Triazine derivatives

Abstract

The invention relates to novel compounds having the general formula (I) wherein n, R1 and Y are as described herein, composition including the compounds and methods of using the compounds.

Description

[0001]P39353 NOVEL COMPOUNDS FIELD OF INVENTION The present invention relates to organic compounds useful for therapy and / orprophylaxis in a mammal, and in particular to compounds that modulate NLRP3 inhibition.The present invention provides novel compounds of formula I I wherein, n is 1 or 2; Y is –O– or –CH2–; R1is –OH or NR2R3; R2and R3are independently selected from H and alkyl, or R2is H and R3is haloalkyl, hydroxyalkyl, cycloalkyl, hydroxycycloalkyl, cycloalkylalkyl, imidazolylalkyl, or oxetanylmethyl, or R2and R3, together with the N atom to which they are attached, form a 4-6 membered ring optionally substituted with halo or –OH, or R2and R3, together with the N atom to which they are attached, form a 6 member ring comprising an additional O-heteroatom; and pharmaceutically acceptable salts thereof. Furthermore, the invention includes all racemic mixtures, all their corresponding enantiomers and / or optical isomers. BACKGROUND OF THE INVENTION The NOD-like receptor (NLR) family, pyrin domain–containing protein 3 (NLRP3) inflammasome is a component of the inflammatory process, and its aberrant activity is pathogenic in inherited disorders such as cryopyrin-associated periodic syndromes (CAPS) and complex diseases such as multiple sclerosis, type 2 diabetes, Alzheimer’s disease and atherosclerosis. NLRP3 is an intracellular signaling molecule that senses many pathogen-derived, environmental and host-derived factors. Upon activation, NLRP3 binds to apoptosis-associated speck-like protein containing a caspase activation and recruitment domain (ASC). ASC then polymerises to form a large aggregate known as an ASC speck. Polymerised ASC in turn interacts with the cysteine protease caspase-1 to form a complex termed the inflammasome. This results in the activation of caspase-1, which cleaves the precursor forms of the proinflammatory cytokines IL-1β and IL-18 (termed pro-IL-1β and pro-IL-18 respectively) to thereby activate these cytokines. Caspase-1 also mediates a type of inflammatory cell death known as pyroptosis. The ASC speck can also recruit and activate caspase-8, which can process pro-IL-1β and pro-IL-18 and trigger apoptotic cell death. Caspase-1 cleaves pro-IL-1β and pro-IL-18 to their active forms, which are secreted from the cell. Active caspase-1 also cleaves gasdermin-D to trigger pyroptosis. Through its control of the pyroptotic cell death pathway, caspase-1 also mediates the release of alarmin molecules such as IL-33 and high mobility group box 1 protein (HMGB1). Caspase-1 also cleaves intracellular IL-1R2 resulting in its degradation and allowing the release of IL-1α. In human cells caspase-1 may also control the processing and secretion of IL-37. A number of other caspase-1 substrates such as components of the cytoskeleton and glycolysis pathway may contribute to caspase-1-dependent inflammation. NLRP3-dependent ASC specks are released into the extracellular environment where they can activate caspase-1, induce processing of caspase-1 substrates and propagate inflammation. Active cytokines derived from NLRP3 inflammasome activation are important drivers of inflammation and interact with other cytokine pathways to shape the immune response to infection and injury. For example, IL-1β signalling induces the secretion of the pro- inflammatory cytokines IL-6 and TNF. IL-1β and IL-18 synergise with IL-23 to induce IL-17 production by memory CD4 Th17 cells and by γδ T cells in the absence of T cell receptor engagement. IL-18 and IL-12 also synergise to induce IFN-γ production from memory T cells and NK cells driving a Th1 response. The inherited CAPS diseases Muckle–Wells syndrome (MWS), familial cold autoinflammatory syndrome (FCAS) and neonatal-onset multisystem inflammatory disease (NOMID) are caused by gain-of-function mutations in NLRP3, thus defining NLRP3 as a critical component of the inflammatory process. NLRP3 has also been implicated in the pathogenesis of a number of complex diseases, notably including metabolic disorders such as type 2 diabetes, atherosclerosis, obesity and gout. A role for NLRP3 in diseases of the central nervous system is emerging, and lung diseases have also been shown to be influenced by NLRP3. NLRP3 has also been suggested tohave a role in a number of central nervous system conditions, including Parkinson's d isease(PD), Alzheimer's disease (AD), dementia, Huntington's disease, cerebral malaria, brain injury from pneumococcal meningitis (Walsh et al., Nature Reviews, 15: 84-97, 2014, and Dempsey et al. Brain. Behav. Immun.201761: 306-316). NLRP3 has also been shown to play a role in a number of lung diseases including chronic obstructive pulmonary disorder (COPD), asthma (including steroid-resistant asthma), asbestosis, and silicosis (De Nardo et al., Am. J. Pathol., 184: 42-54, 2014 and Kim et al. Am J Respir Crit Care Med.2017196(3): 283-97). Furthermore, NLRP3 has a role in the development of liver disease, kidney disease and aging. Many of these associations were defined using Nlrp3− / −mice, but there have also been insights into the specific activation of NLRP3 in these diseases. In type 2 diabetes mellitus (T2D), the deposition of islet amyloid polypeptide in the pancreas activates NLRP3 and IL-1β signalling, resulting in cell death and inflammation. Several small molecules have been shown to inhibit the NLRP3 inflammasome. Glyburide inhibits IL-1β production at micromolar concentrations in response to the activation of NLRP3 but not NLRC4 or NLRP1. Other previously characterised weak NLRP3 inhibitors include parthenolide, 3,4-methylenedioxy-β-nitrostyrene and dimethyl sulfoxide (DMSO),although these agents have limited potency and are nonspecific.Current treatments for NLRP3-related diseases include biologic agents that target IL-1. These are the recombinant IL-1 receptor antagonist anakinra, the neutralizing IL-1β antibody canakinumab and the soluble decoy IL-1 receptor rilonacept. These approaches have proven successful in the treatment of CAPS, and these biologic agents have been used in clinical trials for other IL-1β-associated diseases. DEFINITIONS The term “alkyl” denotes a monovalent linear or branched saturated hydrocarbon group of 1 to 6 carbon atoms. In some embodiments, if not otherwise described, alkyl comprises 1 to 6 carbon atoms (C1-6-alkyl), or 1 to 4 carbon atoms (C1-4-alkyl). Examples of C1-6-alkyl include methyl, ethyl, propyl, isopropyl, n-butyl, iso-butyl, sec-butyl, tert-butyl and pentyl. Particular alkyl groups are methyl, ethyl, isopropyl and isobutyl. "Cycloalkyl" refers to a saturated or partially unsaturated carbocyclic moiety having mono-, bi- (including bridged bicyclic and cycloalkyl spiro moieties) or tricyclic rings and 3 to 10 carbon atoms i.e., (C3-C10)cycloalkyl) in the ring. The cycloalkyl moiety can optionally be substituted with one or more substituents. In particular aspects cycloalkyl contains from 3 to 8 carbon atoms (i.e., (C3-C8)cycloalkyl). In other particular aspects cycloalkyl contains from 3 to 6 carbon atoms (i.e., (C3-C6)cycloalkyl). Examples of cycloalkyl moieties include, but are not limited to, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, and partially unsaturated (cycloalkenyl) derivatives thereof (e.g. cyclopentenyl, cyclohexenyl, and cycloheptenyl), bicyclo[3.1.0]hexanyl, bicyclo[3.1.0]hexenyl, bicyclo[3.1.1]heptanyl, bicyclo[3.1.1]heptenyl and bicyclo[1.1.1]pentane. The cycloalkyl moiety can be attached in a “spiro-cycloalkyl” or “cycloalkyl spiro” fashion such as “spirocyclopropyl”. Particular example is cyclopropyl. The term "cycloalkylalkyl" refers to an alkyl group wherein at least one of the hydrogen atoms of the alkyl group is replaced by a cycloalkyl group. Examples of cycloalkylalkylinclude cyclopropylmethyl, cyclopropylethyl, cyclopropylbutyl, cyclobutylpropyl , 2-cyclopropylbutyl, cyclopentylbutyl, cyclohexylmethyl, cyclohexylethyl, andhydroxycylopropylmethyl. Particular example is cyclobutylmethyl. The term “halogen”, “halide” and “halo” are used interchangeably herein and denotefluoro, chloro, bromo or iodo. Particular halo is fluoro."Haloalkyl" refers to a C1-6-alkyl group wherein at least one of the hydrogen atoms of the C1-6-alkyl group has been replaced by the same or different halogen atoms. Examples of haloalkyl include fluoroethyl, difluoroethyl, and trifluoroethyl. "Hydroxyalkyl" refers to an alkyl group wherein at least one of the hydrogen atoms of the alkyl group has been replaced by a hydroxy group. Examples of hydroxyalkyl includehydroxymethyl, hydroxyethyl, hydroxypropyl, hydroxymethylethyl, hydroxymethylpropyl anddihydroxypropyl. Particular examples of hydroxyalkyl are hydroxyethyl and hydroxy-2-methyl- propyl. "Hydroxycycloalkyl" refers to a cycloalkyl group wherein at least one of the hydrogenatoms of the cycloalkyl group is replaced by a hydroxy group. Representative example is hydroxycyclopentyl. "Imidazolylalkyl" refers to an alkyl group wherein one of the hydrogen atoms of the alkyl group has been replaced by an imidazolyl group. A representative example is imidazolylethyl. "Pharmaceutically acceptable salts" refers to those salts which retain the biological effectiveness and properties of the free bases or free acids, which are not biologically or otherwise undesirable. The salts are formed with inorganic acids such as trifluoroacetic acid, hydrochloric acid, hydrobromic acid, sulfuric acid, nitric acid, phosphoric acid, particularly hydrochloric acid, and organic acids such as formic acid, acetic acid, propionic acid, glycolic acid, pyruvic acid, oxalic acid, maleic acid, malonic acid, succinic acid, fumaric acid, tartaric acid, citric acid, benzoic acid, cinnamic acid, mandelic acid, methanesulfonic acid, ethanesulfonic acid, p-toluenesulfonic acid, salicylic acid, N-acetylcystein. In addition these salts may be prepared from addition of an inorganic base or an organic base to the free acid. Salts derived from an inorganic base include, but are not limited to, the sodium, potassium, lithium, ammonium, calcium, magnesium salts. Salts derived from organic bases include, but are not limited to salts of primary, secondary, and tertiary amines, substituted amines including naturally occurring substituted amines, cyclic amines and basic ion exchange resins, such as isopropylamine, trimethylamine, diethylamine, triethylamine, tripropylamine, ethanolamine, lysine, arginine, N-ethylpiperidine, piperidine, polyamine resins. The compound of formula I can also be present in the form of zwitterions. Particularly preferred pharmaceutically acceptable salts of compounds of formula I are the salts formed with formic acid and the salts formed with hydrochloric acid yielding a hydrochloride, dihydrochloride or trihydrochloride salt. The abbreviation uM means microMolar and is equivalent to the symbol µM. The abbreviation uL means microliter and is equivalent to the symbol µL.The abbreviation ug means microgram and is equivalent to the symbol µg.The compounds of formula I can contain several asymmetric centers and can be present in the form of optically pure enantiomers, mixtures of enantiomers such as, for example, racemates, optically pure diastereoisomers, mixtures of diastereoisomers, diastereoisomeric racemates or mixtures of diastereoisomeric racemates. According to the Cahn-Ingold-Prelog Convention the asymmetric carbon atom can be of the "R" or "S" configuration. Also an embodiment of the present invention provides compounds according to formula I as described herein and pharmaceutically acceptable salts or esters thereof, in particular compounds according to formula I as described herein and pharmaceutically acceptable saltsthereof, more particularly compounds according to formula I as described herein.BRIEF DESCRIPTION OF THE DRAWINGS FIG. 1 Voltage pattern utilized in hERG screening assay.DETAILED DESCRIPTION An embodiment of the present invention provides novel compounds of formula II I wherein, n is 1 or 2; R1is –OH or NR2R3; R2and R3are independently selected from H and alkyl, or R2is H and R3is haloalkyl, hydroxyalkyl, cycloalkyl, hydroxycycloalkyl, cycloalkylalkyl, imidazolylalkyl, or oxetanylmethyl, or R2and R3, together with the N atom to which they are attached, form a 4-6 membered ring optionally substituted with halo or –OH, or R2and R3, together with the N atom to which they are attached, form a 6 member ring comprising an additional O-heteroatom; and pharmaceutically acceptable salts thereof. An embodiment of the present invention provides compounds according to formula I as described herein, wherein R1is NR2R3. An embodiment of the present invention provides compounds according to formula I as described herein, wherein n is 2. An embodiment of the present invention provides compounds according to formula I as described herein, wherein R2and R3are independently selected from H and alkyl, or R2is H and R3is hydroxyalkyl, cycloalkyl, hydroxycycloalkyl, cycloalkylalkyl, imidazolylalkyl, or oxetanylmethyl, or R2and R3, together with the N atom to which they are attached, form a 4-5 membered ring optionally substituted with halo or –OH, or R2and R3, together with the N atom to which they are attached, form a 6 member ring comprising an additional O-heteroatom. An embodiment of the present invention provides compounds according to formula I as described herein, wherein R2and R3are independently selected from H and alkyl, or R2is H and R3is hydroxyalkyl, cycloalkyl, hydroxycycloalkyl, cycloalkylalkyl, or oxetanylmethyl, or R2and R3, together with the N atom to which they are attached, form a 4-5 membered ring optionally substituted with halo, or R2and R3, together with the N atom to which they are attached, form a 6 member ring comprising an additional O-heteroatom. In a preferred embodiment, the compound of formula I is a compound of formula IIa or IIb IIb. A to formula I as described herein, wherein n is 1 or 2; Y is –O– or –CH2–; R1is –OH or NR2R3; R2and R3are independently selected from H and alkyl, or R2is H and R3is hydroxyalkyl, cycloalkyl, hydroxycycloalkyl, cycloalkylalkyl, imidazolylalkyl, or oxetanylmethyl, or R2and R3, together with the N atom to which they are attached, form a 4-5 membered ring optionally substituted with halo or –OH, or R2and R3, together with the N atom to which they are attached, form a 6 member ring comprising an additional O-heteroatom; and pharmaceutically acceptable salts thereof. A particular embodiment of the present invention provides compounds according to formula IIa or IIb as described herein, wherein Y is –O– or –CH2–; R1is NR2R3; R2and R3are independently selected from H and alkyl, or R2is H and R3is hydroxyalkyl, cycloalkyl, hydroxycycloalkyl, cycloalkylalkyl, imidazolylalkyl, or oxetanylmethyl, or R2and R3, together with the N atom to which they are attached, form a 4-5 membered ring optionally substituted with halo or –OH, or R2and R3, together with the N atom to which they are attached, form a 6 member ring comprising an additional O-heteroatom; and pharmaceutically acceptable salts thereof. A particular embodiment of the present invention provides compounds according to formula IIa or IIb as described herein, wherein Y is –O– or –CH2–; R1is NR2R3; R2and R3are independently selected from H and alkyl, or R2is H and R3is hydroxyalkyl, cycloalkyl, hydroxycycloalkyl, cycloalkylalkyl, or oxetanylmethyl, or R2and R3, together with the N atom to which they are attached, form a 4-5 membered ring optionally substituted with halo, or R2and R3, together with the N atom to which they are attached, form a 6 member ring comprising an additional O-heteroatom; and pharmaceutically acceptable salts thereof. Particular examples of compounds of formula I as described herein are selected from (1S,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4-triazin-3- yl]amino]cyclohexanecarboxylic acid; (1S,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4-triazin-3- yl]amino]cyclohexanecarboxylic acid;2,2,2-trifluoroacetic acid; (3-fluoroazetidin-1-yl)-[(1S,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5- methyl-1,2,4-triazin-3-yl]amino]cyclohexyl]methanone; (1S,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4-triazin-3- yl]amino]-N-isobutyl-cyclohexanecarboxamide; (1S,3R)-N-(cyclobutylmethyl)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl- 1,2,4-triazin-3-yl]amino]cyclohexanecarboxamide; (1S,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4-triazin-3- yl]amino]-N-(oxetan-3-ylmethyl)cyclohexanecarboxamide; (1S,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4-triazin-3- yl]amino]-N-(2-hydroxyethyl)cyclohexanecarboxamide; (1S,3R)-N-cyclopropyl-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4- triazin-3-yl]amino]cyclohexanecarboxamide; (1S,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4-triazin-3- yl]amino]-N-methyl-cyclohexanecarboxamide; (1S,3R)-N-ethyl-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4-triazin- 3-yl]amino]cyclohexanecarboxamide; [(1S,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4-triazin-3- yl]amino]cyclohexyl]-pyrrolidin-1-yl-methanone; (1R,3S)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4-triazin-3- yl]amino]-N-isopropyl-cyclohexanecarboxamide; (1S,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4-triazin-3- yl]amino]-N-isopropyl-cyclohexanecarboxamide; (1S,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4-triazin-3- yl]amino]-N-isopropyl-cyclohexanecarboxamide; [(1S,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4-triazin-3- yl]amino]cyclohexyl]-morpholino-methanone; (1S,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4-triazin-3- yl]amino]-N,N-dimethyl-cyclohexanecarboxamide; 3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4-triazin-3-yl]amino]-N- isopropyl-cyclopentanecarboxamide; (3-hydroxyazetidin-1-yl)-[(1S,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5- methyl-1,2,4-triazin-3-yl]amino]cyclohexyl]methanone;2,2,2-trifluoroacetic acid; (3-hydroxyazetidin-1-yl)-[(1S,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5- methyl-1,2,4-triazin-3-yl]amino]cyclohexyl]methanone; (1R,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4-triazin-3- yl]amino]cyclohexanecarboxylic acid; (3-hydroxyazetidin-1-yl)-[(1R,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5- methyl-1,2,4-triazin-3-yl]amino]cyclohexyl]methanone;2,2,2-trifluoroacetic acid; (3-hydroxyazetidin-1-yl)-[(1R,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5- methyl-1,2,4-triazin-3-yl]amino]cyclohexyl]methanone; azetidin-1-yl-[(1S,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4- triazin-3-yl]amino]cyclohexyl]methanone; azetidin-1-yl-[(1R,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4- triazin-3-yl]amino]cyclohexyl]methanone;2,2,2-trifluoroacetic acid azetidin-1-yl-[(1R,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4- triazin-3-yl]amino]cyclohexyl]methanone; (1R,3R)-3-[[6-(4-hydroxyindan-5-yl)-5-methyl-1,2,4-triazin-3-yl]amino]-N-isopropyl- cyclohexanecarboxamide;2,2,2-trifluoroacetic acid; (1R,3R)-3-[[6-(4-hydroxyindan-5-yl)-5-methyl-1,2,4-triazin-3-yl]amino]-N-isopropyl- cyclohexanecarboxamide; (1S,3R)-3-[[6-(4-hydroxyindan-5-yl)-5-methyl-1,2,4-triazin-3-yl]amino]-N-isopropyl- cyclohexanecarboxamide;2,2,2-trifluoroacetic acid; (1S,3R)-3-[[6-(4-hydroxyindan-5-yl)-5-methyl-1,2,4-triazin-3-yl]amino]-N-isopropyl- cyclohexanecarboxamide; [(1R,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4-triazin-3- yl]amino]cyclohexyl]-morpholino-methanone;2,2,2-trifluoroacetic acid; [(1R,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4-triazin-3- yl]amino]cyclohexyl]-morpholino-methanone; (1S,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4-triazin-3- yl]amino]-N-(2-hydroxy-2-methyl-propyl)cyclohexanecarboxamide; (1S,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4-triazin-3- yl]amino]-N-(2-imidazol-1-ylethyl)cyclohexanecarboxamide; (1S,3R)-N-[(1S,2R)-2-hydroxycyclopentyl]-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5- yl)-5-methyl-1,2,4-triazin-3-yl]amino]cyclohexanecarboxamide; and pharmaceutically acceptable salts thereof. Preferred examples of compounds of formula I as described herein are selected from (3-fluoroazetidin-1-yl)-[(1S,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5- methyl-1,2,4-triazin-3-yl]amino]cyclohexyl]methanone; (1S,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4-triazin-3- yl]amino]-N-isobutyl-cyclohexanecarboxamide; (1S,3R)-N-(cyclobutylmethyl)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl- 1,2,4-triazin-3-yl]amino]cyclohexanecarboxamide; (1S,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4-triazin-3- yl]amino]-N-(oxetan-3-ylmethyl)cyclohexanecarboxamide; (1S,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4-triazin-3- yl]amino]-N-(2-hydroxyethyl)cyclohexanecarboxamide; (1S,3R)-N-cyclopropyl-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4- triazin-3-yl]amino]cyclohexanecarboxamide; (1S,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4-triazin-3- yl]amino]-N-methyl-cyclohexanecarboxamide; (1S,3R)-N-ethyl-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4-triazin- 3-yl]amino]cyclohexanecarboxamide; [(1S,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4-triazin-3- yl]amino]cyclohexyl]-pyrrolidin-1-yl-methanone; (1S,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4-triazin-3- yl]amino]-N-isopropyl-cyclohexanecarboxamide; [(1S,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4-triazin-3- yl]amino]cyclohexyl]-morpholino-methanone; (1S,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4-triazin-3- yl]amino]-N,N-dimethyl-cyclohexanecarboxamide; (3-hydroxyazetidin-1-yl)-[(1S,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5- methyl-1,2,4-triazin-3-yl]amino]cyclohexyl]methanone;2,2,2-trifluoroacetic acid; (3-hydroxyazetidin-1-yl)-[(1S,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5- methyl-1,2,4-triazin-3-yl]amino]cyclohexyl]methanone; (3-hydroxyazetidin-1-yl)-[(1R,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5- methyl-1,2,4-triazin-3-yl]amino]cyclohexyl]methanone;2,2,2-trifluoroacetic acid; (3-hydroxyazetidin-1-yl)-[(1R,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5- methyl-1,2,4-triazin-3-yl]amino]cyclohexyl]methanone; azetidin-1-yl-[(1S,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4- triazin-3-yl]amino]cyclohexyl]methanone; azetidin-1-yl-[(1R,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4- triazin-3-yl]amino]cyclohexyl]methanone;2,2,2-trifluoroacetic acid; azetidin-1-yl-[(1R,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4- triazin-3-yl]amino]cyclohexyl]methanone; (1R,3R)-3-[[6-(4-hydroxyindan-5-yl)-5-methyl-1,2,4-triazin-3-yl]amino]-N-isopropyl- cyclohexanecarboxamide;2,2,2-trifluoroacetic acid; (1R,3R)-3-[[6-(4-hydroxyindan-5-yl)-5-methyl-1,2,4-triazin-3-yl]amino]-N-isopropyl- cyclohexanecarboxamide; (1S,3R)-3-[[6-(4-hydroxyindan-5-yl)-5-methyl-1,2,4-triazin-3-yl]amino]-N-isopropyl- cyclohexanecarboxamide;2,2,2-trifluoroacetic acid; (1S,3R)-3-[[6-(4-hydroxyindan-5-yl)-5-methyl-1,2,4-triazin-3-yl]amino]-N-isopropyl- cyclohexanecarboxamide; (1S,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4-triazin-3- yl]amino]-N-(2-hydroxy-2-methyl-propyl)cyclohexanecarboxamide; (1S,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4-triazin-3- yl]amino]-N-(2-imidazol-1-ylethyl)cyclohexanecarboxamide; (1S,3R)-N-[(1S,2R)-2-hydroxycyclopentyl]-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5- yl)-5-methyl-1,2,4-triazin-3-yl]amino]cyclohexanecarboxamide; and pharmaceutically acceptable salts thereof. Most preferred examples of compounds of formula I as described herein are selected from (3-fluoroazetidin-1-yl)-[(1S,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5- methyl-1,2,4-triazin-3-yl]amino]cyclohexyl]methanone; (1S,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4-triazin-3- yl]amino]-N-isobutyl-cyclohexanecarboxamide; (1S,3R)-N-(cyclobutylmethyl)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl- 1,2,4-triazin-3-yl]amino]cyclohexanecarboxamide; (1S,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4-triazin-3- yl]amino]-N-(oxetan-3-ylmethyl)cyclohexanecarboxamide; (1S,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4-triazin-3- yl]amino]-N-(2-hydroxyethyl)cyclohexanecarboxamide; (1S,3R)-N-cyclopropyl-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4- triazin-3-yl]amino]cyclohexanecarboxamide; (1S,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4-triazin-3- yl]amino]-N-methyl-cyclohexanecarboxamide; (1S,3R)-N-ethyl-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4-triazin- 3-yl]amino]cyclohexanecarboxamide; (1S,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4-triazin-3- yl]amino]-N-isopropyl-cyclohexanecarboxamide; [(1S,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4-triazin-3- yl]amino]cyclohexyl]-morpholino-methanone; azetidin-1-yl-[(1S,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4- triazin-3-yl]amino]cyclohexyl]methanone; (1S,3R)-3-[[6-(4-hydroxyindan-5-yl)-5-methyl-1,2,4-triazin-3-yl]amino]-N-isopropyl- cyclohexanecarboxamide;2,2,2-trifluoroacetic acid; (1S,3R)-3-[[6-(4-hydroxyindan-5-yl)-5-methyl-1,2,4-triazin-3-yl]amino]-N-isopropyl- cyclohexanecarboxamide; (1S,3R)-N-[(1S,2R)-2-hydroxycyclopentyl]-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5- yl)-5-methyl-1,2,4-triazin-3-yl]amino]cyclohexanecarboxamide; and pharmaceutically acceptable salts thereof. Pharmaceutical compositions and administration Another embodiment of the invention provides a pharmaceutical composition or medicament containing a compound of the invention and a therapeutically inert carrier, diluentor excipient, as well as a method of using the compounds of the invention to prepare suchcomposition and medicament. In one example, the compound of formula I may be formulated by mixing at ambient temperature at the appropriate pH, and at the desired degree of purity, with physiologically acceptable carriers, i.e., carriers that are non-toxic to recipients at the dosages and concentrations employed into a galenical administration form. The pH of the formulation depends mainly on the particular use and the concentration of compound, but preferably ranges anywhere from about 3 to about 8. In one example, a compound of formula I is formulated in an acetate buffer, at pH 5. In another embodiment, the compound of formula I is sterile. The compound may be stored, for example, as a solid or amorphous composition, as a lyophilized formulation or as an aqueous solution. Compositions are formulated, dosed, and administered in a fashion consistent with good medical practice. Factors for consideration in this context include the particular disorder being treated, the particular mammal being treated, the clinical condition of the individual patient, the cause of the disorder, the site of delivery of the agent, the method of administration, thescheduling of administration, and other factors known to medical practitioners.The compounds of the invention may be administered by any suitable means, including oral, topical (including buccal and sublingual), rectal, vaginal, transdermal, parenteral, subcutaneous, intraperitoneal, intrapulmonary, intradermal, intrathecal and epidural and intranasal, and, if desired for local treatment, intralesional administration. Parenteral infusions include intramuscular, intravenous, intraarterial, intraperitoneal, or subcutaneous administration. The compounds of the present invention may be administered in any convenient administrative form, e.g., tablets, powders, capsules, solutions, dispersions, suspensions,syrups, sprays, suppositories, gels, emulsions, patches, etc. Such compositions may con taincomponents conventional in pharmaceutical preparations, e.g., diluents, carriers, pH modifiers,sweeteners, bulking agents, and further active agents. A typical formulation is prepared by mixing a compound of the present invention and a carrier or excipient. Suitable carriers and excipients are well known to those skilled in the art and are described in detail in, e.g., Ansel, Howard C., et al., Ansel’s Pharmaceutical Dosage Forms and Drug Delivery Systems. Philadelphia: Lippincott, Williams & Wilkins, 2004; Gennaro, Alfonso R., et al. Remington: The Science and Practice of Pharmacy. Philadelphia: Lippincott, Williams & Wilkins, 2000; and Rowe, Raymond C. Handbook of Pharmaceutical Excipients. Chicago, Pharmaceutical Press, 2005. The formulations may also include one or more buffers, stabilizing agents, surfactants, wetting agents, lubricating agents, emulsifiers, suspending agents, preservatives, antioxidants, opaquing agents, glidants, processing aids, colorants, sweeteners, perfuming agents, flavoring agents, diluents and other known additives to provide an elegant presentation of the drug (i.e., a compound of the present invention or pharmaceutical composition thereof) or aid in the manufacturing of the pharmaceutical product (i.e., medicament). The compounds of formula I and their pharmaceutically acceptable salts can be processed with pharmaceutically inert, inorganic or organic adjuvants for the production oftablets, coated tablets, hard gelatin capsules, injection solutions or topical formula tionsLactose, corn starch or derivatives thereof, talc, stearic acid or its salts etc. can be used, forexample, as such adjuvants for tablets and hard gelatin capsules.Suitable adjuvants for soft gelatin capsules, are, for example, vegetable oils, waxes, fats, semi-solid substances and liquid polyols, etc. Suitable adjuvants for the production of solutions and syrups are, for example, water, polyols, saccharose, invert sugar, glucose, etc. Suitable adjuvants for injection solutions are, for example, water, alcohols, polyols, glycerol, vegetable oils, etc. Suitable adjuvants for suppositories are, for example, natural or hardened oils, waxes, fats, semi-solid or liquid polyols, etc. Suitable adjuvants for topical ocular formulations are, for example, cyclodextrins,mannitol or many other carriers and excipients known in the art. Moreover, the pharmaceutical preparations can contain preservatives, solubilizers, viscosity-increasing substances, stabilizers, wetting agents, emulsifiers, sweeteners, colorants,flavorants, salts for varying the osmotic pressure, buffers, masking agents or antioxidants. Theycan also contain still other therapeutically valuable substances.The dosage can vary in wide limits and will, of course, be fitted to the individual requirements in each particular case. In general, in the case of oral administration a daily dosage of about 0.1 mg to 20 mg per kg body weight, preferably about 0.5 mg to 4 mg per kg body weight (e.g. about 300 mg per person), divided into preferably 1-3 individual doses, which can consist, for example, of the same amounts, should it be appropriate. In the case of topical administration, the formulation can contain 0.001% to 15% by weight of medicament and the required dose, which can be between 0.1 and 25 mg in can be administered either by single dose per day or per week, or by multiple doses (2 to 4) per day, or by multiple doses per week It will, however, be clear that the upper or lower limit given herein can be exceeded when this is shown to be indicated. Indications An embodiment of the present invention is a compound according to formula I asdescribed herein for use as a therapeutically active substance.An embodiment of the present invention is a compound according to formula I as described herein for use in the treatment or prevention of a disease, disorder or condition,wherein the disease, disorder or condition is responsive to NLRP3 inhibition.An embodiment of the present invention is a compound according to formula I as described herein for the treatment or prophylaxis of a disease, disorder or condition, wherein the disorder or condition is responsive to NLRP3 inhibition. As used herein, the term “NLRP3 inhibition” refers to the complete or partial reduction in the level of activity of NLRP3 and includes, for example, the inhibition of active NLRP3 and / or the inhibition of activation of NLRP3. There is evidence for a role of NLRP3-induced IL-1 and IL-18 in the inflammatory responses occurring in connection with, or as a result of, a multitude of different disorders (Menu et al., Clinical and Experimental Immunology, 166: 1-15, 2011; Strowig et al., Nature, 481: 278-286, 2012). In one embodiment, the disease, disorder or condition is selected from: (i) inflammation; (ii) an auto-immune disease; (iii) cancer; (iv) an infection; (v) a metabolic disease; (vi) a cardiovascular disease; (vii) a respiratory disease; (viii) a liver disease; (ix) a renal disease; (x) an ocular disease; (xi) a skin disease; (xii) a lymphatic condition; (xiii) graft versus host disease; (xiv) allodynia; (xv) a condition associated with diabetes; and (xvi) any disease where an individual has been determined to carry a germline or somatic non-silent mutation in NLRP3 In another embodiment, the disease, disorder or condition is selected from: (i) cancer; (ii) an infection; (iii) a cardiovascular disease; (iv) a liver disease; (v) an ocular disease; and (vi) a skin disease. In a further typical embodiment of the invention, the disease, disorder or condition is inflammation. Examples of inflammation that may be treated or prevented includeinflammatory responses occurring in connection with, or as a result of:(i) a skin condition such as contact hypersensitivity, bullous pemphigoid, sunburn, psoriasis, atopical dermatitis, contact dermatitis, allergic contact dermatitis, seborrhoetic dermatitis, lichen planus, scleroderma, pemphigus, epidermolysis bullosa, urticaria, erythemas, or alopecia; (ii) a joint condition such as osteoarthritis, systemic juvenile idiopathic arthritis, adult -onset Still’s disease, relapsing polychondritis, rheumatoid arthritis, juvenile chronic arthritis, gout, or a seronegative spondyloarthropathy (e.g. ankylosing spondylitis, psoriatic arthritis or Reiter’s disease); (iii) a muscular condition such as polymyositis or myasthenia gravis;(iv) a gastrointestinal tract condition such as inflammatory bowel disease (including Crohn’s disease and ulcerative colitis), colitis, gastric ulcer, Coeliac disease, proctitis, pancreatitis, eosinopilic gastro-enteritis, mastocytosis, antiphospholipid syndrome, or a food-related allergy which may have effects remote from the gut (e.g., migraine, rhinitis or eczema);(v) a respiratory system condition such as chronic obstructive pulmonary disease (COPD), asthma (including eosinophilic, bronchial, allergic, intrinsic, extrinsic or dust asthma, and particularly chronic or inveterate asthma, such as late asthma and airways hyper- responsiveness), bronchitis, rhinitis (including acute rhinitis, allergic rhinitis, atrophic rhinitis, chronic rhinitis, rhinitis caseosa, hypertrophic rhinitis, rhinitis pumlenta, rhinitis sicca, rhinitis medicamentosa, membranous rhinitis, seasonal rhinitis e.g. hay fever, and vasomotor rhinitis), sinusitis, idiopathic pulmonary fibrosis (IPF), sarcoidosis, farmer’s lung, silicosis, asbestosis, volcanic ash induced inflammation, adult respiratory distress syndrome, hypersensitivity pneumonitis, or idiopathic interstitial pneumonia; (vi) a vascular condition such as atherosclerosis, Behcet’s disease, vasculitides, or Wegener’s granulomatosis; (vii) an autoimmune condition such as systemic lupus erythematosus, Sjögren’s syndrome, systemic sclerosis, Hashimoto’s thyroiditis, type I diabetes, idiopathic thrombocytopenia purpura, or Graves disease; (viii) an ocular condition such as uveitis, allergic conjunctivitis, or vernal conjunctivitis;(ix) an infection or infection-related condition, such as Acquired Immunodeficiency Syndrome (AIDS), acute or chronic bacterial infection, acute or chronic parasitic infection,acute or chronic viral infection, acute or chronic fungal infection, meningitis , hepatitis (A, B orC, or other viral hepatitis), peritonitis, pneumonia, epiglottitis, malaria, dengue hemorrhagic fever, leishmaniasis, streptococcal myositis, mycobacterium tuberculosis (including mycobacterium tuberculosis and HIV co-infection), mycobacterium avium intracellulare, pneumocystis carinii pneumonia, orchitis / epidydimitis, legionella, Lyme disease, influenza A, Epstein-Barr virus infection, viral encephalitis / aseptic meningitis, or pelvic inflammatory disease; (x) a renal condition such as mesangial proliferative glomerulonephritis, nephrotic syndrome, nephritis, glomerular nephritis, obesity related glomerulopathy, acute renal failure, acute kidney injury, uremia, nephritic syndrome, kidney fibrosis including chronic crystal nephropathy, or renal hypertension; (xi) a lymphatic condition such as Castleman’s disease;(xii) a condition of, or involving, the immune system, such as hyper IgE syndrome, lepromatous leprosy, familial hemophagocytic lymphohistiocytosis, or graft versus host disease; (xiii) a hepatic condition such as chronic active hepatitis, non-alcoholic steatohepatitis (NASH), alcohol-induced hepatitis, non-alcoholic fatty liver disease (NAFLD), alcoholic fatty liver disease (AFLD), alcoholic steatohepatitis (ASH), primary biliary cirrhosis, fulminant hepatitis, liver fibrosis, or liver failure; (xiv) a cancer, including those cancers listed above; (xv) a burn, wound, trauma, haemorrhage or stroke; (xvi) radiation exposure; (xvii) a metabolic disease such as type 2 diabetes (T2D), atherosclerosis, obesity, gout or pseudo-gout; and / or (xiii) pain such as inflammatory hyperalgesia, pelvic pain, allodynia, neuropathic pain, or cancer-induced bone pain. An embodiment of the present invention is a compound according to formula I as described herein for the treatment or prophylaxis of a disease, disorder or condition selected from: inflammation; an auto-immune disease; cancer; an infection; a metabolic disease; a cardiovascular disease; a respiratory disease; a liver disease; a renal disease; an ocular disease; a skin disease; a lymphatic condition; graft versus host disease; allodynia; a condition associated with diabetes; and any disease where an individual has been determined to carry a germline or somatic non-silent mutation in NLRP3. An embodiment of the present invention is the use of a compound according to formula I as described herein in the treatment or prophylaxis of a disease, disorder or condition,wherein the disease, disorder or condition is responsive to NLRP3 inhibition.An embodiment of the present invention is the use of a compound according to formula Ib as described herein in the treatment or prophylaxis of a disease, disorder or conditionselected from Alzheimer’s disease and Parkinson’s disease.An embodiment of the present invention is the use a compound according to formula I as described herein for use in the treatment or prophylaxis of a disease, disorder or condition selected from Asthma and COPD. An embodiment of the present invention is the use a compound according to formula I as described herein for use in the treatment or prophylaxis of a cardiovascular disease, disorder or condition. An embodiment of the present invention is the use a compound according to formula I as described herein for use in the treatment or prophylaxis of a cardiometabolic disease, disorder or condition. An embodiment of the present invention is the use a compound according to formula I as described herein for use in the treatment or prophylaxis of a disease, disorder or condition selected from Cryopyrin-associated periodic syndromes. An embodiment of the present invention is a compound according to formula I as described herein for the treatment or prophylaxis of a disease, disorder or condition selected from Alzheimer’s disease and Parkinson’s disease. An embodiment of the present invention is a compound according to formula I as described herein for the treatment or prophylaxis of a disease, disorder or condition selected from Asthma and COPD. An embodiment of the present invention is a compound according to formula I as described herein for the treatment or prophylaxis of a cardiovascular disease, disorder or condition. An embodiment of the present invention is a compound according to formula I as described herein for the treatment or prophylaxis of a cardiometabolic disease, disorder or condition. An embodiment of the present invention is a compound according to formula I as described herein for the treatment or prophylaxis of a disease, disorder or condition selected from Cryopyrin-associated periodic syndromes. An embodiment of the present invention is the use of a compound according to formula I as described herein for the preparation of a medicament for the treatment or prophylaxis of a disease, disorder or condition selected from Alzheimer’s disease and Parkinson’s disease. An embodiment of the present invention is the use of a compound according to formula I as described herein for the preparation of a medicament for the treatment or prophylaxis of a disease, disorder or condition selected from Asthma and COPD. An embodiment of the present invention is the use of a compound according to formula I as described herein for the preparation of a medicament for the treatment or prophylaxis of a cardiovascular disease, disorder or condition. An embodiment of the present invention is the use of a compound according to formula I as described herein for the preparation of a medicament for the treatment or prophylaxis of a cardiometabolic disease, disorder or condition. An embodiment of the present invention is the use of a compound according to formula I as described herein for the preparation of a medicament for the treatment or prophylaxis of a disease, disorder or condition selected from Cryopyrin-associated periodic syndromes. An embodiment of the present invention is a method of treatment or prophylaxis of a disease, disorder or condition selected from Alzheimer’s disease and Parkinson’s disease, which method comprises administering an effective amount of a compound according to formula I as described herein. An embodiment of the present invention is a method of treatment or prophylaxis of a disease, disorder or condition selected from Asthma and COPD, which method comprises administering an effective amount of a compound according to formula I as described herein. An embodiment of the present invention is a method of treatment or prophylaxis of a cardiovascular disease, disorder or condition, which method comprises administering aneffective amount of a compound according to formula I as described herein.An embodiment of the present invention is a method of treatment or prophylaxis of a cardiometabolic disease, disorder or condition, which method comprises administering aneffective amount of a compound according to formula I as described herein.An embodiment of the present invention is a method of treatment or prophylaxis of a disease, disorder or condition selected from Cryopyrin-associated periodic syndromes, which method comprises administering an effective amount of a compound according to formula I as described herein. An embodiment of the present invention relates to a method of inhibiting NLRP3, which method comprises administering an effective amount of a compound according to formula I as described herein. Also an embodiment of the present invention are compounds of formula I as describedherein, when manufactured according to any one of the described processes.An embodiment of the present invention is a pharmaceutical composition comprising a compound according to formula I as described herein and a therapeutically inert carrier. Experimental part The invention will now be illustrated by the following examples which have no limiting character. In case the preparative examples are obtained as a mixture of enantiomers or diastereoisomers, the pure enantiomers or diastereomers can be obtained by methods described herein or by methods known to those skilled in the art, such as e.g. chiral chromatography or crystallization. The salt free compounds can be made analogues to the described examples yielding salts. Examples Experimental Methods Abbreviations: ACN, MeCN Acetonitrile DIEA N,N-Diisopropylethylamine DMF N,N-dimethylformamide DMSO Dimethyl sulfoxide EtOAc Ethyl acetate FA Formic acid h, hrs hour, hours HATU Hexafluorophosphate Azabenzotriazole Tetramethyl Uronium HPLC High-performance liquid chromatography min(s) Minute(s) NMR Nuclear magnetic resonance spectroscopy prep Preparative RP Reverse phase rt Room temperature TBTU 2-(1H-Benzotriazole-1-yl)-1,1,3,3-tetramethylaminium tetrafluoroborate TEA Triethylamine THF Tetrahydrofuran TFA Trifluoroacetic acid All examples and intermediates were prepared under nitrogen atmosphere if not specified otherwise. Example 1 (1S,3R)-3-[[6-(4-Hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4-triazin-3- yl]amino]cyclohexanecarboxylic acid Step A: Methyl-(1S,3R)-3- cis-(1S,3R)-3-(Tert-butoxycarbonylamino)cyclohexanecarboxylic acid (CAS # 222530-34-9, 2.0 g, 7.97 mmol, 1.0 eq) was dissolved in dichloromethane (90 mL) and methanol (30 mL). Then 4 M HCl in 1,4-dioxane (16.0 mL, 63.8 mmol, 8.0 eq) was added to the reaction mixture, and it was stirred under argon for 16 h. The reaction solution was evaporated to dryness to afford the title compound (1.64 g, quant. yield) as a white solid. LCMS: m / z 158.1 [M+H]+, ESI pos. Step B: Methyl-(1S,3R)-3-[(6-chloro-5-methyl-1,2,4-triazin-3-yl)amino]cyclohexanecarboxylate To a mixture of aforementioned methyl-(1S,3R)-3-aminocyclohexanecarboxylate;hydrochloride (1.64 g, 8.05 mmol, 1.10 eq) in 1,4-dioxane (20 mL) and N,N-dimethylformamide (5 mL) was added at rt N,N-diisopropylethylamine (3.78 g, 4.98 mL, 29.27 mmol, 4.00 eq). After stirring for 5 mins 3,6- dichloro-5-methyl-1,2,4-triazine (CAS #132434-82-3, 1.20 g, 7.32 mmol, 1.00 eq) was added in one portion as a solid, resulting in a greenish solution. The reaction mixture was stirred at 23 °C for 60 h. The reaction mixture was then quenched with half saturated NaHCO3 solution (100 mL) and extracted with ethyl acetate (2 x 100 mL). The organic layers were washed with water (100 mL) and brine (100 mL). The combined organic extracts were dried over sodium sulfate, filtered off and evaporated. The crude product was purified by flash chromatography on silica gel, (gradient 0% to 30 % ethyl acetate in heptane) to afford the title compound (1.59 g, 73% yield) as a light yellow solid. LCMS: m / z 285.1 ([{35Cl}M+H]+), 287.1 ([{37Cl }M+H]+), ESI pos. Step C: -3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4-triazin-3- yl]amino] In a sealable tube, a mixture of aforementioned methyl-(1S,3R)-3-[(6-chloro-5-methyl-1,2,4-triazin- 3-yl)amino]cyclohexanecarboxylate (551 mg, 1.94 mmol, 1.00 eq), 5-(4,4,5,5-tetramethyl-1,3,2- dioxaborolan-2-yl)coumaran-4-ol (CAS# 2923540-32-1, 710.1 mg, 2.71 mmol, 1.40 eq) and cesium carbonate (1.89 g, 5.81 mmol, 3.0 eq) in 1,4-dioxane (8 mL) and water (2 mL) was set under argon, and XPhos Pd G3 gt (CAS # 1445085-55-1, 245.7 mg, 0.290 mmol, 0.15 eq) was added. The reaction mixture was stirred at 90 °C in a sealed tube for 3 h. Afterwards, the reaction mixture was cooled to rt, quenched with water (10 mL) and sat. NH4Cl solution (5 mL) and extracted with ethyl acetate (2 x 30 mL). The organic layers were washed with brine (20 mL), dried over Na2SO4, filtered off and concentrated in vacuo. The crude product was purified by flash chromatography on silica gel (gradient 0% to 60% ethyl acetate in heptane) to afford the title compound (775 mg, 94% yield) as a yellow oil. LCMS: m / z 385.4 [M+H]+, ESI pos. Step D: (1S,3R)-3-[[6-(4-Hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4-triazin-3- yl]amino]cyclohexanecarboxylic acid To a solution of aforementioned methyl-(1S,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5- methyl-1,2,4-triazin-3-yl]amino]cyclohexanecarboxylate (775 mg, 1.81 mmol, 1.0 eq) in tetrahydrofuran (8 mL) and methanol (4 mL) was added at ambient temperature 1 M lithium hydroxide in water (5.4 mL, 5.4 mmol, 3.0 eq) dropwise via syringe. The yellow reaction mixture was stirred at 23 °C for 2 h. The reaction mixture was neutralized with 5% citric acid and set to pH=3-4 and extracted with ethyl acetate (2 x 60 mL). The organic layers were washed with brine (60 mL), dried over Na2SO4, filtered off and concentrated in vacuo to afford the title compound (724 mg, 97% yield) as a yellow foam. LCMS: m / z 369.2 [M-H]-, ESI neg. Example 2 (3-Fluoroazetidin-1-yl)-[(1S,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4- triazin-3-yl]amino]cyclohexyl]methanone To a solution of aforementioned (1S,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl- 1,2,4-triazin-3-yl]amino]cyclohexanecarboxylic acid (example 1, 42 mg, 0.11 mmol, 1.0 eq) and N,N- dimethylformamide (0.70 mL) was added at rt, N,N-diisopropylethylamine (73.3 mg, 0.096 mL, 0.57 mmol, 5.00 eq) followed by HATU (66.7 mg, 0.17 mmol, 1.50 eq). The yellow solution was stirred for 5 mins, then 3-fluoroazetidine;hydrochloride (CAS # 617718-46-4, 21.3 mg, 0.18 mmol, 1.60 eq) was added. The reaction mixture was stirred at 23 °C for 16 h. The reaction mixture was quenched with water (5 mL) and extracted with ethyl acetate (2 x 20 mL). The organic layers were washed with brine (20 mL), dried over Na2SO4, filtered off and concentrated in vacuo. The crude product was purified by flash chromatography on silica gel (gradient 0% to 10% methanol in ethyl acetate) followed by preparative HPLC (column: YMC Triart C18, 12 nm, 5 µm, 100 x 30 mm; elution: 20% to 80% water / acetonitrile + 0.1% triethylamine) to afford the title compound (9.0 mg, 18% yield) as a light yellow amorphous freeze-dried solid. LCMS: m / z 428.3[M+H]+, ESI pos. Example 3 (1S,3R)-3-[[6-(4-Hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4-triazin-3-yl]amino]-N- isobutyl-cyclohexanecarboxamide To a solution of 5-yl)-5-methyl- 1,2,4-triazin-3-yl]amino]cyclohexanecarboxylic acid (example 1, 43 mg, 0.12 mmol, 1.00 eq) and N,N-dimethylformamide (0.70 mL) was added at rt N,N-diisopropylethylamine (75.0 mg, 0.099 mL, 0.580 mmol, 5.00 eq ) followed by HATU (68.3 mg, 0.17 mmol, 1.50 eq). The yellow solution was stirred for 5 min, then isobutylamine (14.3 mg, 0.019 mL, 0.186 mmol, 1.60 eq ) was added. The reaction mixture was stirred at 23 °C for 16 h. The reaction mixture was quenched with water (5 mL) and extracted with ethyl acetate (2 x 20 mL). The organic layers were washed with brine (20 mL), dried over Na2SO4, filtered off and concentrated in vacuo. The crude product was purified by flash chromatography on silica gel (gradient 0% to 10% methanol in ethyl acetate) followed by preparative HPLC (column: Phenomenex Gemini NX C18, 12 nm, 5 µm, 100 x 30 mm; elution: 20% to 80% water / acetonitrile + 0.1% formic acid) to afford the title compound (17 mg, 33% yield) as a light yellow amorphous freeze-dried solid. LCMS: m / z 426.3 [M+H]+, ESI pos. Example 4 (1S,3R)-N-(Cyclobutylmethyl)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4- triazin-3-yl]amino]cyclohexanecarboxamide To a solution of aforement ydrobenzofuran-5-yl)-5-methyl- 1,2,4-triazin-3-yl]amino]cyclohexanecarboxylic acid (example 136 mg, 0.097 mmol, 1.0 eq) and N,N- dimethylformamide (0.70 mL) was added at rt, N,N-diisopropylethylamine (62.8 mg, 0.083 mL, 0.486 mmol, 5.0 eq ) followed by HATU (57.2 mg, 0.145 mmol, 1.50 eq). The yellow solution was stirred for 5 mins, then cyclobutylmethylamine;hydrochloride (20.0 mg, 0.155 mmol, 1.6 eq) was added. The reaction mixture was stirred at 23 °C for 16 h. The reaction mixture was quenched with water (5 mL) and extracted with ethyl acetate (2 x 20 mL). The organic layers were washed with brine (20 mL), dried over Na2SO4, filtered off and concentrated in vacuo. The crude product was purified by flash chromatography on silica gel (gradient 0% to 10% methanol in ethyl acetate) followed by preparative HPLC (column: YMC Triart C18, 12 nm, 5 µm, 100 x 30 mm; elution: 20% to 80% water / acetonitrile + 0.1% formic acid) to afford the title compound (15 mg, 34% yield) as a light yellow amorph freeze- dried solid. LCMS: m / z 438.5 [M+H]+, ESI pos. Example 5 (1S,3R)-3-[[6-(4-Hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4-triazin-3-yl]amino]-N- (oxetan-3-ylmethyl)cyclohexanecarboxamide To a solution of - 5-yl)-5-methyl- 1,2,4-triazin-3-yl]amino]cyclohexanecarboxylic acid (example 137 mg, 1.00 mmol, 1.0 eq) and N,N- dimethylformamide (0.70 mL) was added at rt, N,N-diisopropylethylamine (65 mg, 0.085 mL, 0.500 mmol, 5.0 eq) followed by HATU (58.7 mg, 0.150 mmol, 1.50 eq). The yellow solution was stirred for 5 mins, then oxetan-3-ylmethylamine (15.0 mg, 0.160 mmol, 1.60 eq) was added. The reaction mixture was stirred at 23 °C for 16 h. The reaction mixture was quenched with water (5 mL) and extracted with ethyl acetate (2 x 20 mL). The organic layers were washed with brine (20 mL), dried over Na2SO4, filtered off and concentrated in vacuo. The crude product was purified by flash chromatography on silica gel (gradient 0% to 10% methanol in ethyl acetate) followed by preparative HPLC (column: Phenomenex Gemini NX C18, 12 nm, 5 µm, 100 x 30 mm; elution: 50% to 100% water / acetonitrile + 0.1% triethylamine) to afford the title compound (4.0 mg, 9% yield) as a light yellow amorph freeze-dried solid. LCMS: m / z 440.3 [M+H]+, ESI pos. Example 6 (1S,3R)-3-[[6-(4-Hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4-triazin-3-yl]amino]-N- (2-hydroxyethyl)cyclohexanecarboxamide To a solution of 5-yl)-5-methyl- 1,2,4-triazin-3-yl]amino]cyclohexanecarboxylic acid (example 1, 50 mg, 0.12 mmol, 1.0 eq) and N,N- dimethylformamide (0.80 mL) was added at rt N,N-diisopropylethylamine (78.5 mg, 0.10 mL, 0.61 mmol, 5.0 eq) followed by HATU (71.4 mg, 0.18 mmol, 1.50 eq). The yellow solution was stirred for 5 mins, then ethanolamine (11.9 mg, 0.012 mL, 0.19 mmol, 1.60 eq) was added. The reaction mixture was stirred at 23 °C for 16 h. The reaction mixture was quenched with water (5 mL) and extracted with ethyl acetate (2 x 20 mL). The organic layers were washed with brine (20 mL), dried over Na2SO4, filtered off and concentrated in vacuo. The crude product was purified by flash chromatography on silica gel (gradient 0% to 10% methanol in ethyl acetate) to afford the title compound (19 mg, 34% yield) as a light yellow amorph freeze-dried solid. LCMS: m / z 414.2 [M+H]+, ESI pos. Example 7 (1S,3R)-N-Cyclopropyl-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4-triazin- 3-yl]amino]cyclohexanecarboxamide To a solution of aforementioned (1S,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl- 1,2,4-triazin-3-yl]amino]cyclohexanecarboxylic acid (example 153 mg, 0.143 mmol, 1.0 eq) and N,N- dimethylformamide, extra dry (0.700 mL) was added at rt, N,N-diisopropylethylamine (92 mg, 0.121 mL, 0.715 mmol, 5.00 eq) followed by HATU (84 mg, 0.21 mmol, 1.50 eq). The yellow solution was stirred for 5 minutes, then cyclopropylamine (13 mg, 0.016 mL, 0.229 mmol, 1.60 eq) was added. The reaction mixture was stirred at 23 °C for 60 h. The reaction mixture was quenched with water (5 mL) and extracted with ethyl acetate (2 x 20 mL). The organic layers were washed with brine (20 mL), dried over Na2SO4, filtered off and concentrated in vacuo. The crude product was purified by flash chromatography on silica gel (gradient 0% to 10% methanol in ethyl acetate) followed by preparative HPLC (column: Phenomenex Gemini NX C18, 12 nm, 5 µm, 100 x 30 mm; elution: 50% to 100% water / acetonitrile + 0.1% triethylamine) to afford the title compound (22 mg, 36% yield) as a light yellow amorph freeze-dried solid. LCMS: m / z 410.3 [M+H]+, ESI pos. Example 8 (1S,3R)-3-[[6-(4-Hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4-triazin-3-yl]amino]-N- methyl-cyclohexanecarboxamide To a solution of 5-yl)-5-methyl-1,2,4-triazin-3- yl]amino]cyclohexanecarboxylic acid (example 1,38 mg, 100 mmol, 1.0 eq) and N,N- dimethylformamide, extra dry (0.32 mL) was added at rt, N,N-diisopropylethylamine (64 mg, 0.085 mL, 0.45 mmol, 5.0 eq) followed by HATU (59 mg, 0.149 mmol, 1.5 eq). The yellow solution was stirred for 5 minutes, then methylamine hydrochloride (CAS # 593-51-1, 12 mg, 0.18 mmol, 1.8 eq) was added. The reaction mixture was stirred at 23 °C for 6 h. The reaction mixture was quenched with water (5mL) and extracted with ethyl acetate (2 x 10 mL). The organic layers were washed with brine (10 mL), dried over Na2SO4, filtered off and concentrated in vacuo. The crude product was then purified by preparative HPLC (Column: YMC-Triart C18, 12 nm, 5 um, 100 x 30 mm; Condition: ACN / water + 0.1% HCOOH; Gradient: ACN in water, runtime 4.5 min) to afford the title compound (7 mg, 17% yield) as a yellow solid. LCMS: m / z 384.3 [M+H]+, ESI pos. Example 9: (1S,3R)-N-Ethyl-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4-triazin-3- yl]amino]cyclohexanecarboxamide To a solution of 5-yl)-5-methyl-1,2,4-triazin-3- yl]amino]cyclohexanecarboxylic 0.108 mmol, 1.0 eq) and N,N- dimethylformamide, extra dry (0.347 mL) was added at rt, N,N-diisopropylethylamine (70 mg, 0.092 mL, 0.54 mmol, 5.0 eq) followed by HATU (64 mg, 0.162 mmol, 1.5 eq). The yellow solution was stirred for 5 minutes, then ethylamine (2M in MeOH; CAS # 75-04-7, 0.097 mL, 0.195 mmol, 1.8 eq) was added. The reaction mixture was stirred at 23 °C for 15 h. The reaction mixture was quenched with water (2 mL) and extracted with ethyl acetate (2 x 10 mL). The organic layers were washed with brine (5 mL), dried over Na2SO4, filtered off and concentrated in vacuo. The crude product was then purified by preparative HPLC (Column: Phenomenex Gemini NX C18, 12 nm, 5 um, 100 x 30 mm; Condition: ACN / water + 0.1% HCOOH; Gradient: ACN in water, runtime 4.5 min) to afford the title compound (19 mg, 43% yield) as yellow solid. LCMS: m / z 398.4 [M+H]+, ESI pos. Example 10: [(1S,3R)-3-[[6-(4-Hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4-triazin-3- yl]amino]cyclohexyl]-pyrrolidin-1-yl-methanone To a solution of - 5-yl)-5-methyl-1,2,4-triazin-3- yl]amino]cyclohexanecarboxylic acid (Example 1, 40 mg, 0.108 mmol, 1.0 eq) and N,N- dimethylformamide, extra dry (0.347 mL) was added at rt, N,N-diisopropylethylamine (70 mg, 0.092 mL, 0.540 mmol, 5.0 eq) followed by HATU (64 mg, 0.162 mmol, 1.5 eq). The yellow solution was stirred for 5 mins, then pyrrolidine (CAS # 123-75-1, 14 mg, 0.016 mL, 0.195 mmol, 1.8 eq) was added. The reaction mixture was stirred at 23 °C for 15 h. The reaction mixture was quenched with water (2 mL) and extracted with ethyl acetate (2 x 10 mL). The organic layers were washed with brine (5 mL), dried over Na2SO4, filtered off and concentrated in vacuo. The crude product was then purified by preparative HPLC (Column: Phenomenex Gemini NX C18, 12 nm, 5 um, 100 x 30 mm; Condition: ACN / water + 0.1% HCOOH; Gradient: ACN in water, runtime 4.5 min) to afford the title compound (15 mg, 30% yield) as yellow solid. LCMS: m / z 424.4 [M+H]+, ESI pos. Example 11: (1S,3R)-3-[[6-(4-Hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4-triazin-3-yl]amino]-N- isopropyl-cyclohexanecarboxamide To a solution of 5-yl)-5-methyl-1,2,4-triazin-3- yl]amino]cyclohexanecarboxylic acid (example 1, 40 mg, 0.108 mmol, 1.0 eq) and N,N- dimethylformamide, extra dry (0.347 mL) was added at rt, N,N-diisopropylethylamine (70 mg, 0.092 mL, 0.54 mmol, 5.0 eq) followed by HATU (64 mg, 0.162 mmol, 1.5 eq). The yellow solution was stirred for 5 mins, then isopropylamine (CAS # 75-31-0, 11.5 mg, 0.007 mL, 0.195 mmol, 1.8 eq) was added. The reaction mixture was stirred at 23 °C for 15 h. Then, the reaction mixture was quenched with water (2 mL) and extracted with ethyl acetate (2 x 10 mL). The organic layers were washed with brine (5 mL), dried over Na2SO4, filtered off and concentrated in vacuo. The crude product was then purified by preparative HPLC (Column: Phenomenex Gemini NX C18, 12 nm, 5 um, 100 x 30 mm; Condition: ACN / water + 0.1% HCOOH; Gradient: ACN in water, runtime 4.5 min) to afford the title compound (21 mg, 43% yield) as yellow solid. LCMS: m / z 412.5[M+H]+, ESI pos. Example 12: [(1S,3R)-3-[[6-(4-Hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4-triazin-3- yl]amino]cyclohexyl]-morpholino-methanone To a solution of cis-(1S,3R)-3-[[6-(4-hydroxycoumaran-5-yl)-5-methyl-1,2,4-triazin-3- yl]amino]cyclohexanecarboxylic acid (example 1, 40 mg, 108 mmol, 1.0 eq) and N,N- dimethylformamide, extra dry (347.29 uL) was added at rt, N,N-diisopropylethylamine (70 mg, 0.092 mL, 0.540 mmol, 5.0 eq) followed by HATU (64 mg, 0.162 mmol, 1.5 eq). The yellow solution was stirred for 5 minutes, then morpholine (CAS # 110-91-8, 17 mg, 0.017 mL, 0.195 mmol, 1.8 eq) was added. The reaction mixture was stirred at 23 °C for 15 h. The reaction mixture was quenched with water (2 mL) and extracted with ethyl acetate (2 x 10 mL). The organic layers were washed with brine (5 mL), dried over Na2SO4, filtered off and concentrated in vacuo. The crude product was then purified by preparative HPLC (Column: Phenomenex Gemini NX C18, 12 nm, 5 um, 100 x 30 mm; Condition: ACN / water + 0.1% HCOOH; Gradient: ACN in water, runtime 4.5 min) to afford the title compound (13 mg, 27% yield) as yellow solid. LCMS: m / z 440.3[M+H]+, ESI pos. Example 13: (1S,3R)-3-[[6-(4-Hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4-triazin-3-yl]amino]- N,N-dimethyl-cyclohexanecarboxamide To a solution of 5-yl)-5-methyl-1,2,4-triazin-3- yl]amino]cyclohexanecarboxylic acid (example 1, 40 mg, 0.108 mmol, 1.0 eq) and N,N- dimethylformamide, extra dry (0.347 mL) was added at rt, N,N-diisopropylethylamine (70 mg, 0.092 mL, 0.54 mmol, 5.0 eq) followed by HATU (64 mg, 0.162 mmol, 1.5 eq). The yellow solution was stirred for 5 minutes, then dimethylamine (2M in THF; CAS # 124-40-3, 87 mg, 0.097 mL, 0.195 mmol, 1.8 eq) was added. The reaction mixture was stirred at 23 °C for 15 h. Then, the reaction mixture was quenched with water (2 mL) and extracted with ethyl acetate (2 x 10 mL). The organic layers were washed with brine (5 mL), dried over Na2SO4, filtered off and concentrated in vacuo. The crude product was then purified by preparative HPLC (Column: Phenomenex Gemini NX C18, 12 nm, 5 um, 100 x 30 mm; Condition: ACN / water + 0.1% HCOOH; Gradient: ACN in water, runtime 4.5 min) to afford the title compound (22 mg, 50% yield) as yellow solid. LCMS: m / z 398.3 [M+H]+, ESI pos. Example 14: 3-[[6-(4-Hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4-triazin-3-yl]amino]-N-isopropyl- cyclopentanecarboxamide Step A: Benzyl N-[3-(isopropylcar ate To a solution of 3-(benzyloxycarbonylamino)cyclopentanecarboxylic acid (CAS # 1427475-13-5; 0.50 g, 1.9 mmol, 1.0 eq), TBTU (0.85 g, 2.66 mmol, 1.4 eq) and propan-2-amine (0.17 g, 2.85 mmol, 1.5 eq) in DMF (5 mL) was added DIEA (1.56 mL, 9.5 mmol, 5.0 eq). The mixture was stirred at 25 °C for 30 mins. The reaction mixture was then diluted with water (20 mL) and extracted with EtOAc (2 x 10 mL). The combined extracts were washed with brine (20 mL), dried over Na2SO4, filtered and the filtrate was concentrated under reduced pressure. The residue was purified by column chromatography on silica gel (petroleum ether: ethyl acetate =1:0 to 1:1) to give the title compound (430 mg, 73% yield) as a brown solid. LCMS: m / z 305.2 [M+H]+, ESI pos. Step B: 3-Amino-N-isopropyl-cyclopentanecarboxamide A mixture of Pd(OH)2 / C (10% purity on carbon, 31.3 mg), Pd / C (10% purity on carbon, 31.3 mg) and aforementioned benzyl N-[3-(isopropylcarbamoyl)cyclopentyl]carbamate (300.0 mg, 0.99 mmol, 1.0 eq) in methanol (15 mL) was stirred at 20 °C for 1 h under H2(1100 mmHg). The reaction mixture was filtered, the filtrate was concentrated under reduced pressure to give the title compound (230 mg, 96% yield) as a white solid.1H NMR (400 MHz, CD3OD) δ [ppm]: 3.96 - 3.89 (m, 1H), 3.26 - 3.18 (m, 1H), 2.63 (dd, 1H), 2.10 - 1.99 (m, 1H), 1.90 - 1.73 (m, 3H), 1.57 - 1.44 (m, 2H), 1.08 (d, 6H). Step C: 3-[(6-Chloro-5-methyl-1,2,4-triazin-3-yl)amino]-N-isopropyl-cyclopentanecarboxamide To a solution of 3,6-dichloro-5-methyl-1,2,4-triazine (CAS# 132434-82-3, 200.0 mg, 1.22 mmol, 1.0 eq) and DIEA (0.4 mL, 2.44 mmol, 2.0 eq) in 1,4-dioxane (5 mL) was added aforementioned 3-amino- N-isopropyl-cyclopentanecarboxamide (207.6 mg, 1.22 mmol, 1.0 eq). Then the mixture was stirred at 20 °C for 3 h. The reaction mixture was diluted with water (10 mL), and extracted with EtOAc (10 mL x 2). The combined extracts were washed with brine (20 mL), dried over Na2SO4and filtered. The filtrate was concentrated under reduced pressure to give the title compound (220.0 mg, 56% yield) as a brown solid. LCMS: m / z 298.1 [M+H]+, ESI pos. Step D: 3- (4-Hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4-triazin-3-yl]amino]-N- isopropyl- To a solution of aforementioned 3-[(6-chloro-5-methyl-1,2,4-triazin-3-yl)amino]-N-isopropyl- cyclopentanecarboxamide (100.0 mg, 0.34 mmol, 1.0 eq) and 5-(4,4,5,5-tetramethyl-1,3,2- dioxaborolan-2-yl)-2,3-dihydrobenzofuran-4-ol (CAS# 2923540-32-1, 114.4 mg, 0.44 mmol, 1.3 eq), CsF (102.0 mg, 0.67 mmol, 2.0 eq) in 1,4-dioxane (1 mL) and water (0.1 mL) was added XPhos Pd G3 (56.8 mg, 0.07 mmol, 0.2 eq) under N2. Then the mixture was stirred at 95 °C for 9 h under N2. The reaction mixture was filtered, and the filtrate was concentrated under reduced pressure. The residue was purified by prep-HPLC (column: Xtimate C18, 250mm*50mm*10μm; mobile phase: [water (0.1% FA v / v)-MeCN]; B%: 5%-58%, 10 mins) to afford the title compound (43.4 mg, 30% yield) as a yellow solid. LCMS: m / z 398.2 [M+H]+, ESI pos. Example 15: (3-Hydroxyazetidin-1-yl)-[(1S,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl- 1,2,4-triazin-3-yl]amino]cyclohexyl]methanone;2,2,2-trifluoroacetic acid Step A: Tert-butyl N-[(1R,3S)- carbamate To a solution of (1S,3R)-3-(BOC-amino)cyclohexane-1-carboxylic acid (CAS # 222530-34-9, 200.0 mg, 0.82 mmol, 1.0 eq), DIEA (0.27 mL, 1.64 mmol, 2.0 eq) and HATU (468.9 mg, 1.23 mmol, 1.5 eq) in DMF (2 mL) was added azetidin-3-ol (72.1 mg, 0.99 mmol, 1.2 eq). The reaction mixture was stirred at 25 °C for 1 h. Upon reaction completion, the reaction mixture was diluted with water (5 mL), and extracted with ethyl acetate (30 mL x 6). The combined extracts were washed with brine (20 mL x 2), dried over Na2SO4, filtered, and the filtrate was concentrated in vacuum. The residue was purified by column chromatography on silica gel (ethyl acetate: methanol = 1:0 to 10:1) to afford the title compound (150.0 mg, 37% yield) as colorless oil.1H NMR (400 MHz, CD3OD) δ [ppm]: 4.56 (m, 1H), 4.52 - 4.38 (m, 1H), 4.21 - 4.10 (m, 1H), 1H), 3.77 - 3.71 (m, 1H), 3.23 (m, 2H), 2.37 (m, 2H), 1.91 - 1.80 (m, 3H), 1.72 - 1.62 (m, 1H), 1.43 (s, 9H), 1.27 - 1.20 (m, 1H), 1.18 - 1.08 (m, 1H). Step B: [(1S,3R)-3-Aminocyclohexyl]-(3-hydroxyazetidin-1-yl)methanone A mixture of tert-butyl N-[(1R,3S)-3-(3-hydroxyazetidine-1-carbonyl)cyclohexyl]carbamate (150.0 mg, 0.5 mmol, 1.0 eq) in HCl / dioxane (2M, 1.5 mL) was stirred at 25 °C for 1 h. Upon reaction completion, the reaction mixture was concentrated in vacuum to afford the title compound (HCl salt, 120.0 mg, 71% yield) as yellow oil.1H NMR (400 MHz, CD3OD) δ [ppm]: 4.59 (m, 1H), 4.45 (m, 1H), 4.24 - 4.12 (m, 1H), 4.06 - 3.95 (m, 1H), 3.79 - 3.73 (m, 2H), 3.22 - 3.10 (m, 2H), 2.48 (m, 1H), 2.13 - 1.86 (m, 3H), 1.78 (m, 1H), 1.34 - 1.25 (m, 2H). Step C: [(1S,3R)-3-[(6-Chloro-5-methyl-1,2,4-triazin-3-yl)amino]cyclohexyl]-(3-hydroxyazetidin-1- yl)methanone To a solution of aforementioned [(1S,3R)-3-aminocyclohexyl]-(3-hydroxyazetidin-1-yl)methanone (HCl salt, 107.4 mg, 0.46 mmol, 1.5 eq), DIEA (157.3 mg, 1.22 mmol, 4.0 eq) in DMF (1 mL) was added 3,6-dichloro-5-methyl-1,2,4-triazine (50.0 mg, 0.3 mmol, 1.0 eq). The reaction mixture was stirred at 25 °C for 1 h. Upon reaction completion, the reaction mixture was diluted with water (5 mL), and extracted with ethyl acetate (3 x 30 mL). The combined extracts were washed with brine (60 mL), dried over Na2SO4, filtered, and the filtrate was concentrated in vacuum. The residue was purified by column chromatography on silica gel (ethyl acetate: methanol = 1:0 to 10:1) to afford the title compound (60.0 mg, 48% yield) as green oil. LCMS: m / z 326.0 [M+H]+, ESI pos. Step D: (3-Hydroxyazetidin-1-yl)-[(1S,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl- 1,2,4-triazin-3-yl]amino]cyclohexyl]methanone;2,2,2-trifluoroacetic acid To a solution of [(1S,3R)-3-[(6-chloro-5-methyl-1,2,4-triazin-3-yl)amino]cyclohexyl]-(3- hydroxyazetidin-1-yl)methanone (40.0 mg, 0.12 mmol, 1.0 eq) and 5-(4,4,5,5-tetramethyl-1,3,2- dioxaborolan-2-yl)-2,3-dihydrobenzofuran-4-ol (41.8 mg, 0.16 mmol, 1.3 eq), CsF (37.3 mg, 0.25 mmol, 2.0 eq) in 1,4-dioxane (1 mL) and water (0.2 mL) was added XPhos Pd G3 (20.8 mg, 0.02 mmol, 0.2 eq) under N2. The mixture was stirred at 95 °C for 2 h under N2. Upon reaction completion, the reaction mixture was cooled to room temperature and concentrated in vacuum. The residue was purified by prep-HPLC (column: Phenomenex Gemini, 150 mm*30mm*15µm; mobile phase: [water (0.1% TFA, V / V)-MeCN]; B%: 0%-30%, 10 minutes) to afford the title compound (36.1 mg, 68% yield) as a yellow solid. LCMS: m / z 426.1 [M+H]+, ESI pos. Example 16: (1R,3R)-3-[[6-(4-Hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4-triazin-3- yl]amino]cyclohexanecarboxylic acid Step A: Methyl (1R,3R)-3-[(6-chlo -yl)amino]cyclohexanecarboxylate To a solution of methyl (1R,3R)-3-aminocyclohexane-1-carboxylate (CAS # 1821656-06-7; 0.8 g, 4.13 mmol, 1.0 DIEA (2.0 mL, 12.39 mmol, 3.0 eq) in DMF (10 mL) was added 3,6-dichloro- 5-methyl-1,2,4-triazine (0.81 g, 4.96 mmol, 1.2 eq) and the mixture was stirred at 25 °C for 12 h. Upon reaction completion, the mixture was diluted with water (80 mL), and extracted with ethyl acetate (3 x 100 mL). The combined organic phases were washed with brine (100 mL), dried over anhydrous sodium sulfate, filtered and the filtrate was concentrated under reduced pressure. The residue was purified by column chromatography on silica gel (petroleum ether: ethyl acetate = 1:0 to 0:1) to afford the title compound (740 mg, 62% yield) as yellow oil. LCMS: m / z 285.1 [M+H]+, ESI pos. Step B: Methyl (1R,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4-triazin-3- yl]amino]cyclohexanecarboxylate To a solution of aforementioned methyl (1R,3R)-3-[(6-chloro-5-methyl-1,2,4-triazin-3- yl)amino]cyclo-hexanecarboxylate (300.0 mg, 1.05 mmol, 1.0 eq), 5-(4,4,5,5-tetramethyl-1,3,2- dioxaborolan-2-yl)-2,3-dihydrobenzofuran-4-ol (359.0 mg, 1.37 mmol, 1.3 eq) and CsF (320.1 mg, 2.11 mmol, 2.0 eq) in 1,4-dioxane (3 mL) and water (0.6 mL) was added XPhos Pd G3 (178.5 mg, 0.21 mmol, 0.2 eq) under N2. The mixture was stirred at 95 °C for 2 h under N2. Upon reaction completion, the mixture was cooled to rt, diluted with water (50 mL) and extracted with ethyl acetate (3 x 50 mL). The combined organic phases were washed with brine (50 mL), dried over anhydrous sodium sulfate, filtered and the filtrate was concentrated under reduced pressure. The residue was purified by column chromatography on silica gel (petroleum ether: ethyl acetate = 1:0 to 3:1) to afford the title compound (120 mg, 21% yield) as a yellow solid. LCMS: m / z 385.3 [M+H]+, ESI pos. Step C: (1R,3R)-3-[[6-(4-Hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4-triazin-3- yl]amino] acid To a solution of aforementioned methyl (1R,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5- methyl-1,2,4-triazin-3-yl]amino]cyclohexanecarboxylate (150.0 mg, 0.39 mmol, 1.0 eq) in THF (2 mL) and water (0.4 mL) was added LiOH•H2O (81.9 mg, 1.95 mmol, 5.0 eq). The mixture was stirred at 25 °C for 2 h. Upon reaction completion, the reaction mixture was concentrated in vacuum. The residue was purified by reversed phase flash (column: Phenomenex Gemini, 150mm*30mm*15µm; mobile phase: [water (0.1% TFA, V / V)-MeCN]; B%: 20%-50%, 12 mins), to afford the title compound (140.0 mg, 63% yield) as a yellow solid. LCMS: m / z 371.1 [M+H]+, ESI pos. Example 17 (3-Hydroxyazetidin-1-yl)-[(1R,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl- 1,2,4-triazin-3-yl]amino]cyclohexyl]methanone;2,2,2-trifluoroacetic acid To a solution of 5-yl)-5-methyl- 1,2,4-triazin-3-yl]amino]cyclohexanecarboxylic acid (example 16, 45.0 mg, 0.09 mmol, 1.0 eq), DIEA (0.06 mL, 0.37 mmol, 4.0 eq) and HATU (52.9 mg, 0.14 mmol, 1.5 eq) in DMF (0.5 mL) was added azetidin-3-ol (8.1 mg, 0.11 mmol, 1.2 eq). The reaction mixture was stirred at 25 °C for 1 h. Upon reaction completion, the mixture was purified by prep-HPLC (column: Phenomenex luna C18, 150mm*25mm*10µm; mobile phase: [water (0.1% TFA, V / V)-ACN]; B%: 0%-28%, 10 mins) to afford the title compound (10.2 mg, 19% yield) as a yellow solid. LCMS: m / z 426.2 [M+H]+, ESI pos. Example 18: Azetidin-1-yl-[(1S,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4-triazin-3- yl]amino]cyclohexyl]methanone To a solution of aforementioned - dihydrobenzofuran-5-yl)-5-methyl- 1,2,4-triazin-3-yl]amino]cyclohexanecarboxylic acid (example 16, 25.0 mg, 0.05 mmol, 1.0 eq; Example 1, step D), DIEA (0.03 mL, 0.21 mmol, 4.0 eq) and HATU (29.4 mg, 0.08 mmol, 1.5 eq) in DMF (0.5 mL) was added azetidine (3.5 mg, 0.06 mmol, 1.2 eq). The reaction mixture was stirred at 25 °C for 1 h. Upon reaction completion, the reaction mixture was purified by prep-HPLC (Column Waters Xbridge, 150mm*25mm*5µm; mobile phase: [water (0.1% NH4HCO3, V / V)-MeCN]; B%: 22%-52%, 9 mins) to afford the title compound (14.3 mg, 67% yield) as a yellow solid. LCMS: m / z 410.3 [M+H]+, ESI pos. Example 19 Azetidin-1-yl-[(1R,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4-triazin-3- yl]amino]cyclohexyl]methanone;2,2,2-trifluoroacetic acid To a solution of 5-yl)-5-methyl- 1,2,4-triazin-3-yl]amino]cyclohexanecarboxylic acid (example 16, 35.0 mg, 0.07 mmol, 1.0 eq), DIEA (0.05 mL, 0.29 mmol, 4.0 eq) and HATU (41.2 mg, 0.11 mmol, 1.5 eq) in DMF (0.5 mL) was added azetidine (5.0 mg, 0.09 mmol, 1.2 eq). The reaction mixture was stirred at 25 °C for 1 h. Upon reaction completion, the mixture was purified by prep-HPLC (column: Phenomenex luna C18, 150mm*25mm*10µm; mobile phase: [water (0.1% TFA, V / V)-MeCN]; B%: 8%-38%, 10 mins) to afford the title compound (22.0 mg, 57% yield) as a yellow solid. LCMS: m / z 410.2 [M+H]+, ESI pos. Example 20 (1R,3R)-3-[[6-(4-Hydroxyindan-5-yl)-5-methyl-1,2,4-triazin-3-yl]amino]-N-isopropyl- cyclohexanecarboxamide;2,2,2-trifluoroacetic acid Step A: tert-Butyl N-[ - To solution of -3-(tert-butoxycarbonylamino)cyclohexanecarboxylic acid (CAS # 218772-92-0; 500.0 mg, 2.06 mmol, 1.0 eq), DIEA (0.68 mL, 4.11 mmol, 2.0 eq) and HATU (1172.1 mg, 3.08 mmol, 1.5 eq) in DMF (10 mL) was added propan-2-amine (145.7 mg, 2.47 mmol, 1.2 eq). The mixture was stirred at 25 °C for 1 h under N2. The reaction mixture was quenched with water (10 mL) at 25 °C, and extracted with EtOAc (3 x 50 m). The combined organic layers were washed with brine (3 x 50 mL), dried over Na2SO4, filtered and the filtrate was concentrated under reduced pressure. The residue was purified by column chromatography on silica gel (petroleum ether: ethyl acetate = 1:0 to 1:1) to afford the title compound (580.0 mg, 99% yield) as a white solid.1H NMR (400 MHz, DMSO-d6) δ [ppm]: 7.36 (d, 1H), 6.53 (d, 1H), 3.82 - 3.77 (m, 1H), 3.68 - 3.66 (m, 1H), 2.36 - 2.33 (m, 1H), 1.59 - 1.52 (m, 1H), 1.46-1.48 (m, 6H), 1.38 (s, 9H), 1.36 - 1.32 (m, 1H), 1.02 (d, 6H). Step B: (1R,3R)-3-Amino-N-isopropyl-cyclohexanecarboxamide A mixture of aforementioned tert-butyl N-[(1R,3R)-3-(isopropylcarbamoyl)cyclohexyl]carbamate (200.0 mg, 0.7 mmol, 1.0 eq) in HCl / dioxane (2.5 mL, 2M) was stirred at 25 °C for 1 h. The mixture was concentrated under reduced pressure to give the title compound (120.0 mg, 93% yield, HCl salt) as a white solid.1H NMR (400 MHz, DMSO-d6) δ [ppm]: 8.01 (s, 2H), 7.68 (d, 1H), 3.87 (m, 1H), 3.49 - 3.58 (m, 1H), 1.92 - 2.07 (m, 1H), 1.77 - 1.90 (m, 1H), 1.38 - 1.76 (m, 7H), 1.02 - 1.11 (m, 6H). Step C: (1R,3R)-3-[(6-Chloro-5-methyl-1,2,4-triazin-3-yl)amino]-N-isopropyl- cyclohexanecarboxamide A mixture of (1R,3R)-3-amino-N-isopropyl-cyclohexanecarboxamide (120.0 mg, 0.66 mmol, 1.0 eq) in DMF (4 mL) was added DIEA (252 mg, 1.96 mmol, 3.0 eq) and 3,6-dichloro-5-methyl-1,2,4- triazine (CAS # 132434-82-3, 135 mg, 0.78 mmol, 1.2 eq). Then the mixture was stirred at 25 °C for 1 h. The reaction mixture was diluted with water (50 mL) and extracted with EtOAc (3 x 50 mL). The combined organic layers were washed with brine (3 x 50 mL), dried over Na2SO4, filtered and the filtrate was concentrated under reduced pressure. The residue was purified by column chromatography on silica gel (petroleum ether: ethyl acetate = 1:0 to 1:1) to give the title compound (154.0 mg, 91% yield) as a yellow solid.1H NMR (400 MHz, DMSO-d6) δ [ppm]: 7.57 (s, 1H), 7.41(s, 1H), 3.83 - 3.78 (m, 1H), 2.47 - 2.42 (m, 1H), 2.36 (s, 3H), 1.74 - 1.71 (m, 2H), 1.61 - 1.52 (m, 6H), 1.48 - 1.35 (m, 1H), 1.02 (dd, 6H). Step D: (1R,3R)-3-[[6-(4-Hydroxyindan-5-yl)-5-methyl-1,2,4-triazin-3-yl]amino]-N-isopropyl- trifluoroacetic acid To a solution of aforementioned (1R,3R)-3-[(6-chloro-5-methyl-1,2,4-triazin-3-yl)amino]-N- isopropyl-cyclohexanecarboxamide (50.0 mg, 0.16 mmol, 1.0 eq) and 5-(4,4,5,5-tetramethyl-1,3,2- dioxaborolan-2-yl)indan-4-ol (CAS # 2795101-92-5; 54.2 mg, 0.21 mmol, 1.3 eq) in 1,4-dioxane (1 mL) and water (0.1 mL) was added CsF (48.7 mg, 0.32 mmol, 2.0 eq) and XPhos Pd G3 (27.1 mg, 0.03 mmol, 0.2 eq) under N2. Then the mixture was stirred at 95 °C for 2 h under N2 atmosphere. Upon reaction completion, the mixture was cooled to 20 °C and concentrated under reduced pressure. The residue was purified by prep-HPLC (column: Phenomenex Gemini, 150mm*30mm*15µm; mobile phase: [water (0.1% TFA, V / V)-MeCN]; B%: 22%-53%, 10 mins) to afford the title compound (27.4 mg, 32% yield) as a white solid. LCMS: m / z 410.2 [M+H]+, ESI pos. Example 21: (1S,3R)-3-[[6-(4-Hydroxyindan-5-yl)-5-methyl-1,2,4-triazin-3-yl]amino]-N-isopropyl- cyclohexanecarboxamide;2,2,2-trifluoroacetic acid Step A: tert-Butyl N-[ To a mixture of propan-2-amine (145.7 mg, 2.47 mmol, 1.2 eq), (1S,3R)-3-(BOC-amino)cyclohexane- 1-carboxylic acid (CAS # 222530-34-9; 500.0 mg, 2.06 mmol, 1.0 eq) and HATU (937.1 mg, 2.47 mmol, 1.2 eq) in DMF (10 mL) was added DIEA (530.2 mg, 4.11 mmol, 2.0 eq) and the reaction mixture was stirred at 25 °C for 1 h. Then, the reaction mixture was poured into 10 mL of water. A white solid precipitate was formed and the mixture was filtered, the filter cake was collected and dried to give the title compound (500.0 mg, 86% yield) as a white solid.1H NMR (400 MHz, DMSO-d6) δ [ppm]: 7.56 (d, 1H), 6.76 (d, 1H), 3.80 - 3.73 (m, 1H), 3.21 - 3.16 (m, 1H), 2.11 - 2.05 (m, 1H), 1.73 - 1.71 (m, 3H), 1.57 - 1.55 (m, 1H), 1.37 (s, 9H), 1.25 - 1.14 (m, 4H), 1.01 (d, 6H). Step B: (1S,3R)-3-Amino-N-isopropyl-cyclohexanecarboxamide A mixture of aforementioned tert-butyl N-[(1R,3S)-3-(isopropylcarbamoyl)cyclohexyl]carbamate (500.0 mg, 1.76 mmol, 1.0 eq) in HCl / dioxane (6 mL, 2M) was stirred at 25 °C for 1 h. The mixture was concentrated in vacuum and dried to give the title compound (450.0 mg, quant., HCl salt) as a white solid.1H NMR (400 MHz, CD3OD) δ [ppm]: 3.85 - 3.80 (m, 1H), 3.51 - 3.45 (m, 1H), 1.98 - 1.94 (m, 1H), 1.80 - 1.76 (m, 1H), 1.65 - 1.56 (m, 2H), 1.54 - 1.49 (m, 4H), 1.48 - 1.35 (m, 1H), 1.03 (dd, 6H). Step C: (1S,3R)-3-[(6-Chloro-5-methyl-1,2,4-triazin-3-yl)amino]-N-isopropyl- cyclohexanecarboxamide To a mixture of 3,6-dichloro-5-methyl-1,2,4-triazine (CAS # 132434-82-3, 200.0 mg, 1.22 mmol, 1.0 eq) and DIEA (530.2 mg, 4.11 mmol, 2.0 eq) in DMF (4 mL) was added aforementioned (1S,3R)-3- amino-N-isopropyl-cyclohexanecarboxamide (337.1 mg, 1.83 mmol, 1.5 eq) and the mixture was stirred at 25 °C for 1 h. Afterwards, the reaction mixture was quenched with water (50 mL) and extracted with EtOAc (3 x 50 mL). The combined organic layers were washed with brine (3 x 50 mL), dried over Na2SO4, filtered and the filtrate was concentrated under reduced pressure. The residue was purified by column chromatography on silica gel (petroleum ether: ethyl acetate = 1:0 to 1:1) to give the title compound (190.0 mg, 50% yield) as a yellow solid. LCMS: m / z 312.2 [M+H]+, ESI pos. Step D: (1S,3R)-3-[[6-(4-Hydroxyindan-5-yl)-5-methyl-1,2,4-triazin-3-yl]amino]-N-isopropyl- trifluoroacetic acid To a mixture of (1S,3R)-3-[(6-chloro-5-methyl-1,2,4-triazin-3-yl)amino]-N- isopropyl-cyclohexanecarboxamide (50.0 mg, 0.16 mmol, 1.0 eq) and 5-(4,4,5,5-tetramethyl-1,3,2- dioxaborolan-2-yl)indan-4-ol (CAS # 2795101-92-5; 54.23 mg, 0.21 mmol, 1.3 eq) in 1,4-dioxane (1 mL) and water (0.1 mL) was added CsF (48.7 mg, 0.32 mmol, 2.0 eq) and Xphos Pd G3 (27.1 mg, 0.03 mmol, 0.2 eq) under N2. Then the mixture was stirred at 95 °C for 2 h under N2. Upon reaction completion, the mixture was cooled to 20 °C and concentrated in vacuum. The residue was purified by prep-HPLC (column: Phenomenex Gemini, 150mm*25mm*10µm; mobile phase: [water (0.1% TFA, V / V)-MeCN]; B%: 22%-52%, 12 mins) to afford the title compound (16.1 mg, 19% yield) as a yellow solid. LCMS: m / z 410.4 [M+H]+, ESI pos. Example 22 [(1R,3R)-3-[[6-(4-Hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4-triazin-3- yl]amino]cyclohexyl]-morpholino-methanone;2,2,2-trifluoroacetic acid To a solution of - 5-yl)-5-methyl- 1,2,4-triazin-3-yl]amino]cyclohexanecarboxylic acid (example 16, 40.0 mg, 0.08 mmol, 1.0 eq), DIEA (0.05 mL, 0.33 mmol, 4.0 eq) and HATU (47.1 mg, 0.12 mmol, 1.5 eq) in DMF (0.5 mL) was added morpholine (CAS # 110-91-8, 8.6 mg, 0.1 mmol, 1.2 eq). The reaction mixture was stirred at 25 °C for 1 h. Upon reaction completion, the mixture was purified by prep-HPLC (column: Phenomenex luna C18, 150mm*25mm*10µm; mobile phase: [water (0.1% TFA, V / V)-MeCN]; B%: 5%-35%, 10 mins) to afford the title compound (10.2 mg, 22% yield) as a yellow solid. LCMS: m / z 440.2 [M+H]+, ESI pos. Example 23 (1S,3R)-3-[[6-(4-Hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4-triazin-3-yl]amino]-N- (2-hydroxy-2-methyl-propyl)cyclohexanecarboxamide To a solution of - dihydrobenzofuran-5-yl)-5-methyl- 1,2,4-triazin-3-yl]amino]cyclohexanecarboxylic acid (example 1, 50 mg, 0.121 mmol, 1.0 eq) and N,N-dimethylformamide (0.70 mL) was added at rt N,N-diisopropylethylamine (78.5 mg, 0.103 mL, 0.607 mmol, 5.0 eq) followed by HATU (71.4 mg, 0.182 mmol, 1.50 eq). The yellow solution was stirred at 23 °C for 5 mins, then 1-amino-2-methyl-propan-2-ol (17.3 mg, 0.017 mL, 0.194 mmol, 1.600 eq) was added. The reaction mixture was stirred at 23 °C for 16 h. The reaction mixture was quenched with water (5 mL) and extracted with ethyl acetate (2 x 20 mL). The organic layers were washed with brine (20 mL), dried over Na2SO4, filtered off and concentrated in vacuo. The crude product was purified by flash chromatography on silica gel (gradient 0% to 10% methanol in ethyl acetate) followed by preparative HPLC (column: Phenomenex Gemini NX C18, 12 nm, 5 µm, 100 x 30 mm; elution: 50% to 100% water / acetonitrile + 0.1% formic acid) to afford the title compound (21 mg, 37%) as a light yellow amorphous freeze-dried solid. LCMS: m / z 442.4 [M+H]+, ESI pos. Example 24 (1S,3R)-3-[[6-(4-Hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4-triazin-3-yl]amino]-N- (2-imidazol-1-ylethyl)cyclohexanecarboxamide To a solution of aforementioned (1S,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl- 1,2,4-triazin-3-yl]amino]cyclohexanecarboxylic acid (example 1, 50 mg, 0.121 mmol, 1.0 eq) and N,N-dimethylformamide (0.70 mL) was added at rt, N,N-diisopropylethylamine (94.2 mg, 0.123 mL, 0.729 mmol, 6.00 eq) followed by HATU (71.4 mg, 0.182 mmol, 1.50 eq). The yellow solution was stirred at 23 °C for 5 mins, then 2-imidazol-1-ylethylamine-dihydrochloride (40.3 mg, 0.218 mmol, 1.800 eq) was added. The reaction mixture was stirred at 23 °C for 16 h. The reaction mixture was quenched with water (5 mL) and extracted with ethyl acetate (2 x 20 mL). The organic layers were washed with brine (20 mL), dried over Na2SO4, filtered off and concentrated in vacuo. The residue was purified by reversed-phase chromatography (RP C18; 0% to 40% acetonitrile in water) to afford the title compound (17 mg, 28%) as a light yellow amorph freeze-dried solid. LCMS: m / z 464.3 [M+H]+, ESI pos. Example 25 (1S,3R)-N-[(1S,2R)-2-hydroxycyclopentyl]-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5- methyl-1,2,4-triazin-3-yl]amino]cyclohexanecarboxamide To a solution of dihydrobenzofuran-5-yl)-5-methyl- 1,2,4-triazin-3-yl]amino]cyclohexanecarboxylic acid (example 1, 44 mg, 0.106 mmol, 1.00 eq) and N,N-dimethylformamide (0.70 mL) was added at rt, N,N-diisopropylethylamine (82.9 mg, 0.109 mL, 0.641 mmol, 6.00 eq) followed by HATU (62.9 mg, 0.160 mmol, 1.50 eq). The yellow solution was stirred at 23 °C for 5 min, then (1S,2R)-2-aminocyclopentanolhydrochloride (26.5 mg, 0.192 mmol, 1.80 eq) was added. The reaction mixture was stirred at 23 °C for 16 h. The reaction mixture was quenched with water (5 mL) and extracted with ethyl acetate (2 x 20 mL). The organic layers were washed with brine (20 mL), dried over Na2SO4, filtered off and concentrated in vacuo. The residue was purified by reversed-phase chromatography (RP C18; 0% to 40% acetonitrile in water) to afford the title compound (11 mg, 22%) as a light yellow amorphous freeze-dried solid. LCMS: m / z 454.3 [M+H]+, ESI pos. BIOLOGICAL ASSAYS NLRP3 and Pyroptosis It is well established that the activation of NLRP3 leads to cell pyroptosis and this feature plays an important part in the manifestation of clinical disease (Yan-gang Liu et al., Cell Death & Disease, 2017, 8(2), e2579; Alexander Wree et al., Hepatology, 2014, 59(3), 898-910; Alex Baldwin et al., Journal of Medicinal Chemistry, 2016, 59(5), 1691-1710; Ema Ozaki et al., Journal of Inflammation Research, 2015, 8, 15-27; Zhen Xie & Gang Zhao, Neuroimmunology Neuroinflammation, 2014, 1(2), 60-65; Mattia Cocco et al., Journal of Medicinal Chemistry, 2014, 57(24), 10366-10382; T. Satoh et al., Cell Death & Disease, 2013, 4, e644). Therefore, itis anticipated that inhibitors of NLRP3 will block pyroptosis, as well as the release of pro -inflammatory cytokines (e.g. IL-1β) from the cell. THP-1 Cells: Culture and Preparation THP-1 cells (ATCC # TIB-202) were grown in RPMI containing L-glutamine (Gibco #11835) supplemented with 1mM sodium pyruvate (Sigma # S8636) and penicillin (100units / ml) / streptomycin (0.1mg / ml) (Sigma # P4333) in 10% Fetal Bovine Serum (FBS)(Sigma # F0804). The cells were routinely passaged and grown to confluency (~106cells / ml).On the day of the experiment, THP-1 cells were harvested and resuspended into RPMI medium (without FBS). The cells were then counted and viability (>90%) checked by Trypan blue (Sigma # T8154). Appropriate dilutions were made to give a concentration of 625,000cells / ml. To this diluted cell solution was added LPS (Sigma # L4524) to give a 1µg / ml Final Assay Concentration (FAC). 40µl of the final preparation was aliquoted into each well of a 96-well plate. The plate thus prepared was used for compound screening. THP-1 Cells Pyroptosis Assay The following method step-by-step assay was followed for compound screening. Seed THP-1 cells (25,000cells / well) containing 1.0µg / ml LPS in 40µl of RPMI medium (without FBS) in 96-well, black walled, clear bottom cell culture plates coated with poly-D- lysine (VWR # 734-0317) Add 5µl compound (8 points half-log dilution, with 10µM top dose) or vehicle (DMSO 0.1% FAC) to the appropriate wells Incubate for 3 hours at 37 °C, 5% CO2Add 5µl nigericin (Sigma # N7143) (FAC 5µM) to all wells Incubate for 1hr at 37°C, 5% CO2 At the end of the incubation period, spin plates at 300xg for 3mins and remove supernatant Then add 50µl of resazurin (Sigma # R7017) (FAC 100 µM resazurin in RPMI medium without FBS) and incubate plates for a further 1-2 hours at 37 °C and 5% CO2Plates were read in an Envision reader at Ex 560nm and Em 590nm IC50 data is fitted to a non-linear regression equation (log inhibitor vs response-variable slope 4-parameters) The results of the pyroptosis assay are summarised in Table 1 below as THP IC50. Human Whole Blood IL-1β Release Assay For systemic delivery, the ability to inhibit NLRP3 when the compounds are present within the bloodstream is of great importance. For this reason, the NLRP3 inhibitory activity ofa number of compounds in human whole blood was investigated in accordance wi th thefollowing protocol. Human whole blood in Li-heparin tubes was obtained from healthy donors from a volunteer donor panel. Plate out 80µl of whole blood containing 1µg / ml of LPS in 96-well, clear bottom cell culture plate (Corning # 3585) Add 10µl compound (8 points half-log dilution with 10µM top dose) or vehicle (DMSO 0.1% FAC) to the appropriate wells Incubate for 3 hours at 37 °C, 5% CO2 Add 10µl nigericin (Sigma # N7143) (10µM FAC) to all wells Incubate for 1hr at 37°C, 5% CO2 At the end of the incubation period, spin plates at 300xg for 5mins to pellet cells and remove 20µl of supernatant and add to 96-well v-bottom plates for IL-1β analysis (note: these plates containing the supernatants can be stored at -80°C to be analysed at a later date) IL-1β was measured according to the manufacturer protocol (Perkin Elmer-AlphaLisa IL-1 Kit AL220F-5000) IC50 data is fitted to a non-linear regression equation (log inhibitor vs response-variable slope 4-parameters) The results of the human whole blood assay are summarised in Table 1 below as HWB IC50. Microsomal Stability: Incubations of test compounds at 1 µM in microsomes (0.5 mg / mL) plus cofactor NADPH are performed in 96 well plates at 37°C on a TECAN (Tecan Group Ltd, Switzerland) automated liquid handling system. After a 10 minutes pre-incubation step of the test compound with the microsomes, the enzymatic reaction is started by the addition of cofactors. At 1, 3, 6, 9, 15, 25, 35 and 45 minutes, aliquots of the incubations are removed and quenched with 1:3 (v / v) acetonitrile containing internal standard. Samples are then cooled and centrifuged before analysis of the supernatant by LC-MS / MS 2. Metabolic Stability in Hepatocytes: Assay descriptions: Biological materials. Cryopreserved hepatocytes [mouse, rat, rabbit, monkey and human (male and female; mixed)] are obtained. Viability of hepatocytes after reconstitution is at least 80% throughout the study. Ready-to-use rat / human HepatoPac® cultures [long-term hepatocyte co-cultures; pooled (n=5 for male and n=5 for female for human)] with stromal mouse fibroblasts (negative control; pooled) with the plates for incubations, application medium and maintenance medium are acquired. Metabolism by suspended hepatocytes. Primary pooled cryopreserved hepatocytes are reconstituted in pre-warmed William’s E media containing 10% FCS, 0.05 mg / mL streptomycin and 50 U / mL penicillin and 0.4 mM L-glutamine; and 0.01 mg / mL gentamicin, 0.048 mg / mL hydrocortisone and 0.004 mg / mL insulin, to a final suspension density of 1×106 cells / mL. The incubation was performed fully automatically with Liquid Handling System (Tecan) equipped with a CO2 incubator with an orbital shaker. After the addition of a test compound at e.g.1 µM to the wells (1×105 cells / well), the 96-well hepatocyte suspension culture plates are incubated in a 5% CO2 at 37°C. Samples are quenched by addition of acetonitrile (including an internal standard) to the incubation well at the designated time points up to 2 h. Metabolism by HepatoPac®. Incubations for a test article (at e.g.1 µM, 0.1% v / v DMSO) as conducted in suspension assays are performed in 96-well plates containing either a co-culture of adherent hepatocytes with mouse fibroblast control cells or control cells alone (5% CO2 atmosphere and 37°C). The incubation media in human HepatoPac® is identical with that in suspended hepatocytes. At defined time points (2, 18, 26, 48, 72 and 96 h), whole wells are quenched with ice-cold acetonitrile containing an internal standard. Samples are then centrifuged appropriately and the supernatant analyzed by LC-MS / MS. The incubation is conducted in n=1 or 2. hERG screening assay In the drug development process of small molecules, one of the most frequent adverse side effects, leading to the failure of drugs, is the cardiac arrhythmias. Such failure is often related to the capacity of the drug to inhibit the human ether-à-go-go-related gene (hERG) cardiac potassium channel. Having no or low inhibition of the hERG cardiac potassium channel is therefore considered as beneficial. Cells The CHO crelox hERG cell line (ATCC reference Nr. PTA-6812, female Chinese hamster cells) was generated and validated at Roche. Ready-to-use frozen instant CHO-hERGcells were cryopreserved at Evotec (Germany) and used directly in the experiments.Experimental solutions The extracellular solution contains (in mM): NaCl 150; KCl 4; CaCl21; MgCl21; HEPES 10; pH 7.2-7.4 with NaOH, osmolarity 290-330 mOsm. The internal solution contains (in mM): KCl, 10; KF, 100; NaCl, 10; HEPES, 10; EGTA, 20; pH = 7.0-7.4 with KOH, osmolarity 260-300 mOsm. Electrophysiology The effects of a compound on hERG K+-currents parameters will be evaluated at 2 concentrations in at least 4 cells. The hERG test is performed using automated patch clamp system SynchroPatch® 384 (Nanion Technologies GmbH, Germany). K+ currents are measured with the patch-voltage- clamp technique in the whole-cell configuration at 35-37°C. Cells were held at a resting voltage of -80 mV and they were stimulated by a voltage pattern shown in Figure 1 (pulse pattern used to elicit outward K+current at 35-37°C) to activate hERG channels and conduct outward IKhERG current, at a stimulation frequency of 0.1 Hz (6 bpm) Data analysis The amplitudes of IKhERG were recorded in each concentration of drug and they were compared to the vehicle control values (taken as 100%) to define fractional blocks. The concentration-response data were fitted with the following relationship: where C is the concentration, IC50is the concentration producing 50% block h is the Hill coefficient. Concentration-response curves were fitted by non-linear regression analysis using EworkBook suite (ID Business Solutions Ltd, UK). Data fit was done with the 4 ParameterLogistic Model (fit = (A+(B / (1+((x / C)^D)))), where A=0 and B=100).The results of the hERG assay are summarised in Table 2 below as hERG IC 20.Transcellular P-gp Assay: The general assay uses transfected LLC-PK1 cells (porcine kidney epithelial cells) over- expressing human or mouse P-gp, cultured on 96 well semi-permeable filter membrane plates, where they form a polarized monolayer with tight junctions, and act as a barrier between the apical and basolateral compartment. P-gp is expressed in the apical-facing membrane of the monolayer. The tightness of the cell monolayer and functional activity of P-gp are confirmed by addition of a cell-impermeable marker, Lucifer yellow, and a reference P-gp substrate, edoxaban, respectively. J. Pharmacol. Exp Ther., 2021, 376, 322–329. PAMPA: PAMPA (Parallel Artificial Membrane Permeability Assay) is a first line permeability screen for drug candidates. The PAMPA assay mimics the transcellular absorption conditions using an artificial phospholipid membrane. This assay determines a permeability value that can be used for compound optimization and ranking purposes as well as input parameters for in silico models to predict intestinal absorption. The donor concentration is measured at t-start (reference) and compared with the donor and acceptor concentration after a certain time (t-end) to calculate the extent of passage of the compound through the membrane. Bacterial Reverse Mutation Test (AMES): The testing of compounds is conducted as outlined in this guideline: Test No. 471:Bacterial Reverse Mutation Test | OECD Guidelines for the Testing of Chemicals, Section 4 : Health Effects | OECD iLibrary (oecd-ilibrary.org) Bacteria culture: The bacterial strains used are TA98, TA100, TA1535, TA97a and TA102. Batches of each strain, are maintained as frozen stocks. Vials are thawed and used to inoculate cultures in nutrientbroth. The cultures are placed in an incubator set to 37°C with agitat ion for approximately 10hours to provide a working culture of at least 108 cells per mL. To ensure cultures are at the appropriate phase of growth and culture density, a sample is taken from each culture at the end of the incubation period and assessed for culture density by either viability plating or OD650 assessment. Treatment: 3 replicates per concentration of compound and positive controls and 6 replicates per vehicle controls are included. Formulations are prepared using DMSO to allow maximum exposure up to the solubility limit or 1000 μg / well for a freely soluble test article. This concentration is equivalent to 5000μg / plate as used in the usual plate incorporation Ames assay.Concentrations are usually separated by half-log intervals in a single experiment. Forsoluble compounds, concentrations will be 0, 3.2, 10, 32, 100, 320, 1000 μg / well.Positive controls used are: Abbreviation Name Used for strain 2NF 2-Nitrofluorene TA98 –S-9 NaN3 Sodium Azide TA100 and TA1535 –S-9 AAC 9-Aminoacridine TA97a –S-9 MMC Mitomycin C TA102 –S-9 B[a]P Benzo[a]pyrene TA98 +S-9 AAN Aminoanthracene TA100, TA1535,TA97a and TA102 +S-9 Platings will be achieved by the following sequence of additions to 400 μL supplemented molten agar at 45±1°C: • 20 μL of bacterial culture •20 μL of test article solution / vehicle control / positive control• 100 μL of 10% S-9 mix or buffer solution followed by rapid mixing and pouring onto mutation plates (wells).When set, the plates will be inverted and incubated protected from light for 2 to 3 days in an incubator set to 37 °C. Toxicity: Toxicity is detected by the following parameters: • Diminution of background lawn •Marked reduction in revertants compared to the concurrent vehicle controls• Reduction in mutagenic response. Scoring: Scoring of bacteria colonies is performed manually or electronically using automated colony counter. In Vitro Mammalian Cell Micronucleus Test: The testing of compounds is conducted as outlined in this guideline: Test No. 487: In Vitro Mammalian Cell Micronucleus Test | OECD Guidelines for the Testing of Chemicals, Section 4 : Health Effects | OECD iLibrary (oecd-ilibrary.org) Cell culture: Cultures are maintained in tissue culture flasks containing HEPES-buffered RPMI 1640 medium with GlutaMAX-1 including 10% (v / v) heat inactivated foetal calf serum, 100 Units / mL / 100 µg / mL penicillin / streptomycin in a humidified incubator set to 37°C, 5% (v / v) CO2 in air. Cells will be subcultured at low to medium density at least once prior to treatment. On the day prior to treatment, cells will be subcultured at a density of approximately 7 x 104 cells / mL. Cells will be maintained at 37°C, 5% (v / v) CO2 in air, in a humidified environment prior to treatment. Treatment: Cultured human lymphoblastoid TK6 cells will be exposed to the compound for 3 hours in the presence of S-9, followed by a recovery period of 24 hours. In addition, a continuous 27 hour treatment in the absence of S-9 will be included as a number of chemicals have been reported as only exerting positive effects following prolonged treatment. This is equivalent to approximately 1.5-2.0 times the average generation time of the TK6 cells used in this laboratory (cell cycle approximately 15 hours). All cultures will be sampled 27 hours after the beginning of treatment. Dilutions will be prepared in DMSO that allow maximum exposure up to the solubility limit, 1 mM or 500 µg / mL, whichever is lower. Normally, at least 12 concentrations separated by 0.7-fold intervals, ranging down from the upper limit (for soluble compounds with a MW ≥ 500, concentrations will be 9.887, 14.12, 20.18, 28.82, 41.18, 58.82, 84.04, 120.1, 171.5, 245, 350 and 500 µg / mL). The finalconcentration of DMSO will be 1% v / v. Positive controls are Noscapine in the absence of S -9and Cyclophosphamide in the presence of S-9. 2 replicates per concentration of compound and multiple concurrent vehicle and positive controls will be included per treatment in 96-well plates and incubated for the treatment time at 37°C, 5% (v / v) CO2. 3 hour treatment cultures will bewashed once and reincubated with fresh medium for 24 hours.Harvesting: At the defined sampling time an aliquot of cell suspension from designated cultures will be taken for determination of cell number by using a Coulter Counter. Cultures designated for analysis will be centrifuged at approximately 200 g, 5 minutes. Cells will be resuspended in 0.075 M KCl prior to fixation in fresh, cold methanol / glacial acetic acid (7:1 v / v). Fixed cells will be stored in fixative at 2-8°C prior to slide preparation. Slides will be air-dried prior to staining by immersion in 12.5 µg / mL Acridine Orange in phosphate buffered saline (PBS), pH 6.8 forapproximately 10 minutes, following by a wash with PBS (with agitation) for a few seconds.Cytotoxicity readout and selection of concentrations:Toxicity is expressed as Population Doubling (PD) relative to vehicle controls. PD will be calculated for each concentration as follows: PD = [log (N / X0)] / log 2 Where N = mean final cell count / culture at each concentration X0= starting (baseline) count The highest concentration for micronucleus analysis should either not exceed (approximately) 50% cytotoxicity, be the highest concentration tested, or, be the lowestprecipitating concentration observed by eye at the end of the treatment incubation period. Slidesfrom the highest selected concentration and at least two lower concentrations will be analysed, such that a range of cytotoxicity from maximum to little or none is covered, where appropriate. A minimum of 1000 mononucleate cells from each culture (2000 per concentration) will be analysed for micronuclei. Evaluation criteria: The compound will be considered to induce clastogenic and / or aneugenic events if: - A statistically significant increase in the frequency of MNMON cells at one or more concentrations is observed. - The incidence of cells with micronuclei at such a concentration exceeds the normal range in both replicates. - A concentration-related increase in the proportion of cells with micronuclei is observed (positive trend test). The compound will beconsidered positive in this assay if all of the above criteria are met . The compound will beconsidered negative in this assay if none of the above criteria are met. Results which only partially satisfy the above criteria will be dealt with on a case-by-case basis, but in the context of the screening study, will be concluded as either positive, negative or equivocal. Evidence of a concentration-related effect is considered useful but not essential in the evaluation of a positive result. Biological relevance will be taken into account, for example consistency of response within and between concentrations and (if applicable) between experiments, or effects occurring only at very toxic concentrations. Table 1: NLRP3 inhibitory activity THP-1 pyroptosis Example Assay No. IC50 (nM) 338 27 25 24 31 35 25 29 27 64 30 30 64 366 83 586 154 27 144 46 11 355 48 91 30

Claims

CLAIMS 1. A compound of formula I I wherein,n is 1 or 2; Y is –O– or –CH2–; R1is –OH or NR2R3; R2and R3are independently selected from H and alkyl; or R2is H and R3is haloalkyl, hydroxyalkyl, cycloalkyl, hydroxycycloalkyl, cycloalkylalkyl, imidazolylalkyl, or oxetanylmethyl; or R2and R3, together with the N atom to which they are attached, form a 4-6 membered ring optionally substituted with halo or –OH; or R2and R3, together with the N atom to which they are attached, form a 6 member ring comprising an additional O-heteroatom; and pharmaceutically acceptable salts thereof.

2. The compound of claim 1 wherein n is 2.

3. The compound of claim 2, wherein the compound of formula I is a compound of formula IIa or IIb IIb.

4. The compound of any of claims 1 to 3, wherein R1is NR2R3.

5. The compound of any one of claims 1 to 4 wherein R2and R3are independently selected from H and alkyl,or R2is H and R3is hydroxyalkyl, cycloalkyl, hydroxycycloalkyl, cycloalkylalkyl, imidazolylalkyl, or oxetanylmethyl, or R2and R3, together with the N atom to which they are attached, form a 4-5 membered ring optionally substituted with halo or –OH, or R2and R3, together with the N atom to which they are attached, form a 6 member ring comprising an additional O-heteroatom.

6. The compound of any one of claims 1 to 5 wherein R2and R3are independently selected from H and alkyl, or R2is H and R3is hydroxyalkyl, cycloalkyl, hydroxycycloalkyl, cycloalkylalkyl, or oxetanylmethyl, or R2and R3, together with the N atom to which they are attached, form a 4-5 membered ring optionally substituted with halo, or R2and R3, together with the N atom to which they are attached, form a 6 member ring comprising an additional O-heteroatom.

7. The compound of claim 1 wherein n is 1 or 2; Y is –O– or –CH2–; R1is –OH or NR2R3; R2and R3are independently selected from H and alkyl, or R2is H and R3is hydroxyalkyl, cycloalkyl, hydroxycycloalkyl, cycloalkylalkyl, imidazolylalkyl, or oxetanylmethyl, or R2and R3, together with the N atom to which they are attached, form a 4-5 membered ring optionally substituted with halo or –OH, or R2and R3, together with the N atom to which they are attached, form a 6 member ring comprising an additional O-heteroatom; and pharmaceutically acceptable salts thereof.

8. The compound of claim 3 wherein Y is –O– or –CH2–; R1is NR2R3; R2and R3are independently selected from H and alkyl,or R2is H and R3is hydroxyalkyl, cycloalkyl, hydroxycycloalkyl, cycloalkylalkyl, imidazolylalkyl, or oxetanylmethyl, or R2and R3, together with the N atom to which they are attached, form a 4-5 membered ring optionally substituted with halo or –OH, or R2and R3, together with the N atom to which they are attached, form a 6 member ring comprising an additional O-heteroatom; and pharmaceutically acceptable salts thereof.

9. The compound claim 3 or claim 8, wherein Y is –O– or –CH2–; R1is NR2R3; R2and R3are independently selected from H and alkyl, or R2is H and R3is hydroxyalkyl, cycloalkyl, hydroxycycloalkyl, cycloalkylalkyl, or oxetanylmethyl, or R2and R3, together with the N atom to which they are attached, form a 4-5 membered ring optionally substituted with halo, or R2and R3, together with the N atom to which they are attached, form a 6 member ring comprising an additional O-heteroatom; and pharmaceutically acceptable salts thereof.

10. The compound of claim 1 wherein the compound is selected from (1S,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4-triazin-3- yl]amino]cyclohexanecarboxylic acid; (1S,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4-triazin-3- yl]amino]cyclohexanecarboxylic acid;2,2,2-trifluoroacetic acid; (3-fluoroazetidin-1-yl)-[(1S,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5- methyl-1,2,4-triazin-3-yl]amino]cyclohexyl]methanone; (1S,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4-triazin-3- yl]amino]-N-isobutyl-cyclohexanecarboxamide; (1S,3R)-N-(cyclobutylmethyl)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl- 1,2,4-triazin-3-yl]amino]cyclohexanecarboxamide; (1S,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4-triazin-3- yl]amino]-N-(oxetan-3-ylmethyl)cyclohexanecarboxamide;(1S,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4-triazin-3- yl]amino]-N-(2-hydroxyethyl)cyclohexanecarboxamide; (1S,3R)-N-cyclopropyl-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4- triazin-3-yl]amino]cyclohexanecarboxamide; (1S,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4-triazin-3- yl]amino]-N-methyl-cyclohexanecarboxamide; (1S,3R)-N-ethyl-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4-triazin- 3-yl]amino]cyclohexanecarboxamide; [(1S,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4-triazin-3- yl]amino]cyclohexyl]-pyrrolidin-1-yl-methanone; (1R,3S)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4-triazin-3- yl]amino]-N-isopropyl-cyclohexanecarboxamide; (1S,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4-triazin-3- yl]amino]-N-isopropyl-cyclohexanecarboxamide; (1S,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4-triazin-3- yl]amino]-N-isopropyl-cyclohexanecarboxamide; [(1S,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4-triazin-3- yl]amino]cyclohexyl]-morpholino-methanone; (1S,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4-triazin-3- yl]amino]-N,N-dimethyl-cyclohexanecarboxamide; 3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4-triazin-3-yl]amino]-N- isopropyl-cyclopentanecarboxamide; (3-hydroxyazetidin-1-yl)-[(1S,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5- methyl-1,2,4-triazin-3-yl]amino]cyclohexyl]methanone;2,2,2-trifluoroacetic acid; (3-hydroxyazetidin-1-yl)-[(1S,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5- methyl-1,2,4-triazin-3-yl]amino]cyclohexyl]methanone; (1R,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4-triazin-3- yl]amino]cyclohexanecarboxylic acid; (3-hydroxyazetidin-1-yl)-[(1R,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5- methyl-1,2,4-triazin-3-yl]amino]cyclohexyl]methanone;2,2,2-trifluoroacetic acid; (3-hydroxyazetidin-1-yl)-[(1R,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5- methyl-1,2,4-triazin-3-yl]amino]cyclohexyl]methanone;azetidin-1-yl-[(1S,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4- triazin-3-yl]amino]cyclohexyl]methanone; azetidin-1-yl-[(1R,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4- triazin-3-yl]amino]cyclohexyl]methanone;2,2,2-trifluoroacetic acid azetidin-1-yl-[(1R,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4- triazin-3-yl]amino]cyclohexyl]methanone; (1R,3R)-3-[[6-(4-hydroxyindan-5-yl)-5-methyl-1,2,4-triazin-3-yl]amino]-N-isopropyl- cyclohexanecarboxamide;2,2,2-trifluoroacetic acid; (1R,3R)-3-[[6-(4-hydroxyindan-5-yl)-5-methyl-1,2,4-triazin-3-yl]amino]-N-isopropyl- cyclohexanecarboxamide; (1S,3R)-3-[[6-(4-hydroxyindan-5-yl)-5-methyl-1,2,4-triazin-3-yl]amino]-N-isopropyl- cyclohexanecarboxamide;2,2,2-trifluoroacetic acid; (1S,3R)-3-[[6-(4-hydroxyindan-5-yl)-5-methyl-1,2,4-triazin-3-yl]amino]-N-isopropyl- cyclohexanecarboxamide; [(1R,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4-triazin-3- yl]amino]cyclohexyl]-morpholino-methanone;2,2,2-trifluoroacetic acid; [(1R,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4-triazin-3- yl]amino]cyclohexyl]-morpholino-methanone; (1S,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4-triazin-3- yl]amino]-N-(2-hydroxy-2-methyl-propyl)cyclohexanecarboxamide; (1S,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4-triazin-3- yl]amino]-N-(2-imidazol-1-ylethyl)cyclohexanecarboxamide; (1S,3R)-N-[(1S,2R)-2-hydroxycyclopentyl]-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5- yl)-5-methyl-1,2,4-triazin-3-yl]amino]cyclohexanecarboxamide; and pharmaceutically acceptable salts thereof.

11. The compound of claim 1 or 10 wherein the compound is selected from (3-fluoroazetidin-1-yl)-[(1S,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5- methyl-1,2,4-triazin-3-yl]amino]cyclohexyl]methanone; (1S,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4-triazin-3- yl]amino]-N-isobutyl-cyclohexanecarboxamide; (1S,3R)-N-(cyclobutylmethyl)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl- 1,2,4-triazin-3-yl]amino]cyclohexanecarboxamide;(1S,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4-triazin-3- yl]amino]-N-(oxetan-3-ylmethyl)cyclohexanecarboxamide; (1S,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4-triazin-3- yl]amino]-N-(2-hydroxyethyl)cyclohexanecarboxamide; (1S,3R)-N-cyclopropyl-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4- triazin-3-yl]amino]cyclohexanecarboxamide; (1S,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4-triazin-3- yl]amino]-N-methyl-cyclohexanecarboxamide; (1S,3R)-N-ethyl-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4-triazin- 3-yl]amino]cyclohexanecarboxamide; [(1S,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4-triazin-3- yl]amino]cyclohexyl]-pyrrolidin-1-yl-methanone; (1S,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4-triazin-3- yl]amino]-N-isopropyl-cyclohexanecarboxamide; [(1S,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4-triazin-3- yl]amino]cyclohexyl]-morpholino-methanone; (1S,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4-triazin-3- yl]amino]-N,N-dimethyl-cyclohexanecarboxamide; (3-hydroxyazetidin-1-yl)-[(1S,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5- methyl-1,2,4-triazin-3-yl]amino]cyclohexyl]methanone;2,2,2-trifluoroacetic acid; (3-hydroxyazetidin-1-yl)-[(1S,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5- methyl-1,2,4-triazin-3-yl]amino]cyclohexyl]methanone; (3-hydroxyazetidin-1-yl)-[(1R,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5- methyl-1,2,4-triazin-3-yl]amino]cyclohexyl]methanone;2,2,2-trifluoroacetic acid; (3-hydroxyazetidin-1-yl)-[(1R,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5- methyl-1,2,4-triazin-3-yl]amino]cyclohexyl]methanone; azetidin-1-yl-[(1S,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4- triazin-3-yl]amino]cyclohexyl]methanone; azetidin-1-yl-[(1R,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4- triazin-3-yl]amino]cyclohexyl]methanone;2,2,2-trifluoroacetic acid; azetidin-1-yl-[(1R,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4- triazin-3-yl]amino]cyclohexyl]methanone;(1R,3R)-3-[[6-(4-hydroxyindan-5-yl)-5-methyl-1,2,4-triazin-3-yl]amino]-N-isopropyl- cyclohexanecarboxamide;2,2,2-trifluoroacetic acid; (1R,3R)-3-[[6-(4-hydroxyindan-5-yl)-5-methyl-1,2,4-triazin-3-yl]amino]-N-isopropyl- cyclohexanecarboxamide; (1S,3R)-3-[[6-(4-hydroxyindan-5-yl)-5-methyl-1,2,4-triazin-3-yl]amino]-N-isopropyl- cyclohexanecarboxamide;2,2,2-trifluoroacetic acid; (1S,3R)-3-[[6-(4-hydroxyindan-5-yl)-5-methyl-1,2,4-triazin-3-yl]amino]-N-isopropyl- cyclohexanecarboxamide; (1S,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4-triazin-3- yl]amino]-N-(2-hydroxy-2-methyl-propyl)cyclohexanecarboxamide; (1S,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4-triazin-3- yl]amino]-N-(2-imidazol-1-ylethyl)cyclohexanecarboxamide; (1S,3R)-N-[(1S,2R)-2-hydroxycyclopentyl]-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5- yl)-5-methyl-1,2,4-triazin-3-yl]amino]cyclohexanecarboxamide; and pharmaceutically acceptable salts thereof.

12. The compound of any one of claims 1 or 10-11 wherein the compound is selected from (3-fluoroazetidin-1-yl)-[(1S,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5- methyl-1,2,4-triazin-3-yl]amino]cyclohexyl]methanone; (1S,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4-triazin-3- yl]amino]-N-isobutyl-cyclohexanecarboxamide; (1S,3R)-N-(cyclobutylmethyl)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl- 1,2,4-triazin-3-yl]amino]cyclohexanecarboxamide; (1S,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4-triazin-3- yl]amino]-N-(oxetan-3-ylmethyl)cyclohexanecarboxamide; (1S,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4-triazin-3- yl]amino]-N-(2-hydroxyethyl)cyclohexanecarboxamide; (1S,3R)-N-cyclopropyl-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4- triazin-3-yl]amino]cyclohexanecarboxamide; (1S,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4-triazin-3- yl]amino]-N-methyl-cyclohexanecarboxamide; (1S,3R)-N-ethyl-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4-triazin- 3-yl]amino]cyclohexanecarboxamide;(1S,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4-triazin-3- yl]amino]-N-isopropyl-cyclohexanecarboxamide; [(1S,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4-triazin-3- yl]amino]cyclohexyl]-morpholino-methanone; azetidin-1-yl-[(1S,3R)-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5-yl)-5-methyl-1,2,4- triazin-3-yl]amino]cyclohexyl]methanone; (1S,3R)-3-[[6-(4-hydroxyindan-5-yl)-5-methyl-1,2,4-triazin-3-yl]amino]-N-isopropyl- cyclohexanecarboxamide;2,2,2-trifluoroacetic acid; (1S,3R)-3-[[6-(4-hydroxyindan-5-yl)-5-methyl-1,2,4-triazin-3-yl]amino]-N-isopropyl- cyclohexanecarboxamide; (1S,3R)-N-[(1S,2R)-2-hydroxycyclopentyl]-3-[[6-(4-hydroxy-2,3-dihydrobenzofuran-5- yl)-5-methyl-1,2,4-triazin-3-yl]amino]cyclohexanecarboxamide; and pharmaceutically acceptable salts thereof.

13. A pharmaceutical composition comprising a compound according to any one of claims 1 to 12 and a therapeutically inert carrier.

14. The compound of any one of claims 1 to 12 for use as a therapeutically active substance.

15. A compound according to any one of claims 1 to 12 for use in the treatment or prevention of a disease, disorder or condition, wherein the disease, disorder or condition is responsive to NLRP3 inhibition.

16. A compound according to any one of claims 1 to 12 for the treatment or prophylaxis of a disease, disorder or condition selected from Asthma or COPD.

17. A compound according to any one of claims 1 to 12 for the treatment or prophylaxis of a cardiovascular disease, disorder or condition.

18. A compound according to any one of claims 1 to 12 for the treatment or prophylaxis of a cardiometabolic disease, disorder or condition.

19. A compound according to any one of claims 1 to 12 for the treatment or prophylaxis of a disease, disorder or condition selected from Parkinson’s Disease or Alzheimer’s Disease.

20. The use of a compound according to any one of claims 1 to 12 for the treatment or prophylaxis of a disease, disorder or condition, wherein the disease, disorder or condition is responsive to NLRP3 inhibition.

21. The use of a compound according to any one of claims 1 to 12 in the treatment or prophylaxis of a disease, disorder or condition selected from Asthma or COPD.

22. The use of a compound according to any one of claims 1 to 12 in the treatment or prophylaxis of a cardiovascular disease, disorder or condition.

23. The use of a compound according to any one of claims 1 to 12 in the treatment or prophylaxis of a cardiometabolic disease, disorder or condition.

24. The use of a compound according to any one of claims 1 to 12 in the treatment or prophylaxis of a disease, disorder or condition selected from Parkinson’s Disease or Alzheimer’s Disease.

25. The use of a compound according to any one of claims 1 to 12 for the preparation of a medicament for the treatment or prophylaxis of a disease, disorder or condition selected from Asthma or COPD.

26. The use of a compound according to any one of claims 1 to 12 for the preparation of a medicament for the treatment or prophylaxis of a cardiovascular disease, disorder or condition.

27. The use of a compound according to any one of claims 1 to 12 for the preparation of a medicament for the treatment or prophylaxis of a cardiometabolic disease, disorder or condition.

28. The use of a compound according to any one of claims 1 to 12 for the preparation of a medicament for the treatment or prophylaxis of a disease, disorder or condition selected from Parkinson’s Disease or Alzheimer’s Disease.

29. A method of inhibiting NLRP3, which method comprises administering an effective amount of a compound as claimed in any one of claims 1 to 12 to inhibit NLRP3.

30. A method for the treatment or prophylaxis of a disease, disorder or condition, which method comprises administering an effective amount of a compound according to any one of claims 1to 12 wherein the disease, disorder or condition is selected from Asthma or COPD.

31. A method for the treatment or prophylaxis of a cardiovascular disease, disorder orcondition, which method comprises administering an effective amount of a compound according to any one of claims 1 to 12.

32. A method for the treatment or prophylaxis of a cardiometabolic disease, disorder orcondition, which method comprises administering an effective amount of a compound according to any one of claims 1 to 12.

33. A method for the treatment or prophylaxis of a disease, disorder or condition, which method comprises administering an effective amount of a compound according to any one of claims 1 to 12 wherein the disease, disorder or condition is selected from Parkinson’s Disease or Alzheimer’s Disease.

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