-2H-benzo[d]imidazol-2-one (186); 5-(7,8-dimethyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-isopropyl-1-((1s,4s)-4-((tetrahydro-2H-pyran-4-yl)amino)cyclohexyl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (187); 5-(7,8-dimethyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-isopropyl-1-((1s,4s)-4-(oxetan-3-ylamino)cyclohexyl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (188); 5-(7,8-dimethyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-isopropyl-1-((1s,4s)-4-(oxetan-3-ylamino)cyclohexyl)-1,3-dihydro-2H-benzo[d]imidazol-2-one; Lysin-6-yl)-1-((1s,4s)-4-(ethylamino)cyclohexyl)-6-isopropyl-1,3-dihydro-2H-benzo[d]imidazol-2-one (189); 5-(7,8-dimethyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-isopropyl-1-((1s,4s)-4-(neopentylamino)cyclohexyl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (190); 1-((1s,4s)-4-(dimethylamino)cyclohexyl)- 6-Isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (191); 6-Isopropyl-1-((1s,4s)-4-(isopropylamino)cyclohexyl)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (192); 6-Isopropyl-5-(8-methoxy-[1,2,4]triazolo[1, 5-a]pyridin-6-yl)-1-((1s,4s)-4-((tetrahydro-2H-pyran-4-yl)amino)cyclohexyl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (193); 1-((1s,4s)-4-((2-ethylbutyl)amino)cyclohexyl)-6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (194); 6-isopropyl-5-(8-methoxy 6-Isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-((1s,4s)-4-(((tetrahydro-2H-pyran-4-yl)methyl)amino)cyclohexyl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (196);6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-((1s,4s)-4-(neopentylamino)cyclohexyl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (197); 5-(7,8-dimethyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-((1s,4s)-4-((2-ethylbutyl)amino)cyclohexyl)-6-isopropyl-1,3-dihydro-2H-benzo[d]imidazol-2-one (198); -(7,8-dimethyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-((1s,4s)-4-(dipropylamino)cyclohexyl)-6-isopropyl-1,3-dihydro-2H-benzo[d]imidazol-2-one (199); 5-(7,8-dimethyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-isopropyl-1-((1s,4s)-4-(((tetrahydro-2H-pyran-4-yl)methyl)amino)cyclohexyl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (199); 6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-((1r,4r)-4-(oxetan-3-ylamino)cyclohexyl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (201); 1-((1r,4r)-4-(dimethylamino)cyclohexyl)-6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (202); -one (202); 6-isopropyl-1-((1r,4r)-4-(isopropylamino)cyclohexyl)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (203); 1-((1r,4r)-4-(isobutylamino)cyclohexyl)-6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (204);1-((1r,4r)-4-(diisobutylamino)cyclohexyl)-6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (205); 1-((1r,4r)-4-(bis(cyclopropylmethyl)amino)cyclohexyl)-6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (20 6); 6-isopropyl-1-((1r,4r)-4-((1-isopropylpiperidin-4-yl)amino)cyclohexyl)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (207); (R)-1-(1-(3,3-dimethylbutyl)piperidin-3-yl)-6-ethyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol- 2-one (208); (R)-1-(1-(cyclopentylmethyl)piperidin-3-yl)-6-ethyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (209); (R)-1-(1-(3,3-dimethylbutyl)piperidin-3-yl)-6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (21 0); (R)-1-(1-(cyclopentylmethyl)piperidin-3-yl)-6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (211); 6-ethyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-((3R)-1-(tetrahydrofuran-3-yl)piperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (212);6-Ethyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-((3R)-1-(tetrahydrofuran-3-yl)piperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (213); 6-Ethyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-((3R)-1-(tetrahydro-2H-pyran-3-yl)piperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (214-2 15); 6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-((3R)-1-(tetrahydrofuran-3-yl)piperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (216-217); 6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-((3R)-1-(tetrahydro-2H-pyran-3-yl)piperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazo (S)-2-(3-(6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-2-oxo-2,3-dihydro-1H-benzo[d]imidazol-1-yl)piperidin-1-yl)acetamide (220); (S)-6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-(2-methoxyethyl)piperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2 -one (221); (S)-6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-(2-(methylsulfonyl)ethyl)piperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (222); 6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-(2-methoxyethyl)piperidin-4-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (223);6-Isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-(2-(methylsulfonyl)ethyl)piperidin-4-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (224); (R)-6-Isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-(2-methoxyethyl)piperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (22 5); (R)-6-ethyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(1-(2-methoxyethyl)piperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (227); (R)-1-(1-(dimethylglycyl)piperidin-3-yl)-6-ethyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (228); 1-(4 -(4,4-difluoropiperidin-1-yl)cyclohexyl)-6-isopropyl-5-(8-methoxy-7-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (229-230); 6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(4-(pyrrolidin-1-yl)cyclohexyl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (23 1); 6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(4-(pyrrolidin-1-yl)cyclohexyl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (232); 6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(4-(3-oxopiperazin-1-yl)cyclohexyl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (233-234);1-(4-(7-oxa-2-azaspiro[3.5]nonan-2-yl)cyclohexyl)-6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (235-236); 6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(4-(3-methoxyazetidin-1-yl)cyclohexyl)-1,3-dihydro-2H-benzo[d]imidazo 1-(4-(2-oxa-7-azaspiro[3.5]nonan-7-yl)cyclohexyl)-6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (239-240); 1-(4-(3-hydroxy-3-(trifluoromethyl)azetidin-1-yl)cyclohexyl)-6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]; 6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(4-(3-oxopiperazin-1-yl)cyclohexyl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (241-242); 6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(4-(3-oxopiperazin-1-yl)cyclohexyl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (243); 1-(4-(2,2-dioxido-2-thia-6-azaspiro[3.3]heptan-6-yl)cyclohexyl)-6-isopropyl-5-(8- Methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (244-245); 1-(4-(4,4-difluoropiperidin-1-yl)cyclohexyl)-6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (246-247); 6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5 6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(4-thiomorpholinocyclohexyl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (248-249); 6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(4-thiomorpholinocyclohexyl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (250-251); 1-(4-(3-oxa-8-azabicyclo[3.2.1]octyl) 1-(4-(2-oxa-6-azaspiro[3.3]heptan-6-yl)cyclohexyl)-6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (252-253); 1-(4-(2-oxa-6-azaspiro[3.3]heptan-6-yl)cyclohexyl)-6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (254);6-Isopropyl-5-(8-methoxy-7-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(4-((2-methoxyethyl)amino)cyclohexyl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (257-258); 6-Isopropyl-5-(8-methoxy-7-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(4-(((1-(methylsulfonyl)cyclopropyl)methyl)amino)cyclohexyl)-1,3- Dihydro-2H-benzo[d]imidazol-2-one (259-260); 1-(4-(1,4-oxazepan-4-yl)cyclohexyl)-6-isopropyl-5-(8-methoxy-7-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (261-262); 1-(4-(3-fluoroazetidin-1-yl)cyclohexyl)-6-isopropyl-5-(8-methoxy-7-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)- 6-isopropyl-5-(8-methoxy-7-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(4-(3-methoxyazetidin-1-yl)cyclohexyl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (265-266); 1-(4-(2-oxa-7-azaspiro[3.5]nonan-7-yl)cyclohexyl)-6- Isopropyl-5-(8-methoxy-7-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (267-268); 1-(4-(2-oxa-6-azaspiro[3.3]heptan-6-yl)cyclohexyl)-6-isopropyl-5-(8-methoxy-7-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (269-270);1-(4-(1,4-oxazepan-4-yl)cyclohexyl)-5-(7,8-dimethyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-isopropyl-1,3-dihydro-2H-benzo[d]imidazol-2-one (271-272); 5-(7,8-dimethyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(4-(3-fluoropiperidin-1-yl)cyclohexyl)-6-isopropyl-1,3-dihydro-2H-benzo[d]imidazol-2-one (273-274); 1-(4- (4,4-difluoropiperidin-1-yl)cyclohexyl)-5-(7,8-dimethyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-isopropyl-1,3-dihydro-2H-benzo[d]imidazol-2-one (275-276); 5-(7,8-dimethyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-isopropyl-1-(4-(3-methoxyazetidin-1-yl)cyclohexyl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (277-278); 5-(7,8 -Dimethyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(4-(3-fluoroazetidin-1-yl)cyclohexyl)-6-isopropyl-1,3-dihydro-2H-benzo[d]imidazol-2-one (279-280); 1-(4-(2-oxa-6-azaspiro[3.3]heptan-6-yl)cyclohexyl)-5-(7,8-dimethyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-isopropyl-1,3-dihydro-2H-benzo[d]imidazol-2-one (281); 1-( 4-(2-oxa-7-azaspiro[3.5]nonan-7-yl)cyclohexyl)-5-(7,8-dimethyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-isopropyl-1,3-dihydro-2H-benzo[d]imidazol-2-one (282-283); 6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(4-(3-methoxypyrrolidin-1-yl)cyclohexyl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (284-285);(S)-1-(4-(3-fluoropyrrolidin-1-yl)cyclohexyl)-6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (286-287); 6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(4-(3-(methylsulfonyl)pyrrolidin-1-yl)cyclohexyl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (288 -289); (R)-6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(4-(3-(methoxymethyl)pyrrolidin-1-yl)cyclohexyl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (290-291); 1-(4-((3S,4R)-3,4-difluoropyrrolidin-1-yl)cyclohexyl)-6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d ]imidazol-2-one (292-293); 1-(4-(3,3-difluoropyrrolidin-1-yl)cyclohexyl)-6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (294-295); 1-(4-(3,3-difluoroazetidin-1-yl)cyclohexyl)-6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo [d]imidazol-2-one (296); 1-(4-(2-oxa-6-azaspiro[3.3]heptan-6-yl)cyclohexyl)-5-(7,8-dimethyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-isopropyl-1,3-dihydro-2H-benzo[d]imidazol-2-one (297); 5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-methyl-1-(piperidin-4-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (1E);6-Methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(piperidin-4-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (1EA); 5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(piperidin-4-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (1EB); 6-Methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(piperidin-3-yl)- 1,3-dihydro-2H-benzo[d]imidazol-2-one (1EC); (R)-6-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(piperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (1ED); 1-((1r,4r)-4-aminocyclohexyl)-6-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (1EF); 1-((1s ,4s)-4-aminocyclohexyl)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-methyl-1,3-dihydro-2H-benzo[d]imidazol-2-one (1EI); (R)-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-methyl-1-(piperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (1EH); 5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(piperidine-3-yl)- lysine-4-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (1EG); 7-methyl-5-(8-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(piperidin-4-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (106F); (S)-6-isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(piperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (119H);6-Isopropyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(piperidin-4-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (119HA); (R)-6-ethyl-5-(8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-(piperidin-3-yl)-1 ,3-dihydro-2H-benzo[d]imidazol-2-one (119HB); or (R)-5-(7,8-dimethyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-6-isopropyl-1-(piperidin-3-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one (119HC), or a pharma- ceutically acceptable salt thereof;

6. A pharmaceutical composition comprising a compound according to any one of claims 1 to 5 or a pharma- ceutically acceptable salt thereof and a pharma- ceutically acceptable carrier.

7. A pharmaceutical composition comprising a compound according to any one of claims 1 to 5 or a pharma- ceutically acceptable salt thereof for treating an autoimmune disease or a chronic inflammatory disease.

8. 8. The pharmaceutical composition of claim 7, wherein the autoimmune disease or chronic inflammatory disease is selected from systemic lupus erythematosus (SLE), rheumatoid arthritis, multiple sclerosis (MS) and Sjogren's syndrome.

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