COMPOUNDS, COMPOSITIONS AND METHODS OF INCREASING CFTR

ACTIVITY

CROSS-REFERENCE TO RELATED APPLICATIONS

[0001] This application claims priority to provisional applications U.S. S.N. 62/014,400, filed June 19, 2014; U.S.S.N. 62/014,409, filed June 19, 2014; U.S.S.N. 62/096,389, filed December 23, 2014 and U.S.S.N. 62/102,230, filed January 12, 2015, each of which is hereby incorporated by reference in their entirety.

BACKGROUND

[0002] Cells normally maintain a balance between protein synthesis, folding, trafficking, aggregation, and degradation, referred to as protein homeostasis, utilizing sensors and networks of pathways (Sitia et al, Nature 426: 891-894, 2003; Ron et al, Nat Rev Mol Cell Biol 8: 519- 529, 2007). The cellular maintenance of protein homeostasis, or proteostasis, refers to controlling the conformation, binding interactions, location and concentration of individual proteins making up the proteome. Protein folding in vivo is accomplished through interactions between the folding polypeptide chain and macromolecular cellular components, including multiple classes of chaperones and folding enzymes, which minimize aggregation (Wiseman et al, Cell 131: 809-821, 2007). Whether a given protein folds in a certain cell type depends on the distribution, concentration, and subcellular localization of chaperones, folding enzymes, metabolites and the like (Wiseman et al). Cystic fibrosis and other maladies of protein misfolding arise as a result of an imbalance in the capacity of the protein homeostasis

(proteostasis) environment to handle the reduced energetic stability of misfolded, mutated proteins that are critical for normal physiology (Balch et al, Science 319, 916-9 (2008);

Powers, et al, Annu Rev Biochem 78, 959-91 (2009); Hutt et al, FEB S Lett 583, 2639-46 (2009)).

[0003] Cystic Fibrosis (CF) is caused by mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene which encodes a multi-membrane spanning epithelial chloride channel (Riordan et al, Annu Rev Biochem 11, 701-26 (2008)). Approximately ninety percent of patients have a deletion of phenylalanine (Phe) 508 (AF508) on at least one allele. This mutation results in disruption of the energetics of the protein fold leading to degradation of CFTR in the endoplasmic reticulum (ER). The AF508 mutation is thus associated with defective folding and trafficking, as well as enhanced degradation of the mutant CFTR protein (Qu et al, J Biol Chem 111, 15739-44 (1997)). The loss of a functional CFTR channel at the plasma membrane disrupts ionic homeostasis (Cl ^~ , Na ⁺ , HCO ₃ ^" ) and airway surface hydration leading to reduced lung function (Riordan et al). Reduced periciliary liquid volume and increased mucus viscosity impede mucociliary clearance resulting in chronic infection and inflammation, phenotypic hallmarks of CF disease (Boucher, J Intern Med 261, 5-16 (2007)). In addition to respiratory dysfunction, AF508 CFTR also impacts the normal function of additional organs (pancreas, intestine, gall bladder), suggesting that the loss-of-function impacts multiple downstream pathways that will require correction.

[0004] In addition to cystic fibrosis, mutations in the CFTR gene and/or the activity of the CFTR channel has also been implicated in other conditions, including for example, congenital bilateral absence of vas deferens (CBAVD), acute, recurrent, or chronic pancreatitis, disseminated bronchiectasis, asthma, allergic pulmonary aspergillosis, smoking-related lung diseases, such as chronic obstructive pulmonary disease (COPD), dry eye disease, Sjogren's syndrome and chronic sinusitis, (Sloane et al. (2012), PLoS ONE 7(6):

e39809.doi: 10.1371/journal. pone.0039809; Bombieri et al. (201 1), J Cyst Fibros. 201 1 Jun; 10 Suppl 2:S86-102; (Albert et al. (2008). Clinical Respiratory Medicine, Third Ed., Mosby Inc.; Levin et al. (2005), Invest Ophthalmol Vis Sci., 46(4): 1428-34; Froussard (2007), Pancreas 35(1): 94-5).

[0005] There remains a need in the art for compounds, compositions and methods of increasing CFTR activity as well as for methods of treating CF, other CFTR-related diseases, and other maladies of protein misfolding.

SUMMARY

[0006] The present disclosure is based, in part, on the discovery that disclosed compounds such as those having the formulas as disclosed herein increase cystic fibrosis transmembrane conductance regulator (CFTR) activity as measured in human bronchial epithelial (hBE) cells.

[0007] Disclosed herein, in an embodiment, are compounds having the formula:

and pharmaceutically acceptable salts, stereoisomers, and prodrugs thereof, wherein:

R22 is selected, independently, for each occurrence, from the group consisting of hydrogen, halogen, and Ci- ₄ alkyl (optionally substituted by one, two or three halogens); pp is 0, 1, 2, 3, 4 or 5; R31 is selected from the group consisting of hydrogen, halogen, and C _1-4 alkyl;

Li is selected from the group consisting of C3-9 cycloalkylene, Cialkylene -C3-9 cycloalkylene- and -C3_ ₉ cycloalkylene-Cialkylene, wherein Li may be optionally substituted by one, two or three substituents selected from the group consisting of halogen, hydroxyl, and Ci- 3alkyl (optionally substituted by one, two or three substituents each selected independently from Rf _f );

R44 is selected from the group consisting of -C(0)-OR', 4 to 6 membered heterocycloalkyl, a 5-6 membered monocyclic heteroaryl, and a 9-10 membered bicyclic heteroaryl, wherein the heteroaryl has one, two or three heteroatoms each selected from O, N, and S; and wherein the heteroaryl or heterocycloalkyl may be optionally substituted by one or two substituents each selected independently from R _gg ;

Rff is selected for each occurrence from group consisting of halogen, hydroxyl, Ci_ ₄ alkyl, Ci- ₄ alkyoxy, C ₂ - ₄ alkenyl, oxo, -NR'R", -NR'-S(0)w-Ci- ₃ alkyl, S(0) _w -NR'R", and - S(0) _w -Ci_ ₃ alkyl, where w is 0, 1, or 2, wherein Ci_ ₄ alkyl, Ci_ ₄ alkyoxy, and C2- ₄ alkenyl may be optionally substituted by one, two or three substituents each independently selected from the group consisting of halogen, hydroxyl, -NR'R", -NR'-S(0) _w -Ci_ ₃ alkyl, S(0) _w -NR'R", and - S(0) _w -C ₁ _ ₃ alkyl;

Rgg is selected for each occurrence from group consisting of halogen, hydroxyl, Ci- ealkyl, Ci_ ₆ alkoxy, C ₂ _ ₆ alkenyl, C ₃ - ₆ cycloalkyl, -O-C(O)- Ci_ ₆ alkyl, -C(0)-0- Ci_ ₆ alkyl, -C(O)- O- phenyl, -0-C(0)-phenyl, phenyl, 4 to 6 membered heterocycloalkyl, -NR'R", oxo, -NR'- S(0) _w -Ci_ ₃ alkyl, S(0) _w -NR'R", and -S(0) _w -Ci_ ₃ alkyl, where w is 0, 1, or 2, wherein d_ ₆ alkyl, Ci_ ₆ alkyoxy, C2- ₆ alkenyl C3_ ₆ cycloalkyl, phenyl and heterocycloalkyl may each be optionally substituted by one, two or three substituents each independently selected from the group consisting of halogen, d_ ₆ alkyl, Ci_ ₆ alkoxy, hydroxyl, C(0)OH, -C(0)OCi_ ₆ alkyl, -0-C(0)Ci_ ₆ alkyl, 0-C(0)-phenyl, -C(0)0-NR'-Ci_ ₆ alkyl,-0-C ₃ - ₆ cycloalkyl, -O-heterocycle, phenyl, -O- heteroaryl, -O-phenyl, -NR'R", -NR'-S(0) _w -Ci_ ₃ alkyl, S(0) _w -NR'R", and -S(0) _w -Ci_ ₃ alkyl, where w is 0, 1, or 2; and

R' and R" are each independently selected for each occurrence from H and Ci- ₄ alkyl or taken together with a nitrogen to which they are attached form a heterocyclic ring. [0008] Also contemplated herein are pharmaceutical compositions that include a disclosed compound and a pharmaceutically acceptable carrier or excipient. In certain embodiments, the compositions can include at least one additional CFTR modulator as described anywhere herein or at least two additional CFTR modulators, each independently as described anywhere herein.

[0009] In additional embodiments, a method of enhancing (e.g., increasing) cystic fibrosis transmembrane conductance regulator (CFTR) activity in a subject in need thereof is provided comprising administering to said subject an effective amount of a compound disclosed herein.

[0010] In certain of these embodiments, the activity of one or more (e.g., one or two) mutant CFTRs (e.g., AF508, S549N, G542X, G551D, R117H, N1303K, W1282X, R553X, 621+1G>T, 1717-1G>A, 3849+lOkbOT, 2789+5G>A, 3120+1OA, I507del, R1162X, 1898+lOA, 3659delC, G85E, D1152H, R560T, R347P, 2184insA, A455E, R334W, Q493X, and 2184delA CFTR) is enhanced (e.g., increased). In certain embodiments, AF508 CFTR activity is enhanced (e.g., increased). In other embodiments, the activities of two mutant CFTRs (e.g., AF508 and G551D; AF508 and A455E; or G542X; A508F) are enhanced (e.g., increased). [0011] In certain of these embodiments, the subject (e.g., a human patient) is suffering from a disease associated with decreased CFTR activity (e.g., cystic fibrosis, congenital bilateral absence of vas deferens (CBAVD), acute, recurrent, or chronic pancreatitis, disseminated bronchiectasis, asthma, allergic pulmonary aspergillosis, chronic obstructive pulmonary disease (COPD), chronic sinusitis, dry eye disease, protein C deficiency, Α-β-lipoproteinemia, lysosomal storage disease, type 1 chylomicronemia, mild pulmonary disease, lipid processing deficiencies, type 1 hereditary angioedema, coagulation-fibrinolyis, hereditary

hemochromatosis, CFTR-related metabolic syndrome, chronic bronchitis, constipation, pancreatic insufficiency, hereditary emphysema, Sjogren's syndrome, familial

hypercholesterolemia, I-cell disease/pseudo-Hurler, mucopolysaccharidoses, Sandhof/T ay- Sachs, Crigler-Najjar type II, polyendocrinopathy/hyperinsulemia, Diabetes mellitus, Laron dwarfism, myleoperoxidase deficiency, primary hypoparathyroidism, melanoma, glycanosis CDG type 1, congenital hyperthyroidism, osteogenesis imperfecta, hereditary

hypofibrinogenemia, ACT deficiency, Diabetes insipidus (DI), neurophyseal DI, nephrogenic DI, Charcot-Marie Tooth syndrome, Perlizaeus-Merzbacher disease, Alzheimer's disease, Parkinson's disease, amyotrophic lateral sclerosis, progressive supranuclear palsy, Pick's disease, Huntington's disease, spinocerebellar ataxia type I, spinal and bulbar muscular atrophy, dentatorubral pallidoluysian, myotonic dystrophy, hereditary Creutzfeldt- Jakob disease (due to prion protein processing defect), Fabry disease, and Straussler-Scheinker syndrome). In certain embodiments, a method is provided for treating cystic fibrosis in a patient in need thereof comprising administering a disclosed compound. In another embodiment, a method is provided for treatin chronic obstructive pulmonary disease (COPD), in a patient in need thereof comprising administering a disclosed compound.

[0012] In yet additional aspects, the disclosure is directed to treating a patient suffering from cystic fibrosis comprising administering to said patient an effective amount of a disclosed compound.

[0013] In some embodiments, the methods described herein can further include administering an additional therapeutic agent or administering at least two additional CFTR therapeutic agents. In some embodiments, the methods described herein can further include administering an additional CFTR modulator or administering at least two additional CFTR modulators. In certain embodiments, at least one CFTR modulator is a CFTR corrector (e.g., VX-809, VX-661, VX-983, GLPG2222 and) or potentiator (e.g., ivacaftor, genistein and GLPG1837). In certain of these embodiments, one of the at least two additional therapeutic agents is a CFTR corrector (e.g., VX-809, VX-661 and VX-983) and the other is a CFTR potentiator (e.g., ivacaftor and genistein). In certain of these embodiments, one of the at least two additional therapeutic agents is a CFTR corrector (e.g., GLPG2222) and the other is a CFTR potentiator (e.g., GLPG1837).

[0014] In a further aspect, a method of identifying a candidate agent that increases CFTR activity is provided, which includes: (i) contacting a cell that expresses a CFTR protein with the candidate agent and a disclosed compound; (ii) measuring the CFTR activity in the cell in the presence of the candidate agent and the disclosed compound; and (iii) comparing the CFTR activity to that in the absence of the test agent, wherein an increase in CFTR activity in the presence of the test agent indicates that the agent increases CFTR activity. In certain embodiments, the cell expresses a mutant CFTR protein. In certain embodiments, CFTR activity is measured by measuring chloride channel activity of the CFTR, and/or other ion transport activity. In certain of these embodiments, the method is high-throughput. In certain of these embodiments, the candidate agent is a CFTR corrector or a CFTR potentiator.

DETAILED DESCRIPTION

[0015] As used herein, the words "a" and "an" are meant to include one or more unless otherwise specified. For example, the term "an agent" encompasses both a single agent and a combination of two or more agents.

[0016] As discussed above, the present disclosure is directed in part to compounds as described herein having e.g., the above formula or e.g., Formula 1(a), (Ila), (lib), (lie), (lid), (Ilia), and (Illb), or a pharmaceutically acceptable salt, prodrug or solvate thereof,

pharmaceutical compositions, methods of increasing CFTR activity and methods of treating cystic fibrosis.

[0017] For example, provided herein are compounds having the Formula (la):

or a pharmaceutically acceptable salt, solvate, clathrate or prodrug thereof, wherein:

Ri-a is selected from the group consisting of optionally substituted Ci-Cio alkyl, optionally substituted C2-C1 ₀ alkenyl, optionally substituted C2-C1 ₀ alkynyl, optionally substituted C3-C12 cycloalkyl, optionally substituted C3-C12 cycloalkenyl, optionally substituted aryl, halo, ORc, NR _d R _d , C(0)ORc, N0 ₂ , CN, C(0)R _c , C(0)C(0)R _c , C(0)NRdRd, NRdC(0)R _c , NR _d S(0) _n R _c , NR _d (COOR _c ), NR _d C(0)C(0)R _c , NR _d C(0)NR _d R _d , NR _d S(0) _n NR _d R _d , NR _d S(0) _n R _c , S(0) _n R _c , S(0) _n NR _d R _< i, OC(0)OR _c, (C=NR _d )R _c , optionally substituted heterocyclic and optionally substituted heteroaryl;

Z is an optionally substituted C3-C7 cycloalkyl; Each R ₂ is independently selected from the group consisting of hydrogen, halo, CN, and optionally substituted C1-C1 ₀ alkyl;

R3 is hydrogen or fluoro; each R _b is independently selected from the group consisting of hydrogen, halo, optionally substituted C1-C1 ₀ alkyl, and optionally substituted C ₃ -C6 cycloalkyl, or two geminal R _b groups are independently taken together with the carbon atom to which they are attached to form an optionally substituted heterocyclic or an optionally substituted heteroaryl; each R _c is independently selected from the group consisting of hydrogen, optionally substituted C1-C1 ₀ alkyl, optionally substituted C2-C1 ₀ alkenyl, optionally substituted C2-C1 ₀ alkynyl, optionally substituted C ₃ -C12 cycloalkyl, optionally substituted C ₃ -C12 cycloalkenyl, optionally substituted heterocyclic, optionally substituted aryl and optionally substituted heteroaryl; each R _d is independently selected from the group consisting of hydrogen, optionally substituted C1-C1 ₀ alkyl, optionally substituted C2-C1 ₀ alkenyl, optionally substituted C2-C1 ₀ alkynyl, optionally substituted C1-C1 ₀ alkoxy, optionally substituted C ₃ -C12 cycloalkyl, optionally substituted C ₃ -C12 cycloalkenyl, optionally substituted heterocyclic, optionally substituted aryl and optionally substituted heteroaryl; or two geminal Rj groups are taken together with the nitrogen atom to which they are attached to form an optionally substituted heterocyclic or an optionally substituted heteroaryl; Rf is selected from the group consisting of hydrogen, optionally substituted Ci-Cio alkyl, optionally substituted C2-C1 ₀ alkenyl, optionally substituted C2-C1 ₀ alkynyl, optionally substituted C1-C10 alkoxy, optionally substituted C3-C12 cycloalkyl, optionally substituted C3- C12 cycloalkenyl, optionally substituted heterocyclic, optionally substituted aryl and optionally substituted heteroaryl; m is 0, 1 or 2; each n is independently 0, 1 or 2; and p is 0, 1 or 2.

[0018] Disclosed herein, in an embodiment, are compounds such as those having the Formula (Ila) or (lib):

Ri-b is selected from the group consisting of optionally substituted Ci-Cio alkyl, optionally substituted C2-C1 ₀ alkenyl, optionally substituted C2-C1 ₀ alkynyl, optionally substituted C3-C12 cycloalkyl, optionally substituted C3-C12 cycloalkenyl, optionally substituted aryl, halo, ORe, NR _d R _d , C(0)ORc, N0 ₂ , CN, C(0)R _c , C(0)C(0)R _c , C(0)NRdRd, NRdC(0)R _c , NR _d S(0) _n Rc, NRd(COORc), NRdC(0)C(0)R _c , NR _d C(0)NRdRd, NR _d S(0) _n NR _d R _d , NR _d S(0) _n Rc, S(0) _n Rc, S(0) _n NR _d R _< i, OC(0)ORc, optionally substituted heterocyclic and optionally substituted heteroaryl (e.g., wherein C1-C1 ₀ alkyl, C2-C1 ₀ alkenyl, C2-C1 ₀ alkynyl, C3-C12 cycloalkyl, C3-C12 cycloalkenyl, heterocyclic, phenyl and heteroaryl may each be optionally substituted by one, two or three substituents each independently selected from R ^tt ); each R ₂ is independently selected from the group consisting of hydrogen, halo, CN, and optionally substituted C1-C1 ₀ alkyl;

R3 is hydrogen or fluoro; each R4 is independently selected from the group consisting of hydrogen, optionally substituted C1-C1 ₀ alkyl, optionally substituted C2-C1 ₀ alkenyl, optionally substituted C2-C1 ₀ alkynyl, optionally substituted C ₃ -C12 cycloalkyl, optionally substituted C ₃ -C12 cycloalkenyl, optionally substituted aryl, halo, ORc, NR _d R _d , C(0)ORc, N0 ₂ , CN, C(0)R _c , C(0)C(0)R _c , C(0)NR _d R _d , NRdC(0)R _c , NR _d S(0) _n R _c , NRd(COOR _c ), NR _d C(0)C(0)Rc, NRdC(0)NR _d R _d , NR _d S(0) _n NR _d R _d , NR _d S(0) _n R _c , S(0) _n Rc, S(0) _n NR _d R _d , OC(0)OR _c , (C=NR _d )R _c , optionally substituted heterocyclic and optionally substituted heteroaryl; alternatively, two geminal R4 groups are taken together with the carbon atom to which they are attached to form a spiro C ₃ - C12 cycloalkyl, a spiro C ₃ -C12 cycloalkenyl, a spiro heterocyclic, a spiro aryl or spiro heteroaryl, each optionally substituted; or yet alternatively, two vicinal R4 groups are taken together with the carbon atoms to which they are attached to form a fused, optionally substituted cyclic group selected from the group consisting of C4-C ₈ cycloalkyl, C4-C ₈ cycloalkenyl, 4- to 8-membered heterocyclic, substituted aryl and heteroaryl, each optionally substituted; or further

alternatively, two R4 groups attached to non-adjacent carbon atoms are taken together with the carbon atoms to which they are attached to form a bridged cyclic group selected from the group consisting of C4-C ₈ cycloalkyl, C4-C ₈ cycloalkenyl, and 4- to 8-membered heterocyclic, each optionally substituted; each ¾ is independently selected from the group consisting of hydrogen, halo, optionally substituted Ci-Cio alkyl, and optionally substituted C3-C6 cycloalkyl, or two geminal R _b groups are independently taken together with the carbon atom to which they are attached to form an optionally substituted heterocyclic or an optionally substituted heteroaryl; each R _e is independently selected from the group consisting of hydrogen, optionally substituted C1-C1 ₀ alkyl, optionally substituted C2-C1 ₀ alkenyl, optionally substituted C2-C1 ₀ alkynyl, optionally substituted C3-C12 cycloalkyl, optionally substituted C3-C12 cycloalkenyl, optionally substituted heterocyclic, optionally substituted aryl and optionally substituted heteroaryl; each Ra is independently selected from the group consisting of hydrogen, optionally substituted C1-C1 ₀ alkyl, optionally substituted C2-C1 ₀ alkenyl, optionally substituted C2-C1 ₀ alkynyl, optionally substituted C1-C1 ₀ alkoxy, optionally substituted C3-C12 cycloalkyl, optionally substituted C3-C12 cycloalkenyl, optionally substituted heterocyclic, optionally substituted aryl and optionally substituted heteroaryl; or two geminal Ra groups are taken together with the nitrogen atom to which they are attached to form an optionally substituted heterocyclic or an optionally substituted heteroaryl;

R _e is selected from the group consisting of optionally substituted C1-C1 ₀ alkyl, optionally substituted C2-C1 ₀ alkenyl, optionally substituted C2-C1 ₀ alkynyl, optionally substituted C3-C12 cycloalkyl, optionally substituted C3-C12 cycloalkenyl, optionally substituted heterocyclic, optionally substituted aryl and optionally substituted heteroaryl;

Rf is selected from the group consisting of hydrogen, optionally substituted C1-C10 alkyl, optionally substituted C2-C1 ₀ alkenyl, optionally substituted C2-C1 ₀ alkynyl, optionally substituted C1-C1 ₀ alkoxy, optionally substituted C3-C12 cycloalkyl, optionally substituted C3- C12 cycloalkenyl, optionally substituted heterocyclic, optionally substituted aryl and optionally substituted heteroaryl;

R ^tt is independently selected for each occurrence from the group consisting of: C1-C6 alkyl (optionally substituted by one, two or three substituents selected from the group consisting of: heterocyclic, -F, -CI, -Br, -I, -OH, -N0 ₂ , -N ₃ , -CN, -NH ₂ , NHR _d , -NRaRj, NRdC(0)Ra , - RdSOnRj and -ORc), -C2-C6 alkenyl (optionally substituted by one, two or three substituents selected from the group consisting of: heterocyclic, -F, -CI, -Br, -I, -OH, - N0 ₂ , -N ₃ , -CN, -NH ₂ , NHRd, -NRdRj, NR _d C(0)R _d , -NR _d SO _n R _d and -OR _c ), -C ₂ -C ₆ alkynyl (optionally substituted by one, two or three substituents selected from the group consisting of: heterocyclic, -F, -CI, -Br, -I, -OH, -N0 ₂ , -N ₃ , -CN, -NH ₂ , NHR _d , -NRdRj, NR _d C(0)R _d , - NR _d SO _n R _d and -OR _c ), -C3-C6 cycloalkyl (optionally substituted by one, two or three substituents selected from the group consisting of: heterocyclic, C1-C6 alkyl, -F, -CI, -Br, -I, - OH, -NO2, -N ₃ , -CN, -NH ₂ , NHRd, -NR _d R _d , NR _d C(0)R _d , -NR _d SO _n R _d and -OR _c ), - heterocyclic (optionally substituted by one, two or three substituents selected from the group consisting of: d-C ₆ alkyl, heterocyclic, -F, -CI, -Br, -I, -OH, -N0 ₂ , -N ₃ , -CN, -NH ₂ , NHR _f , - NR _f R _f , NR _f C(0)R _f , -NR _f SO _n R _f and -OR _c ), -F, -CI, -Br, -I, -OH, -N0 ₂ , -N ₃ , -CN, -NH ₂ , oxo, thioxo, -NHR _d , -NR _d R _d , -OR _c , -C(0)R _c , -C(0)C(0)R _c , -OC0 ₂ Rc, -OC(0)R _c , OC(0)C(0)Rc, - NHC(0)R _c , -NHC0 ₂ R _c , -NHC(0)C(0)R _c , NHC(S)NH ₂ , -NHC(S)NHR _d , -NHC(NH)NH ₂ , - NHC(NH)NHR _c , -NHC(NH)R _c , -C(NH)NHR _C , and (C=NR _C )R _C ; -NRcC(0)R _c , - NR _x C(0)N(R _x ) ₂ , -NRcC0 ₂ R _y , -NRcC(0)C(0)R _y , -NRcC(S)NH ₂ , -NR _C C(S)NHR _C , - NR _X C(NH)NH ₂ , -NR _X C(NH)NHR _X , -NR _X C(NH)R _X , -C(NR _X )NHR _X -S(0)R _y , -NHS0 ₂ R _c , - CH ₂ NH ₂ , -CH ₂ S0 ₂ CH ₃ , -phenyl, and heteroaryl; m is 0, 1 or 2; each n is independently 0, 1 or 2; and p is 0, 1 or 2.

[0019] In some embodiments, contemplated compounds have the Formula (Ila). In other embodiments, contemplated compounds has the Formula (lib).

[0020] For example, in some embodiments, R _f is hydrogen and/or R ₃ is hydrogen.

[0021] In some embodiments, a disclosed compound has the Formula (lie):

(lie).

(lid).

[0023] In some embodiments, Ri_ _b is selected from the group consisting of optionally substituted heteroaryl, optionally substituted heterocyclic, Ci-Cio alkyl substituted with OR _c , NR _d C(0)R _c , or NRdS(0) _n Rc, and Ci-C _w alkenyl substituted with ORc, NRdC(0)R _c , or NR _d S(0) _n R _c. In certain embodiments, Ri_ _b is an optionally substituted heteroaryl or an optionally substituted heterocyclic, e.g., an optionally substituted heteroaryl.

[0024] In certain embodiments, Ri_ _b can be selected from the group consisting of:

wherein: each X is independently O, S or NR _g ; each R _g is independently selected from the group consisting of hydrogen, optionally substituted Ci-Cio alkyl, optionally substituted C2-C1 ₀ alkenyl, optionally substituted C2-C1 ₀ alkynyl, optionally substituted C3-C12 cycloalkyl, optionally substituted C3-C12 cycloalkenyl, optionally substituted heterocyclic, optionally substituted aryl and optionally substituted heteroaryl; and each of R5 _; R6 and R7 is independently selected from the group consisting of hydrogen, optionally substituted C1-C10 alkyl, optionally substituted C2-C10 alkenyl, optionally substituted C2-C10 alkynyl, optionally substituted C3-C12 cycloalkyl, optionally substituted C3-C12 cycloalkenyl, optionally substituted aryl, halo, ORc, NR _d R _d , C(0)ORc, N0 ₂ , CN, C(0)Rc, C(0)C(0)Rc, C(0)NR _d Rd, NRdC(0)R _c , NR _d S(0) _n Rc, NRd(COOR _c ), NRdC(0)C(0)R _c , NR _d C(0)NRdRd, NRdS(0) _n NRdRd, NR _d S(0) _n Rc, S(0) _n Rc, S(0) _n NR _d Rd, OC(0)ORc,

(C=NR _d )R _c , optionally substituted heterocyclic and optionally substituted heteroaryl.

[0025] For example, Ri_b can

[0026] In certain embodiments, X is O or S or NR _g .

[0027] In certain embodiments, R5 is optionally substituted Ci- C10 alkyl. For example, R5 can be C1-C10 alkyl substituted with ORc, and is optionally further substituted; e.g., C1-C4 alkyl substituted with OR _c , and is optionally further substituted; e.g., C1-C4 alkyl substituted with OH, and is optionally further substituted.

[0028] In certain embodiments, R ₅ is:

wherein R _8a , Rsb, Rsc, and Rs _d are each independently selected from the group consisting of hydrogen, fluoro, optionally substituted C1-C10 alkyl, and optionally substituted C3-C12 cycloalkyl; or alternatively, a geminal Rs _a and Rsb, or a geminal Rs _c and Rsa, can each independently be taken together with the carbon atom to which they are attached to form an optionally substituted C3-C12 cycloalkyl or an optionally substituted heterocyclic;

Y is O, S or R _; ; t and r are each independently 0, 1, 2 or 3;

R9 is selected from the group consisting of hydrogen, optionally substituted C1-C1 ₀ alkyl, optionally substituted C3-C12 cycloalkyl, halo, optionally substituted heterocyclic, optionally substituted aryl, and optionally substituted heteroaryl; and

Ri is selected from the group consisting of hydrogen, optionally substituted C1-C1 ₀ alkyl, optionally substituted C2-C1 ₀ alkenyl, optionally substituted C2-C1 ₀ alkynyl, optionally substituted C3-C12 cycloalkyl, optionally substituted C3-C12 cycloalkenyl, optionally substituted heterocyclic, optionally substituted aryl and optionally substituted heteroaryl.

[0029] In certain of these embodiments, Rs _a , Rsb, Rs _c , and Rsa are each independently selected from the group consisting of hydrogen and C1-C10 alkyl substituted with ORc, and optionally further substituted. In certain of these embodiments, at least one of Rs _a , Rsb, Rs _c , and Rsa is C1-C1 ₀ alkyl substituted with OR _c , optionally further substituted; e.g., at least one of Rs _a , Rsb, Rs _c , and Re _d is C1-C1 ₀ alkyl substituted with OH, optionally further substituted. In certain of these embodiments, t is 1, 2 or 3. In certain of these embodiments, r is 1, 2 or 3.

[0030] As another example, Ri_b can

[0031] In certain embodiments, at least one of R6 and R7 is optionally substituted C1-C4 alkyl. In certain embodiments, at least one of R6 and R7 is optionally substituted C1-C4 alkyl and the other is hydrogen. For example, at least one of R6 and R7 is C1-C1 ₀ alkyl substituted with OR _c , and is optionally further substituted; at least one of R6 and R7 is C1-C4 alkyl substituted with OR _c , and is optionally further substituted; at least one of R6 and R7 is C1-C4 alkyl substituted with OH, and is optionally further substituted. In certain of these

embodiments, one of 5 and R7 is hydrogen.

[0032] In certain embodiments, at least one of R6 and R7 is independently:

wherein R _8a , Rsb, Rs _c , and Rsa are each independently selected from the group consisting of hydrogen, fluoro, optionally substituted C1-C1 ₀ alkyl, and optionally substituted C3-C12 cycloalkyl; or alternatively, a geminal Rs _a and Rsb, or a geminal Rs _c and Rsa, can each independently be taken together with the carbon atom to which they are attached to form an optionally substituted C3-C12 cycloalkyl or an optionally substituted heterocyclic;

Y is O, S or R _; ; t and r are each independently 0, 1, 2 or 3;

R9 is selected from the group consisting of hydrogen, optionally substituted C1-C1 ₀ alkyl, optionally substituted C3-C12 cycloalkyl, halo, optionally substituted heterocyclic, optionally substituted aryl, and optionally substituted heteroaryl; and

Ri is selected from the group consisting of hydrogen, optionally substituted C1-C1 ₀ alkyl, optionally substituted C2-C1 ₀ alkenyl, optionally substituted C2-C1 ₀ alkynyl, optionally substituted C3-C12 cycloalkyl, optionally substituted C3-C12 cycloalkenyl, optionally substituted heterocyclic, optionally substituted aryl and optionally substituted heteroaryl.

[0033] In certain of these embodiments, Rs _a , Rsb, Rs _c , and Rsa are each independently selected from the group consisting of hydrogen and C1-C10 alkyl substituted with ORc, and optionally further substituted. In certain of these embodiments, at least one of Rs _a , Rsb, Rs _c , and Rsa is C1-C1 ₀ alkyl substituted with OR _c , optionally further substituted; e.g., at least one of Rs _a , Rsb, Rs _c , and Re _d is C1-C1 ₀ alkyl substituted with OH, optionally further substituted. In certain of these embodiments, t is 1, 2 or 3. In certain of these embodiments, r is 1, 2 or 3. [0034] In some embodiments, R ₂ is hydrogen. In other embodiments, R ₂ is fluoro.

[0035] In some embodiments, m is 0. In other embodiments, m is 1. In some embodiments, p is 0. In other embodiments, p is 1.

[0036] In some embodiments, a disclosed compound has the Formula (lie), wherein R ₂ is hydrogen, and in another embodiment, Ri_ _b is

The disclosure thus encompasses compound of Formula (lie), wherein R ₂ is hydrogen and Ri-b is

[0037] Similarly, in some embodiments, a disclosed compound has the Formula (lie), wherein R ₂ is hydrogen, and s described above, the compound has the

Formula (lie), wherein Ri is

The disclosure thus also encompasses compounds of Formula (lie), wherein R ₂ is hydrogen and Ri is

[0038] In some embodiments, a disclosed compound has the following formula:

harmaceutically acceptable salts, stereoisomers, and prodrugs thereof, wherein:

R22 is optional, and is selected, independently, for each occurrence if present from the group consisting of halogen, and Ci-4alkyl (optionally substituted by one, two or three halogens); pp is 0, 1, 2 or 3;

R31 is selected from the group consisting of hydrogen, halogen, and C _1-4 alkyl;

Li is selected from the group consisting of C3-9 cycloalkylene, Cialkylene -C3-9 cycloalkylene- and -C ₃ _ ₉ cycloalkylene-Cialkylene (e.g., C ₃ -8 cycloalkylene, Cialkylene -C ₃ -9 cycloalkylene- and -C ₃ _ ₉ cycloalkylene-Cialkylene), wherein Li may be optionally substituted by one, two or three substituents selected from the group consisting of halogen, hydroxyl, and Ci- ₃ alkyl (optionally substituted by one, two or three substituents each selected independently from Rff);

[0039] R44 is selected from the group consisting of halogen, hydroxyl, -C(O)- OR', 4 to 6 membered heterocycloalkyl, a 5-6 membered monocyclic heteroaryl, and a 9-10 membered bicyclic heteroaryl, wherein the heteroaryl has one, two or three heteroatoms each selected from O, N, and S; and wherein the heteroaryl or heterocycloalkyl may be optionally substituted by one or two substituents each selected independently from R _gg (for example, R44 may be 5-6 membered monocyclic heteroaryl, optionally substituted by one or two substituents each selected independently from R _gg , or R44 may be a 9-10 membered bicyclic heteroaryl, optionally substituted by one or two substituents each selected independently from R _gg .);

Rff is selected for each occurrence from group consisting of halogen, hydroxyl, Ci- ₄ alkyl, Ci_ ₄ alkyoxy, C ₂ - ₄ alkenyl, oxo, -NR'R", -NR'-S(0) _w -Ci_ ₃ alkyl, S(0) _w -NR'R", and - S(0) _w -Ci_ ₃ alkyl, where w is 0, 1, or 2, wherein Ci_ ₄ alkyl, Ci_ ₄ alkyoxy, and C2- ₄ alkenyl may be optionally substituted by one, two or three substituents each independently selected from the group consisting of halogen, hydroxyl, -NR'R", -NR'-S(0) _w -Ci_ ₃ alkyl, S(0) _w -NR'R", and - SCOVd-salkyl;

R _gg is selected for each occurrence from group consisting of halogen, hydroxyl, Ci_ ealkyl, Ci_ ₆ alkoxy, C ₂ _ ₆ alkenyl, C ₃ - ₆ cycloalkyl, -O-C(O)- Ci_ ₆ alkyl, -C(0)-0- Ci_ ₆ alkyl, -C(O)- O- phenyl, -0-C(0)-phenyl, phenyl, 4 to 6 membered heterocycloalkyl, -NR'R", oxo, -NR'- S(0) _w -Ci_ ₃ alkyl, S(0) _w -NR'R", and -S(0) _w -Ci_ ₃ alkyl, where w is 0, 1, or 2, wherein Ci_ ₆ alkyl, Ci- ₆ alkyoxy, C2- ₆ alkenyl C3_ ₆ cycloalkyl, phenyl and heterocycloalkyl may each be optionally substituted by one, two or three substituents each independently selected from the group consisting of halogen, d_ ₆ alkyl, Ci_ ₆ alkoxy, hydroxyl, C(0)OH, -C(0)OCi_ ₆ alkyl, -0-C(0)Ci_ ₆ alkyl, 0-C(0)-phenyl, -C(0)0-NR'-Ci_ ₆ alkyl,-0-C ₃ - ₆ cycloalkyl, -O-heterocycle, phenyl, -O- heteroaryl, -O-phenyl, -NR'R", -NR'-S(0) _w -Ci_ ₃ alkyl, S(0) _w -NR'R", and -S(0) _w -Ci_ ₃ alkyl, where w is 0, 1, or 2; and

R' and R" are each independently selected for each occurrence from H and Ci_ ₄ alkyl or taken together with the nitrogen to which they are attached form a heterocyclic ring.

[0040] In certain embodiments, R22 is selected independently for each occurrence from H (e.g., when pp is 0 and R22 is absent); and F.

[0041] In certain embodiments, pp is 0 or pp is 1.

[0042] Li may be, for example, C ₃ _6 cycloalkylene, e.g., Li may be selected from the group consisting of C ₃ cycloalkylene , -C ₄ cycloalkylene-, Cscycloalkylene, C6cycloalkylene, - bicyclo[l.l. l]pentane-, -bicyclo[2.2.1]heptane -,and bicyclo[3.2.1]octane-. In certain embodimetns, Li is selected from the group consisting of -Cialkylene-C ₄ cycloalkylene, C ₄ cycloalkylene, and C ₄ cycloalkylene-Cialkylene-. For example, Li may be C ₄ cycloalkylene. Li may be substituted by one or two substituents each selected from the group consisting halogen, hydroxyl, and Ci- ₃ alkyl.

[0043] R44, in certain embodiments, may be selected from the group consisting of:

wherein X ₂ independently for each occurrence is selected from the group consisting of O or S; each ¾ _6, R77 and I½ is independently selected for each occurrence from H and R _gg (e.g., ¾6, R-77 and Rss are each independently selected for each occurrence from the group consisting of hydrogen, halogen, hydroxyl, Ci- ₆ alkyl, C3_ ₆ cycloalkyl, and heterocycloalkyl, wherein Ci_ ₆ alkyl, C3_ ₆ cycloalkyl, and heterocycloalkyl are optionally substituted by one, two or three substituents each independently selected from the group consisting of hydroxyl, Ci- ₆ alkyl, Ci_ ₆ alkoxy, -S(0) _w -Ci_ ₃ alkyl (w is 0, 1, or 2) and -NR'S(0) ₂ Ci_ ₆ alkyl; and R' and R" are each independently selected for each occurrence from H and for example, R66, R77 and Rss may each independently selected from the group selected from Ci-4alkyl, optionally substituted by one or two hydroxyls). For example, R44 may be represented by:

[0044] In certain other embodiments, R44 is heterocycloalkyl, e.g., R44 may be represented by:

[0045] In certain embodiments, a disclosed compound is represented by:

R44 may be for example, a 5-membered heteroaryl having two or three nitrogens, e.g., R44 may be a 5 membered heteroaryl having three nitrogens. In other embodiments, R44 is a 5 membered heteroaryl having two nitrogens and additional heteroatom selected from O or S. In certain of these embodiments, R44 is substituted on a free carbon by a substituent selected from the group consisting of: a methyl substituted by one, two or three substituents each selected from halogen, hydroxyl, methoxy and ethoxy, ethyl substituted by one, two or three substituents each selected from halogen, hydroxyl, methoxy and ethoxy, propyl substituted by one, two or three substituents each selected from halogen, hydroxyl, methoxy and ethoxy), isopropyl substituted by one, two or three substituents each selected from halogen, hydroxyl, methoxy and ethoxy, w-butyl substituted by one, two or three substituents each selected from halogen, hydroxyl, methoxy and ethoxy, t- butyl substituted by one, two or three substituents each selected from halogen, hydroxyl, methoxy and ethoxy, s -butyl substituted by one, two or three substituents each selected from halogen, hydroxyl, methoxy and ethoxy and isobutyl substituted by one, two or three substituents each selected from halogen, hydroxyl, methoxy and ethoxy.

[0046] In other embodiments, R44 is substituted on a free carbon by a substituent selected from the group consisting of: (e.g., where a group R-66, R77 or R ₈ 8 may be selected from the group consisting of:) wherein R _ggg is selected from the group consisting of H, Ci- ₆ alkyl, C(0)OH, -C(0)OCi_ alkyl, C(0)0-phenyl, and phenyl.

[0047] As above, R44 may be selected from the group consisting of:

wherein X ₂ independently for each occurrence is selected from the group consisting of O or S; each R66, R77 and Rgs is independently selected for each occurrence from H and R _gg as defined above (e.g., in certain embodiments, each R ₆ 6, R77 and Rss may be independently selected for each occurrence from H, halogen, hydroxyl, and Ci- ₆ alkyl, wherein Ci-6alkyl is optionally substituted by one, two or three substituents each independently selected from the group consisting of hydroxyl, Ci- ₆ alkoxy and -NR'S(0)2Ci_ ₆ alkyl).

[0048] For example, R44 may be represented by:

wherein ¾ ₆ is selected from the group consisting of: a methyl substituted by one, two or three substituents each selected from halogen, hydroxyl, methoxy and ethoxy, ethyl substituted by one, two or three substituents each selected from halogen, hydroxyl, methoxy and ethoxy, propyl substituted by one, two or three substituents each selected from halogen, hydroxyl, methoxy and ethoxy), isopropyl substituted by one, two or three substituents each selected from halogen, hydroxyl, methoxy and ethoxy, w-butyl substituted by one, two or three substituents each selected from halogen, hydroxyl, methoxy and ethoxy, ?-butyl substituted by one, two or three substituents each selected from halogen, hydroxyl, methoxy and ethoxy, s- butyl substituted by one, two or three substituents each selected from halogen, hydroxyl, methoxy and ethoxy, and isobutyl substituted by one, two or three substituents each selected from halogen, hydroxyl, methoxy and ethoxy

[0049] In another embodiment, R44 may be represented by:

wherein R ₇₇ and I½ are each independently selected from the group consisting of: hydrogen, a methyl substituted by one, two or three substituents each selected from halogen, hydroxyl, methoxy and ethoxy, ethyl substituted by one, two or three substituents each selected from halogen, hydroxyl, methoxy and ethoxy, propyl substituted by one, two or three substituents each selected from halogen, hydroxyl, methoxy and ethoxy, isopropyl substituted by one, two or three substituents each selected from halogen, hydroxyl, methoxy and ethoxy, n- butyl substituted by one, two or three substituents each selected from halogen, hydroxyl, methoxy and ethoxy, ?-butyl substituted by one, two or three substituents each selected from halogen, hydroxyl, methoxy and ethoxy, s-butyl substituted by one, two or three substituents each selected from halogen, hydroxyl, methoxy and ethoxy, and isobutyl substituted by one, two or three substituents each selected from halogen, hydroxyl, methoxy and ethoxy.

[0050] Exemplary compounds provided by this disclosure include compounds and pharmaceutically acceptable salts thereof named below and throughout this disclosure, including the examples and the claims.

[0051] For example, contemplated herein is a compound selected from the group consisting of: N-?ra«s-3-(5-(hydroxymethyl)-lH-l,2,3-triazol-l-yl)cyclobut yl)-5-phenylisoxazole-3- carboxamide; N-?raws-3-(4-(hydroxymethyl)- 1H- 1 ,2, 3 -triazol- l-yl)cyclobutyl)-5- phenylisoxazole-3 -carboxamide; N-cis-3 -(5-(hydroxymethyl)- 1H- 1 ,2,3-triazol- 1 -yl) cyclobutyl)-5-phenylisoxazole-3 -carboxamide; N-cis-3 -(4-(hydroxymethyl)- 1 H- 1 ,2,3 -triazol- 1 - yl) cyclobutyl)-5-phenylisoxazole-3 -carboxamide; N-cis-3 -(4-((S)- 1 -hydroxyethyl)- 1 H- 1 ,2,3 - triazol- l-yl)cyclobutyl)-5-phenylisoxazole-3-carboxamide; N-cis-3 -(5 -((S)-l -hydroxy ethyl)- 1 H- 1 ,2,3-triazol- 1 -yl)cyclobutyl)-5 -phenylisoxazole-3 -carboxamide; N-((tran$-3 -(5- (hydroxymethyl)-l,3,4-thiadiazol-2-yl)cyclobutyl)methyl)-5-p henylisoxazole-3-carboxamide; N-((c«-3-(5-(hydroxymethyl)-l,3,4-thiadiazol-2-yl)cyclobuty l)methyl)-5-phenylisoxazole-3- carboxamide; N-((?ra«s-3-((5-(hydroxymethyl)-l,3,4-thiadiazol-2-yl)methy l)cyclobutyl)-5- phenylisoxazole-3 -carboxamide; N-((c«-3-((5-(hydroxymethyl)-l,3,4-thiadiazol-2- yl)methyl)cyclobutyl)-5-phenylisoxazole-3-carboxamide; N-(trans-3 -(5 -((S)-l -hydroxy ethyl)- 1 H- 1 ,2,3-triazol- 1 -yl)cyclobutyl)-5 -phenylisoxazole-3 -carboxamide; N-(trans-3 -(4-((S)- 1 - hydroxyethyl)- 1 H- 1 ,2,3 -triazol- 1 -yl)cyclobutyl)-5-phenylisoxazole-3 -carboxamide; N-(trans-3- (5-((R)- 1 -hydroxyethyl)- 1H- 1 ,2,3 -triazol- 1 -yl)cyclobutyl)-5-phenylisoxazole-3-carboxamide; N-(trans-3 -(4-((R)- 1 -hydroxyethyl)- 1 H- 1 ,2,3-triazol- 1 -yl)cyclobutyl)-5-phenylisoxazole-3 - carboxamide; N-(cis-3 -(5 -((R)- 1 -hydroxyethyl)- 1 H- 1 ,2,3-triazol- 1 -yl)cyclobutyl)-5- phenylisoxazole-3 -carboxamide; N-(cis-3 -(4-((R)- 1 -hydroxyethyl)- 1 H- 1 ,2,3-triazol- 1 - yl)cyclobutyl)-5 -phenylisoxazole-3 -carboxamide; N-(trans-3-(5-((R)-l -hydroxyethyl)- 1, 3,4- oxadiazol-2-yl)cyclobutyl)-5 -phenylisoxazole-3 -carboxamide; N-(trans-3-(5-((S)-l- hydroxyethyl)-l,3,4-oxadiazol-2-yl)cyclobutyl)-5-phenylisoxa zole-3-carboxamide; N-(trans-3- (5-(hydroxymethyl)-l,3,4-oxadiazol-2-yl)cyclobutyl)-5-phenyl isoxazole-3-carboxamide; N- ?ra«s-3-(5-((R)-l-hydroxyethyl)-l,3,4-thiadiazol-2-yl)cyclo butyl)-5-phenylisoxazole-3- carboxamide; N-tra«s-3-(5-((S)-l -hydroxyethyl)- 1, 3,4-thiadiazol-2-yl)cyclobutyl)-5- phenylisoxazole-3 -carboxamide; N-£raws-3-(5-(hydroxymethyl)-l,3,4-thiadiazol-2- yl)cyclobutyl)-5-phenylisoxazole-3-carboxamide; N-czs-3-(5-(hydroxymethyl)-l,3,4-thiadiazol- 2-yl)cyclobutyl)-5-phenylisoxazole-3-carboxamide; N-czs-3-(5-((S)-l-hydroxyethyl)- 1,3,4- thiadiazol-2-yl)cyclobutyl)-5-phenylisoxazole-3-carboxamide; N-cz ^' s-3-(5-((R)-l- hydroxyethyl)-l,3,4-thiadiazol-2-yl)cyclobutyl)-5-phenylisox azole-3-carboxamide; N-cis-3-(5- (hydroxymethyl)-l, 3, 4-oxadiazol-2-yl)cyclobutyl)-5-phenylioxazole-3 -carboxamide; N-cis-3- (5-((R)-l -hydroxyethyl)- l,3,4-oxadiazol-2-yl)cyclobutyl)-5-phenylisoxazole-3-carboxa mide; N-c«-3-(5-((S)-l-hydroxyethyl)-l,3,4-oxadiazol-2-yl)cyclobu tyl)-5-phenylisoxazole-3- carboxamide; N-c«-3-(5-((R)-l,2-dihydroxyethyl)-l,3,4-thiadiazol-2-yl)cy clobutyl)-5- phenylisoxazole-3-carboxamide; (l-cis-3-(5-phenylisoxazole-3-carboxamido)cyclobutyl)-lH-

1.2.3- triazol-4-yl)methyl butylcarbamate; N- trans-3-(4-(R)-l -hydroxy ethyl)- lH-pyrazol-1 - yl)cyclobutyl)-5-phenylisoxazole-3 -carboxamide; N-trans-3 -(4-(S)- 1 -hydroxyethyl)- 1 H- pyrazol- 1 -yl)cyclobutyl)-5 -phenylisoxazole-3 -carboxamide; N-trans-3 -(5-((R)- 1 - hydroxyethyl)- 1 H-pyrazol- 1 -yl)cyclobutyl)-5-phenylisoxazole-3 -carboxamide; N-trans-3-(5- ((S)- 1 -hydroxyethyl)- 1 H-pyrazol- 1 -yl)cyclobutyl)-5 -phenylisoxazole-3 -carboxamide; N-(cis-3- (4-(hydroxymethyl)-l H-pyrazol- l-yl)cyclobutyl)-5 -phenylisoxazole-3 -carboxamide; N-(trans- 3-(4-(hydroxymethyl)-lH-pyrazol-l-yl)cyclobutyl)-5-phenyliso xazole-3-carboxamide; N-cis- 3-(3-(hydroxymethyl)-lH-pyrazol-l-yl)cyclobutyl)-5-phenyliso xazole-3-carboxamide; N- ?ra«s-3-(3-(hydroxymethyl)-lH-pyrazol-l-yl)cyclobutyl)-5-ph enylisoxazole-3-carboxamide; N-?ra«s-3-(3-(hydroxymethyl)-l,2,4-oxadiazol-5-yl)cyclobuty l)-5-phenylisoxazole-3- carboxamide; N-czs-3-(3-(hydroxymethyl)- 1 ,2,4-oxadiazol-5-yl)cyclobutyl)-5-phenylisoxazole- 3 -carboxamide; N-(c¾-3-(5-(hydroxymethyl)-l,2,4-oxadiazol-3-yl)cyclobutyl) -5- phenylisoxazole-3 -carboxamide; N-(?raws-3-(5-(hydroxymethyl)-l,2,4-oxadiazol-3- yl)cyclobutyl)-5 -phenylisoxazole-3 -carboxamide; N-(trans-3 -((5-((S)- 1 -hydroxyethyl)- 1,3,4- thiadiazol-2-yl)methyl)cyclobutyl)-5-phenylisoxazole-3-carbo xamide; N-(cz ^' s-3-((5-((S)-l- hydroxyethyl)-l,3,4-thiadiazol-2-yl)methyl)cyclobutyl)-5-phe nylisoxazole-3-carboxamide; 5- phenyl-N-[(tra«5-3-([5-[(lR)-l-hydroxyethyl]-l,3,4-thiadiaz ol-2- yl]methyl)cyclobutyl]isoxazole-3-carboxamide; 5-phenyl-N-[(czs-3-([5-[(lR)-l-hydroxyethyl]-

1.3.4- thiadiazol-2-yl]methyl)cyclobutyl]isoxazole-3-carboxamide; N-trans-3-(2- hydroxyethyl)cyclobutyl)-5-phenylisoxazole-3 -carboxamide; N-cis-3 -(2- hydroxyethyl)cyclobutyl)-5-phenylisoxazole-3-carboxamide; N-(cis-3-

(methylsulfonamidomethyl)cyclobutyl)-5-phenylisoxazole-3- carboxamide; N-(traws-3-(3-((S)- l-hydroxyethyl)-l,2,4-oxadiazol-5-yl)cyclobutyl)-5-phenyliso xazole-3 -carboxamide; N-(trans- 3 -(3 -((R)- 1 -hydroxy ethyl)- 1 ,2,4-oxadiazol-5 -yl)cyclobutyl)-5 -phenylisoxazole-3 -carboxamide; N-(c«-3-((5-((R)-l-hydroxyethyl)-l,3,4-oxadiazol-2-yl)methy l)cyclobutyl)-5-phenylisoxazole- 3 -carboxamide; N-(trans-3 -((5-((R)- 1 -hydroxyethyl)- 1 ,3 ,4-oxadiazol-2-yl)methyl)cyclobutyl)- 5 -phenylisoxazole-3 -carboxamide; N-((trans-3-((5-((S)-l -hydroxyethyl)- 1,3, 4-oxadiazol-2- yl)methyl)cyclobutyl)-5-phenylisoxazole-3-carboxamide; N-((czs-3-((5-((S)-l-hydroxyethyl)- l,3,4-oxadiazol-2-yl)methyl)cyclobutyl)-5-phenylisoxazole-3- carboxamide; N-(trans-3-(5- ((R)-l-hydroxyethyl)-l,2,4-oxadiazol-3-yl)cyclobutyl)-5-phen ylisoxazole-3-carboxamide; N- (trans-3 -(5 -((S)-l -hydroxy ethyl)- l,2,4-oxadiazol-3-yl)cyclobutyl)-5 -phenylisoxazole-3 - carboxamide; 5-phenyl-N-[?ra«s-3-[5-(l-methylazetidin-3-yl)-l,3,4-oxadia zol-2- yl]cyclobutyl]isoxazole-3-carboxamide; 5-(4-fluorophenyl)-N-[Yra¾s-3-[5-[(lR)-l- hydroxyethyl]-l,3,4-oxadiazol-2-yl]cyclobutyl]isoxazole-3-ca rboxamide; 5-phenyl-N-[trans-3- [5-[(lR)-l-methoxyethyl]-l,3,4-oxadiazol-2-yl]cyclobutyl]iso xazole-3-carboxamide; (1R)-1- [5-[?ra«s-3-(5-phenylisoxazole-3-amido)cyclobutyl]-l,3,4-ox adiazol-2-yl]ethyl acetate; (R)-l- (5-(?ra«s-3-(5-phenylisoxazole-3-carboxamido)cyclobutyl)-l, 3,4-oxadiazol-2-yl)ethyl benzoate; N-(?ra«s-3-(5-((R)-l-isopropoxyethyl)-l,3,4-oxadiazol-2-yl) cyclobutyl)-5- phenylisoxazole-3 -carboxamide; N-(?raws-3-(5-((R)-l-isobutoxyethyl)-l,3,4-oxadiazol-2- yl)cyclobutyl)-5 -phenylisoxazole-3 -carboxamide; tert-butyl 3-(5-(7raws-3-(5-phenylisoxazole- 3 -carboxamido)cyclobutyl)- 1 ,3 ,4-oxadiazol-2-yl)azetidine- 1 -carboxylate; (5-phenyl-N-[?ra«s- 3-[5-(azetidin-3-yl)-l,3,4-oxadiazol-2-yl]cyclobutyl]isoxazo le-3-carboxamide; N-(trans-3-(5- (oxetan-3-yl)-l,3,4-oxadiazol-2-yl)cyclobutyl)-5-phenylisoxa zole-3-carboxamide; N-(trans-3- (l-methyl-lH-benzo[d]imidazol-2-yl)cyclobutyl)-5-phenylisoxa zole-3-carboxamide; 5-(2,4- difluorophenyl)-N-(7raws-3 -(5 -((R)- 1 -hydroxyethyl)- 1 ,3 ,4-oxadiazol-2-yl)cyclobutyl)isoxazole- 3 -carboxamide; 5 -(3 -fluorophenyl)-N-(?ra«s-3 -(5-((R)- 1 -hydroxyethyl)- 1 ,3 ,4-oxadiazol-2- yl)cyclobutyl)isoxazole-3-carboxamide; 5-(2-fluorophenyl)-N-(?raws-3-(5-((R)-l- hydroxyethyl)-l,3,4-oxadiazol-2-yl)cyclobutyl)isoxazole-3-ca rboxamide; 5-(4- hydroxyphenyl)-N-(7raws-3 -(5-((R)- 1 -hydroxyethyl)- 1 ,3 ,4-oxadiazol-2- yl)cyclobutyl)isoxazole-3-carboxamide; 5-(3-hydroxyphenyl)-N-(?ra«s-3-(5-((R)-l- hydroxyethyl)-l,3,4-oxadiazol-2-yl)cyclobutyl)isoxazole-3-ca rboxamide; 5-(3,4- difluorophenyl)-N-(7raws-3 -(5 -((R)- 1 -hydroxyethyl)- 1 ,3 ,4-oxadiazol-2-yl)cyclobutyl)isoxazole- 3 -carboxamide; N-(trans-3 -(5 -((R)- 1 -(methylsulfonyl)ethyl)- 1 ,3 ,4-oxadiazol-2-yl)cyclobutyl)- 5-phenylisoxazole-3-carboxamide; N-(?raws-3-(5-cyclobutyl-l,3,4-oxadiazol-2-yl)cyclobutyl)- 5 -phenylisoxazole-3 -carboxamide; N-(?raws-3-(lH-imidazol-l-yl)cyclobutyl)-5- phenylisoxazole-3 -carboxamide; N-(3-(5-((R)-l-hydroxyethyl)-l,3,4-oxadiazol-2- yl)cyclohexyl)-5-phenylisoxazole-3-carboxamide; N-(3-(4-(hydroxymethyl)-lH-l,2,3-triazol- 1 -yl)cyclohexyl)-5-phenylisoxazole-3 -carboxamide; N-(3 -(5 -(hydroxymethyl)- 1 H- 1 ,2,3 - triazol-l-yl)cyclohexyl)-5-phenylisoxazole-3-carboxamide; N-[3-[5-(hydroxymethyl)- 1,3,4- oxadiazol-2-yl]cyclopentyl]-5-phenylisoxazole-3-carboxamide; N-(cis/trans-4-(5- (hydroxymethyl)-l, 3, 4-oxadiazol-2-yl)cyclohexyl)-5 -phenylisoxazole-3 -carboxamide; 5 -(3 ,4- dihydroxyphenyl)-N-(?ra«s-3-(5-((R)-l-hydroxyethyl)-l,3,4-o xadiazol-2- yl)cyclobutyl)isoxazole-3-carboxamide; N-(?ra«s-3-(lH-benzo[d]imidazol-l-yl)cyclobutyl)-5- phenylisoxazole-3 -carboxamide; N-(trans-3 -(5 -( 1 , 1 -dioxidothietan-3 -yl)- 1 ,3 ,4-oxadiazol-2- yl)cyclobutyl)-5 -phenylisoxazole-3 -carboxamide; N-(3-(4-(hydroxymethyl)-lH-l,2,3-triazol-l- yl)cyclopentyl)-5-phenylisoxazole-3-carboxamide; and N-(3 -(5 -(hydroxymethyl)- 1H- 1,2,3- triazol-l-yl)cyclopentyl)-5-phenylisoxazole-3-carboxamide, and pharmaceutically acceptable salts thereof.

[0052] Also contemplated herein are pharmaceutical compositions that include a disclosed compound such as those compounds having e.g., the above formulas, e.g., Formula la, (Ila), (lib), (lie) (lid), (Ilia), or (Illb) and a pharmaceutically acceptable carrier or excipient. In certain embodiments, the compositions can include at least one additional CFTR modulator as described anywhere herein or at least two additional CFTR modulators, each independently as described anywhere herein.

[0053] Also contemplated herein are compounds represented by: or salt thereof, wherein tt is 0, 1, or 2; rr is 1, 2 or 3; ss is 0 or 1; R55, R56, and R57 are each independently selected from the group consisting of: halogen, hydroxyl, and Ci- ₃ alkyl (optionally substituted by one, two or three substituents each selected independently from Rff) _;

Rff is selected for each occurrence from group consisting of halogen, hydroxyl, Ci_ ₄ alkyl, Ci_ ₄ alkyoxy, C ₂ - ₄ alkenyl, -NR'R", -NR'-S(0) _w -Ci_ ₃ alkyl, S(0) _w -NR'R", and -S(0) _w - Ci_ ₃ alkyl, where w is 0, 1, or 2, wherein Ci_ ₄ alkyl, Ci_ ₄ alkyoxy, and C2- ₄ alkenyl may be optionally substituted by one, two or three substituents each independently selected from the group consisting of halogen, hydroxyl, -NR'R", -NR'-S(0) _w -Ci_ ₃ alkyl, S(0) _w -NR'R", and - S(OVCi-3alkyl;

R' and R" are each independently selected for each occurrence from H and Ci_ ₄ alkyl or taken together with the nitrogen to which they are attached form a heterocyclic ring; and

R45 is selected from the group consisting of:

wherein

X2 independently for each occurrence is selected from the group consisting of O or S; and each ¾ _6, R77 and Rss is independently selected for each occurrence from H and R _gg as defined above, (for example selected from the group consisting of, halogen, hydroxyl, and Ci_ ₆ alkyl, wherein Ci- ₆ alkyl is optionally substituted by one, two or three substituents each independently selected from the group consisting of hydroxyl, Ci- ₆ alkoxy and -NR' S(0)2Ci_ ₆ alkyl).

[0054] It is to be understood that the specific embodiments described herein can be taken in combination with other specific embodiments delineated herein.

[0055] The features and other details of the disclosure will now be more particularly described. Before further description of the present invention, certain terms employed in the specification, examples and appended claims are collected here. These definitions should be read in light of the remainder of the disclosure and as understood by a person of skill in the art. Unless defined otherwise, all technical and scientific terms used herein have the same meaning as commonly understood by a person of ordinary skill in the art.

[0056] It will be appreciated that the description of the disclosure should be construed in congruity with the laws and principals of chemical bonding.

[0057] The term "alkyl", as used herein, unless otherwise indicated, refers to both branched and straight-chain saturated aliphatic hydrocarbon groups having the specified number of carbon atoms; for example, "C1-C1 ₀ alkyl" denotes alkyl having 1 to 10 carbon atoms, and straight or branched hydrocarbons of 1-6, 1-4, or 1-3 carbon atoms, referred to herein as Ci_ ₆ alkyl, and Ci_ ₃ alkyl, respectively. Examples of alkyl include, but are not limited to, methyl, ethyl, n-propyl, i-propyl, n-butyl, i-butyl, sec-butyl, t-butyl, n-pentyl, n-hexyl, 2- methylbutyl, 2-methylpentyl, 2-ethylbutyl, 3-methylpentyl, and 4-methylpentyl.

[0058] The term, "alkenyl", as used herein, refers to both straight and branched-chain moieties having the specified number of carbon atoms and having at least one carbon-carbon double bond. Exemplary alkenyl groups include, but are not limited to, a straight or branched group of 2-6 or 3-4 carbon atoms, referred to herein as C2- ₆ alkenyl, and C3-4alkenyl, respectively. Exemplary alkenyl groups include, but are not limited to, vinyl, allyl, butenyl, pentenyl, etc.

[0059] The term, "alkynyl", as used herein, refers to both straight and branched-chain moieties having the specified number or carbon atoms and having at least one carbon-carbon triple bond. [0060] The term "cycloalkyl," as used herein, refers to saturated cyclic alkyl moieties having 3 or more carbon atoms, for example, 3-10, 3-8, 3-6, or 4-6 carbons, referred to herein as C3_iocycloalkyl, C3- ₆ cycloalkyl or C4- ₆ cycloalkyl, respectively., The term cycloalkyl also includes bridged or fused cycloalkyls. Examples of cycloalkyl include, but are not limited to, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, adamantyl,

bicyclo[l . l . l]pentane-, bicyclo[2.2.1]heptane ,and bicyclo[3.2.1]octane. The term

"cycloalkenyl," as used herein, refers to cyclic alkenyl moieties having 3 or more carbon atoms.

[0061] The term "cycloalkynyl," as used herein, refers to cyclic alkynyl moieties having 5 or more carbon atoms.

[0062] Alkylene" means a straight or branched, saturated aliphatic divalent radical having the number of carbons indicated. "Cycloalkylene" refers to a divalent radical of carbocyclic saturated hydrocarbon group having the number of carbons indicated.

[0063] The term "alkoxy" as used herein refers to a straight or branched alkyl group attached to oxygen (alkyl-O-). Exemplary alkoxy groups include, but are not limited to, alkoxy groups of 1-6 or 2-6 carbon atoms, referred to herein as Ci- ₆ alkoxy, and C2- ₆ alkoxy, respectively. Exemplary alkoxy groups include, but are not limited to methoxy, ethoxy, isopropoxy, etc.

[0064] The term "heterocyclic" or "heterocycle" encompasses heterocycloalkyl, heterocycloalkenyl, heterobicycloalkyl, heterobicycloalkenyl, heteropolycycloalkyl, heteropolycycloalkenyl, and the like unless indicated otherwise. Heterocycloalkyl refers to cycloalkyl groups containing one two, or three heteroatoms within the ring (O, S(0) _w , or NR where w is 0, 1, or 2 and R is e.g., H, Ci_ ₃ alkyl, phenyl) and for example 3, 4, or 5 carbons within the ring. Heterocycloalkenyl as used herein refers to cycloalkenyl groups containing one or more heteroatoms (O, S or N) within the ring. Heterobicycloalkyl refers to bicycloalkyl groups containing one or more heteroatoms (O, S(0) _w or NR) within a ring.

Heterobicycloalkenyl as used herein refers to bicycloalkenyl groups containing one or more heteroatoms (O, S or N) within a ring, a heterocycle can refer to, for example, a saturated or partially unsaturated 4- to 12 or 4-10-membered ring structure, including bridged or fused rings, and whose ring structures include one to three heteroatoms, such as nitrogen, oxygen, and sulfur. Where possible, heterocyclic rings may be linked to the adjacent radical through carbon or nitrogen. Examples of heterocyclic groups include, but are not limited to, pyrrolidine, piperidine, morpholine, morpholine-one, thiomorpholine, piperazine, oxetane, azetidine, thietane dioxide, tetrahydrofuran or dihydrofuran etc.

[0065] Cycloalkyl, cycloalkenyl, heterocyclic, groups also include groups similar to those described above for each of these respective categories, but which are substituted with one or more oxo moieties.

[0066] The term "aryl", as used herein, refers to mono- or polycyclic aromatic carbocyclic ring systems. A polycyclic aryl is a polycyclic ring system that comprises at least one aromatic ring. Polycyclic aryls can comprise fused rings, covalently attached rings or a combination thereof. The term "aryl" embraces aromatic radicals, such as, phenyl, naphthyl, indenyl, tetrahydronaphthyl, and indanyl. An aryl group may be substituted or unsubstituted. In some embodiments, the aryl is a C4-C10 aryl. Examples of optionally substituted aryl are phenyl, substituted phenyl, napthyl and substituted naphthyl.

[0067] The term "heteroaryl", as used herein, refers to aromatic carbocyclic groups containing one or more heteroatoms (O, S, or N) within a ring. A heteroaryl group, unless indicated otherwise, can be monocyclic or polycyclic. A heteroaryl group may additionally be substituted or unsubstituted. The heteroaryl groups of this disclosure can also include ring systems substituted with one or more oxo moieties. A polycyclic heteroaryl can comprise fused rings, covalently attached rings or a combination thereof. A polycyclic heteroaryl is a polycyclic ring system that comprises at least one aromatic ring containing one or more heteroatoms within a ring. Examples of heteroaryl groups include, but are not limited to, pyridinyl, pyridazinyl, imidazolyl, pyrimidinyl, pyrazolyl, triazolyl, pyrazinyl, quinolyl, isoquinolyl, tetrazolyl, furyl, thienyl, isoxazolyl, thiazolyl, oxazolyl, isothiazolyl, pyrrolyl, quinolinyl, isoquinolinyl, indolyl, benzimidazolyl, benzofuranyl, cinnolinyl, indazolyl, indolizinyl, phthalazinyl, triazinyl, isoindolyl, purinyl, oxadiazolyl, thiadiazolyl, furazanyl, benzofurazanyl, benzothiophenyl, benzotriazolyl, benzothiazolyl, benzoxazolyl, quinazolinyl, quinoxalinyl, naphthyridinyl, dihydroquinolyl, tetrahydroquinolyl, dihydroisoquinolyl, tetrahydroisoquinolyl, benzofuryl, furopyridinyl, pyrolopyrimidinyl, thiazolopyridinyl, oxazolopyridinyl and azaindolyl. The foregoing heteroaryl groups may be C-attached or heteroatom-attached (where such is possible). For instance, a group derived from pyrrole may be pyrrol- 1-yl (N-attached) or pyrrol-3-yl (C-attached). In some embodiments, the heteroaryl is 4- to 12-membered heteroaryl. In yet other embodiments, the heteroaryl is a mono or bicyclic 4- to 10-membered heteroaryl.

[0068] The term "substituted" refers to substitution by independent replacement of one, two, or three or more of the hydrogen atoms with substituents including, but not limited to, and unless indicated otherwise, -C1-C12 alkyl, -C ₂ -C ₁₂ alkenyl, -C ₂ -C ₁₂ alkynyl, -C3-C12 cycloalkyl, -C ₃ -C ₁₂ cycloalkenyl, C3-C12 cycloalkynyl, -heterocyclic, -F, -CI, -Br, -I, -OH, -N0 ₂ , -N ₃ , -CN, -NH ₂ , oxo, thioxo, -NHR _X , -NR _X R _X , dialkylamino, -diarylamino, -diheteroarylamino, -OR _x , - C(0)R _y , -C(0)C(0)R _y , -OC0 ₂ R _y , -OC(0)R _y , OC(0)C(0)R _y , -NHC(0)R _y , -NHC0 ₂ R _y , - NHC(0)C(0)R _y , NHC(S)NH ₂ , -NHC(S)NHR _X , -NHC(NH)NH ₂ , -NHC( H)NHR _X , - NHC( H)R _X , -C( H)NHR _X , and (C=NR _X )R _X ; -NRxC(0)R _x , -NR _x C(0)N(R _x ) ₂ , -NRxC0 ₂ R _y , - NRxC(0)C(0)R _y , -NR _X C(S)NH ₂ , -NR _X C(S)NHR _X , -NR _X C(NH)NH ₂ , -NR _X C(NH)NHR _X , - NR _X C( H)R _X , -C( Rx)NHR _x -S(0)R _y , -NHS0 ₂ R _x , -CH ₂ NH ₂ , -CH ₂ S0 ₂ CH ₃ , -aryl, -arylalkyl, - heteroaryl, -heteroarylalkyl, -heterocycloalkyl, -C ₃ -Ci ₂ -cycloalkyl, -polyalkoxyalkyl, - polyalkoxy, -methoxymethoxy, -methoxyethoxy, -SH, -S-R _x , or -methylthiomethyl, wherein R _x is selected from the group consisting of hydrogen, -Ci-Ci ₂ alkyl, -C ₂ -Ci ₂ alkenyl, -C ₂ -Ci ₂ alkynyl, -C ₃ -Ci ₂ cycloalkyl, -aryl, -heteroaryl and -heterocyclic and -R _y is selected from the group consisting of hydrogen, -Ci-Ci ₂ alkyl, -C ₂ -Ci ₂ alkenyl, -C ₂ -Ci ₂ alkynyl, -C ₃ -Ci ₂ cycloalkyl, -aryl, -heteroaryl, -heterocyclic, -NH ₂ , -NH-Ci-Ci ₂ alkyl, -NH-C ₂ -Ci ₂ alkenyl, -NH- C ₂ -Ci ₂ -alkynyl, -NH-C ₃ -Ci ₂ cycloalkyl, -NH-aryl, -NH-heteroaryl and -NH-heterocyclic. It is understood that the aryls, heteroaryls, alkyls, and the like can be further substituted.

[0069] The terms "halo" or "halogen" as used herein refer to F, CI, Br, or I.

[0070] The term "haloalkyl" as used herein refers to an alkyl group having 1 to (2n+l) substituent(s) independently selected from F, CI, Br or I, where n is the maximum number of carbon atoms in the alkyl group. It will be understood that haloalkyl is a specific example of an optionally substituted alkyl.

[0071 ] The terms "hydroxy" and "hydroxyl" as used herein refers to the radical -OH.

[0072] As will be understood by the skilled artisan, "H" is the symbol for hydrogen, "N" is the symbol for nitrogen, "S" is the symbol for sulfur, "O" is the symbol for oxygen. "Me" is an abbreviation for methyl.

[0073] The compounds of the disclosure may contain one or more chiral centers and, therefore, exist as stereoisomers. The term "stereoisomers" when used herein consist of all enantiomers or diastereomers. These compounds may be designated by the symbols "(+)," "(- )," "R" or "S," depending on the configuration of substituents around the stereogenic carbon atom, but the skilled artisan will recognize that a structure may denote a chiral center implicitly. The present disclosure encompasses various stereoisomers of these compounds and mixtures thereof. Mixtures of enantiomers or diastereomers may be designated "(±)" in nomenclature, but the skilled artisan will recognize that a structure may denote a chiral center implicitly.

[0074] The compounds of the disclosure may contain one or more double bonds and, therefore, exist as geometric isomers resulting from the arrangement of substituents around a carbon-carbon double bond. The symbol =: denotes a bond that may be a single, double or triple bond as described herein. Substituents around a carbon-carbon double bond are designated as being in the "Z" or configuration wherein the terms "Z" and "is" are used in accordance with IUPAC standards. Unless otherwise specified, structures depicting double bonds encompass both the "E" and "Z" isomers. Substituents around a carbon-carbon double bond alternatively can be referred to as "cis" or "trans," where "cis" represents substituents on the same side of the double bond and "trans" represents substituents on opposite sides of the double bond.

[0075] Compounds of the disclosure may contain a carbocyclic or heterocyclic ring and therefore, exist as geometric isomers resulting from the arrangement of substituents around the ring. The arrangement of substituents around a carbocyclic or heterocyclic ring are designated as being in the "Z" or "E" configuration wherein the terms "Z" and "E" are used in accordance with IUPAC standards. Unless otherwise specified, structures depicting carbocyclic or heterocyclic rings encompass both "Z" and "E" isomers. Substituents around a carbocyclic or heterocyclic ring may also be referred to as "cis" or "trans", where the term "cis" represents substituents on the same side of the plane of the ring and the term "trans" represents substituents on opposite sides of the plane of the ring. Mixtures of compounds wherein the substituents are disposed on both the same and opposite sides of plane of the ring are designated "cis/trans."

[0076] Individual enantiomers and diasterisomers of compounds of the present disclosure can be prepared synthetically from commercially available starting materials that contain asymmetric or stereogenic centers, or by preparation of racemic mixtures followed by resolution methods well known to those of ordinary skill in the art. These methods of resolution are exemplified by (1) attachment of a mixture of enantiomers to a chiral auxiliary, separation of the resulting mixture of diastereomers by recrystallization or chromatography and liberation of the optically pure product from the auxiliary, (2) salt formation employing an optically active resolving agent, (3) direct separation of the mixture of optical enantiomers on chiral liquid chromatographic columns or (4) kinetic resolution using stereoselective chemical or enzymatic reagents. Racemic mixtures can also be resolved into their component enantiomers by well known methods, such as chiral-phase liquid chromatography or crystallizing the compound in a chiral solvent. Stereoselective syntheses, a chemical or enzymatic reaction in which a single reactant forms an unequal mixture of stereoisomers during the creation of a new stereocenter or during the transformation of a pre-existing one, are well known in the art. Stereoselective syntheses encompass both enantio- and diastereoselective transformations, and may involve the use of chiral auxiliaries. For examples, see Carreira and Kvaerno, Classics in Stereoselective Synthesis, Wiley-VCH: Weinheim, 2009. Where a particular compound is described or depicted, it is intended to encompass that chemical structure as well as tautomers of that structure.

[0077] The term "enantiomerically pure" means a stereomerically pure composition of a compound. For example, a stereochemically pure composition is a composition that is free or substantially free of other stereoisomers of that compound. In another example, for a compound having one chiral center, an enantiomerically pure composition of the compound is free or substantially free of the other enantiomer. In yet another example, for a compound having two chiral centers, an enantiomerically pure composition is free or substantially free of the other diastereomers.

[0078] Where a particular stereochemistry is described or depicted it is intended to mean that a particular enantiomer is present in excess relative to the other enantiomer. A compound has an R-configuration at a specific position when it is present in excess compared to the compound having an S-configuration at that position. A compound has an S-configuration at a specific position when it is present in excess compared to the compound having an R- configuration at that position.

[0079] The compounds disclosed herein can exist in solvated as well as unsolvated forms with pharmaceutically acceptable solvents such as water, ethanol, and the like, and it is intended that the disclosure embrace both solvated and unsolvated forms. In one embodiment, the compound is amorphous. In one embodiment, the compound is a single polymorph. In another embodiment, the compound is a mixture of polymorphs. In another embodiment, the compound is in a crystalline form.

[0080] The disclosure also embraces isotopically labeled compounds of the disclosure which are identical to those recited herein, except that one or more atoms are replaced by an atom having an atomic mass or mass number different from the atomic mass or mass number usually found in nature. Examples of isotopes that can be incorporated into compounds of the disclosure include isotopes of hydrogen, carbon, nitrogen, oxygen, phosphorus, sulfur, fluorine and chlorine, such as ² H, ³ H, ¹³ C, ¹⁴ C, ¹⁵ N, ¹⁸ 0, ¹⁷ 0, ³¹ P, ³² P, ³⁵ S, ¹⁸ F, and ³⁶ C1, respectively. For example, a compound of the disclosure may have one or more H atom replaced with deuterium.

[0081] Certain isotopically-labeled disclosed compounds (e.g., those labeled with ³ H and ¹⁴ C) are useful in compound and/or substrate tissue distribution assays. Tritiated (i.e., ³ H) and carbon-14 (i.e., ¹⁴ C) isotopes are particularly preferred for their ease of preparation and detectability. Further, substitution with heavier isotopes such as deuterium (i.e., ² H) may afford certain therapeutic advantages resulting from greater metabolic stability (e.g., increased in vivo half-life or reduced dosage requirements) and hence may be preferred in some circumstances. Isotopically labeled compounds of the disclosure can generally be prepared by following procedures analogous to those disclosed in the examples herein by substituting an isotopically labeled reagent for a non-isotopically labeled reagent. The term "pharmaceutically acceptable salt(s)" as used herein refers to salts of acidic or basic groups that may be present in a disclosed compounds used in disclosed compositions. Compounds included in the present compositions that are basic in nature are capable of forming a wide variety of salts with various inorganic and organic acids. The acids that may be used to prepare pharmaceutically acceptable acid addition salts of such basic compounds are those that form non-toxic acid addition salts, i.e., salts containing pharmacologically acceptable anions, including, but not limited to, malate, oxalate, chloride, bromide, iodide, nitrate, sulfate, bisulfate, phosphate, acid phosphate, isonicotinate, acetate, lactate, salicylate, citrate, tartrate, oleate, tannate, pantothenate, bitartrate, ascorbate, succinate, maleate, gentisinate, fumarate, gluconate, glucaronate, saccharate, formate, benzoate, glutamate, methanesulfonate, ethanesulfonate, benzenesulfonate, -toluenesulfonate and pamoate (i.e., l, r-methylene-te-(2-hydroxy-3-naphthoate)) salts. Compounds included in the present compositions that are acidic in nature are capable of forming base salts with various pharmacologically acceptable cations. Examples of such salts include alkali metal or alkaline earth metal salts, particularly calcium, magnesium, sodium, lithium, zinc, potassium, and iron salts. Compounds included in the present compositions that include a basic or acidic moiety may also form pharmaceutically acceptable salts with various amino acids. The compounds of the disclosure may contain both acidic and basic groups; for example, one amino and one carboxylic acid group. In such a case, the compound can exist as an acid addition salt, a zwitterion, or a base salt.

[0082] Also included in the present disclosure are methods that include administering prodrugs of the compounds described herein, or a pharmaceutical composition thereof or method of use of the prodrug.

[0083] The term "prodrug" refers to compounds that are transformed in vivo to yield a disclosed compound or a pharmaceutically acceptable salt, hydrate or solvate of the compound. The transformation may occur by various mechanisms (such as by esterase, amidase, phosphatase, oxidative and or reductive metabolism) in various locations (such as in the intestinal lumen or upon transit of the intestine, blood or liver). Prodrugs are well known in the art (for example, see Rautio, Kumpulainen, et al, Nature Reviews Drug Discovery 2008, 7, 255). For example, if a compound of the disclosure or a pharmaceutically acceptable salt, hydrate or solvate of the compound contains a carboxylic acid functional group, a prodrug can comprise an ester formed by the replacement of the hydrogen atom of the acid group with a group such as (Ci_8)alkyl, (C2-i2)alkylcarbonyloxymethyl, 1 -(alkylcarbonyloxy)ethyl having from 4 to 9 carbon atoms, 1 -methyl- 1 -(alky lcarbonyloxy)-ethyl having from 5 to 10 carbon atoms, alkoxycarbonyloxymethyl having from 3 to 6 carbon atoms, 1- (alkoxycarbonyloxy)ethyl having from 4 to 7 carbon atoms, 1 -methyl- 1-

(alkoxycarbonyloxy)ethyl having from 5 to 8 carbon atoms, N-(alkoxycarbonyl)aminomethyl having from 3 to 9 carbon atoms, l-(N-(alkoxycarbonyl)amino)ethyl having from 4 to 10 carbon atoms, 3-phthalidyl, 4-crotonolactonyl, gamma-butyrolacton-4-yl, di-N,N-(Ci_

2)alkylamino(C2-3)alkyl (such as β-dimethylaminoethyl), carbamoyl-(Ci_2)alkyl, N,N-di(Ci_ 2)alkylcarbamoyl-(Ci-2)alkyl and piperidino-, pyrrolidino- or morpholino(C2-3)alkyl. [0084] Similarly, if a compound of the disclosure contains an alcohol functional group, a prodrug can be formed by the replacement of the hydrogen atom of the alcohol group with a group such as (Ci_6)alkylcarbonyloxymethyl, l-((Ci-6)alkylcarbonyloxy)ethyl, 1 -methyl- l-((Ci- 6)alkylcarbonyloxy)ethyl (Ci_6)alkoxycarbonyloxymethyl, N-(Ci_

6)alkoxycarbonylaminomethyl, succinoyl, (Ci_6)alkylcarbonyl, a-amino(Ci_4)alkylcarbonyl, arylalkylcarbonyl and a-aminoalkylcarbonyl, or a-aminoalkylcarbonyl-a-aminoalkylcarbonyl, where each a-aminoalkylcarbonyl group is independently selected from the naturally occurring L-amino acids, P(0)(OH) ₂ , -P(0)(0(Ci_6)alkyl) ₂ or glycosyl (the radical resulting from the removal of a hydroxyl group of the hemiacetal form of a carbohydrate).

[0085] If a compound of the disclosure incorporates an amine functional group, a prodrug can be formed, for example, by creation of an amide or carbamate, an N-alkylcarbonyloxyalkyl derivative, an (oxodioxolenyl)methyl derivative, an N-Mannich base, imine or enamine. In addition, a secondary amine can be metabolically cleaved to generate a bioactive primary amine, or a tertiary amine can metabolically cleaved to generate a bioactive primary or secondary amine. For examples, see Simplicio, et ah, Molecules 2008, 13, 519 and references therein

[0086] The disclosure additionally includes use of clathrates of the compounds described herein, pharmaceutical compositions comprising the clathrates, and methods of use of the clathrates. In some embodiments, the disclosure is directed to clathrates of a disclosed compound of e.g., Formula (Ilia), (III), or (IV), or a pharmaceutical composition thereof topically labeled reagent.

[0087] The disclosure additionally encompasses embodiments wherein one or more of the nitrogen atoms in a disclosed compound are oxidized to N-oxide.

[0088] Representative and exemplary synthetic routes for the preparation of compounds described herein are shown in the schemes below and throughout the Examples section. As will be understood by the skilled artisan, diastereomers can be separated from the reaction mixture using column chromatography. Schemes 1 and 2

Et

Scheme 3

[0089] Compounds of the disclosure can also be prepared using methods described in the literature, including, but not limited to, J. Med. Chem. 2011, 54(B), 4350-64;; Russian Journal of Organic Chemistry, 201 1, 47(8), 1199-1203; U.S. Patent Application Publication No. 2009/0036451 Al; WO2008/046072 A2, and U.S. Patent No. 4,336,264, the contents of each of which are expressly incorporated by reference herein.

Methods of Use

[0090] The disclosure is in part directed to a method of enhancing (e.g., increasing) CFTR activity in a subject (e.g., a subject suffering from any one or more of the conditions described herein) comprising administering a compound of the disclosure in an effective amount. The disclosure also encompasses a method of treating a patient suffering from a condition associated with CFTR activity comprising administering to said patient an effective amount of a compound described herein. In certain embodiments, the disease is cystic fibrosis.

[0091] "Treating" or "treatment" includes preventing or delaying the onset of the symptoms, complications, or biochemical indicia of a disease, alleviating or ameliorating the symptoms or arresting or inhibiting further development of the disease, condition, or disorder. A "subject" is an animal to be treated or in need of treatment. A "patient" is a human subject in need of treatment.

[0092] An "effective amount" refers to that amount of an agent that is sufficient to achieve a desired and/or recited effect. In the context of a method of treatment, an "effective amount" of the therapeutic agent that is sufficient to ameliorate of one or more symptoms of a disorder and/or prevent advancement of a disorder, cause regression of the disorder and/or to achieve a desired effect.

[0093] The term "modulating" encompasses increasing, enhancing, inhibiting, decreasing, suppressing, and the like. The terms "increasing" and "enhancing" mean to cause a net gain by either direct or indirect means. As used herein, the terms "inhibiting" and "decreasing" encompass causing a net decrease by either direct or indirect means.

[0094] For example, CFTR activity in a patient may be enhanced after administration of a compound described herein when there is an increase in the CFTR activity as compared to that in the absence of the administration of the compound. CFTR activity encompasses, for example, chloride channel activity of the CFTR, and/or other ion transport activity (for example, HCO ₃ ^" transport). In certain of these embodiments, the activity of one or more (e.g., one or two) mutant CFTRs (e.g., AF508, S549N, G542X, G551D, R117H, N1303K, W1282X, R553X, 621+1G>T, 1717-lOA, 3849+lOkbOT, 2789+5G>A, 3120+1OA, I507del, R1162X, 1898+1 G>A, 3659delC, G85E, D1152H, R560T, R347P, 2184insA, A455E, R334W, Q493X, and 2184delA CFTR) is enhanced (e.g., increased). Contemplated patients treated by disclosed methods may have a CFTR mutation(s) from one or more classes, such as without limitation, Class I CFTR mutations, Class II CFTR mutations, Class III CFTR mutations, Class IV CFTR mutations, Class V CFTR mutations, and Class VI mutations. Contemplated subject (e.g., human subject) CFTR genotypes include, without limitation, homozygote mutations (e.g., AF508 / AF508 and Rl 17H / Rl 17H) and compound heterozygote mutations (e.g., AF508 / G551D; AF508 / A455E; AF508 / G542X; A508F / W1204X; R553X / W1316X;

W1282X/N1303K, 591Δ18 / E83 IX, F508del/Rl 17H/ N1303K/ 3849+lOkbOT; Δ303Κ/ 384; and DF508/G178R).

[0095] In certain embodiments a patient may have a Class I mutation, e.g., a G542X; a Class II/ 1 mutation, e.g., a AF508 / G542X compound heterozygous mutation. In other embodiments, the mutation is a Class III mutation, e.g., a G551D; a Class II/ Class III mutation, e.g., a AF508 / G551D compound heterozygous mutation. In still other embodiments, the mutation is a Class V mutation, e.g., a A455E; Class II/ Class V mutation, e.g., a AF508 / A455E compound heterozygous mutation. Of the more than 1000 known mutations of the CFTR gene, AF508 is the most prevalent mutation of CFTR which results in misfolding of the protein and impaired trafficking from the endoplasmic reticulum to the apical membrane (Dormer et al. (2001). J Cell Sci 1 14, 4073-4081; http://www.genet.sickkids.on.ca/app). In certain embodiments, AF508 CFTR activity is enhanced (e.g., increased). In certain embodiments, AF508 CFTR activity and/or G542X CFTR activity and/or G551D CFTR activity and/or A455E CFTR activity is enhanced (e.g., increased). An enhancement of CFTR activity can be measured, for example, using literature described methods, including for example, Ussing chamber assays, patch clamp assays, and hBE Ieq assay (Devor et al. (2000), Am J Physiol Cell Physiol 279(2): C461-79; Dousmanis et al. (2002), J Gen Physiol 119(6): 545-59; Bruscia et al. (2005), PNAS 103(8): 2965-2971).

[0096] Also provided herein are methods of treating a patient suffering from a condition associated with CFTR activity, including conditions associated with deficient CFTR activity. In some embodiments, the disclosure is directed to a method of treating a condition associated with deficient or decreased CFTR activity comprising administering an effective amount of a disclosed compound of (e.g., a disclosed formula, e.g., Formula (la) or (lb)) that enhances CFTR activity. Non-limiting examples of conditions associated with deficient CFTR activity are cystic fibrosis, congenital bilateral absence of vas deferens (CBAVD), acute, recurrent, or chronic pancreatitis, disseminated bronchiectasis, asthma, allergic pulmonary aspergillosis, smoking-related lung diseases, such as chronic obstructive pulmonary disease (COPD), chronic sinusitis, dry eye disease, protein C deficiency, Αβ-lipoproteinemia, lysosomal storage disease, type 1 chylomicronemia, mild pulmonary disease, lipid processing deficiencies, type 1 hereditary angioedema, coagulation-fibrinolyis, hereditary hemochromatosis, CFTR-related metabolic syndrome, chronic bronchitis, constipation, pancreatic insufficiency, hereditary emphysema, and Sjogren's syndrome.

[0097] In some embodiments, disclosed methods of treatment that include administering a disclosed compound to a patient may further comprise administering an additional therapeutic agent. For example, in an embodiment, provided herein is a method of administering a disclosed compound and at least one additional therapeutic agent. In certain aspects, the disclosure is directed to a method comprising administering a disclosed compound, and at least two additional therapeutic agents. Additional therapeutic agents include, for example, mucolytic agents, bronchodilators, antibiotics, anti-infective agents, anti-inflammatory agents, ion channel modulating agents (e.g., ENaC inhibitors), therapeutic agents used in gene therapy, CFTR correctors, and CFTR potentiators, or other agents that modulates CFTR activity. In some embodiments, at least one additional therapeutic agent is selected from the group consisting of a CFTR corrector and a CFTR potentiator. Non-limiting examples of CFTR correctors and potentiators include VX-770 (Ivacaftor), VX-809 (3-(6-(l-(2,2- difluorobenzo[d][l,3]dioxol-5-yl)cyclopropanecarboxamido)-3- methylpyridin-2-yl)benzoic acid, VX-661 (l-(2,2-difluoro-l,3-benzodioxol-5-yl)-N-[l-[(2R)-2,3-dihydr oxypropyl]-6- fluoro-2-(2 -hydroxy- 1 , 1 -dimethylethyl)- 1 H-indol-5-yl] - cyclopropanecarboxamide), VX-983 , and Ataluren (PTC124) (3-[5-(2-fluorophenyl)-l,2,4-oxadiazol-3-yl]benzoic acid), FDL169, GLPG1837/ABBV-974 (for example, a CFTR potentiator), GLPG2222 (for example, a corrector); and compounds described in, e.g., WO2014/144860 and 2014/176553, hereby incorporated by reference. Non-limiting examples of modulators include QBW-251, QR-010, NB-124, and compounds described in, e.g., WO2014/045283; WO2014/081821,

WO2014/081820, WO2014/152213; WO2014/ 160440, WO2014/ 160478, US2014027933; WO2014/0228376, WO2013/038390, WO2011/113894, WO2013/038386; and

WO2014/180562, of which the disclosed modulators in those publications are contemplated as additional therapeutic agents and incorporated by reference. Non-limiting examples of antiinflammatory agents include N6022 (3-(5-(4-(lH-imidazol-l-yl) phenyl)- l-(4-carbamoyl-2- methylphenyl)- ¹ H-pyrrol-2-yl) propanoic acid), CTX-4430, N1861, N1785, and N911 15.

[0098] In some embodiments, the methods described herein can further include administering an additional therapeutic agent or administering at least two additional CFTR therapeutic agents. In some embodiments, the methods described herein can further include administering an additional CFTR modulator or administering at least two additional CFTR modulators. In certain embodiments, at least one CFTR modulator is a CFTR corrector (e.g., VX-809, VX-661, VX-983, GLPG2222 and) or potentiator (e.g., ivacaftor, genistein and GLPG1837). In certain of these embodiments, one of the at least two additional therapeutic agents is a CFTR corrector (e.g., VX-809, VX-661 and VX-983) and the other is a CFTR potentiator (e.g., ivacaftor and genistein). In certain of these embodiments, one of the at least two additional therapeutic agents is a CFTR corrector (e.g., GLPG2222) and the other is a CFTR potentiator (e.g., GLPG1837). In certain of these embodiments, one of the at least two additional therapeutic agents is a CFTR corrector (e.g., VX-809 or VX-661) and the other is a CFTR potentiator (e.g., ivacaftor). In certain of these embodiments, at least one CFTR modulator is an agent that enhances read-through of stop codons (e.g., NB 124 or ataluren).

[0099] Accordingly, in another aspect, this disclosure provides a method of treating a condition associated with deficient or decreased CFTR activity (e.g., cystic fibrosis), which includes administering to a subject in need thereof (e.g., a human patient in need thereof) an effective amount of a disclosed compound and at least one or two additional CFTR therapeutic agent(s) (e.g., at least one or two additional CFTR therapeutic agents, e.g., in which one of the at least one or two additional therapeutic agents is optionally a CFTR corrector or modulator (e.g., VX-809, VX-661, VX-983, GLPG2222, NB124, ataluren ) and/or the other is a CFTR potentiator (e.g., ivacaftor, genistein, and GLPG1837); e.g., one of the at least two additional therapeutic agents is GLPG2222, and the other is GLPG1837; or one of the at least two additional therapeutic agents is VX-809 or VX-661, and the other is a ivacaftor). In certain embodiments, the subject's CFTR genotype includes, without limitation, one or more Class I CFTR mutations, one or more Class II CFTR mutations, one or more Class III CFTR mutations, one or more Class IV CFTR mutations, or one or more Class V CFTR mutations, or one or more Class VI CFTR mutations. In certain embodiments, the subject's CFTR genotype includes, without limitation, one or more homozygote mutations (e.g., AF508 / AF508 or Rl 17H / Rl 17H) and/or one or more compound heterozygote mutations (e.g., AF508 / G55 ID; AF508 / A455E; AF508 / G542X; A508F / W1204X; R553X / W1316X; W1282X/N1303K; F508del/R117H; N1303K/ 3849+lOkbOT; AF508/R334W; DF508/G178R. and 591Δ18 / E83 IX). In certain embodiments, the subject's CFTR genotype includes a Class I mutation, e.g., a G542X Class I mutation, e.g., a AF508 / G542X compound heterozygous mutation. In other embodiments, the subject's CFTR genotype includes a Class III mutation, e.g., a G551D Class III mutation, e.g., a AF508 / G551D compound heterozygous mutation. In still other embodiments, the subject's CFTR genotype includes a Class V mutation, e.g., a A455E Class V mutation, e.g., a AF508 / A455E compound heterozygous mutation. In certain embodiments, AF508 CFTR activity and/or G542X CFTR activity and/or G551D CFTR activity and/or A455E activity is enhanced (e.g., increased). In certain embodiments, the enhancement in activity (e.g., increase in activity) provided by the combination of the disclosed compound and one or two additional therapeutic agents is greater than additive when compared to the enhancement in activity provided by each therapeutic component individually.

Class Effect on CFTR protein Example of mutation

I Shortened protein W1282X Instead of inserting the amino acid tryptophan (W), the protein sequence is prematurely stopped (indicated by an X).

II Protein fails to reach cell AF508 A phenylalanine amino acid membrane (F) is deleted

III Channel cannot be regulated G551D A "missense" mutation:

properly instead of a glycine amino acid (G), aspartate (D) is added

IV Reduced chloride conductance R117H Missense

V Reduced due to incorrect splicing 3120+1G>A Splice-site mutation in of gene gene intron 16

VI Reduced due to protein instability N287Y a A ->T at 991 Genotype Description Possible Symptoms

A508F / A508F homozygote Severe lung disease,

pancreatic insufficient

R117H / R117H homozygote Congenital bilateral absence of the vas deferens ; No lung or pancreas disease

WT / A508F heterozygote Unaffected

WT / 3120+1 G>A heterozygote Unaffected

A508F / W1204X compound heterozygote No lung disease, pancreatic insufficient

R553X and W1316X compound heterozygote Mild lung disease,

pancreatic insufficient

591Δ18 / Ε831Χ compound heterozygote No lung or pancreas disease, nasal polyps

[0100] For example, provided herein is a method of treating a patient for e.g., cystic fibrosis, wherein the patient has one or more of the following mutations in the CFTR gene: G1244E. G1349D, G178R, G551S, SI 25 IN, S1255P, S549N, S549R , G970R, or R117H, and/or e.g., a patient with one or two copies of the F508del mutation, or one copy of the AF508 mutation and a second mutation that results in a gating effect in the CFTR protein (e.g., a patient that is heterozygous for AF508 and G55 ID mutation), a patient with one copy of the AF508 mutation and a second mutation that results in residual CFTR activity , or a patient with one copy of the AF508 mutation and a second mutation that results in residual CFTR activity, comprising administering an effective amount of a disclosed compound. As described herein, such exemplary methods (e.g., of a patient having one or mutations such as those described above) may include, for example, administering to such patient a combination therapy, e.g., administering (simultaneously or sequentially) an effective amount of ivacaftor to said patient and an effective amount of disclosed compound that may act as an amplifier. Such administration may result, for example, in increased chloride transport in human bronchial epithelial cells with e.g., one or two copies of mutations, e.g, AF508 mutation, as compared to administration of ivacaftor alone. Another contemplated combination therapy that includes a disclosed compound may also include an effective amount of a readthrough agent (e.g., ataluren, NB 124) and an effective amount of disclosed compound that may act as an amplifier.

[0101] The phrase "combination therapy," as used herein, refers to an embodiment where a patient is co-administered a disclosed compound, a CFTR potentiator agent (e.g., ivacaftor ) and optionally, one or more CFTR corrector agent(s) (e.g, VX-661 and/or lumacaftor ) as part of a specific treatment regimen intended to provide the beneficial effect from the co-action of these therapeutic agents. For example, a beneficial effect of a combination may include, but is not limited to, pharmacokinetic or pharmacodynamic co-action resulting from the combination of therapeutic agents. For example, administration of a disclosed compound with ivacaftor alone or with a CFTR corrector agent (e.g., lumacaftor or VX-661) may result in a level of function (e.g., as measured by chloride activity in HBE cells or patients that have a AF508 mutation, that achieves clinical improvement (or better) as compared to the chloride activity level in cells or patients with a G55 ID mutation receiving ivacaftor alone, or ivacaftor and a corrector agent (lumacaftor or VX-661 ; or for example, administration of a disclosed compound with ivacaftor alone or ivacaftor with a CFTR corrector agent (e.g., lumacaftor or VX-661) may result in a level of function (e.g., as measured by chloride activity in HBE cells or patients that have a A455E mutation, that achieves clinical improvement (or better) as compared to the chloride activity level at e.g., 50% or more of wild type cells; or upon administration of a disclosed compound and ivacaftor to a patient (e.g. having a G55 ID class III mutation) may show e.g., about two times or more improved activity of ivacaftor as compared to administration of ivacaftor alone. Administration of disclosed therapeutic agents in combination typically is carried out over a defined time period (usually a day, days, weeks, months or years depending upon the combination selected). Combination therapy is intended to embrace administration of multiple therapeutic agents in a sequential manner, that is, wherein each therapeutic agent is administered at a different time, as well as administration of these therapeutic agents, or at least two of the therapeutic agents, in a substantially

simultaneous manner. Substantially simultaneous administration can be accomplished, for example, by administering to the subject a single tablet or capsule having a fixed ratio of each therapeutic agent or in multiple, single capsules for each of the therapeutic agents. Sequential or substantially simultaneous administration of each therapeutic agent can be effected by any appropriate route including, but not limited to, oral routes, inhalational routes, intravenous routes, intramuscular routes, and direct absorption through mucous membrane tissues. The therapeutic agents can be administered by the same route or by different routes. For example, a first therapeutic agent of the combination selected may be administered by intravenous injection or inhalation or nebulizer while the other therapeutic agents of the combination may be administered orally. Alternatively, for example, all therapeutic agents may be administered orally or all therapeutic agents may be administered by intravenous injection, inhalation or nebulization.

[0102] Combination therapy also can embrace the administration of the therapeutic agents as described above in further combination with other biologically active ingredients and non- drug therapies. Where the combination therapy further comprises a non-drug treatment, the non-drug treatment may be conducted at any suitable time so long as a beneficial effect from the co-action of the combination of the therapeutic agents and non-drug treatment is achieved. For example, in appropriate cases, the beneficial effect is still achieved when the non-drug treatment is temporally removed from the administration of the therapeutic agents, perhaps by a day, days or even weeks.

[0103] The components of a disclosed combination may be administered to a patient simultaneously or sequentially. It will be appreciated that the components may be present in the same pharmaceutically acceptable carrier and, therefore, are administered simultaneously. Alternatively, the active ingredients may be present in separate pharmaceutical carriers, such as, conventional oral dosage forms, that can be administered either simultaneously or sequentially.

[0104] The disclosure also encompasses the treatment of a condition associated with a dysfunction in proteostasis in a subject comprising administering to said subject an effective amount of a disclosed compound that enhances, improves or restores proteostasis of a protein. Proteostasis refers to protein homeostasis. Dysfunction in protein homeostasis is a result of protein misfolding, protein aggregation, defective protein trafficking or protein degradation. For example, the disclosure encompasses administering a compound of a disclosed formula, e.g., Formula (la) or (lb) that corrects protein misfolding, reduces protein aggregation, corrects or restores protein trafficking and/or affects protein degradation for the treatment of a condition associated with a dysfunction in proteostasis. In some aspects of the disclosure, a compound of Formula (la) or (lb) that corrects protein misfolding and/or corrects or restores protein trafficking is administered. In cystic fibrosis, the mutated or defective enzyme is the cystic fibrosis transmembrane conductance regulator (CFTR). One of the most common mutations of this protein is AF508 which is a deletion (Δ) of three nucleotides resulting in a loss of the amino acid phenylalanine (F) at the 508th (508) position on the protein. As described above, mutated cystic fibrosis transmembrane conductance regulator exists in a misfolded state and is characterized by altered trafficking as compared to the wild type CFTR. Additional exemplary proteins of which there can be a dysfunction in proteostasis, for example that can exist in a misfolded state, include, but are not limited to, glucocerebrosidase, hexosamine A,

aspartylglucosaminidase, a-galactosidase A, cysteine transporter, acid ceramidase, acid a-L- fucosidase, protective protein, cathepsin A, acid β-glucosidase, acid β-galactosidase, iduronate 2-sulfatase, a-L-iduronidase, galactocerebrosidase, acid a -mannosidase, acid β -mannosidase, arylsulfatase B, arylsulfatase A, N-acetylgalactosamine-6-sulfate sulfatase, acid β - galactosidase, N-acetylglucosamine-1 -phosphotransferase, acid sphingmyelinase, NPC-1, acid a-glucosidase, β-hexosamine B, heparin N-sulfatase, a -N-acetylglucosaminidase, a - glucosaminide N-acetyltransferase, N-acetylglucosamine-6-sulfate sulfatase, a -N- acetylgalactosaminidase, a -neuramidase, β -glucuronidase, β-hexosamine A and acid lipase, polyglutamine, a -synuclein, TDP-43, superoxide dismutase (SOD), Αβ peptide, tau protein transthyretin and insulin. The disclosed compounds may be used to restore proteostasis (e.g., correct folding and/or alter trafficking) of the proteins described above.

[0105] Protein conformational diseases contemplated herein encompass gain of function disorders and loss of function disorders. In one embodiment, the protein conformational disease is a gain of function disorder. The terms "gain of function disorder," "gain of function disease," "gain of toxic function disorder" and "gain of toxic function disease" are used interchangeably herein. A gain of function disorder is a disease characterized by increased aggregation-associated proteotoxicity. In these diseases, aggregation exceeds clearance inside and/or outside of the cell. Gain of function diseases include, but are not limited to, neurodegenerative diseases associated with aggregation of polyglutamine, Lewy body diseases, amyotrophic lateral sclerosis, transthyretin-associated aggregation diseases, Alzheimer's disease, Machado-Joseph disease, cerebral B-amyloid angiopathy, retinal ganglion cell degeneration, tautopathies (progressive supranuclear palsy, corticobasal degeneration, frontotemporal lobar degeneration), cerebral hemorrhage with amyloidosis, Alexander disease, Serpinopathies, familial amyloidotic neuropathy, senile systemic amyloidosis, ApoAI amyloidosis, ApoAII amyloidosis, ApoAIV amyloidosis, familial amyloidosis of the Finnish type, lysozyme amyloidosis, fibrinogen amyloidosis, dialysis amyloidosis, inclusion body myositis/myopathy, cataracts, medullary thyroid carcinoma, cardiac atrial amyloidosis, pituitary prolactinoma, hereditary lattice corneal dystrophy, cutaneous lichen amyloidosis, corneal lactoferrin amyloidosis, corneal lactoferrin amyloidosis, pulmonary alveolar proteinosis, odontogenic tumor amyloid, seminal vesical amyloid, sickle cell disease, critical illness myopathy, von Hippel-Lindau disease, spinocerebellar ataxia 1, Angelman syndrome, giant axon neuropathy, inclusion body myopathy with Paget disease of bone, frontotemporal dementia (IBMPFD) and prion diseases. Neurodegenerative diseases associated with aggregation of polyglutamine include, but are not limited to, Huntington's disease,

dentatorubral and pallidoluysian atrophy, several forms of spino-cerebellar ataxia, and spinal and bulbar muscular atrophy. Alzheimer's disease is characterized by the formation of two types of aggregates: extracellular aggregates of Αβ peptide and intracellular aggregates of the microtubule associated protein tau. Transthyretin-associated aggregation diseases include, for example, senile systemic amyloidoses and familial amyloidotic neuropathy. Lewy body diseases are characterized by an aggregation of a-synuclein protein and include, for example, Parkinson's disease, Lewy body dementia (LBD) and multiple system atrophy (SMA). Prion diseases (also known as transmissible spongiform encephalopathies or TSEs) are characterized by aggregation of prion proteins. Exemplary human prion diseases are Creutzfeldt- Jakob Disease (CJD), Variant Creutzfeldt- Jakob Disease, Gerstmann-Straussler-Scheinker Syndrome, Fatal Familial Insomnia and Kuru. In another embodiment, the misfolded protein is alpha- 1 anti-trypsin.

[0106] In a further embodiment methods are provided to treat a protein conformation disease such as loss of function disorder, comprising administering to a patient suffering from same a disclosed compound. The terms "loss of function disease" and "loss of function disorder" are used interchangeably herein. Loss of function diseases are a group of diseases characterized by inefficient folding of a protein resulting in excessive degradation of the protein. Loss of function diseases include, for example, lysosomal storage diseases. Lysosomal storage diseases are a group of diseases characterized by a specific lysosomal enzyme deficiency which may occur in a variety of tissues, resulting in the build-up of molecules normally degraded by the deficient enzyme. The lysosomal enzyme deficiency can be in a lysosomal hydrolase or a protein involved in the lysosomal trafficking. Lysosomal storage diseases include, but are not limited to, aspartylglucosaminuria, Fabry's disease, Batten disease, Cystinosis, Farber, Fucosidosis, Galactasidosialidosis, Gaucher' s disease (including Types 1, 2 and 3), Gml gangliosidosis, Hunter's disease, Hurler-Scheie's disease, Krabbe's disease, a-Mannosidosis, β-Mannosidosis, Maroteaux-Lamy's disease, Metachromatic Leukodystrophy, Morquio A syndrome, Morquio B syndrome, Mucolipidosis II, Mucolipidosis III, Neimann-Pick Disease (including Types A, B and C), Pompe's disease, Sandhoff disease, Sanfilippo syndrome (including Types A, B, C and D), Schindler disease, Schindler-Kanzaki disease, Sialidosis, Sly syndrome, Tay-Sach's disease and Wolman disease.

[0107] In another embodiment, the disease associated with a dysfunction in proteostasis is a cardiovascular disease. Cardiovascular diseases include, but are not limited to, coronary artery disease, myocardial infarction, stroke, restenosis and arteriosclerosis. Conditions associated with a dysfunction of proteostasis also include ischemic conditions, such as,

ischemia/reperfusion injury, myocardial ischemia, stable angina, unstable angina, stroke, ischemic heart disease and cerebral ischemia.

[0108] In yet another embodiment, the disease associated with a dysfunction in proteostasis is diabetes and/or complications of diabetes, including, but not limited to, diabetic retinopathy, cardiomyopathy, neuropathy, nephropathy, and impaired wound healing.

[0109] In a further embodiment, the disease associated with a dysfunction in proteostasis is an ocular disease including, but not limited to, age-related macular degeneration (AMD), diabetic macular edema (DME), diabetic retinopathy, glaucoma, cataracts, retinitis pigmentosa (RP) and dry macular degeneration.

[01 10] In yet additional embodiments, the method of the disclosure is directed to treating a disease associated with a dysfunction in proteostasis, wherein the disease affects the respiratory system, pancreas and/or the kidneys. For example, provided herein are methods of treaing polycystic kidney disease and/or other kidney pathologies, comprising administering a disclosed compound. In certain additional embodiments, the methods of the disclosure encompass treating a condition selected from the group consisting of polyendocrinopathy/hyperinsulinemia, diabetes mellitus, Charcot-Marie Tooth syndrome, Pelizaeus-Merzbacher disease, and Gorham's Syndrome.

[01 11] Additional conditions associated with a dysfunction of proteostasis include hemoglobinopathies, inflammatory diseases, intermediate filament diseases, drug-induced lung damage and hearing loss. The disclosure also encompasses methods for the treatment of hemoglobinopathies (such as sickle cell anemia), an inflammatory disease (such as

inflammatory bowel disease, colitis, ankylosing spondylitis), intermediate filament diseases (such as non-alcoholic and alcoholic fatty liver disease) and drug induced lung damage (such as methotrexate-induced lung damage). The disclosure additionally encompasses methods for treating hearing loss, such as noise-induced hearing loss, aminoglycoside-induced hearing loss, and cisplatin-induced hearing loss.

[01 12] Additional conditions include those associated with a defect in protein trafficking and that can be treated according to methods of the disclosure include: PGP mutations, hERG trafficking mutations, nephrongenic diabetes insipidus mutations in the arginine-vasopressin receptor 2, persistent hyperinsulinemic hypoglycemia of infancy (PHH1) mutations in the sulfonylurea receptor 1, and alAT.

[01 13] In an embodiment, a method of enhancing cystic fibrosis transmembrane conductance regulator (CFTR) activity in a subject in need thereof is provided, which includes administering to said subject an effective amount of a disclosed compound,e.g., having the Formula (Ilia) or (Illb):

(Ilia)

(nib)

or a pharmaceutically acceptable salt, solvate, clathrate or prodrug thereof, wherein:

Rio is selected from the group consisting of hydrogen, optionally substituted Ci-Cio alkyl, optionally substituted C2-C1 ₀ alkenyl, optionally substituted C2-C1 ₀ alkynyl, optionally substituted C3-C12 cycloalkyl, optionally substituted C3-C12 cycloalkenyl, optionally substituted aryl, halo, ORc, NR _d R _d , C(0)ORc, N0 ₂ , CN, C(0)R _c , C(0)C(0)R _c , C(0)NRdRd, NRdC(0)R _c , NR _d S(0) _n Rc, NRd(COORc), NRdC(0)C(0)R _c , NR _d C(0)NRdRd, NR _d S(0) _n NR _d R _d , NR _d S(0) _n Rc, S(0) _n Rc, S(0)nNR _d R _d , OC(0)ORc, optionally substituted heterocyclic and optionally substituted heteroaryl; each R ₂ is independently selected from the group consisting of hydrogen, halo, CN, and optionally substituted C1-C1 ₀ alkyl;

R3 is hydrogen or fluoro; each R4 is independently selected from the group consisting of hydrogen, optionally substituted C1-C10 alkyl, optionally substituted C2-C10 alkenyl, optionally substituted C2-C10 alkynyl, optionally substituted C ₃ -C12 cycloalkyl, optionally substituted C ₃ -C12 cycloalkenyl, optionally substituted aryl, halo, ORc, NR _d R _d , C(0)ORc, N0 ₂ , CN, C(0)R _c , C(0)C(0)R _c , C(0)NR _d R _d , NRdC(0)R _c , NR _d S(0) _n R _c , NRd(COOR _c ), NR _d C(0)C(0)Rc, NRdC(0)NR _d R _d , NR _d S(0) _n NR _d R _d , NR _d S(0) _n R _c , S(0) _n Rc, S(0) _n NR _d R _d , OC(0)OR _c , (C=NR _d )R _c , optionally substituted heterocyclic and optionally substituted heteroaryl; alternatively, two geminal R4 groups are taken together with the carbon atom to which they are attached to form a spiro C ₃ - C12 cycloalkyl, a spiro C3-C12 cycloalkenyl, a spiro heterocyclic, a spiro aryl or spiro heteroaryl, each optionally substituted; or yet alternatively, two vicinal R4 groups are taken together with the carbon atoms to which they are attached to form a fused, optionally substituted cyclic group selected from the group consisting of C4-C8 cycloalkyl, C4-C8 cycloalkenyl, 4- to 8-membered heterocyclic, substituted aryl and heteroaryl, each optionally substituted; or further

alternatively, two R4 groups attached to non-adjacent carbon atoms are taken together with the carbon atoms to which they are attached to form a bridged cyclic group selected from the group consisting of C4-C8 cycloalkyl, C4-C8 cycloalkenyl, and 4- to 8-membered heterocyclic, each optionally substituted;

each ¾ is independently selected from the group consisting of hydrogen, halo, optionally substituted C1-C1 ₀ alkyl, and optionally substituted C3-C6 cycloalkyl, or two geminal Rb groups are independently taken together with the carbon atom to which they are attached to form an optionally substituted heterocyclic or an optionally substituted heteroaryl; each R _c is independently selected from the group consisting of hydrogen, optionally substituted C1-C1 ₀ alkyl, optionally substituted C2-C1 ₀ alkenyl, optionally substituted C2-C1 ₀ alkynyl, optionally substituted C3-C12 cycloalkyl, optionally substituted C3-C12 cycloalkenyl, optionally substituted heterocyclic, optionally substituted aryl and optionally substituted heteroaryl; each Ra is independently selected from the group consisting of hydrogen, optionally substituted C1-C1 ₀ alkyl, optionally substituted C2-C1 ₀ alkenyl, optionally substituted C2-C1 ₀ alkynyl, optionally substituted C1-C1 ₀ alkoxy, optionally substituted C3-C12 cycloalkyl, optionally substituted C3-C12 cycloalkenyl, optionally substituted heterocyclic, optionally substituted aryl and optionally substituted heteroaryl; or two geminal Ra groups are taken together with the nitrogen atom to which they are attached to form an optionally substituted heterocyclic or an optionally substituted heteroaryl;

R _e is selected from the group consisting of optionally substituted C1-C1 ₀ alkyl, optionally substituted C2-C1 ₀ alkenyl, optionally substituted C2-C1 ₀ alkynyl, optionally substituted C3-C12 cycloalkyl, optionally substituted C3-C12 cycloalkenyl, optionally substituted heterocyclic, optionally substituted aryl and optionally substituted heteroaryl;

Rf is selected from the group consisting of hydrogen, optionally substituted C1-C1 ₀ alkyl, optionally substituted C2-C1 ₀ alkenyl, optionally substituted C2-C1 ₀ alkynyl, optionally substituted C1-C1 ₀ alkoxy, optionally substituted C3-C12 cycloalkyl, optionally substituted C3- Ci2 cycloalkenyl, optionally substituted heterocyclic, optionally substituted aryl and optionally substituted heteroaryl; m is 0, 1 or 2; each n is independently 0, 1 or 2; and p is 0, 1 or 2. [01 14] In a further aspect, a method of identifying a candidate agent that increases CFTR activity is provided, which includes: (i) contacting a cell that expresses a CFTR protein with the candidate agent and a disclosed compound; (ii) measuring the CFTR activity in the cell in the presence of the candidate agent and the disclosed compound; and (iii) comparing the CFTR activity to that in the absence of the test agent, wherein an increase in CFTR activity in the presence of the test agent indicates that the agent increases CFTR activity. In certain embodiments, the cell expresses a mutant CFTR protein. In certain embodiments, CFTR activity is measured by measuring chloride channel activity of the CFTR, and/or other ion transport activity. In certain of these embodiments, the method is high-throughput. In certain of these embodiments, a candidate agent is a CFTR corrector or a CFTR potentiator.

Compositions

[01 15] Provided herein in an embodiment, are pharmaceutical compositions comprising a pharmaceutically acceptable carrier or excipient and a compound described herein, and methods of administering such compositions. For example, a disclosed compound, or a pharmaceutically acceptable salt, solvate, clathrate or prodrug thereof, can be administered in pharmaceutical compositions comprising a pharmaceutically acceptable carrier or excipient. The excipient can be chosen based on the expected route of administration of the composition in therapeutic applications. The route of administration of the composition depends on the condition to be treated. For example, intravenous injection may be preferred for treatment of a systemic disorder and oral administration may be preferred to treat a gastrointestinal disorder. The route of administration and the dosage of the composition to be administered can be determined by the skilled artisan without undue experimentation in conjunction with standard dose-response studies. Relevant circumstances to be considered in making those

determinations include the condition or conditions to be treated, the choice of composition to be administered, the age, weight, and response of the individual patient, and the severity of the patient's symptoms. A pharmaceutical composition comprising a disclosed compound or a pharmaceutically acceptable salt, solvate, clathrate or prodrug, can be administered by a variety of routes including, but not limited to, parenteral, oral, pulmonary, ophthalmic, nasal, rectal, vaginal, aural, topical, buccal, transdermal, intravenous, intramuscular, subcutaneous, intradermal, intraocular, intracerebral, intralymphatic, intraarticular, intrathecal and intraperitoneal. The compositions can also include, depending on the formulation desired, pharmaceutically-acceptable, non-toxic carriers or diluents, which are defined as vehicles commonly used to formulate pharmaceutical compositions for animal or human administration. The diluent is selected so as not to affect the biological activity of the pharmacologic agent or composition. Examples of such diluents are distilled water, physiological phosphate-buffered saline, Ringer's solutions, dextrose solution, and Hank's solution. In addition, the

pharmaceutical composition or formulation may also include other carriers, adjuvants, or nontoxic, nontherapeutic, nonimmunogenic stabilizers and the like. Pharmaceutical compositions can also include large, slowly metabolized macromolecules such as proteins, polysaccharides such as chitosan, polylactic acids, polyglycolic acids and copolymers (such as latex functionalized SEPHAROSE™, agarose, cellulose, and the like), polymeric amino acids, amino acid copolymers, and lipid aggregates (such as oil droplets or liposomes).

[01 16] The compositions can be administered parenterally such as, for example, by intravenous, intramuscular, intrathecal or subcutaneous injection. Parenteral administration can be accomplished by incorporating a composition into a solution or suspension. Such solutions or suspensions may also include sterile diluents such as water for injection, saline solution, fixed oils, polyethylene glycols, glycerine, propylene glycol or other synthetic solvents.

Parenteral formulations may also include antibacterial agents such as, for example, benzyl alcohol or methyl parabens, antioxidants such as, for example, ascorbic acid or sodium bisulfite and chelating agents such as EDTA. Buffers such as acetates, citrates or phosphates and agents for the adjustment of tonicity such as sodium chloride or dextrose may also be added. The parenteral preparation can be enclosed in ampules, disposable syringes or multiple dose vials made of glass or plastic.

[01 17] Additionally, auxiliary substances, such as wetting or emulsifying agents, surfactants, pH buffering substances and the like can be present in compositions. Other components of pharmaceutical compositions are those of petroleum, animal, vegetable, or synthetic origin, for example, peanut oil, soybean oil, and mineral oil. In general, glycols such as propylene glycol or polyethylene glycol are preferred liquid carriers, particularly for injectable solutions.

[01 18] Injectable formulations can be prepared either as liquid solutions or suspensions; solid forms suitable for solution in, or suspension in, liquid vehicles prior to injection can also be prepared. The preparation also can also be emulsified or encapsulated in liposomes or micro particles such as polylactide, polyglycolide, or copolymer for enhanced adjuvant effect, as discussed above [Langer, Science 249: 1527, 1990 and Hanes, Advanced Drug Delivery Reviews 28: 97-119, 1997]. The compositions and pharmacologic agents described herein can be administered in the form of a depot injection or implant preparation which can be formulated in such a manner as to permit a sustained or pulsatile release of the active ingredient.

[01 19] Additional formulations suitable for other modes of administration include oral, intranasal, and pulmonary formulations, suppositories, transdermal applications and ocular delivery. For suppositories, binders and carriers include, for example, polyalkylene glycols or triglycerides; such suppositories can be formed from mixtures containing the active ingredient in the range of about 0.5% to about 10%, preferably about 1% to about 2%. Oral formulations include excipients, such as pharmaceutical grades of mannitol, lactose, starch, magnesium stearate, sodium saccharine, cellulose, and magnesium carbonate. Topical application can result in transdermal or intradermal delivery. Transdermal delivery can be achieved using a skin patch or using transferosomes. [Paul et al, Eur. J. Immunol. 25: 3521-24, 1995; Cevc et al, Biochem. Biophys. Acta 1368: 201-15, 1998].

[0120] For the purpose of oral therapeutic administration, the pharmaceutical compositions can be incorporated with excipients and used in the form of tablets, troches, capsules, elixirs, suspensions, syrups, wafers, chewing gums and the like. Tablets, pills, capsules, troches and the like may also contain binders, excipients, disintegrating agent, lubricants, glidants, sweetening agents, and flavoring agents. Some examples of binders include microcrystalline cellulose, gum tragacanth or gelatin. Examples of excipients include starch or lactose. Some examples of disintegrating agents include alginic acid, corn starch and the like. Examples of lubricants include magnesium stearate or potassium stearate. An example of a glidant is colloidal silicon dioxide. Some examples of sweetening agents include sucrose, saccharin and the like. Examples of flavoring agents include peppermint, methyl salicylate, orange flavoring and the like. Materials used in preparing these various compositions should be

pharmaceutically pure and non-toxic in the amounts used. In another embodiment, the composition is administered as a tablet or a capsule.

[0121] Various other materials may be present as coatings or to modify the physical form of the dosage unit. For instance, tablets may be coated with shellac, sugar or both. A syrup or elixir may contain, in addition to the active ingredient, sucrose as a sweetening agent, methyl and propylparabens as preservatives, a dye and a flavoring such as cherry or orange flavor, and the like. For vaginal administration, a pharmaceutical composition may be presented as pessaries, tampons, creams, gels, pastes, foams or spray.

[0122] The pharmaceutical composition can also be administered by nasal administration. As used herein, nasally administering or nasal administration includes administering the composition to the mucus membranes of the nasal passage or nasal cavity of the patient. As used herein, pharmaceutical compositions for nasal administration of a composition include therapeutically effective amounts of the compounds prepared by well-known methods to be administered, for example, as a nasal spray, nasal drop, suspension, gel, ointment, cream or powder. Administration of the composition may also take place using a nasal tampon or nasal sponge.

[0123] For topical administration, suitable formulations may include biocompatible oil, wax, gel, powder, polymer, or other liquid or solid carriers. Such formulations may be administered by applying directly to affected tissues, for example, a liquid formulation to treat infection of conjunctival tissue can be administered dropwise to the subject's eye, or a cream formulation can be administered to the skin.

[0124] Rectal administration includes administering the pharmaceutical compositions into the rectum or large intestine. This can be accomplished using suppositories or enemas.

Suppository formulations can easily be made by methods known in the art. For example, suppository formulations can be prepared by heating glycerin to about 120oC, dissolving the pharmaceutical composition in the glycerin, mixing the heated glycerin after which purified water may be added, and pouring the hot mixture into a suppository mold.

[0125] Transdermal administration includes percutaneous absorption of the composition through the skin. Transdermal formulations include patches, ointments, creams, gels, salves and the like. [0126] In addition to the usual meaning of administering the formulations described herein to any part, tissue or organ whose primary function is gas exchange with the external environment, for purposes of the present disclosure, "pulmonary" will also mean to include a tissue or cavity that is contingent to the respiratory tract, in particular, the sinuses. For pulmonary administration, an aerosol formulation containing the active agent, a manual pump spray, nebulizer or pressurized metered-dose inhaler as well as dry powder formulations are contemplated. Suitable formulations of this type can also include other agents, such as antistatic agents, to maintain the disclosed compounds as effective aerosols.

[0127] A drug delivery device for delivering aerosols comprises a suitable aerosol canister with a metering valve containing a pharmaceutical aerosol formulation as described and an actuator housing adapted to hold the canister and allow for drug delivery. The canister in the drug delivery device has a head space representing greater than about 15% of the total volume of the canister. Often, the compound intended for pulmonary administration is dissolved, suspended or emulsified in a mixture of a solvent, surfactant and propellant. The mixture is maintained under pressure in a canister that has been sealed with a metering valve.

[0128] The disclosure is illustrated by the following examples which are not meant to be limiting in any way.

EXEMPLIFICATION

[0129] The compounds described herein can be prepared in a number of ways based on the teachings contained herein and synthetic procedures known in the art. In the description of the synthetic methods described below, it is to be understood that all proposed reaction conditions, including choice of solvent, reaction atmosphere, reaction temperature, duration of the experiment and workup procedures, can be chosen to be the conditions standard for that reaction, unless otherwise indicated. It is understood by one skilled in the art of organic synthesis that the functionality present on various portions of the molecule should be compatible with the reagents and reactions proposed. Substituents not compatible with the reaction conditions will be apparent to one skilled in the art, and alternate methods are therefore indicated. The starting materials for the examples are either commercially available or are readily prepared by standard methods from known materials. At least some of the compounds identified as "intermediates" herein are contemplated as compounds of the invention. Example 1 : iV-ir««s-3-(5-(hydroxymethyl)-lH-l,2,3-triazol-l-yl)cyclob utyl)-5- phenylisoxazole-3-carboxamide and 7V-ir««s-3-(4-(hydroxymethyl)-lH-l,2,3-triazol-l- yl)cyclobutyl)-5-phenylisoxazole-3-carboxamide:

[0130] Step 1: 3-Amino-cyclobutan-l-one: S0C1 ₂ (15.6 g, 131.46 mmol) was added dropwise to an ice-cooled solution of 3-oxocyclobutane carboxylic acid (5.0 g, 43.82 mmol) in dry DCM (30 mL) and the reaction mixture was refluxed for 3h. The reaction mixture was cooled to room temperature and the volatiles were removed under reduced pressure to get the crude compound which was azeotropically distilled with toluene (20 mL x 2) to remove acidic traces. The crude compound was dissolved in dry acetone (15 mL) and to the resulting solution was added a solution of a ₃ (5.69 g, 87.64 mmol) in water (20 mL) at 0 °C over 30 min. The reaction mixture was stirred for lh at 0 °C and crushed ice was added to the reaction mixture. The aq. phase was extracted with ether (3 x 50 mL), dried over sodium sulfate and concentrated to ~l/4th volume. Then the reaction mixture was added to toluene (70 mL) and heated to 90 °C, until evolution of 2 ceased (-30 min). To the resulting reaction mixture was added 20% HC1 (50 mL) at 0 °C and the reaction mixture was gently heated to 90 °C for 16h. Organic layer was separated off and washed with water (50 mL). The aqueous layer was concentrated under vacuum to get the compound (5g, crude) as a brown solid. ^X H-NMR (400 MHz, CDCI ₃ ) δ 8.75 (br, 3H), 3.92-3.86 (m obscured by solvent signal, 2H), 3.38-3.31 (m, 3H).

[0131] Step 2: tert-butyl (3-oxocyclobutyl) carbamate: TEA (29.72 g, 293.73 mmol) was added dropwise to a solution of 3-aminocyclobutan-l-one (5.0 g, 58.74 mmol) and B0C2O (25.64 g, 117.49 mmol) in DMF (80 mL) and the reaction mixture was stirred at room temperature for 2h. After complete consumption of starting material as indicated by TLC, the reaction mixture was diluted with water (100 mL) and extracted with diethyl ether (70 mL x 6). Combined organic layer was washed with brine (100 mL x 2) and dried over Na ₂ S0 ₄ . The solvent was removed under reduced pressure to get the crude compound which was purified by silica gel (100-200) column chromatography using 30 % ethyl acetate in n-hexane to afford the product (5.3 g, 65% after two steps) as an off-white solid. ¾-NMR (400 MHz, CDC1 ₃ ) δ 4.91 (br, 1H), 4.25 (br, 1H), 3.41-3.34 (m, 2H), 3.07-3.00 (m, 2H), 1.44 (s, 9H).

[0132] Step 3: tert-butyl c s-3-hydroxycyclobutyl)carbamate: a solution of L-Selectride (1M solution in THF) (8.053 mL, 8.05 mmol) was added dropwise over a period of 20 min to a solution of tert-butyl (3-oxocyclobutyl)carbamate (1.0 g, 5.40 mmol) in THF (25 mL) under 2 atmosphere at -78 °C and the reaction mixture was stirred for lh at -78 °C. To the resulting reaction mixture was added a solution of NaOH (3.25 g) in water (4 mL) over a period of 10 min followed by 30% aqueous ¾(¾ (3 mL) over a period of 20 min. The reaction mixture was allowed to warm to room temperature and diluted with ethyl acetate (100 mL). The organic layer was separated off and washed with 10% aq. a ₂ S0 ₃ (40 mL) followed by brine (40 mL). The organic layer dried over Na ₂ S0 ₄ and concentrated under reduced pressure to get the crude compound which was further purified by neutral alumina column chromatography using 50 % ethyl acetate in n-hexane as eluent to afford the desired compound. The compound was washed with n-hexane to get the product (0.750 g, 74%) as white solid, m. p. 1 19 °C (lit. value 117 °C). ^X H NMR (400 MHz, CDC1 ₃ ) δ 4.63 (br, 1H), 4.03-3.96 (m, 1H), 3.66-3.64 (m, 1H), 2.76-2.72 (m, 2H), 1.91 (br, 1H), 1.79-1.76 (m, 2H), 1.42 (s, 9H).

[0133] Step 4: c s-3-((tert-butoxycarbonyl)amino)cyclobutyl methanesulfonate:

triethylamine (1.0 g, 9.93 mmol) was added to a cold (-10 °C ) solution of tert-butyl (cis-3- hydroxycyclobutyl)carbamate (0.62 g, 3.31 mmol) in DCM (30 mL) followed by dropwise addition of methanesulfonyl chloride (0.45 g, 3.97 mmol) and the reaction mixture was stirred at -10 °C for 2h. The reaction mixture was diluted with DCM (100 mL) and washed with water (5 mL) followed by dilute citric acid (30 mL) and brine (30 mL). The organic layer was dried over Na ₂ S0 ₄ , concentrated under reduced pressure to get the product (0.800 g, crude) as white solid which was used as such in next step without further purification. ^X H NMR (400 MHz, CDCI ₃ ) δ 4.73-4.66 (m, 2H), 3.85-3.80 (m, 1H), 2.98 (s, 3H), 2.93-2.86 (m, 2H), 2.20-2.13 (m, 2H), 1.42 (s, 9H).

[0134] Step 5: tert-butyl (ira/is-3-azidocyclobutyl) carbamate: NaN ₃ (0.49 g, 7.54 mmol) was added to a solution of cz ^' s-3-((tert-butoxycarbonyl) amino) cyclobutyl

methanesulfonate (0.8 g, 3.01 mmol) in dry DMF (20 mL) and the mixture was heated at 85 °C for 16h. The reaction mixture was diluted with water (40 mL) and the aqueous phase was extracted with ethyl acetate (50 mL x 3). Combined organic layer was washed with brine (50 mL x 4) and dried over Na ₂ S0 ₄ . The solvent was removed under reduced pressure to get the crude product (0.73 g) as an off-white solid. Although DMF was present in the crude according to ^- MR, it was used as such in the next step without further purification.

[0135] Step 6: tert-butyl ir«ws-3-(5-(hydroxymethyl)-lH-l,2,3-triazol-l- yl)cyclobutyl)carbamate and tert-butyl (trans-3-(4-(hydroxymethyl)-lH-l,2,3-triazol-l- yl)cyclobutyl)carbamate: a solution of tert-butyl ?ra«s-3-azidocyclobutyl)carbamate (0.98 g, 4.62 mmol) in DMF (5 mL) and propargyl alcohol (1.29 g, 23.08 mmol) was heated at 100 °C in a sealed tube for 16h. The mixture was diluted with water (30 mL) and the aqueous phase was extracted with ethyl acetate (25 mL x 7). Combined organic layer was dried over Na ₂ S0 ₄ and solvent was removed under reduced pressure to get the crude compound which was further purified by neutral alumina column chromatography using 80 % ethyl acetate in n-hexane as eluent to afford a fraction of 5-isomer enriched (4/1 ratio of isomers 5/4, 0.350 g, 28%) as an off- white solid and elution with 5 % methanol in DCM afforded a fraction of 4-isomer enriched (1/3 ratio of isomers 5/4, 0.52 g, 42%) as an off-white solid. LC-MS: (M+H) ⁺ = 269.1

7V-ir««s-3-(5-(hydroxymethyl)-lH-l,2,3-triazol-l-yl) cyclobutyl)-5-phenylisoxazole- 3-carboxamide:

[0136] Step 7a: (l-ir««s-3-aminocyclobutyl)-lH-l,2,3-triazol-5-yl)methanol : A suspension of a mixture of (l-((?ra«s-3-aminocyclobutyl)-lH-l,2,3-triazol-5/4-yl)metha nol isomers (4/1 ratio, 0.35 g, 1.30 mmol) and 4M HC1 in dioxane (30 mL) was stirred at room temperature for 24 h. Volatiles were removed under reduced pressure to get compound (0.35 g, crude) as a white solid.

[0137] Step 8a: 7V-ir««s-3-(5-(hydroxymethyl)-lH-l,2,3-triazol-l-yl)cyclob utyl)-5- phenylisoxazole-3-carboxamide: DIPEA (0.47 g, 3.64 mmol) and HATU (0.554 g, 1.45 mmol) were added sequentially to a solution of 5-phenylisoxazole-3-carboxylic acid (0.230 g, 1.21 mmol) in THF (15 mL) and the reaction mixture was stirred for 30 min. The mixture of amine isomers from step 7a was added (0.204 g, 1.21 mmol) to the reaction mixture and stirred at room temperature for 16h. The reaction mixture was diluted with water (30 mL) and the aqueous phase was extracted with ethyl acetate (30 mL x 3). Combined organic layer was dried over Na ₂ S0 ₄ and concentrated under reduced pressure to get crude compound which was purified by neutral alumina column chromatography. Elution with 2.5% MeOH in DCM as eluent afforded the desired compound which was further washed with ethyl acetate (2 mL x 2) to obtain N-((trans-3-(5-(hydroxymethyl)-lH-l,2,3-triazol-l-yl)cyclobu tyl)-5-phenylisoxazole- 3-carboxamide (0.1 10 g).

[0138] Yield: 24% over two steps

[0139] Appearance: white solid

[0140] Analytical data: ^X H-NMR (400 MHz, CDC1 ₃ ) δ 9.38 (d, 1H, J= 7.3 Hz ), 7.96-7.93

(m, 2H), 7.64 (s, 1H), 7.62-7.52 (m, 3H), 7.40 (s, 1H), 5.44-5.41 (t, 1H, J= 5.5 Hz), 5.24-5.17 (m, 1H), 4.80-4.73 (m, 1H), 4.55 (d, 1H, J= 5.5 Hz), 2.89-2.84

(m, 2H), 2.81-2.76 (m, 2H).

[0141] LC-MS: (M+H) ⁺ = 340.0

[0142] HPLC purity: 97.5 % at 220 nm and 97.2% at 254 nm.

7V-((fr«ws-3-(4-(hydroxymethyl)-lH-l,2,3-triazol-l-yl) cyclobutyl)-5- phenylisoxazole-3-carboxamide:

[0143] Step 7b: (l-ir««s-3-aminocyclobutyl)-lH-l,2,3-triazol-4-yl)methanol : A suspension of a mixture of (l-(?ra«s-3-aminocyclobutyl)-lH-l,2,3-triazol-5/4-yl)methan ol isomers (1/3 ratio, 0.52 g, 1.93 mmol) and 4M HC1 in dioxane (30 mL) was stirred at room temperature for 24 h. Volatiles were removed under reduced pressure to get compound (0.52 g, crude) as a white solid.

[0144] Step 8b: /V-ir««s-3-(4-(hydroxymethyl)-lH-l,2,3-triazol-l-yl)cyclob utyl)-5- phenylisoxazole-3-carboxamide: DIPEA (0.650 g, 5.074 mmol) and HATU (0.771 g, 2.03 mmol) were added sequentially to a solution of 5-phenylisoxazole-3-carboxylic acid (0.320 g, 1.69 mmol) in THF (15 mL) and the reaction mixture was stirred for 30 min. The mixture of amine isomers from step 7b was added (0.284 g, 1.69 mmol) to the reaction mixture and stirred at room temperature for 16h. The reaction mixture was diluted with water (30 mL) and the aqueous phase was extracted with ethyl acetate (30 mL x 3). Combined organic layer was dried over Na ₂ S0 ₄ and concentrated under reduced pressure to get crude compound which was purified by neutral alumina column chromatography. Elution with 2.5% MeOH in DCM as eluent afforded the desired compound which was further washed with ethyl acetate (2 mL x 2) to obtain N-((?raws-3-(4-(hydroxymethyl)- 1H- 1 ,2,3-triazol- 1 -yl)cyclobutyl)-5-phenylisoxazole- 3-carboxamide (0.270 g, 41% over two steps).

[0145] Yield: 41% over two steps [0146] Appearance: white solid

[0147] Analytical data: ^- MR (400 MHz, CDC1 ₃ ) δ 9.39-9.37 (d, 1H, J= 7.3 Hz), 8.16

(s, 1H), 7.96-7.93 (m, 2H), 7.59-7.53 (m, 3H), 7.39 (s, 1H), 5.27-5.22 (m, 1H), 5.20-5.17 (t, 1H, J= 5.6 Hz), 4.75-4.69 (m, 1H), 4.53-4.51 (d, 1H, J= 5.6 Hz), 2.84-2.76 (m, 4H). [0148] LC-MS: (M+H) ⁺ = 339.9

[0149] HPLC purity: 99.4 % at 220 nm and 99.7 % at 254 nm.

Example 2: 7V-c s-3-(5-(hydroxymethyl)-lH-l,2,3-triazol-l-yl) cyclobutyl)-5- phenylisoxazole-3-carboxamide and 7V-c s-3-(4-(hydroxymethyl)-lH-l,2,3-triazol-l-yl) cyclobutyl)-5-phenylisoxazole-3-carboxamide:

Boc

[0150] Step 1: ir««s-3-((tert-butoxycarbonyl)amino)cyclobutyl 4-nitrobenzoate: To an ice-cooled solution of tert-butyl (cz ^' s-3-hydroxycyclobutyl)carbamate (1.5 g, 80.11 mmol) and 4-nitrobenzoic acid (1.47 g, 88.12 mmol) in dry THF (60 mL) was added triphenyl phosphine (3.15 g, 12.01 mmol) followed by dropwise addition of DIAD (8.09 g, 40.05 mmol) and the reaction mixture was stirred at room temperature for 2 days. Solvent was removed under reduced pressure to get the crude compound which was purified by silica gel (100-200 mesh) column chromatography. Elution with 50 % ethyl acetate in n-hexane followed by washing with diethyl ether (4 mL x 2) gave the product (2.3 g, 85%) as a white solid. ^X H-NMR (400 MHz, CDC1 ₃ ) δ 8.29-8.27 (q, 2H, J= 8.92 Hz), 8.21-8.19 (q, 2H, J= 8.92 Hz), 5.37-5.32 (m, 1H), 4.77 (br, 1H), 4.41-4.38 (m, 1H), 2.64-2.58 (m, 2H), 2.47-2.40 (m, 2H), 1.44 (s, 9H); LC- MS: (M+H) ⁺ = 336.8 .

[0151] Step 2a: T ms-tert-butyl -3-hydroxycyclobutyl carbamate: trans-3-((tert- butoxycarbonyl) amino) cyclobutyl 4-nitrobenzoate was added (2.3 g, 68.38 mmol) to a suspension of K2CO ₃ (1.41 g, 10.25 mmol) in MeOH (50 mL) and water (10 mL) and the reaction mixture was heated to reflux for 2h. The reaction mixture was cooled and filtered through celite bed. Filtrate was concentrated under reduced pressure to get the crude product (4.2 g, crude) as an off-white solid which was used as such without further purification.

[0152] Step 2b: ir«ws-3-((tert-butoxycarbonyl)amino)cyclobutyl methanesulfonate: triethyl amine (6.8 g, 67.29 mmol) was added to a suspension of iraws-tert-butyl -3- hydroxycyclobutyl carbamate (4.2 g, 22.43 mmol) in DCM (100 mL) followed by dropwise addition of methanesulfonyl chloride (3.08 g, 26.91 mmol) at -10 °C and the reaction mixture was stirred at -10 °C for 2h. The reaction mixture was diluted with DCM (100 mL) and washed with water (50 mL) followed by brine (30 mL). The organic layer was dried over sodium sulfate and concentrated under reduced pressure to obtain the crude product (3.4 g, crude) as a yellow solid which was used as such in next step without purification.

[0153] Step 2c: c/s-tert-butyl (3-azidocyclobutyl)carbamate: sodium azide (2.08 g, 32.035 mmol) was added to a solution of ?raws-3-((tert-butoxycarbonyl)amino)cyclobutyl methanesulfonate (3.4 g, 12.81 mmol) in dry DMF (20 mL) at room temperature and the reaction mixture was heated at 85 °C for 16h. The crude reaction mixture was diluted with water (50 mL) and the aqueous phase was extracted with ethyl acetate (50 mL x 3). The combined organic layer was washed with brine (50 mL x 4) and dried over a ₂ S0 ₄ . The solvent was removed under reduced pressure to give the crude compound which was purified by neutral alumina column chromatography using 10% MeOH in DCM as eluent to afford the product (1.0 g, 68% after two steps) as a white solid. 1H NMR (400 MHz, CDC1 ₃ ) δ 4.66 (br, 1H), 3.86-3.84 (m, 1H), 3.57-3.53 (m, 1H), 2.76-2.69 (m, 2H), 1.92-1.85 (m, 2H), 1.42 (s, 9H). [0154] Step 3: c s-[3-(4/5-Hydroxymethyl-[l,2,3]triazol-l-yl)-cyclobutyl]-car bamic acid tert-butyl ester: a mixture of c/s-tert-butyl (3-azidocyclobutyl)carbamate (0.280 g, 1.32 mmol) and propargyl alcohol (0.221 g, 3.96 mmol) in DMF (5 mL) was heated at 100 °C in a sealed tube for 16h. Solvent was removed under reduced pressure to get crude compound which was purified by neutral alumina column chromatography using 5 % methanol in DCM as eluent to obtain a mixture of 4/5 regioisomers (0.30 g, 84%) as a viscous oil. This mixture was used as such in the next reaction. LC-MS: (M+H) ⁺ = 269.0 .

[0155] Step 4a: (l-c s-3-aminocyclobutyl)-lH-l,2,3-triazol-4/5-yl)methanol (A): A suspension of c s-[3-(4/5-hydroxymethyl-[l,2,3]triazol-l-yl)-cyclobutyl]-car bamic acid tert- butyl ester (0.30 g, 1.12 mmol) in 4M HC1 in dioxane (30 mL) was stirred at room temperature for 24h. Volatiles were removed under reduced pressure to get the crude mixture (0.30 g, crude) as off-white solid which was used as such in next step without further purification. As per ^- MR, it is a 50:50 mixture of two regioisomers.

[0156] Step 4b: 7V-(c s-3-(5-(hydroxymethyl)-lH-l,2,3-triazol-l-yl)cyclobutyl)-5- phenylisoxazole-3-carboxamide and N-(c/s-3-(4-(hydroxymethyl)-lH-l,2,3-triazol-l- yl)cyclobutyl)-5-phenylisoxazole-3-carboxamide: DIPEA (0.69 g, 3.64 mmol) was added to a solution of 5-phenylisoxazole-3-carboxylic acid (0.337 g, 1.78 mmol) in THF (10 mL) followed by HATU (0.813 g, 2.14 mmol) and the reaction mixture was stirred for 30 min. The amine (A) (0.300 g) was added to the mixture and the reaction mixture was stirred at room temperature for 16h. The reaction mixture was diluted with water (30 mL) and the aqueous phase was extracted with ethyl acetate (30 mL x 3). The combined organic layer was dried over Na ₂ S0 ₄ and concentrated under reduced pressure to get the crude mixture which was purified by preparative HPLC to get the two regioisomers:

7V-(c s-3-(5-(hydroxymethyl)-lH-l,2,3-triazol-l-yl) cyclobutyl)-5-phenylisoxazole-3- carboxamide (0.040 g): [0157] Appearance: pale pink solid [0158] Analytical data: ^X H-NMR (400 MHz, CDC1 ₃ ) δ 9.30 (d, 1H, J= 7.4 Hz), 7.92-7.89 (m, 2H), 7.59 (s, 1H), 7.55-7.51 (m, 3H), 7.35 (s, 1H), 5.42 (t, 1H, J= 5.5Hz), 4.81-4.73 (m, 1H), 4.54 (d, 2H, J= 5.5 Hz), 4.39-4.30 (m, 1H), 2.86-2.77 (m, 4H).

[0159] LC-MS: (M+H) ⁺ = 339.9

[0160] HPLC purity: 99.04 % at 220 nm and 99.35 % at 254 nm.

7V-(c s-3-(4-(hydroxymethyl)-lH-l,2,3-triazol-l-yl) cyclobutyl)-5-phenylisoxazole-3- carboxamide (0.040 g):

[0161] Appearance: white solid

[0162] Analytical data: ^X H-NMR (400 MHz, CDC1 ₃ ) δ 9.26 (d, 1H, J= 8.32 Hz), 8.21 (s,

1H), 7.96-7.93 (m, 2H), 7.56-7.54 (m, 3H), 7.39 (s, 1H), 5.22 (t, 1H, J= 5.5 Hz), 4.99-4.91 (m, 1H), 4.54 (d, 2H, J= 5.5 Hz), 4.46-4.41 (m, 1H), 2.95-2.88 (m, 2H), 2.72-2.64 (m, 2H).

[0163] LC-MS: (M+H) ⁺ = 340.0

[0164] HPLC purity: 96.69 % at 220 nm and 97.09 % at 254 nm.

[0165] Yield: 22% over two steps.

Example 3: 7V-C s-3-(4-((S)-l-hydroxyethyl)-lH-l,2,3-triazol-l-yl)cyclobutyl )-5- phenylisoxazole-3-carboxamide and 7V-c s-3-(5-((S)-l-hydroxyethyl)-lH-l,2,3-triazol-l- yl)cyclobutyl)-5-phenylisoxazole-3-carboxamide were prepared by the procedure described in example 2 using (S)-3-butyn-2-ol.

[0166] Yield: 57% over last 2 steps 7V-C/s-3-(5-((S)-l-hydroxyethyl)-lH-l,2,3-triazol-l-yl)cyclo butyl)-5- phenylisoxazole-3-carboxamide Appearance: pale pink solid

[0167] Analytical data: ¾-NMR (400 MHz, CDC1 ₃ ) δ 9.34 (d, 1H, J= 7.5 Hz), 7.95-7.92

(m, 2H), 7.61 (s, 1H), 7.59-7.54 (m, 3H), 7.38 (s, 1H), 5.51 (d, 1H, J= 5.9 Hz), 4.91-4.85 (m, 2H), 4.40-4.34 (m, 1H), 2.88-2.80 (m, 4H), 1.43 (d, 3H, J= 6.5 Hz).

[0168] LC-MS: (M+H) ⁺ = 354.0

[0169] HPLC purity: 99.84 % at 220 nm and 99.80 % at 254 nm

7V-C/s-3-(4-((S)-l-hydroxyethyl)-lH-l,2,3-triazol-l-yl)cy clobutyl)-5- phenylisoxazole-3-carboxamide Appearance: white solid

[0170] 1H-NMR (400 MHz, CDC1 ₃ ) δ 9.26 (d, 1H, J= 8.4 Hz), 8.18 (s, 1H), 7.95-7.93 (m,

2H), 7.59-7.53 (m, 3H), 7.40 (s, 1H), 5.30 (d, 1H, J= 4.8Hz), 4.96-4.92 (m, 1H), 4.86-4.80 (m, 1H), 4.47-4.41 (m, 1H), 2.95-2.88 (m, 2H), 2.71-2.64 (m, 2H), 1.41 (d, 3H, J= 6.5 Hz).

[0171] LC-MS: (M+H) ⁺ = 354.1

[0172] HPLC purity: 99.53 % at 220 nm and 99.54 % at 254 nm.

Example 4: 7V-((ir««s-3-(5-(hydroxymethyl)-l,3,4-thiadiazol-2- yl)cyclobutyl)methyl)-5-phenylisoxazole-3-carboxamide and iV-((c s-3-(5- (hydroxymethyl)-l,3,4-thiadiazol-2-yl)cyclobutyl)methyl)-5-p henylisoxazole-3- carboxamide

[0173] Step la: 3-methylenecyclobutane-l-carboxylic acid: To a solution of 3- methylidenecyclobutane-l-carbonitrile (6 g, 64.43 mmol, 1.00 eq.) in ]¾0/ΕίΟΗ (40/40 mL), was added potassium hydroxide (15 g, 267.33 mmol, 4.00 eq.) in several batches at 105°C in 30 min. The resulting solution was stirred for 2 hours at 105°C. The resulting solution was diluted with water (200 mL) and the pH was adjusted to 2 with cone, hydrogen chloride aqueous (12 M). The resulting solution was extracted with ethyl acetate (2x200 mL) and the organic layers combined. The resulting mixture was washed with brine (2x200 mL), dried over anhydrous sodium sulfate and concentrated under vacuum to give of 3-methylidenecyclobutane-l- carboxylic acid as yellow oil (7 g, 97%).

[0174] Step lb: methyl 3-methylenecyclobutane-l-carboxylate: potassium carbonate (61.5 g, 444.98 mmol, 2.00 eq.) and dimethyl sulfate (33 g, 261.63 mmol, 1.20 eq.) were added to a solution of 3-methylidenecyclobutane-l-carboxylic acid (25 g, 222.96 mmol, 1.00 eq.) in acetone (300 mL). The resulting solution was stirred for 2 hours at 60 °C. The resulting solution was diluted with water (700 mL) and then extracted with ethyl acetate (2x500 mL) and the organic layers combined. The resulting mixture was washed with brine (2x500 mL), dried over anhydrous sodium sulfate and concentrated under vacuum. This resulted in 30 g (crude) of methyl 3-methylidenecyclobutane-l-carboxylate as yellow oil. [0175] Step 1C: methyl 3-(hydroxymethyl)cyclobutane-l-carboxylate: a solution of borane-THF (56 mL, 0.80 eq.) was added dropwise over 30 min to a cold (-10 °C) solution of methyl 3 -methylidenecyclobutane- 1 -carboxylate (10 g, 79.27 mmol, 1.00 eq.) in THF (100 mL). The resulting solution was stirred for 3 hours at 25 °C. The mixture was cooled to -10 °C and methanol (20 mL) was added slowly and the mixture was stirred for 30 min at 25 °C. The reaction mixture was cooled to -10 °C and ¾(¾ (9 g, 79.41 mmol, 1.00 eq., 30%) was added dropwise (5 min) followed by dropwise addition of sodium hydroxide aqueous (12.5 mL) at -10 °C. The resulting solution was stirred for 3 hours at 25 °C. The reaction was then quenched by the addition of a ₂ S0 ₃ aqueous. The resulting solution was diluted with water (300 mL) and then extracted with ethyl acetate (2x300 mL) and the organic layers combined. The resulting mixture was washed with brine (2x300 mL), dried over anhydrous sodium sulfate and concentrated under vacuum to give methyl 3 -(hydroxymethyl)cyclobutane- 1 -carboxylate as colorless oil ( 6.6 g, 58%).

[0176] Step Id: methyl 3-(((tert-butyldimethylsilyl)oxy)methyl)cyclobutane-l- carboxylate: imidazole (5.4 g, 79.41 mmol, 2.00 eq.) and TBDMSCl (9.4 g, 62.38 mmol, 1.50 eq.) were added to a solution of methyl 3 -(hydroxymethyl)cyclobutane- 1 -carboxylate (5 g, 34.68 mmol, 1.00 eq.) in tetrahydrofuran (100 mL) and the resulting solution was stirred for 16 hours at 40 °C. The mixture was diluted with water (200 mL) and then extracted with ethyl acetate (3x200 mL) and the organic layers were combined. The resulting mixture was washed with brine (2x300 mL), dried over anhydrous sodium sulfate and concentrated under vacuum to give methyl 3-[[(tert-butyldimethylsilyl)oxy]methyl]cyclobutane-l -carboxylate as a yellow oil (8 g, 89%).

[0177] Step 2a: 3-(((tert-butyldimethylsilyl)oxy)methyl)cyclobutane-l- carbohydrazide: hydrazine hydrate (20 mL) was added to a solution of methyl 3-[[(tert- butyldimethylsilyl)oxy]methyl]cyclobutane-l -carboxylate (8 g, 30.96 mmol, 1.00 eq.) in ethanol (100 mL). The resulting solution was stirred for 2 hours at 80 °C, diluted with water (300 mL) and then extracted with ethyl acetate (2x300 mL) and the organic layers combined. The resulting mixture was washed with brine (2x200 mL), dried over anhydrous sodium sulfate and concentrated under vacuum to give 3-[[(tert-butyldimethylsilyl)oxy]methyl]cyclobutane-l- carbohydrazide (7.5 g, 94%) as a yellow oil. LC-MS: (M+H) ⁺ :259.1 [M+H] ⁺ . [0178] Step 2b: ethyl 2-(2-(3-(((tert-butyldimethylsilyl)oxy)methyl)cyclobutane-l- carbonyl)hydrazinyl)-2-oxoacetate: ethyl 2-chloro-2-oxoacetate (8.87 g, 64.97 mmol, 1.10 eq.) was added dropwise (in 10 min) to a solution of 3-[[(tert- butyldimethylsilyl)oxy]methyl]cyclobutane-l-carbohydrazide (15.3 g, 59.20 mmol, 1.00 eq.) and TEA (9 g, 88.94 mmol, 1.50 eq.) in dichloromethane (200 mL) at 0 °C. The resulting solution was stirred for 1 hour at 25 °C, diluted with dichloromethane (300 mL) and it was then washed with brine (2x200 mL), dried over anhydrous sodium sulfate and concentrated under vacuum. The residue was applied onto a silica gel column and eluted with petroleum ether/ethyl acetate (2: 1) to give ethyl 2-[(3-[[(tert- butyldimethylsilyl)oxy]methyl]cyclobutyl)formohydrazido]-2-o xoacetate (15 g, 71%) as a yellow oil. LC-MS: 359.0 [M+H] ⁺ .

[0179] Step 2c: ethyl 5-(3-(hydroxymethyl)cyclobutyl)-l,3,4-thiadiazole-2-carboxyl ate:

Lawesson reagent (17 g, 42.03 mmol, 1.00 eq.) was added to a solution of ethyl 2-(2-(3-(((tert- butyldimethylsilyl)oxy)methyl)cyclobutane-l-carbonyl)hydrazi nyl)-2-oxoacetate (15 g, 41.84 mmol, 1.00 eq.) in ACN (150 mL) and the solution was stirred for 2 hours at 50 °C. The reaction mixture was diluted with water (300 mL), extracted with ethyl acetate (2x300 mL) and the organic layers combined. The resulting mixture was washed with brine (2x200 mL), dried over anhydrous sodium sulfate and concentrated under vacuum. The residue was purified by silica gel column with ethyl acetate/petroleum ether (2: 1) followed by purification by Flash- Prep-HPLC using the following conditions (IntelFlash-1): Column, C18 silica gel; mobile phase, X:H ₂ 0 Y:ACN=95/5 increasing to X:H ₂ 0 Y:ACN=40/60 within 50 min; Detector, UV 254 nm. This resulted in 3.4 g (34%) of ethyl 5-[3-(hydroxymethyl)cyclobutyl]-l,3,4- thiadiazole-2-carboxylate as a yellow oil. LC-MS: 243.2 [M+H] ⁺ .

[0180] Step 2d: ethyl 5-(3-((bis((tert-butoxy)carbonyl)amino)methyl)cyclobutyl)-l, 3,4- thiadiazole-2-carboxylate: To a solution of ethyl 5-[3-(hydroxymethyl)cyclobutyl]-l,3,4- thiadiazole-2-carboxylate (1.8 g, 7.43 mmol, 1.00 eq.) in tetrahydrofuran (100 mL) was added triphenyl phosphine (3.9 g, 14.87 mmol, 2.00 eq.) in portions at 0 °C in 10 min. This was followed by the addition of DIAD (3 g, 14.78 mmol, 2.00 eq.) and di-tert-butyl

iminodicarboxylate (2.4 g, 11.05 mmol, 1.50 eq.). The resulting solution was stirred for 3 hours at 2 5°C and then diluted with water (200 mL). The resulting solution was extracted with ethyl acetate (3x200 mL) and the organic layers combined. The mixture was washed with brine (2x200 mL), dried over anhydrous sodium sulfate and concentrated under vacuum. The residue was purified by silica gel column using ethyl acetate/petroleum ether (1 :5) to give the product (1.1 g, 33%) as a yellow solid. LC-MS: [M+H] ⁺ 442.3

[0181] Step 3a: tert-butyl [3-[5-(hydroxymethyl)-l,3,4-thiadiazol-2- yljcyclobutyl] methyl N-[(tert-butoxy)carbonyl]carbamate: NaBH ₄ (310 mg, 8.19 mmol, 1.50 eq.)was added to a solution of ethyl -(3-((bis((tert- butoxy)carbonyl)amino)methyl)cyclobutyl)-l,3,4-thiadiazole-2 -carboxylate (2.4 g, 5.42 mmol, 1.00 eq.) in methanol (50 mL), in portions at 0 °C in 10 min and the reaction mixture was then stirred for 1 hour at 25 °C. The reaction was then quenched with water (200 mL). The resulting solution was extracted with ethyl acetate (2x200 mL) and the organic layers combined. The resulting mixture was washed with brine (2x200 mL), dried over anhydrous sodium sulfate and concentrated under vacuum to give the product (2 g, 92%) of as yellow oil. LC-MS: 400.0 [M+H] ⁺ .

[0182] Step 3b: (5-(3-(aminomethyl)cyclobutyl)-l,3,4-thiadiazol-2-yl)methano l hydrochloride: cone, hydrogen chloride aqueous (4 mL) was added to a solution of tert-butyl [3-[5-(hydroxymethyl)-l,3,4-thiadiazol-2-yl]cyclobutyl]methy l N-[(tert- butoxy)carbonyl]carbamate (2 g, 4.99 mmol, 1.00 eq.) in tetrahydrofuran (20 mL) and the solution was stirred for 16 hours at 25 °C. The resulting mixture was concentrated under vacuum, the solid was washed with 20 mL of ethyl acetate to give the product ( 750 mg, 75%) as a yellow solid. LC-MS: 200.1 [M+H-HC1] ⁺ .

[0183] Step 4a: (5-(3-((5-phenylisoxazole-3-carboxamido)methyl)cyclobutyl)-l ,3,4- thiadiazol-2-yl)methyl 5-phenylisoxazole-3-carboxylate: a solution of [5-[3- (aminomethyl)cyclobutyl]-l,3,4-thiadiazol-2-yl]methanol hydrogen chloride (750 mg, 3.17 mmol, 1.00 eq.), 5 -phenyl- l,2-oxazole-3-carboxylic acid (860 mg, 4.55 mmol, 1.40 eq.), HCTU (1.59 g, 3.82 mmol, 1.20 eq.) and DIEA (1.66 g, 12.84 mmol, 3.00 eq.) in

dichloromethane (50 mL) was stirred for 3 hours at 25 °C. The resulting mixture was concentrated under vacuum. This resulted in 800 mg (crude) [5-(3-[[(5-phenyl-l,2-oxazol-3- yl)formamido]methyl]cyclobutyl)-l,3,4-thiadiazol-2-yl]methyl 5-phenyl-l,2-oxazole-3- carboxylate as a yellow oil. The crude product was used in the next step directly without further purification. LC-MS: 542.0 [M+H] ⁺ . [0184] Step 4b : N-((ir«ws-3-(5-(hydroxymethyl)-l,3,4-thiadiazol-2- yl)cyclobutyl)methyl)-5-phenylisoxazole-3-carboxamide and N-((c s-3-(5- (hydroxymethyl)-l,3,4-thiadiazol-2-yl)cyclobutyl)methyl)-5-p henylisoxazole-3- carboxamide: LiOH (142 mg, 5.93 mmol, 4.00 eq.) was added to a solution of [5-(3-[[(5- phenyl-l,2-oxazol-3-yl)formamido]methyl]cyclobutyl)- l,3,4-thiadiazol-2-yl]methyl 5-phenyl- l,2-oxazole-3-carboxylate (800 mg, 1.48 mmol, 1.00 eq.) in tetrahydrofuran/FLO (20/5 mL) and the solution was stirred for 30 min at 25 °C. The resulting solution was diluted with water (100 mL), extracted with ethyl acetate (2x100 mL) and the organic layers combined. The resulting mixture was washed with brine (2x100 mL) brine, dried over anhydrous sodium sulfate and concentrated under vacuum. The crude product was re-crystallized from petroleum ether/ethyl acetate in the ratio of 5: 1. The solid was separated by Prep-SFC with the following conditions (prep SFC 350-2): Column, Phenomenex Lux 5μ Cellulose-3, 5*25cm, 5um; mobile phase, C0 ₂ (50%), methanol (50%); Detector, UV 220nm.

5-phenyl-N-[[(ir««s-3-[5-(hydroxymethyl)-l,3,4-thiadiaz ol-2-yl]cyclobutyl]methyl]- l,2-oxazole-3-carboxamide:

[0185] Yield: 22%

[0186] Appearance: white solid

[0187] Analytical data: ^X H NMR (300MHz, OMSO-d ₆ , ppm): δ: 8.98-8.94 (m, 1H), 7.95- 7.93 (m, 2H), 7.65-7.55 (m, 3H), 7.37 (s, 1H), 6.15-6.11 (m, 1H), 4.81-4.79 (d, J = 6.0Hz, 2H), 4.06-3.96 (m, 1H), 3.50-3.45 (m, 2H), 2.74-2.62 (m, 1H), 2.38-

2.27 (m, 4H).

[0188] LC-MS: 371.3 [M+H] ⁺

5-phenyl-N- [ [(c s-3- [5-(hydroxymethyl)-l,3,4-thiadiazol-2-yl] cyclobutyl] methyl]- l,2-oxazole-3-carboxamide: [0189] Yield: 21%

[0190] Appearance: white solid

[0191] Analytical data: 'H NMR (300MHZ, OMSO-d ₆ , ppm): δ: 8.92-8.90 (m, 1H), 7.95- 7.92 (m, 2H), 7.64-7.54 (m, 3H), 7.39 (s, 1H), 6.13-6.09 (m, 1H), 4.79-4.77 (d, J = 6.0Hz, 2H), 3.87-3.75 (m, 1H), 3.35-3.31 (m, 3H), 2.73-2.61 (m, 2H), 2.10- 2.1.99 (m, 2H).

[0192] LC-MS 371.3 [M+H] ⁺

Example 5: iV-((ir««s-3-((5-(hydroxymethyl)-l,3,4-thiadiazol-2- yl)methyl)cyclobutyl)-5-phenylisoxazole-3-carboxamide and iV-((c s-3-((5-

(hydroxymethyl)-l,3,4-thiadiazol-2-yl)methyl)cyclobutyl)- 5-phenylisoxazole-3- carboxamide

[0193] Step la: ethyl 2-(3-((tert-butoxycarbonyl)amino)cyclobutylidene)acetate: a solution of tert-butyl N-(3-oxocyclobutyl) carbamate (8 g, 43.19 mmol, 1.00 eq.) and ethyl 2- (triphenyl- ⁵ -phosphanylidene)acetate (16.8 g, 48.22 mmol, 1.10 eq.) in toluene (100 mL) was stirred for 2 hours at 100 °C. The resulting mixture was concentrated under vacuum and the mixture was purified by silica gel column and eluted with ethyl acetate/petroleum ether (0-5%) to give crude (10.5 g) of ethyl 2-(3-[[(tert-butoxy)carbonyl]amino]cyclobutylidene)acetate as a white solid. LC-MS: 256 [M+H] ⁺ . [0194] Step lb: ethyl 2-(3-[[(tert-butoxy)carbonyl]amino]cyclobutyl)acetate: Palladium carbon (210 mg) was added to a solution of ethyl 2-(3-[[(tert- butoxy)carbonyl]amino]cyclobutylidene)acetate (10.5 g, 41.13 mmol, 1.00 eq.) in methanol (150 mL), and the mixture was hydrogenated for 2 h at rt. The solids were filtered out and the mixture was concentrated under vacuum. This resulted in 10.6 g (crude) of ethyl 2-(3-[[(tert- butoxy)carbonyl]amino]cyclobutyl)acetate as a white solid. LC-MS: 258 [M+H] ⁺ .

[0195] Step lc: tert-butyl N-[3-[(hydrazine carbonyl)methyl]cyclobutyl] carbamate: a solution of ethyl 2-(3-[[(tert-butoxy)carbonyl]amino]cyclobutyl)acetate (9.74 g, 37.85 mmol, 1.00 eq.) and hydrazine hydrate (11.4 mL) in ethanol (300 mL) was heated for 17 hours at 80 °C. The resulting solution was diluted with water (500 mL) and then extracted with ethyl acetate (3x300 mL) and the combined organic layer was dried over anhydrous sodium sulfate and concentrated under vacuum. The crude product was re-crystallized from ethyl acetate/petroleum ether in the ratio of 1 :2. This resulted in 6.88 g (crude) of tert-butyl N-[3- [(hydrazine carbonyl)methyl]cyclobutyl]carbamate as a white solid. LC-MS: 244 [M+H] ⁺ .

[0196] Step 2a : ethyl 2- [2-(3- [ [(tert- butoxy)carbonyl] amino] cyclobutyl)acetohydrazido]-2-oxoacetate: ethyl 2-chloro-2- oxoacetate (4.74 g, 34.72 mmol, 1.20 eq.) was added dropwise to a cold solution (0 °C) of tert- butyl N- [3 -[(hydrazine carbonyl)methyl]cyclobutyl]carbamate (7.04 g, 28.94 mmol, 1.00 eq.) and TEA (5.84 g, 57.71 mmol, 2.00 eq.) in tetrahydrofuran (150 mL). The resulting solution was stirred for 1 hour at room temperature, filtered and the resulting mixture was concentrated under vacuum. The residue was applied onto a silica gel column and eluted with ethyl acetate/petroleum ether (4: 1) to give crude (9.5 g) ethyl 2-[2-(3-[[(tert- butoxy)carbonyl]amino]cyclobutyl)acetohydrazido]-2-oxoacetat e as a yellow solid. LC-MS: 344 [M+H] ⁺ .

[0197] Step 2b: ethyl 5-[(3-[[(tert-butoxy)carbonyl]amino]cyclobutyl)methyl]-l,3,4 - thiadiazole-2-carboxylate: a solution of ethyl 2-[2-(3-[[(tert- butoxy)carbonyl]amino]cyclobutyl)acetohydrazido]-2-oxoacetat e (9.5 g, 27.67 mmol, 1.00 eq.) and Lawesson's reagent (11.19 g, 27.67 mmol, 1.00 eq.) in MeCN (200 mL) was heated 16 hours at 50 °C. The reaction was then quenched by the addition of ice-water (300 mL). The resulting solution was extracted with ethyl acetate (4x200 mL). The combined organic layer was dried over anhydrous sodium sulfate and concentrated under vacuum to give crude (1.6 g) ethyl 5-[(3-[[(tert-butoxy)carbonyl]amino]cyclobutyl)methyl]-l,3,4 -thiadiazole-2-carboxylate as a yellow solid. LC-MS: 342.2 [M+H] ⁺ . [0198] Step 2c: tert-butyl 7V-(3-[[5-(hydroxymethyl)-l,3,4-thiadiazol-2- yl] methyl] cyclobutyl)carbamate: NaBH ₄ (399 mg, 10.55 mmol, 3.00 eq.) was added in several batches to a cold solution (0 °C) of ethyl 5-[(3-[[(tert- butoxy)carbonyl]amino]cyclobutyl)methyl]-l,3,4-thiadiazole-2 -carboxylate (1.2 g, 3.51 mmol, 1.00 eq.) in methanol (20 mL). The resulting solution was stirred for 1 hour at 0 °C and then quenched by the addition of water (3 mL). The mixture was filtered and then concentrated under vacuum to give crude (1.146 g) tert-butyl N-(3-[[5-(hydroxymethyl)-l,3,4-thiadiazol-2- yl]methyl]cyclobutyl)carbamate as a yellow solid. LC-MS: 300.1 [M+H] ⁺ .

[0199] Step 2d: [5-[(3-aminocyclobutyl)methyl]-l,3,4-thiadiazol-2-yl]methano l hydrochloride: a solution of tert-butyl N-(3-[[5-(hydroxymethyl)-l,3,4-thiadiazol-2- yl]methyl]cyclobutyl)carbamate (1.45 g, 4.84 mmol, 1.00 eq.) and concentrated hydrogen chloride aqueous (2 mL) in tetrahydrofuran (20 mL) was stirred for 16 hours at room temperature. The resulting mixture was concentrated under vacuum. This resulted in 980 mg (crude) of [5-[(3-aminocyclobutyl)methyl]-l,3,4-thiadiazol-2-yl]methano l hydrogen chloride salt as a yellow solid. LC-MS: 200.0 [M+H-HC1]+.

[0200] Step 3: N-(ir«ws-3-((5-(hydroxymethyl)-l,3,4-thiadiazol-2- yl)methyl)cyclobutyl)-5-phenylisoxazole-3-carboxamide and N-(c s-3-((5- (hydroxymethyl)-l,3,4-thiadiazol-2-yl)methyl)cyclobutyl)-5-p henylisoxazole-3- carboxamide: a solution of [5-[(3-aminocyclobutyl)methyl]-l,3,4-thiadiazol-2-yl]methano l hydrochloride (500 mg, 2.12 mmol, 1.00 eq., 99%), 5-phenyl-l,2-oxazole-3-carboxylic acid (481 mg, 2.54 mmol, 1.20 eq.), HCTU (1.061 g, 2.55 mmol, 1.20 eq.) and DIEA (1.09 g, 8.43 mmol, 1.20 eq.) in dichloromethane (30 mL) was stirred for 2 hours at room temperature. The resulting mixture was concentrated under vacuum. The crude product was purified by Prep- Flash with acetonitrile and water (0-46% within 40 min). The isomers were separated by Prep- SFC with the following conditions (prep SFC 350-2): Column, Phenomenex Lux 5μ Cellulose- 4, 250*50mm; mobile phase, C0 ₂ (50%), MeOH (0.2%DEA) (50%); Detector, UV 220nm.

5-phenyl-7V-[(c s-3-[[5-(hydroxymethyl)-l,3,4-thiadiazol-2-yl]methyl]cyclobu tyl]- l,2-oxazole-3-carboxamide:

[0201] Yield: 37% [0202] Appearance: off-white solid [0203] Analytical data: ^X H NMR (400MHz, OMSO-d ₆ , ppm): δ: 9.06 (d, J= 8.0Hz, 1H),

7.94-7.92 (m, 2H), 7.58-7.54 (m, 3H), 7.35 (s, 1H), 6.14-6.1 1 (m, 1H), 4.80 (d, J = 6.0Hz, 2H), 4.35-4.33 (m, 1H), 3.19-3.17 (m, 2H), 2.43-2.33 (m, 3H), 1.99- 1.93 (m, 2H). [0204] LC-MS: 371.1 [M+H] ⁺

5-phenyl-iV-[(ir««s-3-[[5-(hydroxymethyl)-l,3,4-thiadia zol-2-yl]methyl]cyclobutyl]- l,2-oxazole-3-carboxamide:

[0205] Yield: 37%

[0206] Appearance: light yellow solid [0207] Analytical data: 'H NMR (400MHZ, OMSO-d ₆ , ppm): δ: 9.14 (d, J= 7.2Hz, 1H),

7.94-7.92 (m, 2H), 7.56-7.54 (m, 3H), 7.36 (s, 1H), 6.14-6.1 1 (m, 1H), 4.80 (d, J = 6.0Hz, 2H), 4.63-4.55 (m, 1H), 3.33-3.28 (m, 2H), 2.51-2.49 (m, 1H), 2.33- 2.31 (m, 2H) , 2.14-2.13 (m, 2H).

Example 6: N-(trans-3-(5-((S)-l -hydrox ethyl)-lH-l, 2,3-triazol-l- yl)cyclobutyl)-5-phenylisoxazole-3-carboxamide and 7V-(ir«ws-3-(4-((S)-l-hydroxyethyl)- lH-l,2,3-triazol-l-yl)cyclobutyl)-5-phenylisoxazole-3-carbox amide were prepared by the procedure described in example 1 using (S)-3-butyne-2-ol instead of propargyl alcohol.

7V-(ir««s-3-(5-((S)-l-hydroxyethyl)-lH-l,2,3-triazol-l- yl)cyclobutyl)-5- phenylisoxazole-3-carboxamide [0208] Appearance: white solid

[0209] Analytical data: ^X H-NMR (400 MHz, DMSO) δ 9.40-9.39 (d, J= 7.4 Hz, 1H), 7.96- 7.94 (m, 2H), 7.62 (s, 1H), 7.59-7.54 (m, 3H), 7.40 (s, 1H), 5.49 (d, J= 5.8 Hz, IH), 5.32-5.28 (m, IH), 4.86-4.75 (two overlapped multiplets, 2H), 2.90-2.83 (m, 2H), 2.83-2.76 (m, 2H), 1.43-1.42 (d, J= 6.52 Hz, 3H).

[0210] LC-MS: (M+H) ⁺ = 354.0

[0211] HPLC purity: 99.9 % at 220 nm and 99.89 % at 254 nm.

7V-(ir««s-3-(4-((S)-l-hydroxyethyl)-lH-l,2,3-triazol-l- yl)cyclobutyl)-5- phenylisoxazole-3-carboxamide

[0212] Appearance: white solid

[0213] Analytical data: 1H-NMR (400 MHz, DMSO) δ 9.39-9.38 (d, J= 7.3 Hz, IH), 8.1 1

(s, IH), 7.96-7.93 (m, 2H), 7.59-7.54 (m, 3H), 7.39 (s, IH), 5.25-5.23 (m, 2H), 4.84-4.81 (m, IH), 4.74-4.69 (m, IH), 2.85-2.74 (m, 4H), 1.41 (d, J= 6.52 Hz, 3H).

[0214] LC-MS: (M+H) ⁺ = 353.9

[0215] HPLC purity: 99.84 % at 220 nm and 99.87 % at 254 nm.

[0216] Example 7: 7V-(ir««s-3-(5-((R)-l-hydroxyethyl)-lH-l,2,3-triazol-l- yl)cyclobutyl)-5-phenylisoxazole-3-carboxamide and N-(tmns-3-(4-((R)-l- hydroxyethyl)-lH-l,2,3-triazol-l-yl)cyclobutyl)-5-phenylisox azole-3- carboxamide were prepared by the procedure described in example 1 using (R)- 3-butyne-2-ol instead of propargyl alcohol.

7V-(ir««s-3-(5-((R)-l-hydroxyethyl)-lH-l,2,3-triazol-l- yl)cyclobutyl)-5- phenylisoxazole-3-carboxamide

[0217] Appearance: Of white solid [0218] Analytical data: ^X H-NMR (400 MHz, DMSO) δ 9.37 (d, J

(m, 2H), 7.60 (s, 1H), 7.55 -7.51 (m, 3H), 7.38 (s, 1H), 5.46 (d, J= 5.84 Hz, 1H), 5.30 - 5.22 (m, 1H), 4.82 (t, J= 6.3 Hz, 2H), 4.76 - 4.71 (m, 1H), 2.87 - 2.82 (m, 2H,), 2.78 - 2.71 (m, 2H), 1.40 (d, J= 6.5 Hz, 3H). [0219] LC-MS: (M+H) = 354.1

[0220] HPLC purity: 94.46 % at 200 nm, 95.18 % at 220 nm and 95.14 % at 254 nm

7V-(ir««s-3-(5-((R)-l-hydroxyethyl)-lH-l,2,3-triazol-l- yl)cyclobutyl)-5- phenylisoxazole-3-carboxamide

[0221] Appearance: Of white solid [0222] Analytical data: ^X H-NMR (400 MHz, DMSO) 9.38 (d, J= 7.3 Hz, 1H), 8.11 (s, 1H),

7.96 - 7.93 (m, 2H), 7.57 -7.54 (m, 3H), 7.39 (s, 1H), 5.27 - 5.22 (m, 2H), 4.84 - 4.81 (m, 1H), 4.74 - 4.67 (m, 1H), 2.82 - 2.77 (m, 4H,), 1.41 (d, J= 6.5 Hz, 3H).

[0223] LC-MS: (M+H) ⁺ = 353.9

[0224] HPLC purity: 98.73 % at 200 nm, 98.36 % at 220 nm and 97.83 % at 254 nm

Example 8: 7V-(cis-3-(5-((R)-l-hydroxyethyl)-lH-l,2,3-triazol-l-yl)cycl obutyl)-5- phenylisoxazole-3-carboxamide and 7V-(cis-3-(4-((R)-l-hydroxyethyl)-lH-l,2,3-triazol- l-yl)cyclobutyl)-5-phenylisoxazole-3-carboxamide were prepared by the procedure described in example 2 using (R)-3-butyne-2-ol instead of propargyl alcohol.

7V- c s-3-(5-((R)-l-hydroxyethyl)-lH-l,2,3-triazol-l-yl)cyclobutyl )-5- phenylisoxazole-3-carboxamide:

[0225] Appearance: off white solid [0226] Analytical data: ^X H-NMR (400 MHz, CDC1 ₃ ) : δ 7.80 - 7.76 (m, 2H), 7.56 (s, IH),

7.50 - 7.45 (m, 3H), 7.38 (d, J= 8.4 Hz, IH), 6.95 (s, IH ), 5.01 - 4.96 (m, IH), 4.93 - 4.87 (m, IH), 4.64 - 4.58 (m, IH), 3.16 - 3.05 (m, 2H), 2.96 - 2.87 (m, 2H), 2.23 (d, J= 6.9 Hz, IH ). [0227] LC-MS: (M+H) ⁺ = 353.9

[0228] HPLC purity: 99.48 % at 200 nm, 99.76 % at 220 nm and 99.55 % at 254 nm

[0229] 7V- c s-3-(4-((R)-l-hydroxyethyl)-lH-l,2,3-triazol-l-yl)cyclobutyl )-5- phenylisoxazole-3-carboxamide:

[0230] Appearance: off white solid [0231] Analytical data: ^X H-NMR (400 MHz, CDC1 ₃ ): δ 7.80 - 7.77 (m, 2H), 7.60 (s, IH),

7.51 - 7.46 (m, 3H), 7.30 (d, J= 7.8 Ηζ, ΙΗ), 6.95 (s, IH), 5.1 1 - 5.08 (m, IH), 4.82 - 4.78 (m, IH), 4.54 - 4.50 (m, IH), 3.17 - 3.10 (m, 2H), 2.86 - 2.78 (m, 2H), 2.41 (d, J= 4.1 Ηζ, ΙΗ), 1.60 (d obscured by solvent peak, 3H).

[0232] LC-MS: (M+H) ⁺ = 353.9 [0233] HPLC purity: 98.1 1 % at 200 nm, 97.89 % at 220 nm and 98.57 % at 254 nm.

Example 9: Preparation of Intermediate I: N-trans-3- (hydrazinecarbonyl)cyclobutyl)-5-phenylisoxazole-3-carboxami de hydrochloride:

6. HATU, Et ₃ N,THF, RT, 6h

7. LiOH, THF, RT, 1 h

[0234] Step 1: ethyl 3-oxocyclobutane-l-carboxylate: triethyl orthoacetate (21.31 g, 0.131 mol) was added to a solution of 3-oxocyclobutane-l-carboxylic acid (5.0 g, 0.043 mol) in toluene (100 mL) and the reaction mixture was refluxed for 6 h. The reaction mixture was quenched with a IN HCI solution and the layers were separated off. The organic layer was washed with saturated aHC0 ₃ solution (2 x 50 mL), brine (2 x 50 mL), dried over anhydrous sodium sulfate and concentrated under reduced pressure to get the product (5.3 g, 85%) as a yellow liquid. ^X H NMR (400 MHz, CDC1 ₃ ): δ 4.23-4.17 (q, J= 7.0 Hz, 2H), 3.44-3.37 (m, 2H), 3.32-3.16 (m, 3H), 1.30-1.26 (t, J= 7.0 Hz, 3H).

[0235] Step 2: ethyl c/s-3-hydroxycyclobutane-l-carboxylate: sodium borohydride (1.55 g, 0.041 mol) was added to an iced cold solution of ethyl 3-oxocyclobutane-l-carboxylate (5.3 g, 0.037 mol) in methanol (75 mL) and the reaction mixture was stirred for 1 h. The reaction mixture was quenched with acetone (10 mL) and volatiles were removed under reduced pressure. The crude reaction mixture was suspended in aHC0 ₃ solution (30 mL) and extracted with DCM (100 mL). The organic layer was washed with brine (30 mL), dried over anhydrous sodium sulfate and concentrated under reduced pressure to get the product (3.2 g, 59%) as a yellow oil. ^X H NMR (400 MHz, CDC1 ₃ ): δ 4.20-4.09 (overlapped q and m, 3H), 3.68 (d, J= 2.3 Hz, 1H), 2.62-2.54 (m, 3H), 2.20-2.10 (m, 2H), 1.26-1.22 (t, J= 7.0 Hz, 3H); LC- MS: [M+H] ⁺ 145.1 .

[0236] Step 3: ethyl c s-3-((methylsulfonyl)oxy)cyclobutane-l-carboxylate: Et ₃ N (8.96 mL, 0.0666 mol) was added to a solution of ethyl cz ^' s-3-hydroxycyclobutane-l -carboxylate (3.2 g, 0.0222 mol) in DCM (100 m L) followed by MsCl (3.03 g, 0.0266 mol) drop wise and the resulting reaction mixture was stirred at room temperature for 1 h. The reaction mixture was poured onto ice cold water (50 mL) and extracted with DCM. The organic layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure to get the crude product (5.1 g) as a yellow oil. 'H NMR (400 MHz, CDC1 ₃ ): δ 4.95-4.88 (m, 1H), 4.17-4.12 (q, J= 7.1 Hz, 2H), 3.71 (d, 1H), 2.98 (s, 3H), 2.74-2.66 (m, 3H), 2.60-2.59 (m, 2H), 1.27-1.25 (t, J = 7.1 Hz, 3H); LC-MS: [M+H] ⁺ 223.0 .

[0237] Step 4: ethyl ir«ws-3-azidocyclobutane-l-carboxylate: a mixture of sodium azide (2.98 g, 0.044 mol) and ethyl czs-3-((methylsulfonyl)oxy)cyclobutane-l -carboxylate (5.1 g, 0.022 mol) in DMF (25 mL) was heated to 90°C for 16 h. The reaction mixture was poured onto water (70 mL) and extracted with ethyl acetate (2 x 100 mL). Combined organic layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure to obtain crude product which was chromatographed on 230-400 mesh silica gel using 10% EtOAc in hexane as eluent to afford the product (3.8 g, 100% over two steps) as colorless liquid. ^X H NMR (400 MHz, CDC1 ₃ ): δ 4.18-4.10 (m, 3H), 3.11-3.04 (m, 1H), 2.60-2.53 (m, 2H), 2.36- 2.29 (m, 2H), 1.27-1.22 (t, J= 7.1 Hz, 3H); LC-MS: [M+H] ⁺ 171.1 .

[0238] Step 5a/b: ethyl ir«ws-3-aminocyclobutane-l-carboxylate hydrochloride: a mixture of ethyl iraws-3-azidocyclobutane-l -carboxylate (3.8 g, 0.0221 mol) and 10% Pd/C (1.0 g) in ethanol (50 mL) was hydrogenated (50 psi) for 4 h at room temperature. The reaction mixture was filtered through a celite bed and the filtrate was concentrated under reduced pressure obtain the crude compound. The crude compound was treated with 4 M HC1 in dioxane to afford HC1 salt (3.8 g, 95%) as colorless viscous oil.

[0239] Step 6: ethyl ir««s-3-(5-phenylisoxazole-3-carboxamido)cyclobutane-l- carboxylate: Ets (5.6 mL, 42 mmol) and HATU (4.84 g, 13 mmol) were added to a mixture of ethyl ?ra«s-3-aminocyclobutane-l -carboxylate hydrochloride (1.89 g, 10 mmol) and 5- phenylisoxazole-3-carboxylic acid (2 g, 10 mmol) in TH F (200 mL) at room temperature and the reaction mixture was stirred for 6 h at room temperature. Volatiles were removed under reduced pressure to get the crude compound. The reaction mixture was diluted with water (100 mL) and extracted using ethyl acetate (2 x 75 mL). Combined organic layer was washed with brine (50 mL), dried over anhydrous Na ₂ S0 ₄ and concentrated under reduced pressure. The mixture was purified by flash column chromatography using 30% EtOAc in hexane as eluent to give the product (2.65 g, 80 %) as white solid. ¾ NMR (400 MHz, CDC13) : δ 7.80-7.77 (m, 2H), 7.49-7.46 (m, 3H), 7.00 (d, J= 7.2 Hz, 1H), 6.94 (s, 1H), 4.79-4.73 (m, 1H), 4.17 (q, J = 7.1 Hz, 2H), 3.10-3.09 (m, 1H), 2.78-2.72 (m, 2H), 2.40-2.32 (m, 2H), 1.30-1.26 (t, J= 12 Hz, 3H). LC-MS: [M+H] ⁺ 315.2 [0240] Step 7: ir«ws-3-(5-phenylisoxazole-3-carboxamido)cyclobutane-l-carb oxylic acid: a solution of lithium hydroxide (0.66 g, 15 mmol) in water (20 mL) was added to a solution of ethyl £raws-3-(5-phenylisoxazole-3-carboxamido)cyclobutane-l-carb oxylate (2.5 g, 7.9 mmol) in THF (30 m L) and the reaction mixture was stirred for 1 h at room temperature. Volatiles were removed under reduced pressure and the crude compound was suspended in water (100 mL). The aq. layer was washed with diethyl ether (2 x 50 mL) and acidified with citric acid solution. The resulting reaction mixture was extracted with ethyl acetate (2 x 100 mL). Combined organic layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure to afford the product (2 g, 92%) which was used as such in next step without further purification. ¾ NMR (400 MHz, DMSO-d ₆ ): δ 12.26 (br, 1H), 9.18-9.16(d, J =7 Hz, 1H), 7.94-7.91 (m, 2H), 7.57-7.53 (m, 3H), 7.35 (s, 1H), 4.59-4.54 (m, 1H), 2.97-2.91 (m, 1H), 2.43-2.38 (m, 4H). LC-MS: [M-H] ^" 284.9

[0241] Step 8: tert-butyl 2-ir«ws-3-(5-phenylisoxazole-3-carboxamido)cyclobutane-l- carbonyl)hydrazine-l-carboxylate: TEA (3.66 mL, 28.3 mmol)was added to a mixture of Boc-Hydrazine (1.49 g, 1 1 mmol) and £raws-3-(5-phenylisoxazole-3-carboxamido)cyclobutane- 1-carboxylic acid (2.7 g, 9.4 mmol) in THF (100 mL) followed by addition of T ₃ P ( 12 mL, 18.8 mol). The reaction mixture was stirred for 16h at room temperature. Volatiles were removed under reduced pressure and the crude reaction mixture was diluted with water (100 mL). The reaction mixture was extracted with ethyl acetate (2 x 100 mL). Combined organic layer was washed with brine (100 mL), dried over anhydrous Na ₂ S0 ₄ and concentrated under reduced pressure to afford crude product which was further purified by flash column chromatography using 50% EtOAc in hexane as eluent to afford the product (3.3 g, 99 % ) as a white solid. ^X H NMR (400 MHz, DMSO-d ₆ ): δ 9.49 (s, 1H), 9.15-9.13 (d, J= 7.8 Hz, 2H), 8.72 (s, 1H), 7.94-7.92 (m, 2H), 7.57-7.53 ( m, 3H), 7.36 (s, 1H), 4.63-4.57 ( m, 1H), 2.91 -2.88 (m, 1H), 2.39-2.35 (m, 4H), 1.40 (s, 9H); LC-MS: [M-H]+ 399.1

[0242] Step 9: 7V-ir«ws-3-(hydrazinecarbonyl)cyclobutyl)-5-phenylisoxazole -3- carboxamide hydrochloride: 4 M HC1 in dioxane (30 mL) was added to an ice cooled solution of tert-butyl 2-ira/is-3-(5-phenylisoxazole-3-carboxamido)cyclobutane-l- carbonyl)hydrazine-l-carboxylate (3.8 g, 9.5 mmol) in 1,4 dioxane (50mL)and the reaction mixture was stirred at room temperature for 16 h. Volatiles were removed under reduced pressure and the crude compound was stirred in diethyl ether (100 mL). Solid was filtered and washed with hexane to afford the product (2.5 g, 78 %) as an off white solid. ^X H NMR (400 MHz, DMSO-d ₆ ): δ 10.88 (s, 1H), 10.23 (br, 3H), 9.22-9.20 (d, J= 7.9 Hz, 1H), 7.94-7.92 ( m, 2H), 7.58-7.54 (m, 3H), 7.37 (s, 1H), 4.67-4.61 (m, 1H), 3.08-3.03 (m, 3H), 2.46-2.42 (m, 4H). LC-MS: [M+H] ⁺ 301.0

Example 10: Preparation of 7V-(ir««s-3-(5-((R)-l-hydroxyethyl)-l,3,4-oxadiazol-2- yl)cyclobutyl)-5-phenylisoxazole-3-carboxamide

2. Iodine, PPh ₃ , Et ₃ N, DCM, 0 °C - RT, 1 h

[0243] Step 1: iV-(ir««s-3-(2-((R)-2-((tert-butyldimethylsilyl)oxy)propan oyl)hydrazine- l-carbonyl)cyclobutyl)-5-phenylisoxazole-3-carboxamide: TEA (1.19 mL, 8.9 mmol) and T ₃ P (1.7 ml, 2.6 mmol) were sequentially added to an ice cooled solution of N-iraws-3- (hydrazinecarbonyl)cyclobutyl)-5-phenylisoxazole-3-carboxami de hydrochloride (0.6 g, 1.7 mmol) and (R)-2-((tert-butyldimethylsilyl)oxy) propanoic acid (0.43 g, 2.1 mmol) in 1,4- dioxane (50 mL) were added and the reaction mixture was stirred for 16 h at room temperature. Volatiles were removed under reduced pressure and the crude reaction mixture was diluted with water (100 mL). The reaction mixture was extracted with ethyl acetate (3 x 50 mL).

Combined organic layer was washed with brine (50 mL), dried over anhydrous Na ₂ S0 ₄ and concentrated under reduced pressure to afford crude compound which was further purified by flash column chromatography using 50% EtOAc in hexane as eluent to obtain product (0.3 g, 35 %) as white solid. ¾ NMR (400 MHz, DMSO-d ₆ ): δ 9.83 (s, 1H), 9.44 (s, 1H), 9.16-9.14 (d, J= 7.9 Hz, 1H), 7.94 - 7.92 (m, 2H), 7.58 - 7.53 (m, 3H), 7.34 (s, 1H), 4.65 - 4.59 (m, 1H), 4.29 - 4.24 (m, 1H), 3.01-2.94 (m, 1H), 2.40 - 2.37 (m, 4H), 1.28 (d, J= 6.6 Hz, 3H), 0.88 (s, 9H), 0.09 (s, 6H). LC-MS: [M+H] ⁺ 487.3 .

[0244] Step 2: 7V-(ir««s-3-(5-((R)-l-((tert-butyldimethylsUyl)oxy)ethyl)- l,3,4-oxadiazol-

2- yl)cyclobutyl)-5-phenylisoxazole-3-carboxamide: a solution of triphenyl phosphine (0.32 g, 1.2 mmol) in DCM (20 mL) was added Iodine (0.31 g, 1.2 mmol) and the reaction mixture was stirred for 10 min. Then the reaction mixture was cooled to 0 °C. To the resulting reaction mixture was added TEA (0.40 ml, 3.0 mmol) followed by addition of N-(tra«5-3-(2-((R)-2- ((tert-butyldimethylsilyl)oxy)propanoyl)hydrazine-l-carbonyl )cyclobutyl)-5-phenylisoxazole-

3- carboxamide (0.3 g, 0.6 mmol) and the reaction mixture was stirred for lh at room temperature. Volatiles were removed under reduced pressure and the crude reaction mixture was diluted with ethyl acetate. The precipitate thus obtained was filtered, filtrate concentrated and purified by flash column chromatography using 30 % ethyl acetate in n-hexane as eluent to afford the product (0.180 g, 62 %) as a off-white solid. ^X H NMR (400 MHz, CDC13): δ 7.80- 7.78 (m, 2H), 7.50-7.47 (m, 3H), 7.1 1-7.09 (d, J= 7.3 Hz, 1H), 6.95 (s, 1H), 5.09 - 5.08 (m, 1H), 4.86 - 4.84 (m, 1H), 3.77 - 3.75 (m, 1H), 2.92 - 2.85 (m, 2H), 2.69 - 2.66 (m, 2H), 1.61 (d, J= 6.6 Hz, 3H), 0.89 (s, 9H), 0.12 (s, 3H), 0.07 (s, 3H); LC-MS: [M+H] ⁺ 454.8 .

[0245] Step 3: 7V-(ir««s-3-(5-((R)-l-hydroxyethyl)-l,3,4-oxadiazol-2-yl)c yclobutyl)-5- phenylisoxazole-3-carboxamide: TBAF (1 M solution in THF) (0.7 mL, 0.76 mmol) was added to an ice-cooled solution of N-(?ra«s-3-(5-((R)-l-((tert-butyldimethylsilyl)oxy)ethyl)- l,3,4-oxadiazol-2-yl)cyclobutyl)-5-phenylisoxazole-3-carboxa mide (0.180 g, 0. 38 mmol) in THF (10 mL) was added and the reaction mixture was stirred for 1 h at room temperature. After completion of reaction, volatiles were removed under reduced pressure. The crude reaction mixture was diluted with water (30 mL) and the aq. phase was extracted with ethyl acetate (2 x 30 mL). Combined organic layer was washed with brine (20 mL), dried over anhydrous Na ₂ S0 ₄ and concentrated under reduced pressure to afford crude product which was triturated with diethyl ether (20 mL) and pentane (30 mL) to obtain N-(£raws-3-(5-((R)-l- hydroxyethyl)-l,3,4-oxadiazol-2-yl)cyclobutyl)-5-phenylisoxa zole-3-carboxamide (0.120 g).

[0246] Yield: 88 %

[0247] Appearance: off-white solid

[0248] Analytical data: ^X H NMR (400 MHz, DMSO-d ₆ ): δ 9.33 (d, J= 7.7 Hz, 1H), 7.95 - 7.92 (m, 2H), 7.58 - 7.54 (m, 3H), 7.38 (s, 1H), 5.95 (d, J= 5.6 Hz, 1H), 4.94 - 4.88 ( m, 1H), 4.72 - 4.66 (m, 1H), 3.73 - 3.67 (m, 1H), 2.70 - 2.65 (m, 2H), 2.63 - 2.58 (m, 2H), 1.48-1.47 (d, J= 6.6 Hz, 3H).

[0249] LC-MS: (M+H) ⁺ = 355.0

[0250] HPLC purity: 99.68% at 200 nm and 99.66% at 254 nm.

Example 11 : iV-(ir««s-3-(5-((S)-l-hydroxyethyl)-l,3,4-oxadiazol-2-yl)c yclobutyl)-5- phenylisoxazole-3-carboxamide

[0251] This compound was prepared using a similar procedure as example 10 using (S)-2- ((tert-butyldimethylsilyl)oxy)propanoic acid instead.

[0252] Appearance: white solid [0253] Analytical data: ^X H NMR (400 MHz, DMSO-d ₆ ): δ 9.34-9.32 (d, J= 7.7 Hz, 1H),

7.95 - 7.92 (m, 2H) , 7.58 - 7.53 (m, 3H), 7.38 (s, 1H), 5.96 (d, J= 5.7 Hz, 1H), 4.94 - 4.88 (m, 1H), 4.72 - 4.66 (m, 1H), 3.73 - 3.66 (m, 1H), 2.70 - 2.63 (m, 2H), 2.62 - 2.60 (m, 2H), 1.48 (d, J= 6.6 Hz, 3H). [0254] LC-MS [M+H] ⁺ = 355.2

[0255] HPLC purity: 99.47% at 254 nm and 98.78% at 220 nm.

Example 12 : 7V-(ir««s-3-(5-(hydroxymethyl)-l,3,4-oxadiazol-2-yl)cyclob utyl)-5- phenylisoxazole-3-carboxamide

[0256] Step 1: iV-(ir««s-3-(2-(2-((tert-butyldimethylsilyl)oxy)acetyl)hyd razine-l- carbonyl)cyclobutyl)-5-phenylisoxazole-3-carboxamide: TEA (1.14 ml, 8.5 mmol) and HATU (0.77 g, 2.0 mmol) were added sequentially to a solution of N-traws-(3- (hydrazinecarbonyl)cyclobutyl)-5-phenylisoxazole-3-carboxami de hydrochloride (0.6 g, 1.7 mmol) and 2-((tert-butyldimethylsilyl)oxy)acetic acid (0.5 g, 2.6 mmol) in TH F (50 m L). The reaction mixture was stirred for 4 h at room temperature, volatiles were removed under reduced pressure and the crude compound was diluted with water (100 mL). The aq. phase was extracted with ethyl acetate (3 x 50 mL). Combined organic layer was washed with brine (50 mL), dried over anhydrous Na ₂ S0 ₄ and concentrated under reduced pressure to afford crude compound which was further purified by flash column chromatography using 50% EtOAc in hexane as eluent to obtain the product (0.4 g, 47 %) as off-white solid. ^X H NMR (400 MHz, DMSO-d ₆ ): δ 9.78 (s, 1H), 9.51 (s, 1H), 9.16 - 9.14 (m, 1H), 7.94 - 7.92 (m, 2H), 7.58 - 7.51 (m, 3H), 7.35 (s, 1H), 4.64 - 4.58 (m, 1H), 4.12 (s, 2H), 3.01 -2.94 (m, 1H), 2.41 - 2.37 (m, 4H), 0.89-0.86 (s, 9H), 0.10 (s, 6H); LC-MS [M+H] ⁺ 473.3

[0257] Step 2: iV-(ir««s-3-(5-(((tert-butyldimethylsilyl)oxy)methyl)-l,3, 4-oxadiazol-2- yl)cyclobutyl)-5-phenylisoxazole-3-carboxamide: a mixture of triphenyl phosphine (0.44 g, 1.7 mmol) and iodine (0.43 g, 1.7 mmol) in DCM (20 mL) was stirred for 10 min and then cooled to cooled to 0 C. To the resulting reaction mixture was added TEA (0.57 g, 4.2 mmol) and N-(?ra«s-3-(2-(2-((tert-butyldimethylsilyl)oxy)acetyl)hydra zine-l-carbonyl)cyclobutyl)-5- phenylisoxazole-3-carboxamide (0.4 g, 0.84 mmol) sequentially and the reaction mixture was stirred for lh at room temperature. Volatiles were removed under reduced pressure and the crude reaction mixture was diluted with ethyl acetate. The precipitate thus formed was filtered, filtrate concentrated and purified by flash column chromatography using 30 % ethyl acetate in n-hexane as eluent to afford the product (0.280 g, 73 %) as an off-white solid. ^X H NMR (400 MHz, CDC13): δ 7.80 - 7.78 (m, 2H), 7.50 - 7.47 (m, 3H), 7.10-7.09 (d, J = 7.3 Hz, 1H), 6.95 (s, 1H), 4.87 - 4.83 (m, 3H), 3.79 - 3.75 (m, 1H), 2.93 - 2.86 (m,2H), 2.69 - 2.64 (m, 2H), 0.91 (s, 9H), 0.13 (s, 6H); LC-MS [M+H] ⁺ 454.8.

[0258] Step 3: iV-(ir««s-3-(5-(hydroxymethyl)-l,3,4-oxadiazol-2-yl)cyclob utyl)-5- phenylisoxazole-3-carboxamide: TBAF (1 M solution in THF) (1.2 mL, 1.2 mmol) was added to an ice-cooled solution of N-(?ra«s-3-(5-(((tert-butyldimethylsilyl)oxy)methyl)-l,3,4- oxadiazol-2-yl)cyclobutyl)-5-phenylisoxazole-3-carboxamide (0.280 g, 0. 61 m mol) in THF (10 mL)and the reaction mixture was stirred for 2 h at room temperature. Volatiles were removed under reduced pressure and the crude reaction mixture was diluted with water (30 mL). The aq. phase was extracted with ethyl acetate (2 x 30 mL). Combined organic layer was washed with brine (20 mL), dried over anhydrous Na ₂ S0 ₄ and concentrated under reduced pressure to afford crude product (0.180 g) which was triturated with diethyl ether (20 mL) and pentane (30 mL) to obtain the product (0.150 g).

[0259] Yield: 71 %

[0260] Appearance: off-white solid

[0261] Analytical data: ^X H NMR (400 MHz, DMSO-d ₆ ): δ 9.34-9.32 (d, J

7.95 - 7.92 (m, 2H) , 7.58 -7.53 (m, 3H), 7.38 (s, 1H), 5.89-5.86( t, J= 6.3 Hz, 1H), 4.73 - 4.67 (m, 1H), 4.63 (d, J= 6.2 Hz, 2H), 3.73 - 3.68 (m, 1H), 2.70 - 2.68 (m, 2H), 2.63 - 2.59 (m, 2H).

[0262] LC-MS: [M+H] : 340.8

[0263] HPLC Purity: 99.79% at 269 nm, 99.74% at 254 nm and 99.58% at 220 nm. Example 13: iV-ir««s-3-(5-((R)-l-hydroxyethyl)-l,3,4-thiadiazol-2- yl)cyclobutyl)-5-phenylisoxazole-3-carboxamide

[0264] Step 1: 7V-ir««s-(3-(5-((lR)-l-((tert-butyl(methyl)silyl)oxy)ethyl )-l,3,4- thiadiazol-2-yl)cyclobutyl)-5-phenylisoxazole-3-carboxamide: a solution of intermediate A (0.4g, crude), which was prepared by the procedure described in step 1, example 12 using (R)- 2-((tert-butyldimethylsilyl)oxy)propanoic acid, and Lawesson's reagent (0.499 g, 1.2 mmol) was stirred at room temperature for 3h. Volatiles were removed under reduced pressure to obtain the crude compound which was purified by neutral alumina chromatography using 25% ethyl acetate in hexane to afford N-(?ra«s-3-(5-((lR)-l-((tert-butyl(methyl)silyl)oxy)ethyl)- l,3,4-thiadiazol-2-yl)cyclobutyl)-5-phenylisoxazole-3-carbox amide (0.220 g, 34 % over two steps) as white solid. ^X H NMR (400 MHz, CDC1 ₃ ): δ 7.79 - 7.78 (m, 2H), 7.50 - 7.47 (m, 3H), 7.10 (d, J=7.2 Hz, 2H), 6.95 (s, 1H), 5.27 - 5.22 (m, 1H), 4.86 - 4.84 (m, 2H), 3.97 - 3.95 (m, 1H), 2.93 - 2.87 (m, 2H), 2.73 - 2.66 (m, 2H), 1.60 (t, J= 6.4 Hz, 3H), 0.91 ( s, 9H), 0.12 (s, 3H), 0.07 (s, 3H); LC-MS [M+H] ⁺ 485.3 . [0265] Step 2: 7V-ir««s-3-(5-((R)-l-hydroxyethyl)-l,3,4-thiadiazol-2-yl)c yclobutyl)-5- phenylisoxazole-3-carboxamide: tetra butylammoniunn fluoride (0.68 mL, 0.68 mmol, 1 M in TH F) was added to a cold solution of N-(tra«s-3-(5-((lR)-l-((tert- butyl(methyl)silyl)oxy)ethyl)- 1 ,3 ,4-thiadiazol-2-yl)cyclobutyl)-5-phenylisoxazole-3 - carboxamide in THF (5 mL). The mixture was stirred at 0°C for 2 h, the volatiles were removed under reduced pressure to get the crude compound which was suspended in water (10 mL) and extracted with ethyl acetate (2 xlO mL). Combined organic layer was washed with water followed by brine, dried over anhydrous Na ₂ S0 ₄ and concentrated under reduced pressure to obtain the crude compound. The crude compound was further purified by combiflash using 2% MeOH in DCM as eluent to afford the product (0.1 10 g, 65 %) as off white solid. [0266] Analytical data: ^X H NMR (400 MHz, CDC1 ₃ ): δ 7.79 - 7.78 ( m, 2H), 7.51 - 7.46 (m, 3H), 7.12 (d, J= 7.2 Hz, 1H), 6.95 (s, 1H), 5.30 -5.28 (m, 1H), 4.88 - 4.82 (m, 1H), 4.02 - 3.96 (m, 1H), 2.94 - 2.87 (m, 2H), 2.80 (br, 1H), 2.73 - 2.68 (m, 2H), 1.69 (d, J= 6.6 Hz, 3H).

[0267] LC-MS [M+H] ⁺ 371.1

[0268] HPLC purity: 97.80% at 220 nm and 98.69% at 254 nm.

[0269] Example 14: iV-ir«ws-3-(5-((S)-l-hydroxyethyl)-l,3,4-thiadiazol-2- yl)cyclobutyl)-5-phenylisoxazole-3-carboxamide was prepared by the procedure described in example 13 using (S)-2-((tert- butyldimethylsilyl)oxy)propanoic acid.

[0270] Appearance: white solid

[0271] Analytical data: ^X H NMR (400 MHz, CDC1 ₃ ): δ 7.80 - 7.77 (m, 2H), 7.50-7.47 (m,

3H), 7.13 (d, J = 7.2 Hz, 1H), 6.95 (s, 1H), 5.33 - 5.27 (m, 1H), 4.88 - 4.82 (m, 1H), 4.02 -3.96 (m, 1H), 2.91 - 2.87 (m, 2H), 2.84 (d, J = 4.7 Hz, 1H), 2.73 - 2.70 (m, 2H), 1.69 (d, J = 6.6 Hz, 3H).

[0272] LC-MS: [M+H] ⁺ 370.8

[0273] HPLC purity: 98.85% at 220 nm and 98.74% at 254 nm.

Example 15: Preparation of Intermediate II: 3-(dibenzylamino)cyclobutane-l- carbohydrazide:

3. NH ₂ -NH ₂ H ₂ 0, EtOH, 80°C

[0274] Step 1: ethyl 3-oxocyclobutane-l-carboxylate: triethyl orthoacetate (24.25 g, 104 mmol) was added to a solution of 3-oxo-cyclobutanecarboxylic acid (5.0 g, 34.7 mmol) in toluene (100 mL) and the reaction mixture was heated to reflux for 5h. The reaction mixture was cooled to 0°C and quenched with IN HC1. Organic layer was separated off and the aq. phase was extracted with ethyl acetate (2 x 20 mL). Combined organic layer was washed with saturated aHC0 ₃ solution followed by water (50 mL) and dried over Na ₂ S0 _4. Solvent removal under reduced pressure afforded the product (5.8 g, 93.5 %) as a pale yellow oil. ^X H NMR (400 MHz, CDC1 ₃ ): δ 4.20 (q, J= 7.1 Hz, 2H), 3.44 - 3.37 (m, 2H), 3.31 - 3.17 (m, 3H,), 1.28 (t, J = 7.1 Hz, 3H). [0275] Step 2: ethyl 3-(dibenzylamino)cyclobutane-l-carboxylate: added dibenzyl amine (3.05 g, 15.4 mmol) was added to a solution of ethyl 3-oxocyclobutane-l-carboxylate (2.0 g, 14.4 mmol) in 10% TH F in AcOH (50 m L) and the reaction mixture was stirred at room temperature for 20 min followed by addition of sodium cyanoborohydride (1.77 g, 28 mmol) portion wise. The mixture was stirred at room temperature for 12h, volatiles were removed under reduced pressure and the crude compound was diluted with DCM (50 mL). DCM layer was washed with water and saturated NaHCC solution, dried over Na ₂ S0 ₄ and concentrated under reduced pressure to get the crude compound. The crude compound was purified by combiflash using 10 % ethyl acetate in hexane as eluent to afford the product (2.0 g, 44.4 %) as colorless oil. ^X H NMR (400 MHz, CDC1 ₃ ): δ 7.33 - 7.26 (m, 8H), 7.23 - 7.20 (m, 2H), 4.13 - 4.07 (m, 2H), 3.49 (s, 3H), 3.46 (s, 1H), 3.12 - 3.07 (m, 1H), 2.66 - 2.61 (m, 1H), 2.25 - 2.03 (m, 4H), 1.25 - 1.22 (t obscured by occluded EtOAc, 3H); LC-MS: [M+H] ⁺ 324.4 [0276] Step 3: 3-(dibenzylamino)cyclobutane-l-carbohydrazide: hydrazine hydrate

(0.99 mL, 30.9 mmol) was added to a solution of ethyl 3-(dibenzylamino)cyclobutane-l- carboxylate (2.0 g, 6.19 mmol) in EtOH (20 mL)and the reaction mixture was refluxed for 12h.

The volatiles were removed under reduced pressure and the crude compound was washed with hexane (2 x 20 mL). The residue thus obtained was dried under vacuum to get the product (1.8 g, 94.2 %) as a white solid. ¾ NMR (400 MHz, CDC1 ₃ ): δ 7.31 - 7.26 (m, 8H), 7.25 - 7.20 (m, 2H), 6.80 (s, 1H), 3.83 (br, 2H), 3.50 (s, 4H), 3.13 - 3.05 (m, 1H), 2.51 - 2.42 (m, 1H), 2.23 - 2.10 (m, 4H); LC-MS: [M+H] ⁺ = 309.9

Example 16: iV-ir««s-3-(5-(hydroxymethyl)-l,3,4-thiadiazol-2-yl)cyclob utyl)-5- phenylisoxazole-3-carboxamide and 7V-c/s-3-(5-(hydroxymethyl)-l,3,4-thiadiazol-2- yl)cyclobutyl)-5-phenylisoxazole-3-carboxamide

,

[0277] Step 1: 3-(dibenzylamino)-iV -(2-hydroxyacetyl)cyclobutane-l-carbohydrazide: triethyl amine (2.7 mL, 19 mmol) was added to a solution of glycolic acid (0.5 g, 6.5 mmol) in DCM (20 mL) followed by T ₃ P (3.13 g, 9.8 mmol) and the reaction mixture was stirred for 10 min. 3-(dibenzylamino)cyclobutane-l-carbohydrazide (2.23 g, 7.2 mmol) was added to the resulting reaction mixture and it was stirred at room temperature for 12h. The reaction mixture was diluted with ice-water (20 mL) and the aq. phase was extracted with DCM (2 x 20 mL). Combined organic layer was washed with brine (20 mL), dried over Na ₂ S0 ₄ and concentrated under reduced pressure to get the crude compound. The crude compound was purified by combiflash using 3% MeOH in DCM as eluent to give the product (2.3 g, crude) as a white solid which was used as such in next step without further purification.

[0278] Step 2: 7V-(2-((tert-butyldimethylsilyl)oxy)acetyl)-3-

(dibenzylamino)cyclobutane-l-carbohydrazide: imidazole (0.93 g, 13.7 mmol) was added to a solution of 3-(dibenzylamino)-N'-(2-hydroxyacetyl)cyclobutane-l-carbohyd razide (2.3 g, crude) in dry DM F (5 mL) and the reaction mixture was stirred for 10 minutes under 2 atmosphere. The reaction mixture was cooled in an ice bath, and TBDMSC1 (1.88 g, 12.5 mmol) was added and the resulting reaction mixture was stirred at room temperature for 3h. The reaction mixture was quenched with water (10 mL) and extracted with ethyl acetate (3 x 50 mL). Combined organic layer was dried over Na ₂ S0 ₄ and concentrated under reduced pressure to get the crude compound. The mixture was purified by column chromatography using 30 % ethyl acetate in hexane as eluent to get the product (2.0 g, 57 % over two steps) as a white solid. ^X H NMR (400 MHz, CDC1 ₃ ): δ 8.95 (d, J= 5.9 Hz, 1H), 8.19 (d, J= 6.6 Hz, 1H), 7.30 - 7.28 (m, 8H), 7.26 - 7.27 (m, 2H), 4.20 (s, 2H), 3.50 (s, 4H), 3.15 - 3.11 (m, 1H), 2.61 - 2.57 (m, 1H), 2.24 - 2.20 (m, 4H), 0.92 (s, 9H), 0.1 1 (s, 6H); LC-MS: [M+H] ⁺ 482.0

[0279] Step 3: 3-amino-iV-(2-((tert-butyldimethylsilyl)oxy)acetyl)cyclobuta ne-l- carbohydrazide: 10% Pd-C (0.2 g) was added to a mixture of N-(2-((tert- butyldimethylsilyl)oxy)acetyl)-3-(dibenzylamino)cyclobutane- l-carbohydrazide (2.0 g, 4.15 mmol) in EtOAc - MeOH (30 mL) and the reaction mixture was stirred under ¾ atmosphere for 12h at room temperature. The reaction mixture was filtered and washed with MeOH (2 x 10 mL). Filtrate was concentrated under reduced pressure to get the crude compound. The crude compound was purified by column chromatography using 20 % MeOH in DCM as eluent to afford the product (0.8 g, 64.0 %) as a white solid. ^X H NMR (400 MHz, CDC1 ₃ ): δ 4.2 (s, 2H), 3.47 - 3.35 (m, 1H), 2.67 - 2.58 (m, 1H), 2.55 - 2.48 (m, 2H), 2.03 - 1.96 (m, 2H), 0.93 (s, 9H), 0.11 (s, 6H); LC-MS: [M+H] ⁺ 301.9.

[0280] Step 4: tert-butyl (3-(2-(2-((tert-butyldimethylsilyl)oxy)acetyl)hydrazine-l- carbonyl)cyclobutyl) carbamate: triethyl amine (0.74 mL, 5.31 mmol) was added to an ice cooled solution of 3-amino-N'-(2-((tert-butyldimethylsilyl)oxy)acetyl)cyclobuta ne-l- carbohydrazide (0.8 g, 2.65 mmol) in DCM (10 mL). Boc-anhydride (0.91 mL, 3.98 mmol) was added to the mixture and the reaction mixture was stirred at room temperature for 12h. The reaction was diluted with cold water (20 mL) and extracted with DCM (2 x 10 mL).

Combined organic layer was dried over Na ₂ S0 ₄ and evaporated to dryness under vacuum to get the crude compound. The crude compound was purified by combiflash using 3 % MeOH in DCM as eluent to afford the product (0.9 g, crude) as an off white solid. As per 1H-NMR, compound is not pure and used as such in next step.

[0281 ] Step 5: tert-butyl (3-(5-(((tert-butyldimethylsilyl)oxy)methyl)-l,3,4-thiadiazo l- 2-yl)cyclobutyl) carbamate: Lawesson's reagent (3.52 g, 8.7 mmol) was added to a solution of -butyl (3 -(2-(2-((tert-butyldimethylsilyl)oxy)acetyl)hydrazine- 1 -carbonyl)cyclobutyl) carbamate (0.7 g, 1.74 mmol) in THF (10 mL)and the reaction mixture was heated to 70°C for 30 min. The volatiles were removed under reduced pressure and the crude compound was purified by neutral alumina column chromatography using 15 % EtOAc in hexane to afford the product (0.3 g, 32 % over two steps) as white solid. ^X H NMR (400 MHz, CDC1 ₃ ): δ 5.0 (s, 2H), 4.81-4.80 (br, 1H), 4.21 (m, 1H), 3.58 - 3.49 (m, 1H), 2.92 - 2.87 (m, 2H), 2.28 - 2.20 (m, 2H), 1.43 (s, 9H), 0.92 (s, 9H), 0.1 1 (s, 6H); LC-MS: [M+H] ⁺ 399.6.

[0282] Step 6: (5-(3-aminocyclobutyl)-l,3,4-thiadiazol-2-yl)methanol: trifluoroacetic acid (0.171 g, 1.5 mmol) was added to an ice cooled solution of tert-butyl (3-(5-(((tert- butyldimethylsilyl)oxy)methyl)-l,3,4-thiadiazol-2-yl)cyclobu tyl) carbamate (0.3 g, 7.5 mmol) in DCM (5 mL) and the reaction mixture was stirred at room temperature for 2h. The volatiles were removed under reduced pressure to get the product (0.178 g, crude) as a white solid which was used as such in next step without further purification.

[0283] Step 7: iV-ir««s-3-(5-(hydroxymethyl)-l,3,4-thiadiazol-2-yl)cyclob utyl)-5- phenylisoxazole-3-carboxamide and 7V-c/s-3-(5-(hydroxymethyl)-l,3,4-thiadiazol-2- yl)cyclobutyl)-5-phenylisoxazole-3-carboxamide: EDC.HC1 (0.287 g, 1 mmol), HOBt (0.168 g, 1 1 mmol) were added to a solution of 5-phenylisoxazole-3-carboxylic acid (0.189 g, 1 mmol) in THF (5 mL), followed by addition of : (5-(3-aminocyclobutyl)-l,3,4-thiadiazol-2- yl)methanol (0.3 g, crude) and the mixture was stirred for 10 min. Triethyl amine (0.42 mL, 3 mmol) was added to the mixture and stir at room temperature for 12h. The reaction mixture was diluted with cold water (20 mL) and extracted with DCM (2 x 10 rnL). Combined organic layer was washed with brine and dried over Na ₂ S0 ₄ and concentrated under reduced pressure to get the crude compound. The crude compound was purified by prep HPLC to afford: iV-c s-3-(5-(hydroxymethyl)-l,3,4-thiadiazol-2-yl)cyclobutyl)-5-p henylisoxazole-3- carboxamide (0.05 g):

[0284] Yield: 11 % over two steps

[0285] Appearance: off white solid.

[0286] Analytical data: ^X H NMR (400 MHz, CDC1 ₃ ): δ 7.83 - 7.79 (m, 2H), 7.53 - 7.49 (m,

3H), 7.22 - 7.20 (br, 1H), 6.97 (s, 1H), 5.08 (s, 2H), 4.75 - 4.68 (m, 1H), 3.77 - 3.68 (m, 1H), 3.10 - 3.03 (m, 2H), 2.62 (br, 1H), 2.57 - 2.51 (m, 2H).

[0287] LC-MS: [M+H] ⁺ 356.8

[0288] HPLC purity: 99.19% at 220 nm and 99.11% at 254 nm. iV-ir««s-3-(5-(hydroxymethyl)-l,3,4-thiadiazol-2-yl)cyclob utyl)-5-phenylisoxazole-3- carboxamide (0.01 g):

[0289] Yield: 2 % over two steps

[0290] Appearance: off white solid.

[0291] Analytical data: ^X H NMR (400 MHz, CDC1 ₃ ): δ 7.80 - 7.78 (m, 2H), 7.50 - 7.47 (m,

3H), 7.11 (d, J= 6.8 Hz, 1H), 6.95 (s, 1H), 5.07 (d, J= 5.4 Hz, 2H), 4.88 - 4.83 (m, 1H), 4.02 - 3.98 (m, 1H), 2.95 - 2.88 (m, 2H), 2.76 - 2.69 (m, 2H), 2.51 - 2.48 (m, 1H).

[0292] LC-MS: [M+H] ⁺ 357.1

[0293] HPLC purity: 98.58 % at 220 nm and 98.43 % at 254 nm. Example 17

[0294] Step 1: (S)-7V-(2-((tert-butyldimethylsilyl)oxy)propanoyl)-3- (dibenzylamino)cyclobutane-l-carbohydrazide: HATU (12.0 g, 31.6 mmol) was added to a solution of 2-((tert-butyldimethylsilyl)oxy)propanoic acid (4.3 g, 6.31 mmol) in THF (50 mL)followed by addition of 3-(dibenzylamino)cyclobutane-l-carbohydrazide (6.5 g, 6.31 mmol) and the reaction mixture was stirred for 10 min at room temperature. Triethyl amine (6.3 mL, 63.1 mmol) was added to the reaction mixture and stirring continued for 4h at room temperature. The volatiles were removed under reduced pressure and the reaction mixture was quenched with ice-water (20 mL). The aq. phase was extracted with ethyl acetate (2 x 20 mL). Combined organic layer was washed with brine (20 mL), dried over Na ₂ S0 ₄ and concentrated under reduced pressure to get the crude compound. The crude compound was purified by combiflash using 15% ethyl acetate in hexane to obtain the product (6.2 g, 59.6 %) as off white solid. ^X H NMR (400 MHz, CDC1 ₃ ): δ 9.06 (d, J= 6.2 Hz, 1H), 8.58 (d, J= 6.4 Hz, 1H), 7.29 - 7.27 (m, 8H), 7.23 - 7.18 (m, 2H), 4.31 (q, J = 6.7 Hz, 1H), 3.50 (s, 4H), 3.14 - 3.09 (m, 1H), 2.62 - 2.57 (m, 1H), 2.25 - 2.18 (m, 4H), 1.40 (d, J = 6.7 Hz, 3H), 0.93 (s, 9H), 0.12 - 0.11 (two adjacent singlets, 6H); LC-MS: [M+H] ⁺ 496.0.

[0295] Step 2: (S)-3-amino-iV-(2-((tert-butyldimethylsilyl)oxy)propanoyl)cy clobutane- 1-carbohydrazide: a solution of (S)-N'-(2-((tert-butyldimethylsilyl)oxy)propanoyl)-3- (dibenzylamino)cyclobutane-l-carbohydrazide (6.2 g, 12.5 mmol) and 10% Pd-C (0.6 g) in EtOAc: MeOH (60 : 5 mL) was hydrogenated (150 psi) at 50°C for 12h. The reaction mixture was filtered, washed with MeOH (2 x 10 mL) and filtrate was evaporated to dryness under reduced pressure. The crude compound thus obtained was purified by 100-200 mesh silica gel using 20% MeOH in DCM as eluent to afford the product (2.5 g, crude) as white semisolid. ^X H NMR (400 MHz, CDC1 ₃ ): δ 4.32 (q, J = 6.7 Hz, 1H), 3.41 - 3.37 (m, 1H), 2.67 - 2.55 (m, 1H), 2.54 -2.48 (m, 2H), 2.04 - 2.0 (m, 2H), 1.41 (d, J= 6.7 Hz, 3H), 0.93 (s, 9H), 0.12 - 0.11 (two adjacent singlets, 6H); LC-MS: [M+H] ⁺ 315.7.

Example 18: 7V-c s-3-(5-((S)-l-hydroxyethyl)-l,3,4-thiadiazol-2-yl)cyclobutyl )-5- phenylisoxazole-3-carboxamide:

2 Lawesson's reagent,

THF, RT, 3h

3. TBAF, THF, RT, 3h

[0296] Step 1: (S)-7V-(3-(2-(2-((tert-butyldimethylsilyl)oxy)propanoyl)hydr azine-l- carbonyl)cyclobutyl)-5-phenylisoxazole-3-carboxamide: HATU (3.6 g, 9.5 mmol) was added to a solution of 5-phenylisoxazole-3-carboxylic acid (1.19 g, 6.3 mmol) in TH F (20 m L) followed by addition of (S)-3-amino-N'-(2-((tert- butyldimethylsilyl)oxy)propanoyl)cyclobutane-l-carbohydrazid e (2.0 g, 6.31 mmol). The reaction mixture was stirred for 10 minutes at room temperature and triethyl amine (2.67 mL, 19.0 mmol) was then added. The reaction mixture was stirred at room temperature for 3h, volatiles were removed under reduced pressure and the reaction mixture was quenched with ice-water (20 mL). The aq. phase was extracted with ethyl acetate (3 x 20 mL). Combined organic layer was washed with brine (20 mL), dried over Na ₂ S0 ₄ and concentrated under reduced pressure to get the crude compound. The crude compound thus obtained was purified by combiflash using 45% ethyl acetate in hexane to get the product (2.2 g, 73.3 %) as a white solid. 'H NMR (400 MHz, CDC1 ₃ ): δ 9.10 - 9.05 (m, 1H), 8.43 - 8.39 (m, 1H), 7.79 - 7.27 (m, 2H), 7.50 - 7.46 (m, 3H), 7.20 - 7.16 (m, 1H), 6.92 (s, 1H), 4.63 - 4.57 (m, 1H), 4.37 - 4.32 (m, 4H), 2.84 - 2.81 (m, 5H), 2.72 - 2.70 (m, 1H), 1.42 (d, J = 6.6 Hz, 2H), 0.95 (s, 9H), 0.14 (s, 3H), 0.12 (s, 3H); LC-MS: [M+H] ⁺ 487.3. [0297] Step 2: (S)-7V-(3-(5-(l-((tert-butyldimethylsilyl)oxy)ethyl)-l,3,4-t hiadiazol-2- yl)cyclobutyl)-5-phenylisoxazole-3-carboxamide: Lawesson's reagent (2.7 g, 6.79 mmol) was added to a solution of (S)-N-(3-(2-(2-((tert-butyldimethylsilyl)oxy)propanoyl)hydra zine-l- carbonyl)cyclobutyl)-5-phenylisoxazole-3-carboxamide and the reaction mixture was stirred at room temperature for 3h. Progress of the reaction was monitored by TLC. After completion, volatiles were removed under reduced pressure to obtain the crude compound which was further purified by neutral alumina column chromatography using 20 % ethyl acetate in hexane to afford the product (1.3 g, 59 %) as pale yellow oil. ^X H NMR (400 MHz, CDC1 ₃ ): δ 7.82 - 7.80 (m, 2H), 7.52 - 7.50 (m, 3H), 7.17 (d, J = 8.4 Hz, 1H), 6.97 (s, 1H), 5.29-5.26 (q, J= 6.3 Hz, 1H), 4.75 - 4.71 (m, 1H), 3.71 - 3.66 (m, 1H), 3.07 - 3.02 (m, 2H), 2.52 - 2.47 (m, 2H), 1.62 - 1.56 (m, 3H), 0.91 (s, 9H), 0.15 (s, 3H), 0.10 (s, 3H); LC-MS: [M+H] ⁺ 485.5.

[0298] Step 3: 7V-c s-3-(5-((S)-l-hydroxyethyl)-l,3,4-thiadiazol-2-yl)cyclobutyl )-5- phenylisoxazole-3-carboxamide: TBAF (4.0 mL, 4.0 mmol) was added to a solution of (S)-N- (3-(5-(l-((tert-butyldimethylsilyl)oxy)ethyl)-l,3,4-thiadiaz ol-2-yl)cyclobutyl)-5- phenylisoxazole-3-carboxamide (1.3 g, 2.68 mmol) in THF (10 mL) and the reaction mixture was stirred at room temperature for 3h. The reaction mixture was diluted with cold water, filtered and the solid washed with water followed by hexane and dried under reduced pressure to get the crude compound. The crude compound was purified by prep HPLC to afford the product (0.2 g. 20.2 %) as a white solid. [0299] Analytical data: ^X H NMR (400 MHz, CDC1 ₃ ): δ 7.80 - 7.77 (m, 2H), 7.49 - 7.46 (m,

3H), 7. 20 (d, J= 8 Hz, 1H), 6.94 (s, 1H), 5.28 (q, J= 6.5 Hz, 1H), 4.71 - 4.46 (m, 1H), 3.70 - 3.63 (m, 1H), 3.06 - 2.99 (m, 2H), 2.86 (bs, 1H), 2.55 - 2.46 (m, 2H), 1.68 (d, J= 6.6 Hz, 3H).

[0300] LC-MS: [M+H] ⁺ 371.2 [0301] HPLC purity: 98.09% at 220 nm and 98.44% at 254 nm.

Example 19: iV-c s-3-(5-((R)-l-hydroxyethyl)-l,3,4-thiadiazol-2-yl)cyclobutyl )-5- phenylisoxazole-3-carboxamide ,0 DMS

TBDMSO N-

2. Lawesson's reagent, THF RT, 4h

3. TFA, DCM, 0 °C-RT, 4h

[0302] Step 1: tert-butyl (R)-(3-(2-(2-((tert- butyldimethylsilyl)oxy)propanoyl)hydrazine-l-carbonyl)cyclob utyl)carbamate: triethyl amine (0.8 mL, 5.7 mmol)was added to a cold solution of (R)-3-amino-N'-(2-((tert- butyldimethylsilyl)oxy)propanoyl)cyclobutane-l-carbohydrazid e (0.6 g, 1.9 mmol, prepared using procedure shown in example 17) in DCM (10 mL) followed by boc-anhydride (0.65 mL, 2.85 mmol) and the reaction mixture was stirred at room temperature for 4h. The reaction mixture was diluted with cold water (20 mL) and extracted with DCM (2 x 20 mL). Combined organic layer was dried over Na ₂ S0 ₄ and evaporated to dryness under vacuum. The crude compound was purified by flash column chromatography using 20 % ethyl acetate in hexane to afford the product (0.8 g, crude) as white solid which was used as such in next step. LC-MS: [M+H] ⁺ 415.9

[0303] Step 2: tert-butyl (R)-(3-(5-(l-((tert-butyldimethylsilyl)oxy)ethyl)-l,3,4- thiadiazol-2-yl)cyclobutyl)carbamate: Lawesson's reagent (1.88 g, 4.6 mmol) was added to a solution of tert-butyl (R)-(3-(2-(2-((tert-butyldimethylsilyl)oxy)propanoyl)hydrazi ne-l- carbonyl)cyclobutyl)carbamate (0.8 g, crude) in THF (10 mL) and the reaction mixture stirred at room temperature for 4h. The reaction mixture was purified by neutral alumina column chromatography using 15 % ethyl acetate in hexane as eluent to afford the product (0.42 g, 22 % over three steps) as a colorless oil. ^X H NMR (400 MHz, CDC1 ₃ ): δ 5.21 (q, J= 6.4 Hz, 1H),

4.81 (br, 1H), 4.22 - 4.20 (br, 1H), 3.56 - 3.47 (m, 1H), 2.91 - 2.84 (m, 2H), 2.28 - 2.18 (m, 2H), 1.56 (br obscured by solvent signal, 3H), 1.43 (s, 9H), 0.90 (s, 9H), 0.11 (s, 3H), 0.05 (s, 3H); LC-MS: [M+H] ⁺ 413.6. [0304] Step 3: (R)-l-(5-(3-aminocyclobutyl)-l,3,4-thiadiazol-2-yl)ethan-l-o l:

trifluoroacetic acid (0.233 mL, 3.05 mmol) was added to a solution of tert-butyl (R)-(3-(5-(l- ((tert-butyldimethylsilyl)oxy)ethyl)-l,3,4-thiadiazol-2-yl)c yclobutyl)carbamate (0.42 g, 1.06 mmol) in DCM (5 mL) and the reaction mixture was stirred at room temperature for 4h. The volatiles were removed under reduced pressure to get the product (0.3 g, crude) as colorless oil which was used as such in next step without further purification. LC-MS: [M+H] ⁺ 314.7.

[0305] Steps 4 and 5: N-((lS,3s)-3-(5-((R)-l-hydroxyethyl)-l,3,4-thiadiazol-2- yl)cyclobutyl)-5-phenylisoxazole-3-carboxamide: HATU (0.837 g, 2.2 mmol) was added to a solution of 5-phenylisoxazole-3-carboxylic acid (0.277 g, 1.4 mmol) in THF (5 mL) followed by addition of (R)-l-(5-(3-aminocyclobutyl)-l,3,4-thiadiazol-2-yl)ethan-l-o l (0.46 g, crude) and the resulting reaction mixture was stirred for 10 min. Triethyl amine (0.61 mL, 4.4 mmol) was added to the reaction mixture and stirring continued at room temperature for 12h. Cold water (20 mL) was added to the mixture and then extracted with DCM (2 x 10 mL). Combined organic layer was washed with brine, dried over Na ₂ S0 ₄ and evaporated to dryness under vacuum. The crude compound was dissolved in THF (5 mL) and TBAF solution (1.2 mL, 1.2 mmol) was added and the reaction mixture was stirred for lh. After completion, the reaction mixture was quenched with cold water (20 mL) and extracted with DCM (2 x 5 mL).

Combined organic layer was washed with brine and dried over Na ₂ S0 ₄ and evaporated to dryness under reduced pressure to get the crude compound which was purified by prep HPLC to afford 5-Phenyl-isoxazole-3-carboxylic acid {3-[5-((R)-l-hydroxy-ethyl)-[l, 3,4]thiadiazol- 2-yl]-cyclobutyl} -amide (0.110 g, 15 % over two steps) as an off white solid.

[0306] Analytical data: ^X H NMR (400 MHz, CDC1 ₃ ): δ 7.78 - 7.76 (m, 2H), 7.50 - 7.46 (m,

3H), 7. 20 (d, J= 8 Hz, 1H), 6.94 (s, 1H), 5.28 (q, J= 6.5 Hz, 1H), 4.71 - 4.65 (m, 1H), 3.72 - 3.63 (m, 1H), 3.05 - 2.99 (m, 2H), 2.85 (br, 1H), 2.53 - 2.46 (m, 2H), 1.68 (d, J= 6.5Hz, 3H).

[0307] LC-MS: [M+H] ⁺ 370.9

[0308] HPLC purity: 98.21% at 220 nm and 98.95% at 254 nm.

Example 20: 7V-c/s-3-(hydrazinecarbonyl)cyclobutyl)-5-phenylisoxazole-3- carboxamide

5. Boc-NHNH ₂ , T ₃ P,

Et ₃ N, THF, RT,

[0309] Step 1: ethyl c/s-3-(dibenzylamino)cyclobutane-l-carboxylate: dibenzyl amine (15.72 g, 79.69 mmol) and sodium cyanoborohydride (9.10 g, 144.9 mmol)were added sequentially to a solution of ethyl 3-oxocyclobutane-l-carboxylate (10.3 g, 72.45 mmol) in AcOH - THF (250 mL, 1 : 9) at 10°C and the reaction mixture stirred at room temperature for 16 h. The volatiles were removed under reduced pressure and the crude reaction mixture was diluted with water. The aq. phase was extracted with DCM (50 x 3 mL). Combined organic layer was washed with sodium bicarbonate solution (50 x 2 mL) followed by brine (50 mL) and dried over anhydrous sodium sulfate. Volatiles were removed under reduced pressure to get the crude compound which was purified by combiflash chromatography using 7 % ethyl acetate in n-hexane as eluent to give the product (15 g, 64.04 %) as a colorless oil. 1H-NMR (400 MHz, CDCI ₃ ) δ 7.32 - 7.27 (m, 8H), 7.24 - 7.20 (m, 2H), 4.10 (q, J= 7.1 Hz, 2H), 3.50 (s, 4H), 3.13 - 3.08 (m, 1H), 2.66 - 2.62 (m, 1H), 2.25 - 2.04 (m, 4H), 1.24 (t, J= 7.1 Hz, 3H); LC-MS: (M+H) ⁺ = 323.9 . [0310] Step 2: ethyl c s-3-aminocyclobutane-l-carboxylate hydrochloride: acetic acid (1.77 mL, 30.91 mmol) was added to a solution of ethyl czs-3-(dibenzylamino)cyclobutane-l- carboxylate (10.0 g, 30.91 mmol) in EtOH:H ₂ 0 (510 mL) and the reaction mixture was degassed for 10 min. To the resulting reaction mixture was added Pd/C (3 g) and the reaction mixture was agitated in a Parr shaker under ¾ atmosphere for 16h at room temperature. The reaction mixture was flittered through celite bed and washed with ethanol (2 x 100 mL).

Filtrate was concentrated under reduced pressure to get the crude compound which was treated with 4M HC1 in dioxane to get crude hydrochloride salt of compound 3. The crude compound was washed with diethyl ether to get as a mixture of cis and trans isomers (5 g). The mixture was dissolved in IPA (10 mL). After stirring for lh, the solution was cooled 0-5 °C and filtered. The solid was washed with cold IPA (2 mL) and dried under vacuum to get crude product (3.6 g, 81 %) as off white solid. ^X H-NMR (400 MHz, CDC1 ₃ ) δ 8.20 (br, 3H), 4.07 (q, J= 7.1 Hz, 2H), 3.63 - 3.55 (m, 1H), 2.99 - 2.92 (m, 1H), 2.44 - 2.37 (m, 2H), 2.29 - 2.21 (m, 2H), 1.18 (t, J = 7.1 Hz, 3H); LC-MS: (M+H) ⁺ 144.0 . [0311] Step 3: ethyl c s-3-(5-phenylisoxazole-3-carboxamido)cyclobutane-l- carboxylate: Et ₃ N (5.3 mL, 0.04 mol) followed by HATU (9.16 g, 0.024 mol) were added to a solution of ethyl cz ^' s-3-aminocyclobutane-l -carboxylate hydrochloride (3.63 g, 0.020 mol) and 5-phenylisoxazole-3-carboxylic acid (4.20 g, 0.022 mol) in THF (150 mL)and the reaction mixture was stirred for 6 h at room temperature. Volatiles were removed under reduced pressure and the crude reaction mixture was diluted with water (100 mL). The aq. phase was extracted with ethyl acetate (200 mL). The organic layer was dried over anhydrous a ₂ S0 ₄ and concentrated under reduced pressure to obtain the crude product. The crude compound was purified by silica gel column chromatography using 50% EtOAc in hexane as eluent to afford the product (5.02 g, 79 %) as off white solid. ^X H NMR (400 MHz, CDC1 ₃ ): δ 7.79 -7.77 (m, 2H), 7.50 - 7.46 (m, 3H), 7.08 (d, J= 8.0 Hz, 1H), 6.93 (s, 1H), 4.61 - 4.12 (m, 1H), 4.15 (q, J = 7.1 Hz, 2H), 2.89 - 2.83 (m, 1H), 2.74 - 2.68 (m, 2H), 2.32 - 2.24 (m, 2H), 1.26 (t, J= 7.2 Hz, 2H), LC-MS: [M+H] ⁺ 315.1.

[0312] Step 4: c s-3-(5-phenylisoxazole-3-carboxamido)cyclobutane-l-carboxyli c acid: lithium hydroxide monohydrate (0.800 g, 0.0190 mol) was added to a solution of ethyl cis-3-(5- phenylisoxazole-3-carboxamido)cyclobutane-l-carboxylate (5.0 g, 0.0159 mol) in THF - ¾0 (200 mL, 1 : 1) and the reaction mixture was stirred at room temperature for 2 h. Volatiles were removed under reduced pressure and the crude reaction mixture was poured onto water (50 mL). The aq. phase was washed with ethyl acetate (2 x 10 mL) and the aq. layer was acidified with saturated citric acid solution. The precipitate thus obtained was filtered, washed with water and dried to afford the product (4.14 g, 90%) as a white solid. ^X H NMR (400 MHz, DMSO-d ₆ ): δ 12.14 (br, 1H), 9.1 1 (d, J= 7.7 Hz, 1H), 7.93 - 7.91 (m, 2H), 7.58 - 7.53 (m, 3H), 7.34 (s, 1H), 4.40 - 4.29 (m, 1H), 2.80 - 2.73 (m, 1H), 2.50 - 2.42 (m, 2H), 2.40 - 2.32 (m, 2H); LC-MS: [M+H] ⁺ 287.1 .

[0313] Step 5: tert-butyl 2-c s-3-(5-phenylisoxazole-3-carboxamido)cyclobutane-l- carbonyl)hydrazine-l-carboxylate: Boc -hydrazine (2.2 g, 0.017 mol) was added to a solution of czs-3-(5-phenylisoxazole-3-carboxamido)cyclobutane-l-carboxy lic acid (4.14 g, 0.0144 mol) in THF (100 mL) followed by the addition of Et ₃ N (5.81 mL, 0.043 mol) and T ₃ P in EtOAc (50%, 17.13 mL, 0.0288 mol) and the reaction mixture was stirred at room temperature for 12 h. Volatiles were removed under reduced pressure and the crude reaction mixture was poured onto water (100 mL). The aq. phase was extracted with ethyl acetate (2 x 100 mL). Combined organic layer was washed with saturated aHC0 ₃ solution (2 x 100 mL), dried over anhydrous Na ₂ S0 ₄ and concentrated under reduced pressure to obtain the crude product. The crude compound was purified by silica gel column chromatography using 2% MeOH in EtOAc as eluent to afford the product (5.6 g, 96%) as a white solid. ^X H NMR (400 MHz, DMSO-d ₆ ): δ 9.50 (s, 1H), 9.14 (d, J= 7.5 Hz, 1H), 8.70 (s, 1H), 7.93 - 7.90 (m, 2H), 7.64 - 7.53 (m, 3H), 7.34 (s, 1H), 4.37 - 4.31 (m, 1H), 2.72 - 2.67 (m, 1H), 2.40 - 2.38 (m, 2H), 2.34 - 2.29 (m, 2H), 1.39 (s, 9H); LC-MS: [M+H] ⁺ 400.9.

[0314] Step 6: 7V-c s-3-(hydrazinecarbonyl)cyclobutyl)-5-phenylisoxazole-3- carboxamide: 4 M HC1 in dioxane (40 mL) was added to a solution of tert-butyl 2-cis-3-(5- phenylisoxazole-3-carboxamido)cyclobutane-l-carbonyl)hydrazi ne-l-carboxylate (5.6 g, 0.0139 mol) in 1,4 dioxane (25 mL) and the resulting reaction mixture was stirred at room temperature for 4 h. Volatiles were removed under reduced pressure and the crude compound thus obtained was stirred in diethyl ether (100 mL). The precipitate was filtered, washed with hexane and dried to afford the product (5.4 g, crude) as off white solid. ^X H NMR (400 MHz, DMSO-d ₆ ): δ 10.92 (s, 1H), 10.26 (br, 2H), 9.20 (d, J= 7.5 Hz, 1H), 7.93 - 7.91 (m, 2H), 7.58 - 7.53 (m, 2H), 7.36 (s, 1H), 4.41 - 4.35 (m,lH), 2.87 - 2.83 (m, 1H), 2.49 - 2.41 (m, 2H), 2.39 - 2.29 (m, 2H); LC-MS: [M+H] ⁺ 300.9. Example 21 : 7V-c s-3-(5-(hydroxymethyl)-l,3,4-oxadiazol-2-yl)cyclobutyl)-5- phenylioxazole-3-carboxamide

[0315] iV-c s-3-(5-(hydroxymethyl)-l,3,4-oxadiazol-2-yl)cyclobutyl)-5-ph enylioxazole- 3-carboxamide was prepared using a similar procedure described in example 12 using N-cis-3- (hydrazinecarbonyl)cyclobutyl)-5-phenylisoxazole-3-carboxami de as the starting material (example 20):

[0316] Appearance: off white solid

[0317] Analytical data: ^X H-NMR (400 MHz, DMSO) δ 9.30 (d, J= 7.7 Hz 1H), 7.94 - 7.91

(m, 2H), 7.58 - 7.53 (m, 3H), 7.37 (s, 1H), 5.86 (t, J= 8 Hz, 1H), 4.61 (d, J= 6.2 Hz, 2H), 4.56 - 4.50 (m, 1H), 3.53 - 3.46 (m , 1H) 2.72■■ 2.66 (m, 2H), 2.54 (signal obscured by solvent signal, 2H).

[0318] LC-MS: [M+H 341

[0319] HPLC purity: 97.63 % at 220 nm and 98.48 % at 254 nm.

[0320] Example 22: 7V-c/s-3-(5-((R)-l-hydroxyethyl)-l,3,4-oxadiazol-2-yl)cyclob utyl)-5- phenylisoxazole-3-carboxamide

[0321 ] 7V-c s-3-(5-((R)-l-hydroxyethyl)-l,3,4-oxadiazol-2-yl)cyclobutyl) -5- phenylisoxazole-3-carboxamide was prepared using a similar procedure described in example 12 using N-c«-3-(hydrazinecarbonyl)cyclobutyl)-5-phenylisoxazole-3-c arboxamide as the starting material (example 20):

[0322] Appearance: off white solid

[0323] Analytical data: ^X H-NMR (400 MHz, DMSO) δ 9.29 (d, J= 7.9 Hz 1H), 7.93 - 7.91

(m, 2H), 7.58 - 7.53 (m, 3H), 7.37 (s, 1H), 5.94 (d, J= 5.6 Hz, 1H), 4.92 - 4.86 ( m, 1H), 4.59 - 4.48 (m, 1H), 3.53 - 3.47 (m , 1H), 2.72 - 2.65 (m, 2H), 2.54- 2.59 (signal obscured by solvent signal, 2H), 1.46 (d, J= 6.6 Hz, 3H).

[0324] LC-MS: [M+H] ⁺ 355.1

[0325] HPLC purity: 96.59 % at 220 nm and 97.98 % at 254 nm.

Example 23 : iV-c s-3-(5-((S)-l-hydroxyethyl)-l,3,4-oxadiazol-2-yl)cyclobutyl) -5- phenylisoxazole-3-carboxamide

[0326] 7V-c s-3-(5-((S)-l-hydroxyethyl)-l,3,4-oxadiazol-2-yl)cyclobutyl) -5- phenylisoxazole-3-carboxamide was prepared using a similar procedure described in example 12 using N-c«-3-(hydrazinecarbonyl)cyclobutyl)-5-phenylisoxazole-3-c arboxamide as the starting material (example 20).

[0327] Appearance: off white solid

[0328] Analytical data: ^X H-NMR (400 MHz, DMSO) δ 9.29 (d, J= 7.8 Hz 1H), 7.94 - 7.91

(m, 2H), 7.58 - 7.53 (m, 3H), 7.36 (s, 1H), 5.93 (d, J= 5.6 Hz, 1H), 4.91 - 4.88 ( m, 1H), 4.57 - 4.50 (m, 1H), 3.54 - 3.45 (m , 1H), 2.72 -2.65 (m, 2H), 2.54 - 2.49 (m obscured by solvent signal, 2H), 1.46 (d, J= 6.6 Hz, 3H).

[0329] LC-MS: [M+H] ⁺ 355.0

[0330] HPLC purity: 97.12 % at 220 nm, 98.41 % at 254 nm and 99.02 % at 269 nm. Example 24: 7V-c s-3-(5-((R)-l,2-dihydroxyethyl)-l,3,4-thiadiazol-2-yl)cyclob utyl)-5- phenylisoxazole-3-carboxamide

[0331 ] 7V-c s-3-(5-((R)-l,2-dihydroxyethyl)-l,3,4-thiadiazol-2-yl)cyclob utyl)-5- phenylisoxazole-3-carboxamide was prepared using a similar procedure described in example 12 using N-c«-3-(hydrazinecarbonyl)cyclobutyl)-5-phenylisoxazole-3-c arboxamide as the starting material (example 20).

[0332] Appearance: off white solid

[0333] Analytical data: ^X H NMR (400 MHz, DMSO-d ₆ ): δ 9.27 (d, J= 8.4 Hz, 1H), 7.94 - 7.92 (m, 2H), 7.58 - 7.54 (m, 3H), 7.37 (s, 1H), 6.32 (d, J= 5.0 Hz, 1H), 5.07 - 5.04 (m, 1H), 4.92 - 4.89 (m, 1H), 4.54 - 4.52 (m, 1H), 3.73 - 3.68 (m, 2H), 3.67 - 3.57 (m, 1H), 2.81 - 2.75 (m, 2H), 2.50 - 2.42 (m, 1H).

[0334] LC-MS: [M+H] ⁺ 387.2

[0335] HPLC Purity: 98.16% at 269 nm and 97.06 at 254 nm.

Example 25: (l-cis-3-(5-phenylisoxazole-3-carboxamido)cyclobutyl)-lH-l,2 ,3- triazol-4-yl)methyl butylcarbamate

[0336] Step 1: TV-butyl carbamoyl chloride: solution of n-butyl amine (0.061 g, 0.84 mmol) and pyridine (0.266 g, 3.37 mmol) in DCM (10 mL) was added drop wise an ice-cooled solution of triphosgene (0.5 g, 1.68 mmol) in dry DCM (10 mL) under nitrogen atmosphere. The mixture was stirred for 16 h at 0 °C and filtered through a silica pad. The reaction mixture was eluted with DCM and concentrated under reduced pressure to get crude N-butyl carbamoyl chloride.

[0337] Step 2: to an ice cooled solution of N-czs-3-(4-(hydroxymethyl)-lH-l,2,3-triazol-l- yl)cyclobutyl)-5-phenylisoxazole-3-carboxamide (example 2: 0.07 g, 0.20 mmol) in DMF (2 mL) was added NaH (60%) (0.158 g, 0.41 mmol) portion wise and the reaction mixture were stirred at 0 °C for 10 min. To this resulting reaction mixture was added a solution of N-butyl carbamoyl chloride in DMF (2 mL) drop wise and the reaction mixture was stirred at 0 °C for 2 h. Progress of the reaction was monitored by TLC. After completion, the reaction mixture was diluted with water (15 mL) and extracted with ethyl acetate (15 mL x 3). Combined organic layer was washed with brine, dried over anhydrous sodium sulfate and concentrated under reduced pressure to get the crude compound. The crude compound was purified by neutral alumina column chromatography using 1% MeOH in DCM as eluent to afford desired compound which was further washed with n-pentane (2 mL) followed by diethyl ether (2 mL x 2) to get the product (0.025 g, 27.64%) as white solid. [0338] Analytical data: ^X H-NMR (400 MHz, CDC1 ₃ ) δ 9.27 (d, J= 8.32 Hz, 1H), 8.32 (s,

1H), 7.95 - 7.93 (m, 2H), 7.54 - 7.59 (m, 3H), 7.39 (s, 1H), 7.20 (t, J= 5.6 Hz, 1H), 5.04 (s, 2H), 5.01 - 4.93 (m, 1H), 4.46 - 4.40 (m, 1H), 3.00 - 2.88 (m, 4H), 2.69 - 2.66 (m, 2H), 1.38 - 1.29 (m, 2H), 1.27 - 1.20 (m, 2H), 0.85 (t J= 7.2 Hz, 3H,). [0339] LC-MS: (M+H) ⁺ = 439.2

[0340] HPLC purity: 94.93 % at 254 nm, 94.74 % at 200 nm and 93.79 % at 220 nm.

Example 26: iV-ir««s-3-(4-(R)-l-hydroxyethyl)-lH-pyrazol-l-yl)cyclobut yl)-5- phenylisoxazole-3-carboxamide and iV-ir««s-3-(4-(S)-l-hydroxyethyl)-lH-pyrazol-l- yl)cyclobutyl)-5-phenylisoxazole-3-carboxamide

[0341] Step 1: tert-butyl (3-hydroxycyclobutyl)carbamate: NaBH ₄ (1.02 g, 26.96 mmol, 0.50 eq.) was added slowly to a 0 °C solution of tert-butyl N-(3-oxocyclobutyl)carbamate (10 g, 53.99 mmol, 1.00 eq.) in ethanol (100 mL). The resulting solution was stirred for 1 hour at 25 °C and then concentrated under vacuum. This resulted in 9.9 g (98%) of tert-butyl N-(3- hydroxycyclobutyl)carbamate as a white solid.

[0342] Step 2: 3-((tert-butoxycarbonyl)amino)cyclobutyl methanesulfonate:

methanesulfonyl chloride (6.7 g, 58.49 mmol, 1.10 eq.) was added dropwise (5 min) to a 0°C solution of tert-butyl N-(3 -hydroxy cyclobutyl)carbamate (9.9 g, 52.87 mmol, 1.00 eq.) and TEA (10.8 g, 106.73 mmol, 2.00 eq.) in dichloromethane (200 mL). The resulting solution was stirred for 3 hours at 25 °C, the mixture was diluted with 400 mL of water. The resulting solution was extracted with dichloromethane (3x200 mL) and the organic layers combined. The resulting mixture was washed with brine (3x200 mL), dried over anhydrous sodium sulfate and concentrated under vacuum. This resulted in 11.4 g (81%) of tert-butyl N-[3- (methanesulfonyloxy)cyclobutyl]carbamate as a yellow solid. [0343] Step 3: tert-butyl N-?ra«s-3-(4-formyl-lH-pyrazol-l-yl)cyclobutyl]carbamate: 1H- pyrazole-4-carbaldehyde (1.73 g, 18.00 mmol, 1.20 eq.) and Cs ₂ C0 ₃ (9.78 g, 30.02 mmol, 2.00 eq.) were added to a solution of tert-butyl N-[3-(methanesulfonyloxy)cyclobutyl]carbamate (4 g, 15.08 mmol, 1.00 eq.) in DMF (100 mL). The resulting solution was stirred for 16 hours at 80 °C and then diluted with 300 mL of water. The resulting solution was extracted with ethyl acetate (3x300 niL) and the organic layers combined. The resulting mixture was washed with brine (3x500 mL), dried over anhydrous sodium sulfate and concentrated under vacuum. The crude product was purified by Flash with the following conditions: Column, CI 8 silica gel; mobile phase, X:H ₂ 0 Y:ACN=70/30 increasing to X:H ₂ 0 Y:ACN=20/80 within 30 min; Detector, UV 254 nm. The isomers were separated by Prep-SFC with the following conditions (Prep SFC80-2): Column, Chiralpak IB, 2*25cm, 5um; mobile phase, C0 ₂ (80%), IPA (20%); Detector, UV 220nm. This resulted in 1.2 g (30%) of tert-butyl N-tra«s-3-(4-formyl-lH- pyrazol-l-yl)cyclobutyl]carbamate as a white solid.

[0344] Step 4: tert-butyl iV-ir«ws-3-[4-(l-hydroxyethyl)-lH-pyrazol-l- yl]cyclobutyl]carbamate: into a 100-mL round-bottom flask purged and maintained with an inert atmosphere of nitrogen, was placed a solution of tert-butyl N-£raws-3-(4-formyl-lH- pyrazol- 1 -yl)cyclobutyl]carbamate (750 mg, 2.83 mmol, 1.00 eq.) in tetrahydrofuran (50 mL). This was followed by the addition of methyl magnesium bromide (3 mL, 3.00 eq., 3 mol/L) dropwise with stirring at 0 °C in 10 min. The resulting solution was stirred for 16 hours at 25 °C. The reaction was then quenched by the addition of 100 mL of NH4CI aqueous. The resulting solution was extracted with ethyl acetate (3x100 mL) and the organic layers combined. The resulting mixture was washed with brine (2x200 mL), dried and concentrated under vacuum. This resulted in 600 mg (75%) of tert-butyl N- trans-3-[4-(l -hydroxy ethyl)- 1H- pyrazol-l-yl]cyclobutyl]carbamate as yellow oil. [0345] Step 5: l-[l-trans-3-aminocyclobutyl]-lH-pyrazol-4-yl]ethan-l-ol: into a 50-mL round-bottom flask, was placed a solution of tert-butyl N-[(lr,3r)-3-[4-(l-hydroxyethyl)-lH- pyrazol-l-yl]cyclobutyl]carbamate (600 mg, 2.13 mmol, 1.00 eq.) in dichloromethane (15 mL) and trifluoroacetic acid (3 mL). The resulting solution was stirred for 2 hours at 25°C. The resulting mixture was concentrated under vacuum. This resulted in 226 mg (crude) of 1-[1- [trans-3-aminocyclobutyl]-lH-pyrazol-4-yl]ethan-l-ol as yellow oil.

[0346] Step 6: 5-phenyl-N-[trans-3-[4-[(lS and lR)-l-hydroxyethyl]-lH-pyrazol-l- yl]cyclobutyl]-l,2-oxazole-3-carboxamide: Into a 50-mL round-bottom flask, was placed a solution of l-[l-[trans-3-aminocyclobutyl]-lH-pyrazol-4-yl]ethan-l-ol (226 mg, 1.25 mmol, 1.00 eq.) in DMF (5 mL). To the solution were added 5-phenyl-l,2-oxazole-3-carboxylic acid (282 mg, 1.49 mmol, 1.00 eq.), HATU (700 mg, 1.84 mmol, 1.50 eq.) and DIEA (560 mg, 4.33 mmol, 3.00 eq.). The resulting solution was stirred for 2 hours at 25 °C. The resulting solution was diluted with 100 mL of water. The resulting solution was extracted with ethyl acetate (3x50 mL) and the organic layers combined. The resulting mixture was washed with brine (2x100 mL), dried and concentrated under vacuum. The residue was applied onto a silica gel column with ethyl acetate/petroleum ether (1: 1). The pure isomers were separated by Chiral- Prep-HPLC with the following conditions (Prep-HPLC-004): Column, Phenomenex Lux 5u Cellulose-4 AXIA Packed, 250*21.2mm,5um; mobile phase, Hex and IPA (hold 50.0% IPA in 15 min); Detector, UV 254/220nm. This resulted in 39.6 mg (9%) of 5-phenyl-N-[trans-3-[4- [(lR)-l-hydroxyethyl]-lH-pyrazol-l-yl]cyclobutyl]-l,2-oxazol e-3-carboxamide as a white solid and 39.4 mg (9%) of 5-phenyl-N-[trans-3-[4-[(lS)-l-hydroxyethyl]-lH-pyrazol-l- yl]cyclobutyl]-l,2-oxazole-3-carboxamide as a white solid:

[0347] Isomer 1:

[0348] Analytical data: 'H NMR (300 MHz, DMSO-i¾): δ 9.31-9.28 (d, J= 7.2 Hz, 2H),

7.96- 7.92 (m. 2H), 7.68 (s, 1H), 7.59-7.55 (m, 3H), 7.41 (s, 1H), 7.38 (s, 1H), 5.00-4.89 (m, 1H), 4.88-4.86 (d, J= 4.8Hz, 1H), 4.71-4.64 (m, 2H), 2.76-2.61 (m, 4H), 1.34-1.32 (d, J= 6.3 Hz, 3H).

[0349] LC-MS: (M+H) ⁺ = 353 [0350] HPLC purity: 99.24 at 254 nm [0351] Isomer 2:

[0352] Analytical data: 'H NMR (300 MHz, DMSO-i¾): δ 9.31-9.28 (d, J= 7.5 Hz, 2H),

7.96-7.93 (m, 2H), 7.68 (s, 1H), 7.57-7.55 (m, 3H), 7.41 (s, 1H), 7.38 (s, 1H),

4.97- 4.89 (m, 1H), 4.88-4.86 (d, J= 4.8 Hz, 1H), 4.70-4.64 (m, 2H), 2.72-2.61 (m, 4H), 1.34-1.32 (d, J= 6.6 Hz, 3H).

[0353] LC-MS: (M+H) ⁺ = 353

[0354] HPLC purity: 99.74 at 254 nm. Example 27: iV-ir««s-3-(5-((R)-l-hydroxyethyl)-lH-pyrazol-l-yl)cyclobu tyl)-5- phenylisoxazole-3-carboxamide and 7V-ir««s-3-(5-((S)-l-hydroxyethyl)-lH-pyrazol-l- yl)cyclobutyl)-5-phenylisoxazole-3-carboxamide

[0355] Step 1: tert-butyl 7V-^r««s-3-[3-(l-hydroxyethyl)-lH-pyrazol-l- yl]cyclobutyl]carbamate: Into a 50-mL 3-necked round-bottom flask purged and maintained with an inert atmosphere of nitrogen, was placed a solution of tert-butyl N-ftrans-3 -(3 -formyl- lH-pyrazol-l-yl)cyclobutyl]carbamate (486 mg, 1.83 mmol, 1.00 eq.) in tetrahydrofuran (10 mL). This was followed by the addition of MeMgBr (3M) (1.22 mL, 2.00 eq.) dropwise with stirring at 0 °C. The resulting solution was stirred for 7 hours at room temperature. The reaction was then quenched by the addition of 10 mL of NH ₄ C1 aqueous. The resulting solution was extracted with ethyl acetate (3x10 mL) and the organic layers combined. The solution was dried over anhydrous sodium sulfate and concentrated under vacuum. The crude product was purified by Flash-Prep-HP LC with the following conditions (CombiFlash-1): Column, CI 8 silica gel; mobile phase, MeCN/H ₂ O=50:50 increasing to MeCN/H ₂ O=60:40 within 3 min; Detector, UV 254 nm. This resulted in 233 mg (45%) of tert-butyl N- [trans -3 -[3- (l-hydroxyethyl)-lH-pyrazol-l-yl]cyclobutyl]carbamate as colorless oil.

[0356] Step 2: l-[l-[ir««s-3-aminocyclobutyl]-lH-pyrazol-3-yl]ethan-l-ol

hydrochloride: into a 50-mL round-bottom flask, was placed a solution of tert-butyl N-ftrans- 3-[3-(l-hydroxyethyl)-lH-pyrazol-l-yl]cyclobutyl]carbamate (300 mg, 1.07 mmol, 1.00 eq.) in dichloromethane (10 mL) and hydrogen chloride gas was bubbled into the solution. The resulting solution was stirred for 5 hours at room temperature. The resulting solution was diluted with 20 mL of water. The resulting solution was washed with ethyl acetate (2x20 mL) and the aqueous layer was concentrated under vacuum. This resulted in 271 mg (crude) of 1- [l-[£raws-3-aminocyclobutyl]-lH-pyrazol-3-yl]ethan-l-ol hydrochloride as yellow oil. [0357] Step 3: 5-phenyl-iV-/ir««s-3-[3-(l-hydroxyethyl)-lH-pyrazol-l-yl]c yclobutyl]- l,2-oxazole-3-carboxamide: into a 50-mL round-bottom flask, was placed a solution of 5- phenyl-l,2-oxazole-3-carboxylic acid (177.7 mg, 0.94 mmol, 1.00 eq.), l-[l-[trans-3- aminocyclobutyl]-lH-pyrazol-3-yl]ethan-l-ol hydrochloride (246 mg, 1.13 mmol, 1.20 eq.), HATU (428.8 mg, 1.13 mmol, 1.20 eq.) and DIEA (363.9 mg, 2.82 mmol, 3.00 eq.) in DMF(10 mL). The resulting solution was stirred for 2 hours at room temperature. The reaction was then quenched by the addition of 20 mL of water. The resulting solution was extracted with ethyl acetate (3x20 mL) and the organic combined layers were dried over anhydrous sodium sulfate and concentrated under vacuum. The residue was applied onto a Prep-TLC with ethyl acetate/petroleum ether (2: 1). This resulted in 189 mg (57%) of 5-phenyl-N-/?raws-3-[3-(l- hydroxyethyl)-lH-pyrazol-l-yl]cyclobutyl]-l,2-oxazole-3-carb oxamide as a off-white solid.

[0358] The mixture (210 mg, 0.60 mmol, 1.00 eq.) was purified by Chiral-Prep-HPLC with the following conditions (Prep-HPLC-004): Column, Phenomenex Lux 5u Cellulose-4 AXIA Packed, 250*21.2mm, 5um; mobile phase, Hex and ethanol (hold 25.0% ethanol in 15 min); Detector, UV 254/220nm. This resulted in 5-phenyl-N-/ ^" ?ra«s-3-[3-[(lR or S)-l- hydroxyethyl]-lH-pyrazol-l-yl]cyclobutyl]-l,2-oxazole-3-carb oxamide:

[0359] Isomer 1 (74 mg)

[0360] Appearance: white solid

[0361] Analytical data: ¹ H-NMR: (OMSO-d ₆ , 400 MHz): δ 9.30, 9.28 (d, J= 8.0Hz, 1H),

7.95-7.93 (m, 2H), 7.72, 7.71 (d, J= 4.0Hz, 1H), 7.58-7.54 (m, 3H), 7.37 (m,

1H), 6.19, 6.18 (d, J= 4.0Hz, 1H), 4.98-4.4.92 (m, 2H), 4.73-4.64 (m, 2H), 2.72-2.64 (m, 5H), 1.36, 1.34 (d, J= 8.0Hz, 3H).

[0362] LC-MS: (M+H) ⁺ = 353

[0363] HPLC purity: 99.14% at 254 nm. [0364] Isomer 2 (72 mg)

[0365] Appearance: white solid

[0366] Analytical data: ¹ H-NMR (OMSO-d ₆ , 300 MHz): δ 9.30, 9.28 (d, J= 6.0Hz, 1H),

7.96-7.93 (m, 2H), 7.73, 7.72 (d, J= 3.0Hz, 1H), 7.60-7.55 (m, 3H), 7.38 (s, 1H), 6.19, 6.18 (d, J= 3.0Hz, 1H), 4.99-4.92 (m, 2H) , 4.74-4.63 (m, 2H), 2.78- 2.65 (m, 5H), 1.37,1.35 (d, J= 6.0Hz, 3H).

[0367] LC-MS: (M+H) ⁺ = 353

[0368] HPLC purity: 98.18% at 254 nm.

Example 28: iV-(c s-3-(4-(hydroxymethyl)-lH-pyrazol-l-yl)cyclobutyl)-5- phenylisoxazole-3-carboxamide

[0369] Tert-butyl N-[c s-3-(4-formyl-lH-pyrazol-l-yl)cyclobutyl]carbamate: into a 100-mL round-bottom flask, was placed a solution of tert-butyl N-[3- (methanesulfonyloxy)cyclobutyl]carbamate (2.65 g, 9.99 mmol, 1.00 eq.), lH-pyrazole-4- carbaldehyde (1.152 g, 11.99 mmol, 1.20 eq.) and Cs ₂ C0 ₃ (6.52 g, 20.01 mmol, 2.00 eq.) in DMF (20 mL). The resulting solution was stirred for 4 h at room temperature. The reaction was then quenched by the addition of 100 mL of water. The resulting solution was extracted with 3x100 mL of ethyl acetate and the organic layers combined. The resulting mixture was washed with 100 mL of brine. The mixture was dried over anhydrous sodium sulfate and concentrated under vacuum. The crude product was purified by Flash-Prep-HPLC with the following conditions (CombiFlash-1): Column, CI 8 silica gel; mobile phase,

MeCN/H ₂ O=60:40 increasing to MeCN/H ₂ O=70:30 within 3 min; Detector, UV 254 nm. The crude product was purified by Prep-SFC with the following conditions (prep SFC 350-2): Column: Phenomenex Lux 5u Cellulose-4 250*50mm; mobile Phase A: CO2:70, Mobile Phase B: MeOH-HPLC:30; Flow rate: 150 mL/min; 254 nm; RTL4.53; RT2:5.36. This resulted in - I l l -

712 mg (54%) of tert-butyl N-[c«-3-(4-formyl-lH-pyrazol-l-yl)cyclobutyl]carbamate as a white solid.

[0370] Step 1: tert-butyl N-[c s-3-[4-(hydroxymethyl)-lH-pyrazol-l- yl]cyclobutyl]carbamate: into a 50-mL round-bottom flask, was placed a solution of tert-butyl N-[c«-3-(4-formyl-lH-pyrazol-l-yl)cyclobutyl]carbamate (700 mg, 2.64 mmol, 1.00 eq.) in methanol (15 mL). This was followed by the addition of NaBH ₄ (702.6 mg, 18.57 mmol, 7.04 eq.) in several batches at 0 °C. The resulting solution was stirred for 30 min at room temperature. The reaction was then quenched by the addition of 50 mL of NH ₄ C1 (aq.). The resulting solution was extracted with ethyl acetate (50 mLx3) and the combined organic layers were dried over anhydrous sodium sulfate and concentrated under vacuum. This resulted in 819 mg (crude) of tert-butyl N-[czs-3-[4-(hydroxymethyl)-lH-pyrazol-l- yl]cyclobutyl]carbamate as an off-white solid.

[0371] Step 2: [l-[c s-3-aminocyclobutyl]-lH-pyrazol-4-yl]methanol hydrochloride: into a 50-mL round-bottom flask, was placed a solution of tert-butyl N-[cz ^' s-3-[4- (hydroxymethyl)-lH-pyrazol-l-yl]cyclobutyl]carbamate (819 mg, 3.06 mmol, 1.00 eq.) in tetrahydrofuran (20 mL) and hydrogen chloride gas was bubbled in. The resulting solution was stirred for 3 hours at room temperature. The resulting solution was diluted with 20 mL of water. The resulting solution was extracted with ethyl acetate (2x20 mL) and the combined aqueous layer was concentrated under vacuum. This resulted in 855 mg (crude) of [l-[cis-3- aminocyclobutyl]-lH-pyrazol-4-yl]methanol hydrochloride as a off- white semi-solid.

[0372] Step 3: 5-phenyl-N-[c s-3-[4-(hydroxymethyl)-lH-pyrazol-l-yl]cyclobutyl]-l,2- oxazole-3-carboxamide: into a 50-mL round-bottom flask, was placed a solution of [l-[cis-3- aminocyclobutyl]-lH-pyrazol-4-yl] methanol hydrochloride (408 mg, 2.00 mmol, 1.20 eq.) in DMF (10 mL). To the solution were added DIEA (645 mg, 4.99 mmol, 3.00 eq.), 5-phenyl- l,2-oxazole-3-carboxylic acid (315 mg, 1.67 mmol, 1.00 eq.) and HATU (760 mg, 2.00 mmol, 1.20 eq.). The resulting solution was stirred for 1 hour at room temperature. The reaction was then quenched by the addition of 20 mL of water. The resulting solution was extracted with ethyl acetate (3x20 mL) and the combined organic layers were dried over anhydrous sodium sulfate and concentrated under vacuum. The residue was applied onto a Prep-TLC with ethyl acetate/petroleum ether (2: 1). This resulted in 63 mg (1 1%) of 5-phenyl-N-[cz ^' s-3-[4- (hydroxymethyl)- 1 H-pyrazol- 1 -yl]cyclobutyl]- 1 ,2-oxazole-3 -carboxamide. [0373] Appearance: white solid

[0374] Analytical data: ¹ HNMR (400MHz, DMSO-i¾): δ 9.24, 9.22 (d, J= 8.0Hz, 1H),

7.95-7.92 (m, 2H), 7.80 (s, 1H), 7.59-7.53 (m, 3H), 7.38, 7.36 (d, J= 8.0Hz, 2H), 4.83-4.80 (t, J= 6.0Hz, 1H), 4.60-4.56 (m, 1H), 4.36-4.28 (m, 3H), 2.82- 2.75 (m, 2H), 2.65-2.59 (m, 2H).

[0375] LC-MS: (M+H) ⁺ = 339

[0376] HPLC purity: 99.94% at 254 nm.

Example 29: iV-(ir««s-3-(4-(hydroxymethyl)-lH-pyrazol-l-yl)cyclobutyl) -5- phenylisoxazole-3-carboxamide

[0377] iV-(ir««s-3-(4-(hydroxymethyl)-lH-pyrazol-l-yl)cyclobutyl) -5-phenylisoxazole- 3-carboxamide was prepared using a similar procedure as shown in example 28 using tert- butyl N-[c«-3-(4-formyl-lH-pyrazol-l-yl)cyclobutyl]carbamate as the starting material.

[0378] Analytical data: ^X H NMR (400 MHz, DMSO-i¾): δ 9.31-9.29 (d, J= 7.2 Hz, 1H),

7.95-7.93 (m, 2H), 7.72 (s, 1H), 7.60-7.55 (m, 3H), 7.43 (s, 1H), 7.37 (s, 1H), 4.97-4.93 (m, 1H), 4.69-4.67 (m, 1H), 4.34 (s, 2H), 2.75-2.63 (m, 4H).

[0379] HPLC purity: 99.7% at 254 nm.

Example 30: 7V-c s-3-(3-(hydroxymethyl)-lH-pyrazol-l-yl)cyclobutyl)-5- phenylisoxazole-3-carboxamide

[0380] Step 1: tert-butyl 7V-[3-(3-formyl-lH-pyrazol-l-yl)cyclobutyl]carbamate: into a 100-mL round-bottom flask, was placed a solution of tert-butyl N-[3- (methanesulfonyloxy)cyclobutyl]carbamate (2 g, 7.54 mmol, 1.00 eq.), lH-pyrazole-3- carbaldehyde (725 mg, 7.55 mmol, 1.00 eq.) and Cs ₂ C0 ₃ (4.9 g, 15.04 mmol, 2.00 eq.) in DMF (40 mL). The resulting solution was stirred for 16 hours at 80°C. The reaction was then quenched by the addition of water. The resulting solution was extracted with of ethyl acetate and the organic layers combined. The resulting mixture was washed with brine, dried over anhydrous sodium sulfate and concentrated under vacuum. The residue was applied onto a silica gel column with ethyl acetate/hexane (1 :4). This resulted in 1.9 g (95%) of tert-butyl N- [3-(3-formyl-lH-pyrazol-l-yl)cyclobutyl]carbamate as a white solid. LC-MS: (M+H) ⁺ = 266. Mixture was purified by Prep-SFC with the following conditions (prep SFC 350-2): column, Chiralpak AS-H, 5*25cm, 5um; mobile phase, C0 ₂ (75%), methanol (25%); Detector, UV 220 nm. This resulted in 600 mg (32%) of tert-butyl N-[c s-3 -(3 -formyl-1 H-pyrazol- 1- yl)cyclobutyl]carbamate as yellow oil, and 760 mg (40%) of tert-butyl N-[/raws-3-(3-formyl- 1 H-pyrazol- 1 -yl)cyclobutyl]carbamate as a white solid.

[0381 ] Step 2: tert-butyl 7V-[c s-3-[3-(hydroxymethyl)-lH-pyrazol-l- yl]cyclobutyl]carbamate: into a 50-mL round-bottom flask, was placed a solution of tert-butyl N-[czs-3 -(3 -formyl-1 H-pyrazol- l-yl)cyclobutyl]carbamate (600 mg, 2.26 mmol, 1.00 eq.) in methanol (5 mL). This was followed by the addition of NaBH ₄ (86 mg, 2.34 mmol, 1.00 eq.), in portions. The resulting solution was stirred for 30 min at room temperature. The reaction was then quenched by the addition of water. The resulting solution was extracted with ethyl acetate and the organic layers combined. The resulting mixture was washed with brine, dried over anhydrous sodium sulfate and concentrated under vacuum. This resulted in 600 mg (crude) of tert4outyl N-[c«-3-[3-(hydroxymethyl)-lH-pyrazol-l-yl]cyclobutyl]carba mate as a white solid. LC-MS: (M+H) ⁺ = 268

[0382] Step 3: [l-[c s-3-aminocyclobutyl]-lH-pyrazol-3-yl]methanol hydrochloride: into a 100-mL 3-necked round-bottom flask, was placed a solution of tert-butyl N-[cz ^' s-3-[3- (hydroxymethyl)-lH-pyrazol-l-yl]cyclobutyl]carbamate (600 mg, 2.24 mmol, 1.00 eq.) in ethyl acetate (5 mL). Hydrogen chloride gas was bubbled slowly into the solution. The resulting solution was stirred for 30 min at room temperature. The reaction was concentrated under vacuum. This resulted in 400 mg (88%) of [l-[czs-3-aminocyclobutyl]-lH-pyrazol-3- yl] methanol hydrochloride as a yellow syrup. LC-MS: (M+H) ⁺ = 168

[0383] Step 4: [l-[c s-3-(5-phenyl-l,2-oxazole-3-amido)cyclobutyl]-lH-pyrazol-3- yl] methyl 5-phenyl-l,2-oxazole-3-carboxylate: into a 100-mL round-bottom flask, was placed a solution of [l-[czs-3-aminocyclobutyl]-lH-pyrazol-3-yl]methanol hydrochloride (400 mg, 1.96 mmol, 1.00 eq.), 5-phenyl-l,2-oxazole-3-carboxylic acid (745 mg, 3.94 mmol, 2.00 eq.), HCTU (983 mg, 2.36 mmol, 1.20 eq.) and DIEA (762 mg, 5.90 mmol, 3.00 eq.) in DMF (20 mL). The resulting solution was stirred for 2 hours at room temperature. The reaction was then quenched by the addition of water. The resulting solution was extracted with ethyl acetate and the organic layers combined. The resulting mixture was washed with brine, dried over anhydrous sodium sulfate and concentrated under vacuum. The crude residue was washed with 5 mL of methanol. This resulted in 400 mg (40%) of [l-[cz ^' s-3-(5-phenyl-l,2-oxazole-3- amido)cyclobutyl]-lH-pyrazol-3-yl]methyl 5-phenyl-l,2-oxazole-3-carboxylate as a white solid. LC-MS: (M+H) ⁺ = 510. [0384] Step 5: 5-phenyl-7V-[c s-3-[3-(hydroxymethyl)-lH-pyrazol-l-yl]cyclobutyl]-l,2- oxazole-3-carboxamide: into a 50-mL round-bottom flask, was placed a solution of [l-[cis-3- (5-phenyl-l,2-oxazole-3-amido)cyclobutyl]-lH-pyrazol-3-yl]me thyl 5-phenyl-l,2-oxazole-3- carboxylate (300 mg, 0.59 mmol, 1.00 eq.) in methanol/water (5 mL/5 mL). This was followed by the addition of LiOH (42 mg, 1.75 mmol, 3.00 eq.), in portions. The resulting solution was stirred for 30 min at room temperature. The reaction was then quenched by the addition of water. The resulting solution was extracted with ethyl acetate and the organic layers combined. The resulting mixture was washed with brine, dried over anhydrous sodium sulfate and concentrated under vacuum. The residue was applied onto a silica gel column with ethyl acetate/petroleum ether (1 : 1). This resulted in 120.7 mg (61%) of 5-phenyl-N-[cz ^' s-3-[3- (hydroxymethyl)-lH-pyrazol-l-yl]cyclobutyl]-l,2-oxazole-3-ca rboxamide as a white solid. [0385] LC-MS: (M+H) ⁺ = 339.1

[0386] Analytical data: ^x H NMR(300MHz, DMSO-i¾, ppm): δ 9.25-9.22 (d, J= 7.8 Hz,

1H), 7.95-7.94 (m, 2H), 7.93-7.92 (m, 1H), 7.77-7.55 (m, 3H), 7.38 (s, 1H), 6.22-6.21 (m, 1H), 4.99-4.95 (m, 1H), 4.63-4.52 (m, 1H), 4.42-4.40 (m, 2H), 4.34-4.26(m, 1H), 2.82-2.76 (m, 2H), 2.66-2.56 (m, 2H). [0387] HPLC purity: 98.8% at 254 nm.

Example 31 : iV-ir««s-3-(3-(hydroxymethyl)-lH-pyrazol-l-yl)cyclobutyl)- 5- phenylisoxazole-3-carboxamide

[0388] Into a 100-mL round-bottom flask, was placed a solution of [l-trans-3- aminocyclobutyl]-lH-pyrazol-3-yl]methanol (120 mg, 0.72 mmol, 1.00 eq., prepared using similar procedure as shown in example 29) in dichloromethane (5 mL). To the solution were added 5 -phenyl- l,2-oxazole-3-carboxylic acid (163 mg, 0.86 mmol, 1.20 eq.) and HCTU (360 mg, 0.87 mmol, 1.20 eq.). This was followed by the addition of DIEA (278 mg, 2.15 mmol, 3.00 eq.) dropwise with stirring. The resulting solution was stirred for 1 hour at room temperature. The reaction was then quenched by the addition of water. The resulting solution was extracted with dichloromethane (3x50 mL). The organic layers were combined, dried and concentrated under vacuum. The crude product was purified by Prep-HPLC with the following conditions (Waters): Column, Bridget Prep CI 8 5um OBDTM 19* 100mm; mobile phase, water with 0.05% NH4HCO3 and CH ₃ CN (40.0% CH ₃ CN up to 80.0% in 10 min, up to 95.0% in 1.5min, down to 40.0% in 1.5min); Detector, 254nm. This resulted in 44.7 mg (18%) of 5- phenyl-N-?ra«s-3-[3-(hydroxymethyl)-lH-pyrazol-l-yl]cyclobu tyl]-l,2-oxazole-3-carboxamide as a white solid.

[0389] LC-MS: (M+H) ⁺ = 339

[0390] Analytical data: ^X H NMR (400MHz, OMSO-d ₆ ): δ 9.32-9.30 (d, J= 6.8 Hz, 1H),

7.95-7.94 (d, J= 6.0 Hz, 2H), 7.74 (s, 1H), 7.57-7.55 (m, 3H), 7.38 (s, 1H), 6.20 (s, 1H), 5.02-4.99 (t, J= 5.6Hz, 1H), 4.96-4.95 (m, 1H), 4.71-4.65 (m, 1H), 4.44-4.42 (d, J= 6.0 Hz, 2H), 2.75-2.63 (m, 4H).

[0391] HPLC purity: 98.8% at 254 nm.

Example 32 : 7V-ir«ws-3-(3-(hydroxymethyl)-l,2,4-oxadiazol-5-yl)cyclobut yl)-5- phenylisoxazole-3-carboxamide and 7V-c/s-3-(3-(hydroxymethyl)-l,2,4-oxadiazol-5- yl)cyclobutyl)-5-phenylisoxazole-3-carboxamide

[0392] Step la: (Z)-2-chloro-N-hydroxyethenimidamide: into a 100-mL round-bottom flask, was placed a solution of 2-chloroacetonitrile (8 g, 105.96 mmol, 1.00 eq.) in water (28 mL). To the solution were added NH ₂ OH.HCl (7.36 g, 1.00 eq.) and Na ₂ C0 ₃ (5.6 g, 52.32 mmol, 0.50 eq.). The resulting solution was stirred for 1 hour at room temperature. The resulting solution was diluted with water. The resulting solution was extracted with ethyl acetate (3x100 mL) and the organic layer was dried and concentrated under vacuum. This resulted in 4 g (35%) of (Z)-2-chloro-N-hydroxyethenimidamide as a yellow solid. LC-MS: (M+H) ⁺ = 109.

[0393] Step 1: methyl 3-(l,3-dioxo-2,3-dihydro-lH-isoindol-2-yl)cyclobutane-l- carboxylate: into a 1000-mL round-bottom flask, was placed a solution of methyl 3- hydroxycyclobutane-l-carboxylate (10 g, 76.88 mmol, 1.00 eq.) in tetrahydrofuran (500 mL), 2,3-dihydro-lH-isoindole-l,3-dione (13.2 g, 89.7 mmol, 1.20 eq.), triphenyl phosphine (23.6 g, 90.0 mmol, 1.20 eq.). This was followed by the addition of DEAD (21 g, 120.6 mmol, 1.50 eq.) dropwise with stirring. The resulting solution was stirred for 3 h at room temperature. The reaction was then quenched by the addition of water. The resulting solution was extracted with 3x100 mL of ethyl acetate and the organic layers combined and dried over anhydrous sodium sulfate and concentrated under vacuum. The residue was applied onto a silica gel column with ethyl acetate/petroleum ether (1 : 1). This resulted in 6 g (30%) of methyl 3-(l,3-dioxo-2,3- dihydro-lH-isoindol-2-yl)cyclobutane-l-carboxylate as a white solid. ^X H NMR (300MHz, CDC1 ₃ ): δ 7.85-7.81 (m, 2H), 7.75-7.70 (m, 2H), 5.09-5.03 (t, J= 8.7 Hz, 1H), 3.32-3.29 (m, 1H), 3.18-3.10 (m, 2H), 2.67-2.59 (m, 2H), 1.31-1.24 (m, 3H). LC-MS: (M+H) ⁺ = 260.

[0394] Step 2: 3-(l,3-dioxo-2,3-dihydro-lH-isoindol-2-yl)cyclobutane-l-carb oxylic acid: into a 250-mL round-bottom flask, was placed a solution of methyl 3-(l,3-dioxo-2,3- dihydro-lH-isoindol-2-yl)cyclobutane-l-carboxylate (6 g, 23.14 mmol, 1.00 eq.) in dioxane (100 mL). To the solution was added 6N hydrogen chloride aqueous (30 mL). The resulting solution was stirred for 3 hours at 90 °C in an oil bath. The resulting mixture was concentrated under vacuum. This resulted in 5 g (crude) of 3-(l,3-dioxo-2,3-dihydro-lH-isoindol-2- yl)cyclobutane-l-carboxylic acid as a white solid. LC-MS: (M+H) = 246.

[0395] Step 3: 7V-[(lE)-2-chloro-l-(hydroxyimino)ethyl]-3-(l,3-dioxo-2,3-di hydro-lH- isoindol-2-yl)cyclobutane-l-carboxamide: into a 250-mL round-bottom flask, was placed a solution of 3-(l,3-dioxo-2,3-dihydro-lH-isoindol-2-yl)cyclobutane-l-carb oxylic acid (5 g,

20.38 mmol, 1.00 eq.) in dichloromethane (100 mL). To the mixture were added (Z)-2-chloro- N-hydroxyethenimidamide (2.6 g, 24.00 mmol, 1.20 eq.), HATU (9.2 g, 38.16 mmol, 1.20 eq.) and DIEA (8 g, 60.36 mmol, 3.00 eq.) with stirring. The resulting solution was stirred for 2 hours at room temperature. The reaction was then quenched by the addition of water. The resulting solution was extracted with dichloromethane (3x100 mL) and the organic layer was dried over anhydrous sodium sulfate and concentrated under vacuum. The residue was applied onto a silica gel column with ethyl acetate/hexane (1 : 1). This resulted in 4.4 g (64%) of N- [(lE)-2-chloro-l-(hydroxyimino)ethyl]-3-(l,3-dioxo-2,3-dihyd ro-lH-isoindol-2- yl)cyclobutane-l-carboxamide as a white solid. LC-MS: [M+Hf = 336.

[0396] Step 4: 2-[3-[3-(chloromethyl)-l,2,4-oxadiazol-5-yl]cyclobutyl]-2,3- dihydro-lH- isoindole-l,3-dione: into a 10-mL vial, was placed a solution of N-[(lE)-2-chloro-l-

(hydroxyimino)ethyl]-3-(l,3-dioxo-2,3-dihydro-lH-isoindol -2-yl)cyclobutane-l-carboxamide (4 g, 1 1.92 mmol, 1.00 eq.) in AcOH (15 mL). The final reaction mixture was irradiated with microwave radiation for 30 min at 150 °C. The resulting mixture was concentrated under vacuum. The residue was applied onto a silica gel column with ethyl acetate/hexane (1 : 1). This resulted in 2 g (53%) of 2-[3-[3-(chloromethyl)-l,2,4-oxadiazol-5-yl]cyclobutyl]-2,3- dihydro-lH-isoindole-l,3-dione as a white solid. LC-MS: [M+H] ⁺ = 318.

[0397] Step 5: [5-[3-(l,3-dioxo-2,3-dihydro-lH-isoindol-2-yl)cyclobutyl]-l, 2,4- oxadiazol-3-yl] methyl acetate: into a 100-mL round-bottom flask, was placed a solution of 2- [3 - [3 -(chloromethyl)- 1 ,2,4-oxadiazol-5 -yl]cyclobutyl] -2,3 -dihydro- 1 H-isoindole- 1 ,3 -dione (2 g, 6.60 mmol, 1.00 eq.) and potassium acetate (1.3 g, 13.22 mmol, 2.00 eq.) in DMF (50 mL). The resulting solution was stirred for 2 hours at 60°C in an oil bath. The resulting mixture was concentrated under vacuum. The residue was applied onto a silica gel column with ethyl acetate/petroleum ether (1 : 1). This resulted in 1.4 g (62%) of [5-[3-(l,3-dioxo-2,3-dihydro-lH- isoindol-2-yl)cyclobutyl]-l,2,4-oxadiazol-3-yl]methyl acetate as yellow oil. LC-MS: [M+H] ⁺ = 342.

[0398] Step 6: [5-(3-aminocyclobutyl)-l,2,4-oxadiazol-3-yl] methanol: into a 100-mL round-bottom flask, was placed a solution of [5-[3-(l,3-dioxo-2,3-dihydro-lH-isoindol-2- yl)cyclobutyl]-l,2,4-oxadiazol-3-yl]methyl acetate (1.4 g, 4.1 mmol, 1.00 eq.) in ethanol (40 mL). To the solution was added hydrazine (1 mL). The resulting solution was stirred for 3 hours at 60°C in an oil bath. The solids were filtered out. The resulting mixture was concentrated under vacuum. This resulted in 1 g (crude) of [5-(3-aminocyclobutyl)-l,2,4- oxadiazol-3-yl]methanol as a white solid. LC-MS: [M+H] ⁺ = 170.

[0399] Step 7: 7V-[3-[3-(hydroxymethyl)-l,2,4-oxadiazol-5-yl]cyclobutyl]-5- phenyl-l,2- oxazole-3-carboxamide: into a 250-mL round-bottom flask, was placed a solution of 5- phenyl- l,2-oxazole-3-carboxylic acid (1 g, 5.28 mmol, 1.10 eq.) in dichloromethane (100 mL). To the mixture were added [5-(3-aminocyclobutyl)-l,2,4-oxadiazol-3-yl]methanol (800 mg, 4.52 mmol, 1.00 eq.) and HATU (2.16 g, 8.96 mmol, 1.20 eq.). This was followed by the addition of DIEA (2 g, 14.5 mmol, 3.00 eq.) dropwise with stirring. The resulting solution was stirred for 1 hour at room temperature. The reaction was then quenched by the addition of water. The resulting solution was extracted with dichloromethane (3x100 mL) and the organic layer was dried over anhydrous sodium sulfate and concentrated under vacuum. The residue was applied onto a silica gel column with dichloromethane/methanol (50: 1). This resulted in 1 g (62%) of N-[3-[3-(hydroxymethyl)-l,2,4-oxadiazol-5-yl]cyclobutyl]-5-p henyl-l,2-oxazole-3- carboxamide as a white solid. LC-MS: [M+H] ⁺ = 341. [0400] Step 8: Separation by SFC: the isomers (lg) were separated by Chiral-Prep-HPLC with the following conditions (Prep-HPLC-032): Column, Repaired IA, 21.2* 150mm, 5um; mobile phase, Hex and ethanol (hold 50.0% ethanol in 15 min); Detector, UV 254/220nm. This resulted in 555 mg (37%) of 5-phenyl-N-[?raws-3-[3-(hydroxymethyl)-l,2,4-oxadiazol-5- yl]cyclobutyl]-l,2-oxazole-3-carboxamide and 26.5 mg (3%) of 5-phenyl-N-[cz ^' s-3-[3- (hydroxymethyl)-l,2,4-oxadiazol-5-yl]cyclobutyl]-l,2-oxazole -3-carboxamide as a white solid.

[0401] 5-Phenyl-iV-[ir««s-3-[3-(hydroxymethyl)-l,2,4-oxadiazol-5- yl]cyclobutyl]-l,2- oxazole-3-carboxamide

[0402] Analytical data: ^X H NMR (300MHz, DMSO-i¾): δ 9.34-9.31 (d, J= 7.8 Hz, 1H),

7.96-7.93 (m, 2H), 7.78-7.75 (m, 3H), 7.60-7.55 (m, 3H), 7.38 (s, 1H), 5.72-5.68 (t, J= 6.3 Hz, 1H), 4.81-4.70 (m, 1H), 4.57-4.55 (d, J= 6.3 Hz, 2H), 3.81-3.75

(m, 1H), 2.78-2.71 (m, 2H), 2.68-2.58 (m, 2H).

[0403] HPLC purity: 99.27% at 254 nm.

5-Phenyl-7V-[c s-3-[3-(hydroxymethyl)-l,2,4-oxadiazol-5-yl]cyclobutyl]-l,2- oxazole- 3-carboxamide [0404] Analytical data: ^- MR (400MHz, CD ₃ OD-i¾): δ 7.91-7.88 (m, 2H), 7.57-7.52

(m, 3H), 7.10 (s, 1H), 4.72-4.60 (m, 3H), 3.73-3.58 (m, 1H), 2.91-2.87 (m, 2H), 2.65-2.57 (m, 2H).

[0405] HPLC purity: 98.2% at 254 nm. Example 33 : 7V-(c s-3-(5-(hydroxymethyl)-l,2,4-oxadiazol-3-yl)cyclobutyl)-5- phenylisoxazole-3-carboxamide and 7V-(ir««s-3-(5-(hydroxymethyl)-l,2,4-oxadiazol-3- yl)cyclobutyl)-5-phenylisoxazole-3-carboxamide

[0406] Step 1: oxocyclobutane-l-carbonitrile: into a 500-mL 3-necked round-bottom flask, was placed a solution of 3-methylidenecyclobutane-l-carbonitrile (1.5 g, 16.11 mmol, 1.00 eq.) and RuCl ₃ .H ₂ 0 (360 mg, 1.60 mmol, 0.10 eq.) in DCM/ACN/H ₂ 0 (60/60/90 mL). This was followed by the addition of sodium periodate (5.2 g, 24.31 mmol, 1.50 eq.), in portions at 10°C in 15 min. The resulting solution was stirred for 2 hours at 25 °C. The solids were filtered out. The resulting solution was extracted with dichloromethane (3x100 mL) and the organic layers combined. The resulting mixture was washed with brine (2x200 mL), dried over anhydrous sodium sulfate and concentrated under vacuum. The residue was applied onto a silica gel column with ethyl acetate/petroleum ether (1: 1). This resulted in 1.1 g (72%) of 3- oxocyclobutane-l-carbonitrile as a yellow solid.

[0407] Step 2: 7V-(3-cyanocyclobutyl)-2-methylpropane-2-sulfmamide: into a 500-mL round-bottom flask, was placed a solution of 3 -oxocyclobutane-l-carbonitrile (4 g, 42.06 mmol, 1.00 eq.) tetra(propan-2-yloxy)titanium (14.16 g, 62.90 mmol, 1.50 eq.) and 2- methylpropane-2-sulfinamide (6.12 g, 50.49 mmol, 1.20 eq.) in tetrahydrofuran (200 mL). The resulting solution was stirred for 16 hours at 65°C. The reaction was cooled to 25°C. Then NaBH ₄ (3.2 g, 84.60 mmol, 2.00 eq.) was added. The mixture was stirred for 2 hours at 25°C. The reaction was then quenched by the addition of 200 mL of water. The solids were filtered out and the resulting solution was extracted with ethyl acetate (2x200 mL) and the organic layers were combined. The resulting mixture was washed with brine (2x300 mL), dried over sodium sulfate and concentrated under vacuum. This resulted in 7.2 g (85%) of N-(3- cyanocyclobutyl)-2-methylpropane-2-sulfinamide as a yellow solid.

[0408] Step 3: (Z)-/V-hydroxy-3-[(2-methylpropane-2-sulfinyl)amino]cyclobut -l- carboximidamide: into a 500-mL round-bottom flask, was placed a solution of N-(3- cyanocyclobutyl)-2-methylpropane-2-sulfinamide (7.2 g, 35.95 mmol, 1.00 eq.) in ethanol/H ₂ 0 (200/70 mL). To the solution were added NH ₂ OH HCl (5 g, 71.94 mmol, 2.00 eq.) and sodium carbonate (1 1.43 g, 107.84 mmol, 3.00 eq.). The resulting solution was stirred for 2 hours at 80 °C. The resulting solution was diluted with 400 mL of water. The resulting solution was extracted with ethyl acetate (2x300 mL) and the organic layers combined. The resulting mixture was washed with brine (2x400 mL), dried over anhydrous sodium sulfate and concentrated under vacuum. This resulted in 5 g (60%) of (Z)-N-hydroxy-3-[(2- methylpropane-2-sulfinyl)amino]cyclobut-l-carboximidamide as yellow oil. LC-MS [M+H] ⁺ = 234.

[0409] Step 4: [[Z-hydroxyimino)([3-[(2-methylpropane-2- sulfinyl)amino]cyclobutyl])methyl] carbamoyl] methyl acetate: into a 250-mL round-bottom flask, was placed a solution of (Z)-N-hydroxy-3-[(2-methylpropane-2-sulfinyl)amino]cyclobut- 1 -carboximidamide (3.7 g, 15.86 mmol, 1.00 eq.) in dichloromethane ( mL). To the solution were added TEA (3.2 g, 31.62 mmol, 2.00 eq.) and 2-chloro-2-oxoethyl acetate (2.6 g, 19.04 mmol, 1.20 eq.). The resulting solution was stirred for 1 hour at 25 °C. The resulting solution was diluted with 300 mL of Η ₂ 0 and then it was extracted with ethyl acetate (2x500 mL) and the organic layers combined. The resulting mixture was washed with brine (2x500 mL), dried over anhydrous sodium sulfate and concentrated under vacuum. The residue was applied onto a silica gel column with ethyl acetate/petroleum ether (1 : 1). This resulted in 3.7 g (70%) of [ [Z-hy droxy imino)( [3 - [(2 -methy lpropane-2 - sulfinyl)amino]cyclobutyl])methyl]carbamoyl]methyl acetate as a yellow solid. LC-MS

[M+H] ⁺ = 334. [0410] Step 5: (3-[3-[(2-methylpropane-2-sulfinyl)amino]cyclobutyl]-l,2,4-o xadiazol-5- yl)methyl acetate: into a 50-mL round-bottom flask, was placed a solution of [[(Z)- (hydroxyimino)([3-[(2-methylpropane-2-sulfinyl)amino]cyclobu tyl])methyl]carbamoyl]methyl acetate (3.2 g, 9.60 mmol, 1.00 eq.) in DMF (20 mL). The resulting solution was stirred for 2 hours at 100 °C. The mixture was concentrate and the crude product was purified by Flash- Prep-HPLC with the following conditions (IntelFlash-1): Column, C18; mobile phase, X: H20 Y:ACN=80/20 increasing to X:H ₂ 0 Y:ACN=20/80 within 20 min; Detector, UV 220 nm. This resulted in 1.2 g (40%) of (3-[3-[(2-methylpropane-2-sulfinyl)amino]cyclobutyl]-l,2,4- oxadiazol-5-yl)methyl acetate as a yellow solid. LC-MS [M+Hf = 332.

[0411] Step 6: [3-(3-aminocyclobutyl)-l,2,4-oxadiazol-5-yl]methyl acetate: into a 100- mL 3-necked round-bottom flask, was placed a solution of (3-[3-[(2-methylpropane-2- sulfinyl)amino]cyclobutyl]-l,2,4-oxadiazol-5-yl)methyl acetate (1.2 g, 3.80 mmol, 1.00 eq.) in ethyl acetate (50 mL). To the above solution, the HC1 gas was introduced.

[0412] The resulting solution was stirred for 2 hours at 25 °C. The resulting mixture was concentrated under vacuum. This resulted in 1.1 g (crude) of [3-(3-aminocyclobutyl)-l,2,4- oxadiazol-5-yl]methyl acetate as yellow oil. LC-MS: (M+H) ⁺ = 212. [0413] Step 7: [3-[3-(3-phenyl-l,2-oxazole-5-amido)cyclobutyl]-l,2,4-oxadia zol-5- yljmethyl acetate: into a 100-mL round-bottom flask, was placed a solution of [3-(3- aminocyclobutyl)-l,2,4-oxadiazol-5-yl]methyl acetate (1.1 g, 5.21 mmol, 1.00 eq.) in dichloromethane (50 mL). To the solution were added DIEA (2.02 g, 15.63 mmol, 3.00 eq.), HCTU (3.25 g, 7.80 mmol, 1.50 eq.) and 3-phenyl-l,2-oxazole-5-carboxylic acid (1.18 g, 6.24 mmol, 1.20 eq.). The resulting solution was stirred for 2 hours at 25 °C. The resulting solution was diluted with 150 mL of FLO, extracted with ethyl acetate (2x150 mL) and the organic layers combined. The resulting mixture was washed with brine (2x200 mL), dried over anhydrous sodium sulfate and concentrated under vacuum to give 1.5 g (crude) of [3-[3-(3- phenyl-l,2-oxazole-5-amido)cyclobutyl]-l,2,4-oxadiazol-5-yl] methyl acetate as yellow oil. LC-MS [M+H] ⁺ = 383.

[0414] Step 8: into a 50-mL round-bottom flask, was placed a solution of [3-[3-(3-phenyl- l,2-oxazole-5-amido)cyclobutyl]-l,2,4-oxadiazol-5-yl]methyl acetate (1.5 g, 3.92 mmol, 1.00 eq.) in tetrahydrofuran/H ₂ 0 (12/4 mL). To the solution was added LiOH (480 mg, 20.04 mmol, 5.00 eq.) and the resulting solution was stirred for 1 hour at 25 °C. The solution was diluted with 100 mL of FLO and extracted with ethyl acetate (2x100 mL) and the organic layers combined. The resulting mixture was washed with brine (2x100 mL), dried over anhydrous sodium sulfate and concentrated under vacuum. The residue was applied onto a silica gel column with ethyl acetate/petroleum ether (1 :2). The pure isomers were separated by Prep- SFC with the following conditions (prep SFC 350): Column, Phenomenex Lux 5u Cellulose-3, 5*25cm, 5um; mobile phase, CO ₂ (50%), methanol(50%); Detector, UV 220 nm. This resulted in 26 mg (2%) of 3-phenyl-N-[(tra«5-3-[5-(hydroxymethyl)-l,2,4-oxadiazol-3-y l]cyclobutyl]- l,2-oxazole-5-carboxamide (PH-PTS-002-0048-0) as a white solid and 565.1 mg (42%) of 3- phenyl-N-[c«-3-[5-(hydroxymethyl)-l,2,4-oxadiazol-3-yl]cycl obutyl]-l,2-oxazole-5- carboxamide as a white solid. 3-Phenyl-iV-[(ir««s-3-[5-(hydroxymethyl)-l,2,4-oxadiazol-3 -yl]cyclobutyl]-l,2- oxazole-5-carboxamide:

[0415 ] LC-MS : (M+FTf = 341

[0416] Analytical data: ^X H NMR (400MHz, CDC1 ₃ ): δ 7.83-7.81 (m, 2H), 7.54-7.50 (m,

2H), 7.16-7.14 (d, J= 6.8Hz 1H), 6.99 (s, 1H), 5.00-4.90 (m, 3H), 3.75-3.69 (m,

1H), 2.88-2.81 (m, 2H), 2.68-2.60 (m, 2H).

[0417] HPLC purity: 98.4% at 254 nm.

3-Phenyl-7V-[(c s-3-[5-(hydroxymethyl)-l,2,4-oxadiazol-3-yl]cyclobutyl]-l,2- oxazole- 5-carboxamide:

[0418] LC-MS: (M+H) ⁺ = 341 [0419] Analytical data: ^X H NMR (300 MHz, DMSO-i¾): δ 9.26-9.23 (d, J= 9.3 Hz, 1H),

7.95-7.92 (m, 2H), 7.60-7.51 (m, 3H), 7.36 (s, 1H), 5.99-5.95 (t, J= 6.2 Hz, 1H), 4.72-4.70 (d, J= 6.6 Hz, 2H), 4.56-4.45 (m, 1H), 3.45-3.34 (m, 1H), 2.69- 2.60 (m, 2H), 2.50-2.40 (m, 2H).

[0420] HPLC purity: 99.3% at 254 nm.

Example 34: iV-(ir««s-3-((5-((S)-l-hydroxyethyl)-l,3,4-thiadiazol-2- yl)methyl)cyclobutyl)-5-phenylisoxazole-3-carboxamide and iV-(c s-3-((5-((S)-l- hydroxyethyl)-l,3,4-thiadiazol-2-yl)methyl)cyclobutyl)-5-phe nylisoxazole-3- carboxamide

[0421] Tert-butyl (3-(2-hydrazinyl-2-oxoethyl)cyclobutyl)carbamate was prepared by the procedure described in example 5 , step 1.

[0422] Step 1: methyl (S)-2-((tert-butyldimethylsilyl)oxy)propanoate: a solution of methyl (2S)-2-hydroxypropanoate (5 g, 48.03 mmol, 1.00 eq.) and IH-imidazole (4.9 g, 71.98 mmol, 1.50 eq.) in dichloromethane (100 mL) was placed into a 250-mL round-bottom flask. This was followed by the addition of a solution of tert-butyl(chloro)dimethylsilane (8.69 g, 57.66 mmol, 1.20 eq.) in dichloromethane (50 mL) dropwise with stirring at 0°C. The resulting solution was stirred for 2 hours at room temperature. The reaction was then quenched by the addition of 80 mL of water/ice and extracted with dichloromethane (3x50 mL). The resulting mixture was washed with brine (2x100 mL), dried over anhydrous sodium sulfate and concentrated under vacuum. This resulted in 8 g (76%) of methyl (2S)-2-[(tert- butyldimethylsilyl)oxy]propanoate as a colorless liquid.

[0423] Step 2: lithio (2S)-2-[(tert-butyldimethylsilyl)oxy]propanoate: a solution of methyl (2S)-2-[(tert-butyldimethylsilyl)oxy]propanoate (7.2 g, 32.97 mmol, 1.00 eq.) in THF (50 mL) was placed in a 250 mL round bottom flask. This was followed by the addition of a solution of lithium hydroxide (1.67 g, 39.80 mmol, 1.20 eq.) in H ₂ 0 (30 mL) dropwise with stirring. The resulting solution was stirred for 4 hours at room temperature. The resulting mixture was concentrated under vacuum. This resulted in 5.9 g (85%) of lithio (2S)-2-[(tert- butyldimethylsilyl)oxy]propanoate as a white solid. [0424] Step 3: tert-butyl 7V-[3-([N-[(2S)-2-[(tert- butyldimethylsilyl)oxy]propanoyl]hydrazinecarbonyl]methyl)cy clobutyl]carbamate: a solution of lithio (2S)-2-[(tert-butyldimethylsilyl)oxy]propanoate (5.9 g, 28.06 mmol, 1.00 eq.), tert-butyl N- [3 -[(hydrazine carbonyl)methyl]cyclobutyl]carbamate (7.51 g, 30.87 mmol, 1.10 eq.) and HATU (16 g, 42.1 1 mmol, 1.50 eq.) in DMF (100 mL)were placed in a 250-mL round- bottom flask. This was followed by the addition of DIEA (10.9 g, 84.34 mmol, 3.00 eq.) dropwise with stirring at 0°C. The resulting solution was stirred for 4 hours at room

temperature. The reaction was then quenched by the addition of 100 mL of water/ice and extracted with ethyl acetate (3x100 mL) and the organic layers combined. The resulting mixture was washed with brine (3x80 mL), dried over anhydrous sodium sulfate and concentrated under vacuum. The residue was applied onto a silica gel column with ethyl acetate/hexane (1 : 1). This resulted in 4.4 g (36%) of tert-butyl N-[3-([N-[(2S)-2-[(tert- butyldimethylsilyl)oxy]propanoyl]hydrazinecarbonyl]methyl)cy clobutyl]carbamate as off- white solid. [0425] LC-MS: (M+H) ⁺ = 430.

[0426] Step 4: tert-butyl 7V-[3-([5-[(lS)-l-[(tert-butyldimethylsilyl)oxy]ethyl]-l,3,4 - thiadiazol-2-yl]methyl)cyclobutyl]carbamate:a solution of tert-butyl N-[3-([N-[(2S)-2-[(tert- butyldimethylsilyl)oxy]propanoyl]hydrazinecarbonyl]methyl)cy clobutyl]carbamate (4.4 g, 10.24 mmol, 1.00 eq.) and Lawesson reagent (6.2 g, 15.33 mmol, 1.50 eq.) in toluene (100 mL) were placed in a 250-mL round-bottom flask. The resulting solution was stirred for 2 hours at 80°C in an oil bath. The reaction was then quenched by the addition of 50 mL of water/ice and extracted with ethyl acetate (3x80 mL) and the organic layers combined. The resulting mixture was washed with brine (2x50 mL), dried over anhydrous sodium sulfate and concentrated under vacuum. The residue was applied onto a silica gel column with ethyl acetate/petroleum ether (1 :5). The crude product was purified by Flash-Prep-HPLC with the following conditions (CombiFlash-1): Column, C18 silica gel; mobile phase, H ₂ 0/CH ₃ CN=1 : 1 increasing to H ₂ 0/CH ₃ CN=1 :9 within 30 min; Detector, UV 210 nm. This resulted in 2.1 g (48%) of tert- butyl N-[3-([5-[(l S)-l-[(tert-butyldimethylsilyl)oxy]ethyl]-l,3,4-thiadiazol-2 - yl]methyl)cyclobutyl]carbamate as colorless oil. LC-MS: (M+H) ⁺ = 428. [0427] Step 5: (lS)-l-[5-[(3-aminocyclobutyl)methyl]-l,3,4-thiadiazol-2-yl] ethan-l-ol hydrochloride: a solution of tert-butyl N-[3-([5-[(lS)-l-[(tert-butyldimethylsilyl)oxy]ethyl]- l,3,4-thiadiazol-2-yl]methyl)cyclobutyl]carbamate (2.1 g, 4.91 mmol, 1.00 eq.) in THF (50 niL) was placed in a 100-mL round-bottom flask. To the mixture was added concentrated hydrogen chloride aqueous (5 mL). The resulting solution was stirred for 3 hours at room temperature. The resulting mixture was concentrated under vacuum. This resulted in 1.2 g (crude) of (lS)-l-[5-[(3-aminocyclobutyl)methyl]-l,3,4-thiadiazol-2-yl] ethan-l-ol

hydrochloride as a colorless crude oil. LC-MS: (M+H) ⁺ = 214.

[0428] Step 6: (lS)-l-(5-[[3-(5-phenyl-l,2-oxazole-3-amido)cyclobutyl]methy l]-l,3,4- thiadiazol-2-yl)ethyl 5-phenyl-l,2-oxazole-3-carboxylate: a solution of (lS)-l-[5-[(3- aminocyclobutyl)methyl]-l,3,4-thiadiazol-2-yl]ethan-l-ol hydrochloride (1.2 g, 4.80 mmol, 1.00 eq.), 5-phenyl-l,2-oxazole-3-carboxylic acid (2.36 g, 12.48 mmol, 2.60 eq.) and HCTU (6.0 g, 14.50 mmol, 3.00 eq.) in dichloromethane (50 mL) was placed in a 100-mL round- bottom flask. This was followed by the addition of DIEA (3.1 g, 23.99 mmol, 5.00 eq.) dropwise with stirring at 0°C. The resulting solution was stirred for 4 hours at room

temperature. The reaction was then quenched by the addition of 50 mL of water/ice and extracted with dichloromethane (3x50 mL) and the organic layers combined. The resulting mixture was washed with brine (3x30 mL), dried over anhydrous sodium sulfate and concentrated under vacuum. The residue was applied onto a silica gel column with ethyl acetate/petroleum ether (2: 1). This resulted in 2.1 g (79%) of (lS)-l-(5-[[3-(5-phenyl-l,2- oxazole-3-amido)cyclobutyl]methyl]-l,3,4-thiadiazol-2-yl)eth yl 5-phenyl-l,2-oxazole-3- carboxylate as a off-white solid. LC-MS: (M+H) ⁺ = 556.

[0429] Step 7: 5-phenyl-iV-[(ir««s/c/s-3-([5-[(lS)-l-hydroxyethyl]-l,3,4- thiadiazol-2- yl]methyl)cyclobutyl]-l,2-oxazole-3-carboxamide: a solution of (lS)-l-(5-[[3-(5-phenyl-l,2- oxazole-3-amido)cyclobutyl]methyl]-l,3,4-thiadiazol-2-yl)eth yl 5-phenyl-l,2-oxazole-3- carboxylate (2.1 g, 3.78 mmol, 1.00 eq.) in THF (50 mL) was placed in a 100-mL round- bottom flask. To the solution was added a solution of lithium hydroxide (175 mg, 4.17 mmol, 1.10 eq.) in H ₂ O (5 mL). The resulting solution was stirred for 30 min at room temperature. The resulting solution was diluted with 50 mL of FLO and extracted with ethyl acetate (3x50 mL) and the organic layers combined. The resulting mixture was washed with brine (2x30 mL), dried over anhydrous sodium sulfate and concentrated under vacuum. The isomers were separated by Prep-SFC with the following conditions (prep SFC 350-2): Column, Phenomenex Lux 5u Cellulose-4 AXIA Packed, 250*21.2mm,5um; mobile phase, CO ₂ (50%), ethanol(50%); Detector, UV 220nm. This resulted in 318.3 mg (22%) of 5-phenyl-N-[(?raws-3-([5-[(lS)-l- hydroxyethyl]-l,3,4-thiadiazol-2-yl]methyl)cyclobutyl]-l,2-o xazole-3-carboxamide as a off- white solid and 511.3 mg (39%) of 5-phenyl-N-[c«-3-([5-[(lS)-l-hydroxyethyl]-l,3,4- thiadiazol-2-yl]methyl)cyclobutyl]-l,2-oxazole-3-carboxamide ) as a off-white solid.

[0430] 5-phenyl-7V-[(ir««s-3-([5-[(lS)-l-hydroxyethyl]-l,3,4-thia diazol-2- yl]methyl)cyclobutyl]-l,2-oxazole-3-carboxamide:

[0431] LC-MS: (M+H) ⁺ = 385

[0432] Analytical data: ^X H-NMR (300MHz, DMSO-i¾): 9.14-9.12 (d, J= 7.5 Hz, 1H),

7.95-7.92 (m, 2H), 7.60-7.53 (m, 3H), 6.24 (s, 1H), 5.09-5.02 (q, J= 6.6 Hz, 1H), 4.62-4.54 (m, 1H), 3.29-3.26 (d, J= 7.8 Hz, 2H), 2.69-2.59 (m, 1H), 2.38- 2.28 (m, 2H), 2.17-2.09 (m, 2H), 1.49-1.47 (d, J= 6.6 Hz, 3H).

[0433] HPLC purity: 99.4% at 254 nm

[0434] 5-phenyl-7V-[(c s-3-([5-[(lS)-l-hydroxyethyl]-l,3,4-thiadiazol-2- yl]methyl)cyclobutyl]-l,2-oxazole-3-carboxamide:

[0435] Analytical data: ^X H-NMR (300MHz, DMSO-i¾): δ 9.05-9.03 (d, J= 8.1 Hz, 1H),

7.95-7.92 (m, 2H), 7.58-7.55 (m, 3H), 7.35 (s, 1H), 6.25 (s, 1H), 5.08-5.02 (q, J = 6.6 Hz, 1H), 4.38-4.30 (m, 1H), 3.18-3.16 (d, J= 7.2 Hz, 2H), 2.52-2.32 (m, 3H), 2.00-1.94 (m, 2H), 1.49-1.47 (d, J= 6.6 Hz, 3H).

Example 35: 5-phenyl-iV-[(ir««s-3-([5-[(lR)-l-hydrox ethyl]-l,3,4-thiadiazol-2- yl]methyl)cyclobutyl]-l,2-oxazole-3-carboxamide and 5-phenyWV-[(c s-3-([5-[(lR)-l- hydroxyethyl]-l,3,4-thiadiazol-2-yl]methyl)cyclobutyl]-l,2-o xazole-3-carboxamide

[0436] Compounds were prepared using the methodology shown in example 34 using methyl (R)-2-hydroxypropanoate in step 1. 5-phenyl-iV-[(ir««s-3-([5-[(lR)-l-hydroxyethyl]-l,3,4-thia diazol-2- yl] methyl)cy clobutyl] -1 ,2-oxazole-3-carb oxamide :

[0437] LC-MS: (M+H) ⁺ = 385

[0438] Analytical data: ^X H NMR (300MHz, OMSO-d ₆ ): δ 9.14-9.12 (d, J

7.95-7.92 (m, 2H), 7.60-7.54 (m, 3H), 7.36 (s, 1H), 6.25-6.24 (d, J= 3.9 Hz, 1H), 5.07-5.04 (m, 1H), 4.62-4.54 (m, 1H), 3.29-3.26 (d, J = 7.8 Hz, 2H), 2.65- 2.58 (m, 1H), 2.38-2.28 (m, 2H), 2.17-2.10 (m, 2H), 1.49-1.47 (d, J= 6.6 Hz, 3H).

[0439] HPLC purity: 98.8% at 254 nm.

5-phenyl-7V-[(c s-3-([5-[(lR)-l-hydroxyethyl]-l,3,4-thiadiazol-2- yl] methyl)cy clobutyl] -1 ,2-oxazole-3-carb oxamide :

[0440] LC-MS : (M+H) ⁺ = 385

[0441] Analytical data: ^X H NMR (300MHz, DMSO-i¾): 9.05-9.03 (d, J

7.95-7.92 (m, 2H), 7.60-7.51 (m, 3H), 7.35 (s, 1H), 6.25-6.24 (d, J= 5.1 Hz, 1H), 5.09-5.01 (m, 1H), 4.38-4.27 (m, 1H), 3.18-3.16 (d, J= 6.9 Hz, 2H), 2.52- 2.30 (m, 3H), 2.00-1.94 (m, 2H), 1.49-1.47 (d, J= 6.6 Hz, 3H).

[0442] HPLC purity: 99.74% at 254 nm.

Example 36: 7V-ir«ws-3-(2-hydroxyethyl)cyclobutyl)-5-phenylisoxazole-3- carboxamide and iV-c/s-3-(2-hydroxyethyl)cyclobutyl)-5-phenylisoxazole-3- carboxamide

H

[0443] Step 1: 2-(3-aminocyclobutyl)ethan-l-ol hydrochloride: a solution of ethyl 2-(3 aminocyclobutyl)acetate hydrochloride (2.5 g, 12.91 mmol, 1.00 eq.) in tetrahydrofuran (10 mL) was placed in a 100-mL round-bottom flask. This was followed by the addition of L1AIH ₄ (2.4 g, 63.24 mmol, 4.90 eq.) in several batches at 0°C. The resulting solution was stirred for 1 hour at room temperature. The reaction was then quenched by the addition of 2 g of

Na ₂ S0 ₄ .H ₂ 0. The solids were filtered out. The resulting mixture was concentrated under vacuum. This resulted in 1.8 g (crude) of 2-(3-aminocyclobutyl)ethan-l-ol hydrochloride as a yellow solid. LC-MS: (M+H) ⁺ = 152.

[0444] Step 2: 7V-[3-(2-hydroxyethyl)cyclobutyl]-5-phenyl-l,2-oxazole-3-car boxamide: a solution of 5-phenyl-l,2-oxazole-3-carboxylic acid (850.5 mg, 4.50 mmol, 1.51 eq.) and 2-(3- aminocyclobutyl)ethan-l-ol hydrochloride (452 mg, 2.98 mmol, 1.00 eq.) in dichloromethane (25 mL)was placed in a 100-mL round-bottom flask. HATU (1.368 g, 3.60 mmol, 1.21 eq.) and DIEA (1.161 g, 8.98 mmol, 3.01 eq.) were added to the solution and stirred for 1 hour at room temperature. The resulting solution was diluted with 50 mL of water, extracted with chloromethane (3x30 mL) and the organic layers combined. The resulting mixture was dried over anhydrous sodium sulfate and concentrated under vacuum. The crude product was purified by Flash-Prep-HPLC with the following conditions (CombiFlash-1): Column, C18 silica gel; mobile phase, MeCN/H ₂ 0=55:45 increasing to MeCN/H ₂ O=60:40 within 2 min; Detector, UV 254 nm to give 110 mg (13%) of N-[3-(2-hydroxyethyl)cyclobutyl]-5-phenyl- l,2-oxazole-3-carboxamide as a off-white solid. The isomers were separated by Chiral-Prep- HPLC using the following conditions (Prep-HPLC-009): Column, Repaired IA, 21.2* 150mm, 5um; mobile phase, Hexane and ethanol (hold 20.0% ethanol in 20 min); Detector, UV 254/220 nm. This resulted in 23.8 mg (60%) of 5-phenyl-N-[?ra«s-3-(2-hydroxyethyl)cyclobutyl]-l,2- oxazole-3-carboxamide as a white solid and 35.7 mg (70%) of 5-phenyl-N-[c/s-3-(2- hydroxyethyl)cyclobutyl]-l,2-oxazole-3-carboxamide as a white solid.

[0445] 7V-ir««s-3-(2-hydroxyethyl)cyclobutyl)-5-phenylisoxazole-3 -carboxamide: [0446] LC-MS: (M+H) ⁺ = 287

[0447] Analytical data: 1H NMR (CDC1 ₃ , 400MHz): δ 7.83-7.81 (m, 2H), 7.54-7.49 (m,

3H), 7.05-7.02 (m, 1H), 6.97 (s, 1H), 4.72-4.67 (m, 1H), 3.73-3.68 (t, J= 10.0Hz, 2H), 2.49-2.41 (m, 1H), 2.26-2.21 (m, 4H), 1.87-1.81 (m, 2H).

[0448] HPLC purity: 99.4% at 254 nm. 7V-c s-3-(2-hydroxyethyl)cyclobutyl)-5-phenylisoxazole-3-carboxam ide: [0449] LC-MS: (M+H) ⁺ = 287

[0450] Analytical data: ^X H NMR (CDC1 ₃ , 400MHz): 7.83-7.80 (m, 2H), 7.54-7.49 (m, 3H),

7.02-6.93 (m, 3H), 4.50-4.44 (m, 1H), 3.67-3.63 (t, J= 8.0Hz, 2H), 2.68-2.62 (m, 2H), 2.22-2.13 (m, 1H), 1.76-1.66 (m, 4H). [0451 ] HPLC purity: 99.0% at 254 nm.

Example 37: 7V-(c s-3-(methylsulfonamidomethyl)cyclobutyl)-5-phenylisoxazole-3 - carboxamide

[0452] Step 1: 7V-(c s-3-cyanocyclobutyl)-2-methylpropane-2-sulfmamide: a solution of 3-oxocyclobutane-l-carbonitrile (3.9 g, 41.01 mmol, 1.00 eq.) and 2-methylpropane-2- sulfinamide (4.97 g, 41.01 mmol, 1.00 eq.) in tetrahydrofuran (100 mL) was placed in a 250- mL 3 -necked round-bottom flask and stirred for 16 hours at 70°C. After cooled to room temperature, NaBH ₄ (780 mg, 20.53 mmol, 0.50 eq.) was added in portions and stirred for 30 min at room temperature. The reaction was then quenched by the addition of water. The resulting solution was extracted with ethyl acetate and the organic layers combined. The resulting mixture was washed with brine, dried over anhydrous sodium sulfate and

concentrated under vacuum. This resulted in 7.5 g (91%) of N-(cz ^' s-3-cyanocyclobutyl)-2- methylpropane-2-sulfinamide as a yellow solid. LC-MS: (M+H) ⁺ = 201.

[0453] Step 2: c/s-3-aminocyclobutanecarbonitrile hydrochloride: a solution of N-(cis- 3-cyanocyclobutyl)-2-methylpropane-2-sulfinamide (1 g, 4.99 mmol, 1.00 eq.) in

tetrahydrofuran (15 mL) was placed in a 100-mL round-bottom flask and concentrated hydrogen chloride (lmL) was added. The resulting solution was stirred for 1 hour at room temperature and then concentrated under vacuum. This resulted in 440 mg (crude) of cis-3- aminocyclobutanecarbonitrile hydrochloride as a yellow solid.

[0454] Step 3: 7V-(c s-3-cyanocyclobutyl)-5-phenylisoxazole-3-carboxamide: 3- aminocyclobutanecarbonitrile hydrochloride (440 mg, 4.58 mmol, 1.00 eq.), 5-phenyl-l,2- oxazole-3-carboxylic acid (866 mg, 4.58 mmol, 1.00 eq.) and HATU (2090 mg, 5.50 mmol, 1.20 eq.) in dichloromethane (18 mL) were placed in a 100-mL round-bottom flask. To the mixture was added DIEA (1773 mg, 13.72 mmol, 3.00 eq.) and the mixture was stirred for 2 hours at room temperature. The reaction was then quenched by the addition of water. The resulting solution was extracted with ethyl acetate and the organic layers combined. The resulting mixture was washed with brine, dried over anhydrous sodium sulfate and

concentrated under vacuum. The residue was applied onto a silica gel column with ethyl acetate/petroleum ether (1 :3) to give 600 mg (49%) of N-(cz ^' s-3-cyanocyclobutyl)-5- phenylisoxazole-3-carboxamide as a white solid. LC-MS: (M+H) ⁺ = 268. [0455] Step 4: 5-phenyl-7V-[c s-3-(aminomethyl)cyclobutyl]-l,2-oxazole-3- carboxamide: a solution of N-(czs-3-cyanocyclobutyl)-5-phenylisoxazole-3-carboxamide (400 mg, 1.50 mmol, 1.00 eq.) and ammonia (0.1 mL) in methanol (10 mL) was placed in a 50-mL round-bottom flask and Raney (40 mg) was added. The mixture was hydrogenated for 6 hours at 35°C. The solids were filtered out. The resulting mixture was concentrated under vacuum. This resulted in 180 mg (crude) of 5-phenyl-N-[c«-3-(aminomethyl)cyclobutyl]-l,2- oxazole-3-carboxamide as yellow green oil. LC-MS: (M+H) = 272.

[0456] Step 5: 5-phenyl-7V-[c s-3-(methanesulfonamidomethyl)cyclobutyl]-l,2-oxazole- 3-carboxamide: a solution of 5-phenyl-N-[c«-3-(aminomethyl)cyclobutyl]-l,2-oxazole-3- carboxamide (120 mg, 0.44 mmol, 1.00 eq.) and triethylamine (89 mg, 0.88 mmol, 2.00 eq.) in dichloromethane (3 mL) was placed in a 25 -mL round-bottom flask and methanesulfonyl chloride (55 mg, 0.48 mmol, 1.10 eq.) was added. The resulting solution was stirred for 10 min at room temperature. The reaction was then quenched by the addition of water and extracted with ethyl acetate and the organic layers combined. The resulting mixture was washed with brine, dried over anhydrous sodium sulfate and concentrated under vacuum. The residue was applied onto a silica gel column with ethyl acetate/petroleum ether (1 :2) to give 45.5 mg (29%) of 5-phenyl-N-[cw-3-(methanesulfonamidomethyl)cyclobutyl]-l,2-o xazole-3-carboxamide as a white solid.

[0457] LC-MS: (M+H) ⁺ = 350

[0458] Analytical data: ^X H NMR (300MHz, OMSO-d ₆ , ppm): δ 9.02-8.99 (d, J= 7.8 Hz,

1H), 7.94-7.92 (m, 2H), 7.57-7.55 (m, 3H), 7.34 (s, 1H), 7.00-6.96 (t, J= 5.7 Hz, 1H), 4.35-4.27 (m, 1H), 3.00-2.96 (m, 2H) , 2.91-2.89 (m, 3H), 2.38-2.30 (m, 2H), 2.18-2.08 (m, 1H), 1.90-1.80 (m, 2H).

[0459] HPLC purity: 97.44% at 254 nm.

Example 38: iV-(ir««s-3-(3-((S)-l-hydroxyethyl)-l,2,4-oxadiazol-5-yl)c yclobutyl)-5- phenylisoxazole-3-carboxamide and 7V-(ir««s-3-(3-((R)-l-hydroxyethyl)-l,2,4- oxadiazol-5-yl)cyclobutyl)-5-phenylisoxazole-3-carboxamide

[0460] The compounds were prepared using a similar procedure as shown in example 32 using (E)-2-[(tert-butyldimethylsilyl)oxy]-N-hydroxypropimidamide as the starting material in step 3.

Preparation of (E)-2-((tert-butyldimethylsilyl)oxy)-iV-hydroxypropanimidami de:

[0461] Step A: 2-[(tert-butyldimethylsilyl)oxy]propanenitrile: tert- butyl(chloro)dimethylsilane (6.3 g, 41.80 mmol, 1.50 eq.), imidazole (2.87 g, 42.16 mmol, 1.50 eq.) and 4-dimethylaminopyridine (400 mg, 3.27 mmol, 0.10 eq.) were added to a solution of 2- hydroxypropanenitrile (2 g, 28.14 mmol, 1.00 eq.) in dichloromethane (100 mL). The resulting solution was stirred for 3 hours at room temperature. The reaction was then quenched by the addition of water, extracted with ethyl acetate (3x50 mL) and the combined organic layers were dried over anhydrous sodium sulfate and concentrated under vacuum to give 4 g (crude) of 2- [(tert-butyldimethylsilyl)oxy]propanenitrile as colorless oil. [0462] Step B: (E)-2-[(tert-butyldimethylsilyl)oxy]-N-hydroxypropimidamide:

hydroxylamine hydrochloride (225 mg, 3.24 mmol, 2.00 eq.) and sodium methoxide (390 mg, 4.64 mmol, 3.00 eq.) was added to a solution of 2-[(tert-butyldimethylsilyl)oxy]propanenitrile (3 g, 16.19 mmol, 1.00 eq.) in methanol (100 mL). The resulting solution was stirred overnight at 70°C in an oil bath. The reaction was then quenched by the addition of water. The resulting solution was extracted with ethyl acetate (3x50 mL) and the combined organic layers were dried over anhydrous sodium sulfate and concentrated under vacuum. The residue was applied onto a silica gel column with ethyl acetate/petroleum ether (1 :2). This resulted in 2.4 g (68%) of (E)-2-[(tert-butyldimethylsilyl)oxy]-N-hydroxypropimidamide as a yellow solid. LC-MS: (M+H) ⁺ = 219. [0463] Stepl: 5-phenyl-7V-[c s-3-(3-[l-[(tert-butyldimethylsUyl)oxy]ethyl]-l,2,4- oxadiazol-5-yl)cyclobutyl]-l,2-oxazole-3-carboxamide and 5-phenyl-iV-[ir««s-3-(3-[l- [(tert-butyldimethylsilyl)oxy]ethyl]-l,2,4-oxadiazol-5-yl)cy clobutyl]-l,2-oxazole-3- carboxamide: to a solution of 3-(3-[l-[(tert-butyldimethylsilyl)oxy]ethyl]-l,2,4-oxadiazol -5- yl)cyclobutan-l -amine (1.5 g, 5.04 mmol, 1.00 eq.) in dichloromethane (100 mL)was added 5- phenyl- l,2-oxazole-3-carboxylic acid (1.13 g, 5.97 mmol, 1.20 eq.), HATU (2.28 g, 6.00 mmol, 1.20 eq.) and DIEA (1.93 g, 14.93 mmol, 3.00 eq.). The resulting solution was stirred for 1 hour at room temperature. The reaction was then quenched by the addition of water and extracted with ethyl acetate (3x50 mL) and the combined organic layers were dried over anhydrous sodium sulfate and concentrated under vacuum. The residue was applied onto a silica gel column with ethyl acetate/petroleum ether (1 :50)to give 300 mg (13%) of 5-phenyl- N-[c«-3-(3-[l-[(tert-butyldimethylsilyl)oxy]ethyl]-l,2,4-ox adiazol-5-yl)cyclobutyl]-l,2- oxazole-3-carboxamide as a white solid. The solvent was changed to a mixture of with ethyl acetate/petroleum ether (1 :20) to give 1.4 g (59%) of 5-phenyl-N-[?raws-3-(3-[l-[(tert- butyldimethylsilyl)oxy]ethyl]-l,2,4-oxadiazol-5-yl)cyclobuty l]-l,2-oxazole-3-carboxamide as a white solid. LC-MS: (M+H) ⁺ = 469. [0464] Step 2a: iV-(ir««s-3-(3-((S)-l-hydroxyethyl)-l,2,4-oxadiazol-5-yl)c yclobutyl)-5- phenylisoxazole-3-carboxamide and 7V-(ir««s-3-(3-((R)-l-hydroxyethyl)-l,2,4-oxadiazol-5- yl)cyclobutyl)-5-phenylisoxazole-3-carboxamide:

[0465] 5M hydrogen chloride (15 rnL) was added dropwise to a solution of 5-phenyl-N- [?ra«s-3-(3-[l-[(tert-butyldimethylsilyl)oxy]ethyl]-l,2,4-o xadiazol-5-yl)cyclobutyl]-l,2- oxazole-3-carboxamide (1.4 g, 2.99 mmol, 1.00 eq.) in methanol (30 mL). The resulting solution was stirred for 1 hour at room temperature. The reaction was then quenched by the addition of water. The resulting solution was extracted with dichloromethane (3x50 mL) and the combined organic layers were dried over anhydrous sodium sulfate and concentrated under vacuum. The residue was applied onto a silica gel column with ethyl acetate/petroleum ether (1: 1) to give 1.05 g (99%) of 5-phenyl-N-[?ra«s-3-[3-(l-hydroxyethyl)-l,2,4-oxadiazol-5- yl]cyclobutyl]-l,2-oxazole-3-carboxamide as a white solid.

[0466] Step 3a: SFC separation: the pure isomers were separated by Prep-SFC with the following conditions (prep SFC 350): Column, Chiralpak IA SFC, 5*25cm; mobile phase, CO ₂ (50%), ACN/MeOH=l/l(50%); Detector, UV: 220nm. This resulted in:

[0467] Isomer I: 455 mg (41%) as a white solid

[0468] Analytical data: ^X H NMR (400MHz, DMSO-i¾): δ 9.33-9.31 (d, J= 7.6 Hz, 1H),

7.95-7.93 (m, 2H), 7.59-7.52 (m, 3H), 7.38 (s, 1H), 5.72-5.71 (d, J= 5.6 Hz, 1H), 4.87-4.82 (m, 1H), 4.80-4.71 (m,lH), 3.80-3.74 (m, 1H), 2.76-2.71 (m, 2H), 2.68-2.60 (m, 2H).

[0469] HPLC purity: 99.35 at 254 nm.

[0470] Isomer II: 549 mg (50%) as a white solid [0471] Analytical data: ^X H NMR (400MHz, DMSO-i¾): δ 9.33-9.31 (d, J= 7.6 Hz, 1H), 7.95-7.93 (m, 2H), 7.59-7.52 (m, 3H), 7.38 (s, 1H), 5.72-5.71 (d, J= 5.6 Hz, 1H), 4.86-4.81 (m, 1H), 4.80-4.71 (m,lH), 3.80-3.74 (m, 1H), 2.76-2.71 (m, 2H), 2.68-2.60 (m, 2H). [0472] HPLC purity: 99.5% at 254 nm.

Step 2b : 7V-(c s-3-(3-((S)-l-hydroxyethyl)-l,2,4-oxadiazol-5-yl)cyclobutyl) -5- phenylisoxazole-3-carboxamide and 7V-(c s-3-(3-((R)-l-hydroxyethyl)-l,2,4-oxadiazol- 5-yl)cyclobutyl)-5-phenylisoxazole-3-carboxamide:

[0473] Step 2b: 5M hydrogen chloride (5 rnL) was added dropwise to a solution of 5- phenyl-N-[c«-3-(3-[l-[(tert-butyldimethylsilyl)oxy]ethyl]-l ,2,4-oxadiazol-5-yl)cyclobutyl]- l,2-oxazole-3-carboxamide (300 mg, 0.64 mmol, 1.00 eq.) in methanol (20 mL). The resulting solution was stirred for 1 hour at room temperature and then quenched by the addition of water. The resulting solution was extracted with dichloromethane (3x20 mL) and the combined organic layers were dried over anhydrous sodium sulfate and concentrated under vacuum to give 140 mg (62%) of 5-phenyl-N-[c«-3-[3-(l-hydroxyethyl)-l,2,4-oxadiazol-5-yl]c yclobutyl]- l,2-oxazole-3-carboxamide as a white solid.

[0474] Step 3b: SFC purification: the pure isomers (140 mg, 0.40 mmol, 1.00 eq.) were separated by Chiral-Prep-HPLC using the following conditions (Prep-HPLC-009): Column, Repaired IA, 21.2* 150mm,5um; mobile phase, hexane and ethanol (hold 20.0% ethanol in 20 min); Detector, UV 254/220 nm to give:

[0475] Isomer I: 52.1 mg as a white solid

[0476] LC-MS: (M+H) ⁺ = 355 [0477] Analytical data: ^X H NMR (400MHz, DMSO-i¾): δ 9.28-9.26 (d, J

7.94-7.91 (m, 2H), 7.58-7.53 (m, 3H), 7.36 (s, 1H), 5.68-5.66 (d, J= 5.6 Hz, 1H), 4.84-4.78 (m, 1H), 4.58-4.52 (m, lH), 3.59-3.54 (m, 1H), 2.76-2.71 (m, 2H), 2.68-2.60 (m, 2H), 1.42-1.40 (d, J= 14.8Hz, 3H).

[0478] HPLC purity: 97.9% at 254% nm

[0479] Isomer II: 49.7 mg (36%) as a white solid.

[0480] LC-MS: (M+H) ⁺ = 355

Example 39: 5-phenyl-iV-[ir««s-3-([5-[(lR)-l-hydroxyethyl]-l,3,4-oxadi azol-2- yl]methyl)cyclobutyl]-l,2-oxazole-3-carboxamide and 5-phenyWV-[c s-3-([5-[(lR)-l- hydroxyethyl]-l,3,4-oxadiazol-2-yl]methyl)cyclobutyl]-l,2-ox azole-3-carboxamide

[0481 ] tert-butyl (R)-(3-(2-(2-(2-((tert-butyldimethylsilyl)oxy)propanoyl)hydr azinyl)-2- oxoethyl)cyclobutyl)carbamate was prepared following the procedure shown in example 34 (steps 1-3) using lithium (R)-2-((tert-butyldimethylsilyl)oxy)propanoate as the starting material. [0482] Step 1: tert-butyl 7V-[3-([5-[(lR)-l-[(tert-butyldimethylsilyl)oxy]ethyl]-l,3,4 - oxadiazol-2-yl]methyl)cyclobutyl] carbamate: TEA (7 g, 69.18 mmol, 4.00 eq.) was added dropwise to a solution of tert-butyl N-[3-([N-[(2R)-2-[(tert- butyldimethylsilyl)oxy]propanoyl]hydrazinecarbonyl] methyl)cyclobutyl]carbamate (7.4 g, 17.22 mmol, 1.00 eq.) and 4-methylbenzene-l-sulfonyl chloride (9.85 g, 51.67 mmol, 3.00 eq.) in dichloromethane (100 mL). The resulting solution was stirred for 24 hours at room temperature. The reaction was then quenched by the addition of 100 mL of water/ice. The resulting solution was extracted with dichloromethane (3x100 mL) and the organic layers combined. The resulting mixture was washed with brine (2x50 mL), dried over anhydrous sodium sulfate and concentrated under vacuum. The residue was applied onto a silica gel column with ethyl acetate/petroleum ether (1 :5) to give 4.3 g (61%) of tert-butyl N-[3-([5- [(lR)-l-[(tert-butyldimethylsilyl)oxy]ethyl]-l,3,4-oxadiazol -2-yl]methyl)cyclobutyl]carbamate as colorless oil. LC-MS: (M+H) ⁺ = 412. [0483] Step 2: [3-([5-[(lR)-l-[(tert-butyldimethylsilyl)oxy]ethyl]-l,3,4-ox adiazol-2- yl]methyl)cyclobutyl] amino 2,2,2-trifluoroacetate : trifluoroacetic acid (8 mL) was added to a solution of tert-butyl N-[3-([5-[(lR)-l-[(tert-butyldimethylsilyl)oxy]ethyl]-l,3,4- oxadiazol-2- yl]methyl)cyclobutyl]carbamate (3.2 g, 7.77 mmol, 1.00 eq.) in dichloromethane (50 mL). The resulting solution was stirred for 16 hours at room temperature and then concentrated under vacuum to give 3.2 g (97%) of [3-([5-[(lR)-l-[(tert-butyldimethylsilyl)oxy]ethyl]-l,3,4- oxadiazol-2-yl]methyl)cyclobutyl]amino 2,2,2-trifluoroacetate as colorless crude oil. LC-MS: (M+H) ⁺ = 312.

[0484] Step 3: 7V-[3-([5-[(lR)-l-[(tert-butyldimethylsilyl)oxy]ethyl]-l,3,4 -oxadiazol-2- yl]methyl)cyclobutyl]-5-phenyl-l,2-oxazole-3-carboxamide: a solution of [3-([5-[(lR)-l- [(tert-butyldimethylsilyl)oxy]ethyl]-l,3,4-oxadiazol-2-yl]me thyl)cyclobutyl]amino 2,2,2- trifluoroacetate (3 g, 7.08 mmol, 1.00 eq.), 5 -phenyl- l,2-oxazole-3-carboxylic acid (2.68 g, 14.17 mmol, 2.00 eq.), HCTU (7.3 g, 17.65 mmol, 2.50 eq.) and DIEA (4.6 g, 35.59 mmol, 5.00 eq.) in dichloromethane (100 mL) was stirred for 3 hours at room temperature. The resulting solution was diluted with 100 mL of water, extracted with dichloromethane (3x100 mL) and the organic layers combined. The resulting mixture was washed with brine (3x50 mL), dried over anhydrous sodium sulfate and concentrated under vacuum. The residue was applied onto a silica gel column with ethyl acetate/petroleum ether (1 : 1) to give 2.7 g (79%) of N-[3-([5-[(lR)-l-[(tert-butyldimethylsilyl)oxy]ethyl]-l,3,4- oxadiazol-2-yl]methyl)cyclobutyl]- 5 -phenyl- l,2-oxazole-3-carboxamide as a white solid. LC-MS: (M+H) ⁺ = 483. [0485] Step 4: 7V-[3-([5-[(lR)-l-hydroxyethyl]-l,3,4-oxadiazol-2-yl]methyl) cyclobutyl]- 5-phenyl-l,2-oxazole-3-carboxamide: TBAF (2 mL) in THF (2 mL) was added to a solution ofN-[3-([5-[(lR)-l-[(tert-butyldimethylsilyl)oxy]ethyl]-l,3, 4-oxadiazol-2- yl]methyl)cyclobutyl]-5-phenyl-l,2-oxazole-3-carboxamide (2.7 g, 5.59 mmol, 1.00 eq.) in THF (20 mL). The resulting solution was stirred for 1 hour at room temperature and then diluted with 50 mL of water. The resulting solution was extracted with dichloromethane (3x50 mL) and the combined organic layers were dried over anhydrous sodium sulfate and concentrated under vacuum. The residue was applied onto a silica gel column with ethyl acetate/petroleum ether (1 : 100). The crude product was purified by Flash-Prep-HPLC with the following conditions (CombiFlash-1): Column, CI 8 silica gel; mobile phase, H ₂ 0/CH ₃ CN=9: 1 increasing to H ₂ 0/CH ₃ CN=1 : 1 within 30 min; Detector, UV 254 nm. This resulted in 1.8 g (88%) ofN-[3-([5-[(lR)-l-hydroxyethyl]-l,3,4-oxadiazol-2-yl]methyl )cyclobutyl]-5-phenyl- l,2-oxazole-3-carboxamide as a off-white solid. LC-MS: (M+FTf = 369. The isomers were separated by Prep-SFC with the following conditions (prep SFC 350-2): Column, Phenomenex Lux, 5u Cellulose-4 AXIA Packed, 250*21.2mm, 5um; mobile phase, CO ₂ (50%),

ethanol(0.2%DEA)(50%); Detector, UV 254 nm. This resulted in 460.2 mg (26%) of 5-phenyl- N-[?ra«s-3-([5-[(lR)-l-hydroxyethyl]-l,3,4-oxadiazol-2-yl]m ethyl)cyclobutyl]-l,2-oxazole-3- carboxamide as a off-white solid and 749.4 mg (42%) of 5-phenyl-N-[cz ^' s-3-([5-[(lR)-l- hydroxyethyl]-l,3,4-oxadiazol-2-yl]methyl)cyclobutyl]-l,2-ox azole-3-carboxamide as a off- white solid.

[0486] 5-phenyl-7V-[ir««s-3-([5-[(lR)-l-hydroxyethyl]-l,3,4-oxadi azol-2- yl]methyl)cyclobutyl]-l,2-oxazole-3-carboxamide:

[0487] Analytical data: ^X H NMR (400MHz, CD ₃ OD): δ 7.90-7.87 (m, 2H), 7.56-7.50 (m, 3H), 7.09 (s, 1H), 5.04-4.99 (q, J= 6.8 Hz, 1H), 4.70-4.63 (m, 1H), 3.17-3.15 (d, J= 8 Hz, 2H), 2.88-2.79 (m, 1H), 2.48-2.41 (m, 2H), 2.35-2.30 (m, 2H), 1.61-1.59 (d, J= 6.68 Hz, 3H).

[0488] HPLC purity: 98.6% at 254 nm.

[0489] 5-phenyl-7V-[c s-3-([5-[(lR)-l-hydroxyethyl]-l,3,4-oxadiazol-2- yl]methyl)cyclobutyl]-l,2-oxazole-3-carboxamide:

[0490] Analytical data: ^X H NMR (400MHz, CD ₃ OD): δ 7.89-7.87 (m, 2H), 7.56-7.50 (m,

3H), 7.08 (s, 1H), 5.04-4.99 (q, J= 6.8 Hz, 1H), 4.49-4.41 (m, 1H), 3.07-3.05 (d, J= 7.2 Hz, 2H), 2.66-2.50 (m, 3H), 2.05-1.96 (m, 2H), 1.61-1.59 (d, J= 6.8 Hz, 3H). [0491] HPLC purity: 100% at 254 nm.

Example 40: Preparation of 7V-((ir««s-3-((5-((S)-l-hydroxyethyl)-l,3,4-oxadiazol-2- yl)methyl)cyclobutyl)-5-phenylisoxazole-3-carboxamide and 7V-((c s-3-((5-((S)-l- hydroxyethyl)-l,3,4-oxadiazol-2-yl)methyl)cyclobutyl)-5-phen ylisoxazole-3- carboxamide

[0492] Compounds were prepared following the procedure shown in example 39, using tert-butyl (S)-(3-(2-(2-(2-((tert-butyldimethylsilyl)oxy)propanoyl)hydr azinyl)-2- oxoethyl)cyclobutyl)carbamate. Final products were purified by Chiral-Prep-HPLC with the following conditions (Prep-HPLC-009): Column, Chiral pak AS-H, 2*25CM; mobile phase, hexane and IPA (hold 35.0% IPA in 22 min); Detector, UV 254/220 nm to give 201.8 mg (47%) of 5-phenyl-N-[/ra«s-3-([5-[(lS)-l-hydroxyethyl]-l,3,4-oxadiaz ol-2- yl]methyl)cyclobutyl]-l,2-oxazole-3-carboxamide as a off-white solid and 81.9 mg (19%) of 5- phenyl-N-[c s-3-([5-[(lS)-l-hydroxyethyl]-l,3,4-oxadiazol-2-yl]methyl)cy clobutyl]-l,2- oxazole-3 -carboxamide as a off-white solid.

7V-((ir«/is-3-((5-((S)-l-hydroxyethyl)-l,3,4-oxadiazol-2 -yl)methyl)cyclobutyl)-5- phenylisoxazole-3-carboxamide:

[0493] LC-MS: (M+H) ⁺ = 369

[0494] Analytical data: ^X H NMR (400MHz, CD ₃ OD): δ 7.90-7.87 (m, 2H), 7.57-7.50 (m,

3H), 7.09 (s, 1H), 5.04-4.99 (q, J= 6.8 Hz, 1H), 4.70-4.63 (m, 1H), 3.17-3.15 (d, J= 8.0 Hz, 2H), 2.88-2.80 (m, 1H), 2.48-2.41 (m, 2H), 2.35-2.29 (m, 2H), 1.61- 1.59 (d, J= 6.8 Hz, 3H).

[0495] HPLC purity: 100% at 254 nm. iV-((c s-3-((5-((S)-l-hydroxyethyl)-l,3,4-oxadiazol-2-yl)methyl)cyc lobutyl)-5- phenylisoxazole-3-carboxamide:

[0496] LC-MS: (M+H) ⁺ = 369

[0497] Analytical data: ^X H NMR (400MHz, CD ₃ OD): δ 7.89-7.87 (m, 2H), 7.56-7.50 (m,

3H), 7.08 (s, 1H), 5.04-4.99 (q, J= 6.8 Hz, 1H), 4.49-4.41 (m, 1H), 3.07-3.05 (d, J= 6.8 Hz, 2H), 2.66-2.50 (m, 3H), 2.03-1.96 (m, 2H), 1.61-1.59 (d, J= 6.8 Hz, 3H).

[0498] HPLC purity: 100% at 254 nm.

Example 41 : iV-(ir««s-3-(5-((R)-l-hydroxyethyl)-l,2,4-oxadiazol-3-yl)c yclobutyl)-5- phenylisoxazole-3-carboxamide

[0499] Step la: 3-hydroxycyclobutane-l-carbonitrile: NaBH ₄ (2.4 g, 63.45 mmol, 0.50 eq.) was added slowly to a -70°C solution of 3-oxocyclobutane-l-carbonitrile (12 g, 126.18 mmol, 1.00 eq., prepared according example 33, step 1) in THF (100 mL) and water (5 mL). The resulting solution was stirred for 1 hour at -70°C in a liquid nitrogen bath. The reaction was then quenched by the addition of 50 mL of water/ice. The resulting solution was extracted with ethyl acetate (3x100 mL) and the organic layers combined. The resulting mixture was washed with brine (3x50 mL), dried over anhydrous sodium sulfate and concentrated under vacuum to give 8.13 g (66%) of 3 -hydroxy cyclobutane- 1 -carbonitrile as colorless oil.

[0500] Step 2a: 3-[(tert-butyldimethylsilyl)oxy]cyclobutane-l-carbonitrile: tert- butyl(chloro)dimethylsilane (15.1 g, 100.18 mmol, 1.20 eq.) in dichloromethane (30 mL)was added dropwise to a 0°C solution of 3 -hydroxycyclobutane-1 -carbonitrile (8.1 g, 83.41 mmol, 1.00 eq.) and lH-imidazole (11.3 g, 165.99 mmol, 2.00 eq.) in dichloromethane (150 mL). T he resulting solution was stirred for 1.5 hours at room temperature. The reaction was then quenched by the addition of 100 mL of water/ice and extracted with dichloromethane (3x100 mL) and the organic layers combined. The resulting mixture was washed with brine (3x80 mL), dried over anhydrous sodium sulfate and concentrated under vacuum to give 16.3 g (92%) of 3-[(tert-butyldimethylsilyl)oxy]cyclobutane-l-carbonitrile as colorless crude oil.

[0501] Step 3a: (E)-3-[(tert-butyldimethylsilyl)oxy]-N-hydroxycyclobut-l- carboximidamide: sodium carbonate (18.49 g, 174.4 mmol, 2.30 eq.) and hydroxylamine hydrochloride (10.54 g, 151.66 mmol, 2.00 eq.) were added to a solution of 3-[(tert- butyldimethylsilyl)oxy]cyclobutane-l-carbonitrile (16 g, 75.83 mmol, 1.00 eq.) in ethanol (150 mL) and water (150 mL). The resulting solution was stirred for 20 hours at 80°C in an oil bath. The resulting solution was diluted with 100 mL of water and extracted with ethyl acetate (3x100 mL) and the organic layers combined. The resulting mixture was washed with brine (2x100 mL), dried over anhydrous sodium sulfate and concentrated under vacuum to give 12.95 g (70%) of (E)-3-[(tert-butyldimethylsilyl)oxy]-N-hydroxycyclobut-l-car boximidamide as a off-white solid. LC-MS: (M+H) ⁺ = 245.

[0502] Step 1: (2R)-2-(benzoyloxy)propanoic acid: benzoyl chloride (28 g, 199.19 mmol, 2.00 eq.) Was added dropwise to a 0 °C solution of (2R)-2-hydroxypropanoic acid (9 g, 99.91 mmol, 1.00 eq.) and sodium hydride (9.6 g, 240.02 mmol, 4.00 eq., 60%) in DMF (100 mL). The resulting solution was stirred for 2 hours at room temperature. The reaction was then quenched by the addition of 100 mL of water/ice. The resulting solution was washed with ethyl acetate (3x100 mL). The pH value of the aqueous layer was adjusted to 4 with hydrogen chloride aqueous (6 mol/L) and extracted with ethyl acetate (3x100 mL) and the organic layers combined. The resulting mixture was washed with brine (3x100 mL), dried over anhydrous sodium sulfate and concentrated under vacuum. The residue was applied onto a silica gel column with ethyl acetate/petroleum ether (1 :2) to give 6.2 g (32%) of (2R)-2-

(benzoyloxy)propanoic acid as colorless oil. LC-MS: (M+H) ⁺ = 193. ¾ NMR (400MHz, CDC1 ₃ ): δ 8.10-8.08 (m, 2H), 7.58-7.54 (m, 1H), 7.45-7.42 (m. 2H), 5.38-5.33 (m, 1H), 1.66- 1.65 (d, J= 6.8 Hz, 3H).

[0503] Step 2: (lR)-l-[[(lE)-[3-[(tert- butyldimethylsilyl)oxy] cyclobutyl] (hydroxyimino)methyl] carbamoyl] ethyl benzoate:

DIEA (12 g, 92.85 mmol, 3.00 eq.) was added dropwise to a 0°C solution of (E)-3-[(tert- butyldimethylsilyl)oxy]-N-hydroxycyclobut-l-carboximidamide (8.3 g, 33.96 mmol, 1.10 eq.), (2R)-2-(benzoyloxy)propanoic acid (6 g, 30.90 mmol, 1.00 eq.) and HATU (23.5 g, 61.84 mmol, 2.00 eq.) in DMF (100 mL). The resulting solution was stirred for 1.5 hours at room temperature. The reaction was then quenched by the addition of 100 mL of water/ice and extracted with ethyl acetate (3x100 mL) and the organic layers combined. The resulting mixture was washed with brine (3x100 mL), dried over anhydrous sodium sulfate and concentrated under vacuum. The residue was applied onto a silica gel column with ethyl acetate/petroleum ether (1 :3) to give 6.25 g (48%) of (lR)-l-[[(lE)-[3-[(tert- butyldimethylsilyl)oxy]cyclobutyl](hydroxyimino)methyl]carba moyl]ethyl benzoate as colorless oil. LC-MS: (M+H) ⁺ = 421.

[0504] Step 3: (lR)-l-(3-[3-[(tert-butyldimethylsilyl)oxy]cyclobutyl]-l,2,4 -oxadiazol-5- yl)ethyl benzoate: a solution of (lR)-l-[[(lZ)-[3-[(tert- butyldimethylsilyl)oxy]cyclobutyl](hydroxyimino)methyl] carbamoyl] ethyl benzoate (3.4 g, 8.08 mmol, 1.00 eq.) in DMF(15 mL) was stirred for 3 hours at 100 °C in an oil bath. The resulting solution was diluted with 50 mL of water and extracted with ethyl acetate (3x80 mL) and the organic layers combined. The resulting mixture was washed with brine (2x50 mL), dried over anhydrous sodium sulfate and concentrated under vacuum. The residue was applied onto a silica gel column with ethyl acetate/petroleum ether (1 :6) to give 2.4 g (74%) of (1R)-1- (3-[3-[(tert-butyldimethylsilyl)oxy]cyclobutyl]- 1 ,2,4-oxadiazol-5-yl)ethyl benzoate as colorless oil. LC-MS: (M+H) ⁺ = 403. 'H NMR (300MHZ, CDC1 ₃ ): δ 8.10-8.08 (m, 2H), 7.62-7.57 (m, 1H), 7.50-7.26 (m. 2H), 6.30-6.23 (m, 1H), 4.31-4.25 (m, 1H), 3.09-3.03 (m, 1H), 2.69-2.60 (m, 2H), 2.38-2.31 (m, 2H), 1.83-1.81 (d, J= 6.6 Hz, 3H), 0.89 (s, 9H), 0.05 (s, 6H).

[0505] Step 4: (lR)-l-[3-(3-hydroxycyclobutyl)-l,2,4-oxadiazol-5-yl]ethyl benzoate:

5M hydrogen chloride aqueous (2 mL) was added to a solution of (lR)-l-(3-[3-[(tert- butyldimethylsilyl)oxy]cyclobutyl]-l,2,4-oxadiazol-5-yl)ethy l benzoate (2.4 g, 5.95 mmol, 1.00 eq.) in Dioxane (30 mL). The resulting solution was stirred for 1 hour at room temperature. The resulting solution was diluted with 30 mL of water and extracted with ethyl acetate (3x50 mL) and the organic layers combined. The resulting mixture was washed with brine (3x20 mL), dried over anhydrous sodium sulfate and concentrated under vacuum. The residue was applied onto a silica gel column with ethyl acetate/petroleum ether (1 : 1) to give 1.63 g (95%) of (lR)-l-[3-(3-hydroxycyclobutyl)-l,2,4-oxadiazol-5-yl]ethyl benzoate as colorless oil. LC- MS: (M+H) ⁺ = 289. ^l H NMR (300MHz, CDC1 ₃ ): δ 8.11-8.08 (m, 2H), 7.63-7.60 (m, 1H), 7.47-7.44 (m. 2H), 6.31-6.24 (m, 1H), 4.34-4.30 (m, 1H), 3.21-3.13 (m, 1H), 2.83-2.74 (m, 2H), 2.35-2.25 (m, 2H), 1.84-1.82 (d, J= 6.9 Hz, 3H).

[0506] Step 5: (lR)-l-[3-[3-(l,3-dioxo-2,3-dihydro-lH-isoindol-2-yl)cyclobu tyl]-l,2,4- oxadiazol-5-yl] ethyl benzoate: DIAD (1.83 g, 9.05 mmol, 2.00 eq.)was dropwise to a solution of (lR)-l-[3-(3-hydroxycyclobutyl)-l,2,4-oxadiazol-5-yl]ethyl benzoate (1.3 g, 4.51 mmol, 1.00 eq.), 2,3-dihydro-lH-isoindole-l,3-dione (1.33 g, 9.04 mmol, 2.00 eq.) and triphenyl phosphine (2.37 g, 9.04 mmol, 2.00 eq.) in THF (50 mL) under N ₂ . The resulting solution was stirred for 2.5 hours at room temperature and concentrated under vacuum. The residue was applied onto a silica gel column with ethyl acetate/petroleum ether (1 :5). The crude product was purified by Flash-Prep-HPLC with the following conditions (CombiFlash-1): Column, C18; mobile phase, H ₂ 0/CH ₃ CN=9: 1 increasing to H ₂ 0/CH ₃ CN=1 :9 within 30 min; Detector, UV 254 nm. This resulted in 1.3 g (69%) of (lR)-l-[3-[3-(l,3-dioxo-2,3-dihydro-lH-isoindol- 2-yl)cyclobutyl]-l,2,4-oxadiazol-5-yl]ethyl benzoate as light yellow oil. LC-MS: (M+H) ⁺ = 418.

[0507] Step 6: (lR)-l-[3-(3-aminocyclobutyl)-l,2,4-oxadiazol-5-yl]ethan-l-o l: hydrazine hydrate (5.4 g, 86.30 mmol, 30.00 eq., 80%) was added to a solution of (lR)-l-[3-[3-(l,3- dioxo-2,3-dihydro-lH-isoindol-2-yl)cyclobutyl]-l,2,4-oxadiaz ol-5-yl]ethyl benzoate (1.2 g, 2.87 mmol, 1.00 eq.) in ethanol (50 mL). The resulting solution was stirred for 3.5 hours at room temperature. The solids were filtered out and concentrated under vacuum to give 520 mg (99%) of (lR)-l-[3-(3-aminocyclobutyl)-l,2,4-oxadiazol-5-yl]ethan-l-o l as light yellow oil. LC-MS: (M+H) ⁺ = 184.

[0508] Step 7: (lR)-l-[3-[3-(5-phenyl-l,2-oxazole-3-amido)cyclobutyl]-l,2,4 -oxadiazol- 5-yl]ethyl 5-phenyl-l,2-oxazole-3-carboxylate: DIEA (1.95 g, 15.09 mmol, 5.00 eq.) was added dropwise to a 0°C solution of (lR)-l-[3-(3-aminocyclobutyl)-l,2,4-oxadiazol-5-yl]ethan- l-ol (520 mg, 2.84 mmol, 1.00 eq.), 5-phenyl-l,2-oxazole-3-carboxylic acid (1.14 g, 6.03 mmol, 2.00 eq.) and HCTU (3.1 g, 7.49 mmol, 2.50 eq.) in dichloromethane (60 mL). The resulting solution was stirred for 30 min at room temperature. The resulting solution was diluted with 50 mL of water/ice and extracted with dichloromethane (3x30 mL) and the organic layers combined. The resulting mixture was washed with brine (2x20 mL), dried over anhydrous sodium sulfate and concentrated under vacuum. The residue was applied onto a silica gel column with ethyl acetate/petroleum ether (1: 1) to give 1.3 g (87%) of (lR)-l-[3-[3- (5-phenyl-l,2-oxazole-3-amido)cyclobutyl]-l,2,4-oxadiazol-5- yl]ethyl 5-phenyl-l,2-oxazole-3- carboxylate as light yellow oil. LC-MS: (M+H) ⁺ = 526.

[0509] Step 8: 7V-(3-[5-[(lR)-l-hydroxyethyl]-l,2,4-oxadiazol-3-yl]cyclobut yl)-5- phenyl-l,2-oxazole-3-carboxamide: LiOH(l 15 mg, 2.74 mmol, 1.10 eq.) in ¾0 (10 mL) was added to a solution of (lR)-l-[3-[3-(5-phenyl-l,2-oxazole-3-amido)cyclobutyl]-l,2,4 - oxadiazol-5-yl]ethyl 5 -phenyl- l,2-oxazole-3-carboxylate (1.3 g, 2.47 mmol, 1.00 eq.) in THF (80 mL) and stirred for 30 min at room temperature. The resulting solution was diluted with 50 mL of H ₂ 0 and extracted with ethyl acetate (2x20 mL) and the organic layers combined, dried over anhydrous sodium sulfate and concentrated under vacuum to give 850 mg (97%) of N-(3- [5-[(lR)-l-hydroxyethyl]-l,2,4-oxadiazol-3-yl]cyclobutyl)-5- phenyl-l,2-oxazole-3- carboxamide as a white solid. LC-MS: (M+H) ⁺ = 355. The isomers (850mg) were separated by Prep-SFC using the following conditions (prep SFC 350-2): Column, Chiralpak AS-H, 5*25cm, 5um; mobile phase, C0 ₂ (50%), ethanol (0.2%DEA)(50%); Detector, UV 254 nm. This resulted in 679 mg (80%) of 5-phenyl-N-[?raws-3-[5-[(lR)-l-hydroxyethyl]-l,2,4- oxadiazol-3-yl]cyclobutyl]-l,2-oxazole-3-carboxamide as white solid.

[0510] LC-MS: (M+H) ⁺ = 355

[0511] Analytical data: 'H NMR (300MHZ, DMSO-i¾): δ 9.29-9.26 (d, J= 7.8 Hz, 1H),

7.95-7.92 (m, 2H), 7.58-7.53 (m, 3H), 7.37 (s, 1H), 6.10 (s, 1H), 5.03-4.96 (m, 1H), 4.83-4.72 (m, 1H), 3.64-3.55 (m, 1H), 2.72-2.62 (m, 2H), 2.52-2.46 (m,

2H), 1.51-1.49 (d, J= 6.9 Hz, 3H).

[0512] HPLC purity: 99.2% at 254 nm.

Example 42: iV-(ir««s-3-(5-((S)-l-hydroxyethyl)-l,2,4-oxadiazol-3-yl)c yclobutyl)-5- phenylisoxazole-3-carboxamide was prepared using a similar procedure as shown in example 42 where (2S)-2-hydroxypropanoic acid was used. The product was purified by Prep-SFC with the following conditions (prep SFC 350-2): Column, CHIRALPAK IC SFC, 5*25cm, 5um; mobile phase, CO ₂ (50%), IPA(50%); Detector, UV 220nmto give 282.4 mg (71%) 5-phenyl-N- [?ra«s-3-[5-[(lS)-l-hydroxyethyl]-l,2,4-oxadiazol-3-yl]cycl obutyl]-l,2-oxazole-3-carboxamide as white solid. [0513] LC-MS: (M+H) ⁺ = 355 [0514] Analytical data: ^X H NMR (300MHz, DMSO-i¾): δ 9.29-9.26 (d, J= 7.8 Hz, 1H), 7.96-7.93 (m, 2H), 7.60-7.55 (m, 3H), 7.37 (s, 1H), 6.10-6.08 (d, J= 5.7 Hz, 1H), 5.04-4.96 (m, 1H), 4.83-4.70 (m, 1H), 3.64-3.55 (m, 1H), 2.73-2.63 (m, 2H), 2.55-2.47 (m, 2H), 1.52-1.49 (d, J= 6.9 Hz, 3H). [0515] HPLC purity: 98.9% at 254 nm.

Example 43: 5-phenyl-7V-[ir««s-3-[5-(l-methylazetidin-3-yl)-l,3,4-oxad iazol-2- yl] cyclobutyl] isoxazole-3-carboxamide

Step 1: 5-phenyl-iV-[ir«Hs-3-[[(l-methylazetidin-3-yl)

formohydrazido]carbonyl]cyclobutyl]isoxazole-3-carboxamid e: l-methylazetidine-3- carboxylic acid (172.5 mg, 1.50 mmol, 1.50 eq.), HATU (456 mg, 1.20 mmol, 1.20 eq.) and DIEA (387 mg, 2.99 mmol, 3.00 eq.) were added to a solution of 5-phenyl-N-?ra¾s-3- (hydrazinecarbonyl)cyclobutyl]isoxazole-3-carboxamide (300 mg, 1.00 mmol, 1.00 eq., prepared according to example 20) in DMF (15 mL). The resulting solution was stirred for 3 hours at room temperature and then it was concentrated under vacuum. The crude product was purified by Flash-Prep-HPLC with the following conditions (IntelFlash-1): Column, C18; mobile phase, MeCN/H ₂ 0 = 5:95 increasing to MeCN/H ₂ 0 = 95:5 within 15 min; Detector, UV 254 nm. This resulted in 337 mg (85%) of 5-phenyl-N-[?raws-3-[[(l-methylazetidin-3- yl)formohydrazido]carbonyl]cyclobutyl]isoxazole-3-carboxamid e as a yellow solid. LC-MS (ES, m/z): [M+H] ⁺ = 398. [0516] Step 2: 5-phenyl-/V-[ir««s-3-[5-(l-methylazetidin-3-yl)-l,3,4-oxad iazol-2- yl]cyclobutyl]isoxazole-3-carboxamide: I ₂ (214 mg, 0.84 mmol, 1.44 eq.) was added to a solution of PPI1 ₃ (221 mg, 0.84 mmol, 1.44 eq.) in dichloromethane (20 mL) at 0 °C. Then TEA (340 mg, 3.36 mmol, 5.73 eq.) and 5-phenyl-N-[?raws-3-[[(l-methylazetidin-3- yl)formohydrazido]carbonyl]cyclobutyl]isoxazole-3-carboxamid e (233 mg, 0.59 mmol, 1.00 eq.) were added at 0 °C, respectively. The resulting solution was stirred for 2 hours at room temperature. The resulting mixture was concentrated under vacuum. The residue was applied onto Prep-TLC with ethyl acetate/petroleum ether (1 : 1). The resulted crude product was purified by Prep-HPLC with the following conditions (waters): Column, XBridge Prep CI 8 OBD Column, 5 urn, 19* 150mm; mobile phase, Water with lOmmol NH ₄ HCO ₃ and ACN

(10.0% ACN up to 70.0% in 8 min); Detector, UV 254/220 nm. This resulted in 90 mg (40%) of 5-phenyl-N-[?ra«s-3-[5-(l-methylazetidin-3-yl)-l,3,4-oxadia zol-2-yl]cyclobutyl]isoxazole- 3-carboxamide as a white solid.

[0517] Analytical data: [0518] LC-MS (ES, m/z): [M+H] ⁺ = 380.2

[0519] ¹ H NMR (300 MHz, DMSO-i¾): δ 9.31, 9.29 (d, J= 7.5 Hz, 1H), 7.96-7.92 (m,

2H), 7.59-7.55 (m, 3H), 7.38 (s, 1H), 4.73-4.65 (q, J= 8.1 Hz, 1H), 3.88-3.65 (m, 2H), 3.61-3.56 (m, 2H), 3.32-3.28 (m, 2H), 2.73-2.51 (m, 4H), 2.25 (s, 3H).

Example 44: 5-(4-fluorophenyl)-/V-[ir««s-3-[5-[(lR)-l-hydroxyethyl]-l, 3,4-oxadiazol-2- yl] cyclobutyl] isoxazole-3-carboxamide

[0520] Step 1: ethyl 4-(4-fluorophenyl)-2,4-dioxobutanoate: sodium ethoxide (20 mL, 2.00 eq.) was added to a solution of l-(4-fluorophenyl)ethan-l-one (5 g, 36.20 mmol, 1.00 eq.) and diethyl oxalate (5.29 g, 36.20 mmol, 1.00 eq.) in ethanol (50 mL) at 0°C. The resulting solution was stirred for 5 hours at room temperature, diluted with 500 mL of water and the solids were collected by filtration. This resulted in 7 g (81%) of ethyl 4-(4-fluorophenyl)-2,4- dioxobutanoate as a yellow solid.

[0521] Step 2: ethyl 5-(4-fluorophenyl)isoxazole-3-carboxylate: NH ₂ OH HC1 (2.92 g, 5.00 eq.) was added to a solution of ethyl 4-(4-fluorophenyl)-2,4-dioxobutanoate (2 g, 8.40 mmol, 1.00 eq.) in ethanol (20 mL). The resulting solution was stirred overnight at 90 °C in an oil bath. The solids were filtered and the resulting mixture was concentrated under vacuum. The residue was applied onto a silica gel column with ethyl acetate/petroleum ether (1 :25). This resulted in 518 mg (26%) of ethyl 5-(4-fluorophenyl)isoxazole-3-carboxylate as a white solid. 'H NMR (400MHZ, CDC1 ₃ ): δ 7.85-7.81 (m, 2H), 7.23-7.19 (m, 2H), 6.90 (s, 1H), 4.53- 4.47 (m, 2H), 1.49-1.45 (t, J= 7.2 Hz, 3H). [0522] Step 3: 5-(4-fluorophenyl)isoxazole-3-carboxylic acid: lithium hydroxide (170 mg, 7.10 mmol, 3.00 eq.) in water (3 mL) was added to a solution of ethyl 5-(4- fluorophenyl)isoxazole-3-carboxylate (318 mg, 1.35 mmol, 1.00 eq.) in tetrahydrofuran (20 mL). The resulting solution was stirred overnight at room temperature. The pH of the solution was adjusted to 6 with hydrogen chloride aqueous, the solution was then extracted with ethyl acetate (3x150 mL) and the combined organic layers were dried over anhydrous sodium sulfate and concentrated under vacuum. This resulted in 403 mg (crude) of 5-(4- fluorophenyl)isoxazole-3-carboxylic acid as a white solid. LC-MS (ES, m/z): [M-l] ^" = 206.

[0523] Step 4: 7V-ir««s-(3-[5-[(lR)-l-[(tert-butyldimethylsilyl)oxy]ethyl ]-l,3,4- oxadiazol-2-yl]cyclobutyl)-5-(4-fluorophenyl)isoxazole-3-car boxamide: 5-(4- fluorophenyl)isoxazole-3-carboxylic acid (284 mg, 1.37 mmol, 1.20 eq.), HATU (652.5 mg, 1.50 eq.) and DIEA (443 mg, 3.00 eq.) were added to a solution of N-/Taws-3-5-[(lR)-l-[(tert- butyldimethylsilyl)oxy]ethyl]-l,3,4-oxadiazol-2-ylcyclobutan -l-amine (340 mg, 1.14 mmol, 1.00 eq.) in dichloromethane (6 mL). The resulting solution was stirred for 3 hours at room temperature. The reaction was then quenched by the addition of water. The resulting solution was extracted with ethyl acetate (3x100 mL) and the organic layers combined. The resulting mixture was washed with brine (3x100 mL), dried over anhydrous sodium sulfate and concentrated under vacuum to give 309 mg (56%) of N-?ra«s-(3-[5-[(lR)-l-[(tert- butyldimethylsilyl)oxy]ethyl]-l,3,4-oxadiazol-2-yl]cyclobuty l)-5-(4-fluorophenyl)isoxazole-3- carboxamide as a solid. LC-MS (ES, m/z): [M+l] ⁺ = 487.

[0524] Step 5: 5-(4-fluorophenyl)-iV-[ir««s-3-[5-[(lR)-l-hydroxyethyl]-l, 3,4-oxadiazol- 2-yl]cyclobutyl]isoxazole-3-carboxamide: TBAF (lmol/L in tetrahydrofuran, 1 mL) was added to solution of 5-(4-fluorophenyl)-N-[?raws-3-[5-[(lR)-l-[(tert- butyldimethylsilyl)oxy]ethyl]-l,3,4-oxadiazol-2-yl]cyclobuty l]isoxazole-3-carboxamide (304 mg, 0.62 mmol, 1.00 eq.) in tetrahydrofuran (5 mL). The resulting solution was stirred for 3 hour at room temperature. The resulting mixture was concentrated under vacuum. The residue was applied onto a silica gel column with dichloromethane/methanol (50: 1). This resulted in 129.7 mg (56%) of 5-(4-fluorophenyl)-N-[?ra«s-3-[5-[(lR)-l-hydroxyethyl]-l,3, 4-oxadiazol-2- yl]cyclobutyl]isoxazole-3-carboxamide as a white solid. [0525] Analytical data: [0526] HPLC purity: 97.1 % at 254 nm [0527] LC-MS (ES, m/z): [M+l = 373.2

[0528] ^X H NMR (400MHz, DMSO-i¾): δ 9.33-9.31 (d, J= 7.6 Hz, 1H), 8.04-8.00 (m, 2H),

7.44-7.38 (m, 3H), 5.95-5.94 (d, J= 5.6 Hz, 1H), 4.95-4.89 (m, 1H), 4.73-4.67 (m, 1H), 3.73-3.69 (m, 1H), 2.73-2.66 (m, 2H), 2.64-2.50 (m, 2H), 1.50-1.48 (d,

J= 6.4 Hz, 3H).

Example 45: 5-phenyl-iV-[ir««s-3-[5-[(lR)-l-methoxyethyl]-l,3,4-oxadia zol-2- yl] cyclobutyl] isoxazole-3-carboxamide

Step 1: methyl (2R)-2-methoxypropanoate: Ag ₂ 0 (6.1 g, 26.4 mmol, 1.10 eq.) was added to a solution of iodomethane (27.3 g, 192 mmol, 8.00 eq.) and methyl (2R)-2- hydroxypropanoate (2.5 g, 24 mmol, 1.00 eq.) in acetonitrile (30 mL) and the solution was stirred for 16 hours at 85 °C in an oil bath. The solids were filtered and the mixture was diluted with DCM (100 mL). The resulting mixture was washed with water (3 x 50 mL), dried over anhydrous sodium sulfate and concentrated under vacuum. This resulted in 2 g (70%) of methyl (2R)-2-methoxypropanoate as colorless oil.

[0529] ^X H NMR (400MHz, CDC1 ₃ ): δ 3.92-3.87 (m, 1H), 3.76 (s, 3H), 3.40 (s, 3H), 1.42- 1.40 (d, J= 6.8 Hz, 3H). [0530] Step 2: (2R)-2-methoxypropanehydrazide: a solution of methyl (2R)-2- methoxypropanoate (2 g, 16.93 mmol, 1.00 eq.) and hydrazine hydrate (5.3 g, 84.70 mmol, 5.00 eq.) in ethanol (50 mL) was stirred for 16 hours at 70 °C in an oil bath. The resulting mixture was concentrated under vacuum. This resulted in 2 g (crude) of (2R)-2- methoxypropanehydrazide as light yellow oil. LC-MS (ES, m/z): [M+l] ⁺ = 1 19.

[0531] Step 3: (2R)-2-methoxy-iV-[ir««s-3-(l,3-dioxo-2,3-dihydro-lH-isoin dol-2- yl)cyclobutyl]carbonyl]propanehydrazide: DIEA (3 g, 23.21 mmol, 3.00 eq.) was added to a solution of ?ra«s-3-(l,3-dioxo-2,3-dihydro-lH-isoindol-2-yl)cyclobutane -l-carboxylic acid (1.9 g, 7.75 mmol, 1.00 eq.), (2R)-2-methoxypropanehydrazide (1.37 g, 1 1.60 mmol, 1.50 eq.) and HATU (5.3 g, 13.95 mmol, 1.80 eq.) in THF (80 mL). The resulting solution was stirred for 1 hour at room temperature, it was then diluted with 100 mL of water/ice. The resulting solution was extracted with ethyl acetate (3x100 mL) and the organic layers combined. The resulting mixture was washed with brine (2x50 mL), dried over anhydrous sodium sulfate and concentrated under vacuum. The residue was applied onto a silica gel column with

dichloromethane/methanol (30: 10) to give 2.2 g (82%) of (2R)-2-methoxy-N-[£ra¾s-3-(l,3- dioxo-2,3-dihydro-lH-isoindol-2-yl)cyclobutyl]carbonyl]propa nehydrazide as colorless oil. LC-MS (ES, m/z): [M+l = 346.

[0532] Step 4: 2-[ir««s-3-[5-[(lR)-l-methoxyethyl]-l,3,4-oxadiazol-2-yl]c yclobutyl]- 2,3-dihydro-lH-isoindole-l,3-dione: a solution of TsCl (3.64 g, 19.09 mmol, 3.00 eq.) in dichloromethane (100 mL) was added dropwise to a cold solution of (2R)-2-methoxy-N-[?raws- 3-(l,3-dioxo-2,3-dihydro-lH-isoindol-2-yl)cyclobutyl]carbony l]propanehydrazide (2.2 g, 6.37 mmol, 1.00 eq.) and TEA (3.22 g, 31.82 mmol, 5.00 eq.) in dichloromethane (50 mL) at 0°C. The resulting solution was stirred for 15 hours at room temperature, it was then washed with water (3x50 mL) and brine (1x50 mL), dried over anhydrous sodium sulfate and concentrated under vacuum. The crude product was purified by Flash-Prep-HPLC with the following conditions (IntelFlash-1): Column, C18; mobile phase, H ₂ 0/CH ₃ CN = 100: 1 increasing to H ₂ 0/CH ₃ CN = 1 : 100 within 30 min; Detector, UV 254 nm. This resulted in 800 mg (38%) of 2-[tra«5-3-[5-[(lR)-l-methoxyethyl]-l,3,4-oxadiazol-2-yl]cy clobutyl]-2,3-dihydro-lH- isoindole-l,3-dione as colorless oil. LC-MS (ES, m/z): [M+l] ⁺ = 328. [0533] Step 5: ir««s-3-[5-[(lR)-l-methox ethyl]-l,3,4-oxadiazol-2-yl]cyclobutan-l- amine: a solution of 2-[?ra«s-3-[5-[(lR)-l-methoxyethyl]-l,3,4-oxadiazol-2-yl]cy clobutyl]- 2,3-dihydro-lH-isoindole-l,3-dione (800 mg, 2.44 mmol, 1.00 eq.) and hydrazine hydrate (3.06 g, 48.90 mmol, 20.00 eq., 80%) in ethanol (50 mL) was stirred for 4 hours at room temperature. The reaction mixture was filtered and then concentrated under vacuum. This resulted in 480 mg (crude) of ?ra«s-3-[5-[(lR)-l-methoxyethyl]-l,3,4-oxadiazol-2-yl]cyclo butan-l-amine as colorless oil. LC-MS (ES, m/z): [M+l = 198.

[0534] Step 6: 5-phenyl-iV-[ir««s-3-[5-[(lR)-l-methoxyethyl]-l,3,4-oxadia zol-2- yl]cyclobutyl]isoxazole-3-carboxamide: DIEA (943 mg, 7.30 mmol, 3.00 eq.) was added dropwise to a cold solution of 5-phenylisoxazole-3-carboxylic acid (550 mg, 2.91 mmol, 1.20 eq.), ?ra«s-3-[5-[(lR)-l-methoxyethyl]-l,3,4-oxadiazol-2-yl]cyclo butan-l-amine (480 mg, 2.43 mmol, 1.00 eq.) and HATU (1.387 g, 3.65 mmol, 1.50 eq.) in dichloromethane (50 mL) at 0 °C. The resulting solution was stirred for 1 hour at room temperature and then diluted with 50 mL of dichloromethane. The resulting mixture was washed with water (2x50 mL) and brine (1x50 mL), dried over anhydrous sodium sulfate and concentrated under vacuum. The residue was applied onto a silica gel column with ethyl acetate/petroleum ether (1 : 1) to give 628 mg (70%) of 5-phenyl-N-[?ra«s-3-[5-[(lR)-l-methoxyethyl]-l,3,4-oxadiazo l-2-yl]cyclobutyl]isoxazole-3- carboxamide as an off-white solid.

[0535] Analytical data:

[0536] HPLC purity: 98.9% at 254 nm

[0537] LC-MS (ES, m/z): [M+l] ⁺ = 369 [0538] ^X H NMR (400MHz, DMSO-i¾): 9.33-9.31 (d, J= 7.6 Hz, 1H), 7.96-7.94 (t, J= 5.6

Hz, 2H), 7.59-7.56 (m, 3H), 7.38 (s, 1H), 4.74-4.67 (m, 2H), 3.76-3.70 (m, 1H), 3.29 (s, 3H), 2.74-2.61 (m, 4H), 1.51-1.49 (d, J= 6.8 Hz, 3H).

Example 46: (lR)-l-[5-[ir««s-3-(5-phenylisoxazole-3-amido)cyclobutyl]- l,3,4- oxadiazol-2-yl] ethyl acetate

[0539] Acetyl chloride (60.3 mg, 0.77 mmol, 2.02 eq.) was added to a solution of 5-phenyl- N- [trans-3 - [5 - [( 1 R)- 1 -hydroxyethyl] - 1 ,3 ,4-oxadiazol-2-yl]cyclobutyl] isoxazole-3 -carboxamide (135 mg, 0.38 mmol, 1.00 eq.) and TEA (115.6 mg, 1.14 mmol, 3.00 eq.) in dichloromethane (10 mL). The resulting solution was stirred for 3 hours at room temperature and it was then concentrated under vacuum. The residue was applied onto a silica gel column with ethyl acetate/petroleum ether (1 : 1). The crude product was purified by Flash-Prep-HPLC with the following conditions (IntelFlash-1): Column, C18; mobile phase, MeCN/H20 = 5:95 increasing to MeCN/H20 = 95:5 within 20 min; Detector, UV 254 nm to give 65 mg (43%) of (lR)-l-[5-[?ra«s-3-(5-phenylisoxazole-3-amido)cyclobutyl]-l ,3,4-oxadiazol-2-yl]ethyl acetate as a white solid.

[0540] Analytical data:

[0541] HPLC purity: 98.1% at 254 nm

[0542] LC-MS (ES, m/z): [M+H]+ = 397.1

[0543] 'H NMR (400 MHz, DMSO-d6, ppm): δ 9.32-9.3 l(d, J = 7.6 Hz, 1H), 7.96-7.94 (m,

2H), 7.59-7.56 (m, 3H), 7.38 (s, 1H), 6.05-6.00 (m, 1H), 4.72-4.66 (m, 1H),

3.73-3.70 (m, 1H), 2.73-2.60 (m, 4H), 2.11 (s, 3H), 1.63-1.61 (d, J = 6.8 Hz, 3H).

Example 47: (R)-l-(5-(ir««s-3-(5-phenylisoxazole-3-carboxamido)cyclobu tyl)-l,3,4- oxadiazol-2-yl)ethyl benzoate

[0544] Compound was prepared using a similar procedure as described in example 46.

Yield: 66%

[0545] Analytical data:

[0546] HPLC purity: 97.1% at 254 nm

[0547] Appearance: white solid [0548] LC-MS (ES, m/z): [M+H = 459.1

[0549] 'H NMR (400 MHz, OMSO-d _6, ppm) 59.31-9.29 (d, J= 7.6 Hz, 1H), 8.03-8.01(m,

2H), 7.96-7.94 (m, 2H), 7.73-7.70 (m, 1H), 7.59-7.53 (m, 5H), 7.38-7.36 (d, J= 6.0 Hz, 1H), 6.33-6.28 (m, 1H), 4.74-4.64 (m, 1H), 3.76-3.70 (m, 1H), 2.73-2.63 (m, 4H), 1.78-1.76 (d, J= 6.8 Hz, 3H).

Example 48: iV-(ir««s-3-(5-((R)-l-isopropoxyethyl)-l,3,4-oxadiazol-2-y l)cyclobutyl)-5- phenylisoxazole-3-carboxamide

Step 1: 5-phenyl-iV-[(ir««s-3-[5-[(lS)-l-bromoethyl]-l,3,4-oxadiaz ol-2- yl]cyclobutyl]isoxazole-3-carboxamide: a solution of PPh ₃ (1.66 g, 6.33 mmol, 1.50 eq.), CBr ₄ (2.1 g, 6.33 mmol, 1.49 eq.) and 5-phenyl-N-[ira/w-3-[5-[(lR)-l-hydroxyethyl]-l,3,4- oxadiazol-2-yl]cyclobutyl]isoxazole-3-carboxamide (1.5 g, 4.23 mmol, 1.00 eq.) in tetrahydrofuran (50 mL) was stirred for 2 hours at room temperature. The resulting solution was diluted with dichloromethane, it washed with brine, dried over anhydrous sodium sulfate and concentrated under vacuum. The residue was applied onto a silica gel column with ethyl acetate/petroleum ether (1 :5) to give 2.36 g (crude) of 5-phenyl-N-[(?ra«s-3-[5-[(l S)-l- bromoethyl]-l,3,4-oxadiazol-2-yl]cyclobutyl]isoxazole-3-carb oxamide as a white solid. LC- MS (ES, m/z): [M+H] ⁺ = 417.0.

[0550] Step 2: iV-(ir««s-3-(5-((R)-l-isopropoxyethyl)-l,3,4-oxadiazol-2-y l)cyclobutyl)- 5-phenylisoxazole-3-carboxamide: a suspension ofNa (1.1 g, 47.83 mmol, 1.00 eq.) in propan-2-ol (70 mL) was stirred overnight at 70 °C. The resulting mixture was concentrated under vacuum to get 3.95 g (crude) of sodium propan-2-olate as a white solid. Into another 100-mL round-bottom flask, was placed a solution of 5-phenyl-N-[?ra«s-3-[5-[(l S)-l- bromoethyl]-l,3,4-oxadiazol-2-yl]cyclobutyl]isoxazole-3-carb oxamide (1 g, 2.40 mmol, 1.00 eq.) in DMF (30 mL). To the solution was added the freshly prepared sodium propan-2-olate (3.95 g, 48.13 mmol, 20.08 eq., crude). The resulting solution was stirred for 30 min at 50 °C. The resulting mixture was concentrated under vacuum, the mixture was diluted with ethyl acetate and the resulting solution was washed with water and concentrated under vacuum. The residue was applied onto a Prep-TLC with ethyl acetate/petroleum ether (1 : 1) and the crude product was purified by Prep-HPLC using the following conditions (waters): Column, XBridge C18 OBD; mobile phase, water with 0.05% NH4HCO3 and CH ₃ CN (10% CH ₃ CN up to 70% CH ₃ CN in 10 min, up to 95% CH ₃ CN in 1.5 min, down to 10% CH ₃ CN in 1.5 min); Detector, UV 220&254 nm. 100 mg product was obtained. The crude product (100 mg) was purified by Chiral-Prep-HPLC with the following conditions (Prep-HPLC-032): Column, Phenomenex Lux 5u Cellulose- AXIA Packed, 250*21.2mm, 5um; mobile phase, hexane (0.2% DEA) and ethanol (hold 30.0% ethanol in 25 min); Detector, UV 254 nm. This resulted in 61 mg (6%) of 5-phenyl-N-[?ra«s-3-[5-[(lR)-l-(propan-2-yloxy)ethyl]-l,3,4 -oxadiazol-2- yl]cyclobutyl]isoxazole-3-carboxamide as a white solid.

[0551] Analytical data:

[0552] HPLC purity: 99.8% at 254 nm [0553] LC-MS (ES, m/z): [M+H] ⁺ = 397.1

[0554] ^X H NMR (300 MHz, DMSO-i¾): δ 9.33-9.30 (d, J= 7.8 Hz, 1H), 7.96-7.93 (m, 2H),

7.60-7.55 (m, 3H), 7.38 (s, 1H), 4.90-4.83 (m, 1H), 4.74-4.66 (m, 1H), 3.76-3.64 (m, 2H), 2.75-2.30 (m, 4H), 1.48-1.46 (d, J= 6.6 Hz, 3H), 1.1 1-1.09 (d, J= 6.0 Hz, 3H), 1.01-0.99 (d, J= 6.0 Hz, 3H). Example 49: iV-(ir««s-3-(5-((R)-l-isobutoxyethyl)-l,3,4-oxadiazol-2-yl )cyclobutyl)-5- phenylisoxazole-3-carboxamide

[0555] The compound was prepared using a similar procedure as reported in example 48 using sodium 2-methylpropan-l-olate. The crude product was purified by Flash-Prep-HPLC with the following conditions (IntelFlash-1): Column, C18; mobile phase, MeCN/H ₂ 0 = 5:95 increasing to MeCN/H ₂ 0 = 95:5 within 20 min; Detector, UV 254 nm. 300 mg product was obtained. The crude product (300 mg) was purified by Prep-HPLC with the following conditions (l#-Pre-HPLC-005 (Waters)): Column, XBridge CI 8 OBD; mobile phase, water with 0.05% NH ₄ HCO ₃ and CH ₃ CN (10% CH ₃ CN up to 70% CH ₃ CN in 10 min, up to 95% CH ₃ CN in 1.5 min, down to 10% CH ₃ CN in 1.5 min; Detector, UV 220&254 nm. 150 mg product was obtained. The crude product (150 mg) was purified by Chiral-Prep-HPLC with the following conditions (Prep-HPLC -004): Column, Phenomenex Lux, 5u Cellulose-4 AXIA

Packed, 250*21.2mm, 5um; mobile phase, hexane and ethanol (hold 30.0% ethanol in 30 min); Detector, UV 254 nm. This resulted in 41.9 mg (5%) of 5-phenyl-N-[?raws-3-[5-[(lR)-l-(2- methylpropoxy)ethyl]-l,3,4-oxadiazol-2-yl]cyclobutyl]isoxazo le-3-carboxamide as a white semi-solid. [0556] Analytical data:

[0557] LC-MS (ES, m/z): [M+H] ⁺ = 41 1.3

[0558] HPLC purity: 97.4% at 254 nm

[0559] 'H NMR (300 MHz, CDC1 ₃ ): 57.82-7.79 (m, 2H), 7.50-7.48 (m, 3H), 7.21-7.18 (m,

1H), 6.97 (s, 1H), 4.82-4.67 (m, 2H), 3.57-3.45 (m, 1H), 3.28-3.17(m, 2H), 3.02-2.92 (m, 2H), 2.56-2.46 (m, 2H), 1.91-1.82 (m, 1H), 1.61-1.59 (d, J = 6.6 Hz, 3H), 0.91-0.86 (m, 6H) 2H), 2.56-2.46(m, 2H), 1.91-77(m, 1H), 1.61, 1.59(d, J=6 Hz, 3H), 0.97-0.85(m, 6H).

Example 50: Tert-butyl 3-(5-(ir«ws-3-(5-phenylisoxazole-3-carboxamido)cyclobutyl)- l,3,4-oxadiazol-2yl)azetidine-l-carboxylate

[0560] Step 1: tert-butyl 3-(iV-[[ir«/is-3-(5-phenylisoxazole-3- amido)cyclobutyl]carbonyl]hydrazinecarbonyl)azetidine-l-carb oxylate: l-[(tert- butoxy)carbonyl]azetidine-3-carboxylic acid (402 mg, 2.00 mmol, 1.50 eq.), HATU (608 mg, 1.60 mmol, 1.20 eq.) and DIEA (516 mg, 3.99 mmol, 3.00 eq.) were added to a solution of 5- phenyl-N-[?ra«s-3-(hydrazinecarbonyl)cyclobutyl]isoxazole-3 -carboxamide (prepared according to example 9, 400 mg, 1.33 mmol, 1.00 eq.) in DMF (10 mL). The resulting solution was stirred for 2 hours at room temperature and the crude product was purified by Flash-Prep- HPLC with the following conditions (IntelFlash-1): Column, C18; mobile phase, MeCN/H ₂ 0 = 5:95 increasing to MeCN/H^O = 95:5 within 10 min; Detector, UV 254 nm. This resulted in 400 mg (62%) of tert-butyl 3-(N-[[/Taws-3-(5-phenylisoxazole-3- amido)cyclobutyl]carbonyl]hydrazinecarbonyl)azetidine-l-carb oxylate as a white solid. LC- MS (ES, m/z): [M+H] ⁺ = 484.2.

[0561] 'H NMR (300 MHz, DMSO-i¾): δ 9.92-9.80 (m, 1H), 9.15-9.12 (d, J= 7.8 Hz, 2H),

7.95-7.92 (m, 2H), 7.57-7.55 (m, 3H), 7.36 (s, 1H), 4.65-4.60 (m, 1H), 4.01-3.96 (m, 2H), 3.86 (br, 2H), 3.36-3.30 (m, 1H), 3.00-2.96 (m, 1H), 2.42-2.38 (t, J =

7.5 Hz, 3H), 1.38 (s, 9H).

[0562] Step 2: tert-butyl 3-[5-[ir««s-3-(5-phenylisoxazole-3-amido)cyclobutyl]-l,3,4 - oxadiazol-2-yl]azetidine-l-carboxylate: 2-(diphenylphosphanyl)pyridine (308.7 mg, 1.17 mmol, 1.50 eq.) was added to solution of tert-butyl 3-(TSf-[?ra¾s-3-(5-phenylisoxazole-3- amido)cyclobutyl]carbonyl]hydrazinecarbonyl)azetidine-l-carb oxylate (378 mg, 0.78 mmol, 1.00 eq.), (298.2 mg, 1.17 mmol, 1.50 eq.) and TEA (474.3 mg, 4.69 mmol, 6.00 eq.) in dichloromethane (30 niL) at 0 °C. The resulting solution was stirred for 2 hours at room temperature and it was then concentrated under vacuum. The residue was applied onto a silica gel column with ethyl acetate/petroleum ether (2: 1). The crude product was purified by Prep- HP LC with the following conditions (Waters): Column, XBridge Prep C18 OBD Column, 19* 150mm, 5um; mobile phase, water with 0.05% NH ₄ HCO ₃ and ACN (30.0% ACN up to 90.0% in 8 min); Detector, UV 254 nm. This resulted in 270 mg (74%) of tert-butyl 3-[5- [?ra«s-3-(5-phenylisoxazole-3-amido)cyclobutyl]-l,3,4-oxadi azol-2-yl]azetidine-l-carboxylate as a white solid.

[0563] Analytical data: [0564] LC-MS (ES, m/z): [M+H-Boc] ⁺ = 366.2

[0565] HPLC purity: 99.2% at 254 nm

[0566] 'H NMR (400 MHz, DMSO-i¾): δ 9.31-9.30 (d, J= 7.6 Hz, 1H), 7.96-7.93 (m, 2H),

7.59-7.54 (m, 3H), 7.38 (s, 1H), 4.71-4.69 (m, 1H), 4.26 (s, 2H), 4.1 1-4.08 (m, 3H), 3.70-3.68 (m, 1H), 2.69-2.65 (m, 4H), 1.40 (s, 9H). Example 51: Tert-butyl 3-(5-(ir«ws-3-(5-phenylisoxazole-3-carboxamido)cyclobutyl)- l,3,4-oxadiazol-2-yl)azetidine-l-carboxylate

Boc _s

[0567] A solution of tert-butyl 3-[5-[/raws-3-(5-phenylisoxazole-3-amido)cyclobutyl]- l,3,4-oxadiazol-2-yl]azetidine-l-carboxylate (200 mg, 0.43 mmol, 1.00 eq.) and hydrogen chloride (gas) in dichloromethane (10 mL) was stirred for 2 hours at room temperature. The resulting mixture was concentrated under vacuum and the crude product was purified by Prep- HP LC with the following conditions (Waters): Column, XBridge Prep C18 OBD Column, 5um, 19* 150mm; mobile phase, Water with 0.05% NH ₄ HCO ₃ and ACN (15.0% ACN up to 80.0% in 8 min); Detector, UV 254/220 nm. This resulted in 85 mg (54%) of 5-phenyl-N- [?ra«s-3-[5-(azetidin-3-yl)-l,3,4-oxadiazol-2-yl]cyclobutyl ]isoxazole-3-carboxamide as a white solid.

[0568] Analytical data:

[0569] LC-MS (ES, m/z): [M+H] ⁺ = 366.1

[0570] HPLC purity: 98.5% at 254 nm

[0571] ^X H NMR (400 MHz, DMSO-ί/ή, ppm): δ 9.33-9.31 (d, J= 7.6 Hz, 1H), 7.96-7.93

(m, 2H), 7.59-7.52 (m, 3H), 7.38 (s, 1H), 4.74-4.64 (m, 1H), 4.23-4.08 (m, 2H), 3.81-3.59 (m, 5H), 2.72-2.63 (m, 4H).

Example 52 : 7V-(ir«ws-3-(5-(oxetan-3-yl)-l,3,4-oxadiazol-2-yl)cyclobuty l)-5- phenylisoxazole-3-carboxamide

Step 1 : 5-phenyl-iV-[ir««s-3-[(oxetan-3-ylformohydrazido)carbonyl] cyclobutyl]isoxazole- 3-carboxamide: HCTU (1.16 g, 2.78 mmol, 2.00 eq.), oxetane-3-carboxylic acid (141 mg, 1.38 mmol, 1.00 eq.) and DIEA (537 mg, 4.16 mmol, 3.00 eq.) were added to a solution of 5- phenyl-N-[?ra«s-3-(hydrazinecarbonyl)cyclobutyl]isoxazole-3 -carboxamide (417 mg, 1.39 mmol, 1.00 eq.) in DMF (10 mL) and the mixture was stirred for 70 min at room temperature. The reaction was then quenched by the addition of water. The resulting solution was extracted with ethyl acetate and the organic layers combined. The resulting mixture was washed with brine, dried over anhydrous sodium sulfate and concentrated under vacuum. This resulted in 0.3 g (56%) of 5-phenyl-N-[?ra¾s-3-[(oxetan-3- ylformohydrazido)carbonyl]cyclobutyl]isoxazole-3-carboxamide as an orange solid. LC-MS ES, m/z): [M+H] ⁺ = 385.1.

[0572] Step 2: 5-phenyWV-[ir«ws-3-[5-(oxetan-3-yl)-l,3,4-oxadiazol-2- yl]cyclobutyl]isoxazole-3-carboxamide: I ₂ (298 mg, 1.17 mmol, 1.50 eq.), TEA (473 mg, 4.67 mmol, 6.00 eq.) and 5-phenyl-N-[/raws-3-[(oxetan-3- ylformohydrazido)carbonyl]cyclobutyl]isoxazole-3-carboxamide (270 mg, 0.70 mmol, 1.00 eq.) were added to a solution of triphenylphosphine (307 mg, 1.17 mmol, 1.50 eq.) in dichloromethane (5 mL). The resulting solution was stirred for 1 hour at room temperature and it was then quenched by the addition of 10 mL of water. The resulting solution was extracted with ethyl acetate (3x25 mL) and the organic layers combined. The resulting mixture was washed with brine (3x20 mL), dried over anhydrous sodium sulfate and concentrated under vacuum. The crude product was purified by Prep-HP LC with the following conditions (Waters): Column, X-Bridge Prep CI 8 OBD Column, 19* 150mm 5um 13nm; mobile phase, Water with 0.05% NH ₄ HCO ₃ and ACN (20.0% ACN up to 70.0% in 8 min); Detector, UV 254/220 nm. This resulted in 63.5 mg (25%) of 5-phenyl-N-[/raws-3-[5-(oxetan-3-yl)-l,3,4- oxadiazol-2-yl]cyclobutyl]isoxazole-3-carboxamide as a white solid.

[0573] Analytical data:

[0574] LC-MS (ES, m/z): [M+H] ⁺ = 367.1

[0575] HPLC purity: 99.9% at 254 nm [0576] ^X H NMR (DMSO-ifc, 300MHz): δ 9.32-9.29 (d, J= 8.1 Hz, 1H), 7.96-7.93 (m, 2H),

7.59-7.55 (m, 3H), 7.38 (s, 1H), 4.95-4.90 (m, 2H), 4.83-4.78 (m, 2H), 4.74-4.53 (m, 2H), 3.72-3.68 (m, 1H), 2.70-2.65 (m, 4H).

Example 53: 7V-(ir««s-3-(l-methyl-lH-benzo[d]imidazol-2-yl)cyclobutyl) -5- phenylisoxazole-3-carboxamide

[0577] Step 1: 5-phenyWV-[""«ws-3-[[2-

(methylamino)phenyl] carbamoyl] cyclobutyl]isoxazole-3-carboxamide: HATU (797 mg, 2.10 mmol, 1.20 eq.), l-N-methylbenzene-l,2-diamine (426 mg, 3.49 mmol, 2.00 eq.) and DIEA (676 mg, 5.23 mmol, 3.00 eq.) were added to a solution of ?raws-3-(5-phenylisoxazole-3- amido)cyclobutane-l-carboxylic acid (500 mg, 1.75 mmol, 1.00 eq.) in dichloromethane (30 mL). The resulting solution was stirred for 6 hours at room temperature and it was then quenched by the addition of water. The resulting solution was extracted with dichloromethane and the organic layers combined. The resulting mixture was washed with brine, dried over anhydrous sodium sulfate and concentrated under vacuum. The residue was applied onto a silica gel column with ethyl acetate/petroleum ether (1 : 15) to give 200 mg (29%) of 5-phenyl- N-[?ra«s-3-[[2-(methylamino)phenyl]carbamoyl]cyclobutyl]iso xazole-3-carboxamide as a white solid. LC-MS (ES, m/z): [M+H] ⁺ = 391.1.

[0578] Step 2: iV-(ir««s-3-(l-methyl-lH-benzo[d]imidazol-2-yl)cyclobutyl) -5- phenylisoxazole-3-carboxamide: solution of 5-phenyl-N-[?raws-3-[[2- (methylamino)phenyl]carbamoyl]cyclobutyl]isoxazole-3-carboxa mide (200 mg, 0.51 mmol, 1.00 eq.) in acetic acid (5 mL) was placed in a microwave reactor for 1 hour at 120°C. The reaction was then quenched by the addition of 10 mL of water and the resulting solution was extracted with ethyl acetate (3x15 mL) and the organic layers combined. The resulting mixture was washed with brine (3x20 mL), dried over anhydrous sodium sulfate and concentrated under vacuum. The crude product was purified by Prep-HP LC with the following conditions

(Waters): Column, XBridge CI 8 OBD Prep Column,, 5 um, 19 mm X 250 mm; mobile phase, Water with 0.05% NH ₄ HCO ₃ and ACN (30.0% ACN up to 75.0% in 8 min); Detector, UV 254 nm. The crude product was purified by Chiral-Prep-HPLC with the following conditions (Prep-HPLC-032): Column, CHIRALPAK IC, 2*25cm, 5um; mobile phase, hexane and ethanol (hold 40.0% ethanol in 15 min); Detector, UV 254/220 nm to give 41.5 mg (22%) of 5- phenyl-N-[£raws-3 -( 1 -methyl- 1 H- 1 ,3 -benzodiazol-2-yl)cyclobutyl] isoxazole-3 -carboxamide as a white solid.

[0579] Analytical data:

[0580] LC-MS (ES, m/z): [M+H] ⁺ = 373.2

[0581] HPLC purity: 99.5% at 254 nm [0582] 1H NMR (CD ₃ OD-i¾, 400 MHz): δ 7.91-7.89 (m, 2H), 7.65-7.63 (m, 1H), 7.58-

7.50 (m, 3H), 7.49-7.47 (m, 1H), 7.32-7.24 (m, 2H), 7.12 (s, 1H), 4.79-4.70 (m, 1H), 3.81(s, 3H), 3.75-3.66 (m, 1H), 3.01-2.95 (m, 2H), 2.66-2.58 (m, 2H).

Example 54: 5-(2,4-difluorophenyl)-/V-(ir««s-3-(5-((R)-l-hydroxyethyl) -l,3,4-oxadiazol- 2-yl)cyclobutyl)isoxazole-3-carboxamide

[0583] A solution of pyridine hydrogen fluoride (1 mL) and 5-(2,4-difluorophenyl)-N- [?ra«s-3-[5-[(lR)-l-[(tert-butyldimethylsilyl)oxy]ethyl]-l, 3,4-oxadiazol-2- yl]cyclobutyl]isoxazole-3-carboxamide (140 mg, 0.28 mmol, 1.00 eq., prepared according to example 44) in methanol (4 mL) was stirred for 2 hours at room temperature. The mixture was filtered and it was then concentrated under vacuum. The residue was applied onto a silica gel column with dichloromethane/methanol (50: 1). The crude product was purified by Flash-Prep- HPLC with the following conditions (IntelFlash-1): Column, C18; mobile phase, H ₂ 0/ACN = 80:20 increasing to H ₂ 0/ACN = 20:80 within 20 min; Detector, UV 254 nm to give 23.4 mg (22%) of 5-(2,4-difluorophenyl)-N-[?ra«s-3-[5-[(l S)-l-hydroxyethyl]-l,3,4-oxadiazol-2- yl]cyclobutyl]isoxazole-3-carboxamide as a white solid. [0584] Analytical data: [0585] LC-MS (ES, m/z): [M+H = 391.2 [0586] HPLC purity: 98.8% at 254 nm

[0587] ^X H NMR (400MHz, DMSO- d ₆ ): δ 9.36-9.35 (d, J= 7.6 Hz, 1H,), 8.08-8.07 (m,

1H), 7.61-7.59 (m, 1H), 7.36-7.34 (m, 1H), 7.18-7.17 (d, J= 2.4 Hz, 1H), 5.96- 5.94 (d, J= 5.6 Hz, 1H), 4.94-4.90 (m, 1H), 4.70-4.69 (m, 1H), 3.73-3.71 (m,

1H), 2.70-2.62 (m, 4H), 1.49-1.48 (d, J= 6.4 Hz, 3H).

Example 55: 5-(3-fluorophenyl)-iV-(ir««s-3-(5-((R)-l-hydroxyethyl)-l,3 ,4-oxadiazol-2- yl)cyclobutyl)isoxazole-3-carboxamide

[0588] Asolution of TEA.3HF (5 mL) and N-[?raws-3-(5-[(lR)-[(tert- butyldimethylsilyl)oxy]ethyl]-l,3,4-oxadiazol-2-yl)cyclobuty l]-5-(3-fluorophenyl)isoxazole-3- carboxamide (500 mg, 1.03 mmol, 1.00 eq.) in methanol (20 mL) was stirred for 3 hours at room temperature. The resulting mixture was concentrated under vacuum and the crude product was purified by Flash-Prep-HPLC with the following conditions (IntelFlash-1):

Column, CI 8; mobile phase, MeCN/water = 20% increasing to MeCN/water = 90%> within 25 min; Detector, UV 254 nm to give 1 12.1 mg of 5-(3-fluorophenyl)-N-[?ra«s-3-[5-(l- hydroxyethyl)-l,3,4-oxadiazol-2-yl]cyclobutyl]isoxazole-3-ca rboxamide as a white solid.

[0589] Analytical data:

[0590] LC-MS (ES, m/z): [M+l] ⁺ = 373.1

[0591] HPLC purity: 98.5% at 254 nm [0592] ^X H NMR (DMSO-i¾, 300MHz): 59.35-9.32 (d, J= 7.8 Hz, 1H), 7.87 - 7.74 (m,

2H), 7.61-7.59 (m, 1H), 7.51 (s, 1H), 7.41-7.33 (m, 1H), 5.94-5.92 (d, J= 5.7 Hz, 1H), 4.98 - 4.83 (m, 1H), 4.75-4.62 (m, 1H), 3.73-3.67 (m, 1H), 2.77 - 2.52 (m, 4H), 1.49-1.46 (d, J= 6.6 Hz, 3H). Example 56: 5-(2-fluorophenyl)-iV-(ir««s-3-(5-((R)-l-hydroxyethyl)-l,3 ,4-oxadiazol-2- yl)cyclobutyl)isoxazole-3-carboxamide

[0593] The compound was prepared using the method methodology described in example 55. The crude product (150 mg) was purified by Flash-Prep-HPLC with the following conditions (IntelFlash-1): Column, C18 silica gel; mobile phase, H ₂ O/CH ₃ CN = 85: 15 increasing to H ₂ 0/CH ₃ CN = 15:85 within 20 min; Detector, UV 254 nm. This resulted in 59.3 mg (62%) of 5-(2-fluorophenyl)-N-[?ra«s-3-[5-[(lR)-l-hydroxyethyl]-l,3, 4-oxadiazol-2- yl]cyclobutyl]isoxazole-3-carboxamide as a white solid.

[0594] Analytical data:

[0595] LC-MS (ES, m/z): [M+l] ⁺ = 373.0

[0596] HPLC purity: 98.6% at 254 nm

[0597] ^X H ΜΡν (DMSO-ifc, 400MHz): 59.35 (d, J= 7.6 Hz, 1H), 8.03-7.98 (m, 1H), 7.66- 7.61 (m, 1H), 7.51-7.43 (m, 2H), 7.19-7.18 (d, J= 2.8 Hz, 1H), 5.95 (d, J= 5.6 Hz, 1H), 4.94-4.88 (m, 1H), 4.72-4.66 (m, 1H), 3.73-3.68 (m, 1H), 2.73-2.49 (m, 4H), 1.48 (d, J= 6.4 Hz, 3H).

Example 57: 5-(4-hydroxyphenyl)-7V-(ir««s-3-(5-((R)-l-hydroxyethyl)-l, 3,4-oxadiazol- 2-yl)cyclobutyl)isoxazole-3-carboxamide

[0598] The compound was prepared using the method methodology described in example 54. The crude mixture was purified by Prep-HPLC with the following conditions (Waters): Column, XBridge CI 8 OBD Prep Column, 19 mm X 250 mm; mobile phase, Water With 0.08% NH ₄ HCO ₃ and CH ₃ CN (35% CH ₃ CN up to 70% CH ₃ CN in 10 min, up to 95% in 2 min and down to 35% in 2 min); Detector, UV 254. This resulted in 23 mg (46%) of N-(trans-3-[5- [(lR)-l-hydroxyethyl]-l,3,4-oxadiazol-2-yl]cyclobutyl)-5-(4- hydroxyphenyl)isoxazole-3- carboxamide as a white solid.

[0599] Analytical data:

[0600] LC-MS (ES, m/z): [M+H] ⁺ = 371.1

[0601] HPLC purity: 100% at 254 nm

[0602] 'H NMR (400MHZ, DMSO- d ₆ ): δ 10.15 (s, 1H), 9.26-9.24 (d, 1H, J = 7.6 Hz),

7.77-7.75 (d, 2H, J = 8.8 Hz), 7.12 (s, 1H), 6.92-6.90 (d, 2H, J= 8.8 Hz), 5.95- 5.94 (d, 1H, J = 5.6 Hz), 4.93-4.89 (m, 1H), 4.71-4.65 (m, 1H), 3.73-3.69 (m, 1H), 2.68-2.60 (m, 4H), 1.49-1.48 (d, 3H, J= 6.4 Hz).

Example 58: 5-(3-hydroxyphenyl)-iV-(ir««s-3-(5-((R)-l-hydroxyethyl)-l, 3,4-oxadiazol 2-yl)cyclobutyl)isoxazole-3-carboxamide

[0603] The compound was prepared using the method methodology described in example 54. The crude product was purified by Prep-HPLC with the following conditions (Waters): Column, XBridge CI 8 OBD Prep Column, 19 mm X 250 mm; mobile phase, Water with 0.08% NH ₄ HCO ₃ and CH ₃ CN (35% CH ₃ CN up to 70% CH ₃ CN in 10 min, up to 95% in 2 min and down to 35% in 2 min; Detector, 254 nm. This resulted in 36.6 mg (31%) of 5-(3- hydroxyphenyl)-N-[?ra«s-3-[5-[(lS)-l-hydroxyethyl]-l,3,4-ox adiazol-2- yl]cyclobutyl]isoxazole-3-carboxamide as a white solid.

[0604] Analytical data: [0605] LC-MS (ES, m/z): [M+H] ⁺ = 371.0

[0606] HPLC purity: 98.0% at 254 nm

[0607] ^X H ΜΡν (400MHz, DMSO- d ₆ , ppm): δ 9.84 (s, 1H), 9.31-9.29 (d, 1H, J= 7.6 Hz),

7.36-7.35 (d, 2H, J= 5.2 Hz), 7.28 (s, 2H), 6.95-6.92 (m, 1H), 5.96-5.94 (d, 1H, J= 5.6 Hz), 4.94-4.90 (m, 1H), 4.72-4.66 (m, 1H), 3.73-3.69 (m, 1H), 2.70-2.59 (m, 4H), 1.50-1.48 (d, 3H, J= 6.4 Hz).

Example 59: 5-(3,4-difluorophenyl)-iV-(ir««s-3-(5-((R)-l-hydroxyethyl) -l,3,4-oxadiazol- 2-yl)cyclobutyl)isoxazole-3-carboxamide

[0608] The compound was prepared using the method methodology described in example 55. The mixture was purified by Prep-TLC with ethyl acetate/petroleum ether (1 : 1) to give 112 mg (94%) 5-(3,4-difluorophenyl)-N-(?ra«s-3-(5-((R)-l-hydroxyethyl)-l ,3,4-oxadiazol-2- yl)cyclobutyl)isoxazole-3-carboxamide as a white solid.

[0609] Analytical data:

[0610] LC-MS (ES, m/z): [M+H] ⁺ = 391.1

[0611] HPLC purity: 98.8% at 254 nm

[0612] 'H NMR (400 MHz, DMSO-i¾): 59.36-9.34 (d, J= 8.0 Hz, 1H), 8.12-8.08 (m, 1H),

7.84-7.83 (m, 1H), 7.69-7 ^' .62 (m, 1H), 7.46 (s, 1H), 5.95-5.94 (d, J= 5.6 Hz, 1H), 4.95-4.90 (m, 1H), 4.74-4.64 (m, 1H), 3.73-3.68 (m, 1H), 2.73-2.60 (m, 4H), 1.49-1.48 (d, J= 6.8 Hz, 3H).

Example 60: iV-(ir««s-3-(5-((R)-l-(methylsulfonyl)ethyl)-l,3,4-oxadiaz ol-2- yl)cyclobutyl)-5-phenylisoxazole-3-carboxamide

[0613] Step 1: (lS)-l-[5-[ir««s-3-(5-phenylisoxazole-3-amido)cyclobutyl]- l,3,4- oxadiazol-2-yl] ethyl 4-nitrobenzoate: DEAD (30 g, 1.50 eq.) was added dropwise to a solution of 5-phenyl-N-[?ra«s-3-[5-[(lR)-l-hydroxyethyl]-l,3,4-oxadiazo l-2- yl]cyclobutyl]isoxazole-3-carboxamide (35 g, 98.77 mmol, 1.00 eq.), 4-nitrobenzoic acid (20 g, 119.68 mmol, 1.20 eq.) and triphenylphosphine (38.85 g, 148.12 mmol, 1.50 eq.) in tetrahydrofuran (500 mL). The resulting solution was stirred for 2 hours at room temperature. The resulting solution was diluted with 500 ml of ethyl acetate, washed with brine (2x200 mL) and concentrated under vacuum. The residue was applied onto a silica gel column with ethyl acetate/petroleum ether (1 :4). This resulted in 43 g of (lS)-l-[5-[?ra«s-3-(5-phenylisoxazole-3- amido)cyclobutyl]-l,3,4-oxadiazol-2-yl]ethyl 4-nitrobenzoate as a white solid. LC-MS (ES, m/z): [M+H] ⁺ = 504.1.

[0614] Step 2: 5-phenyl-7V-[ir««s-3-[5-[(lS)-l-hydroxyethyl]-l,3,4-oxadia zol-2- yl]cyclobutyl]isoxazole-3-carboxamide: solution of LiOH (8 g, 334.06 mmol, 2.00 eq.) in water (100 mL) was added to a solution of (lS)-l-[5-[?ra¾s-3-(5-phenylisoxazole-3- amido)cyclobutyl]-l,3,4-oxadiazol-2-yl]ethyl 4-nitrobenzoate (48 g, 95.34 mmol, 1.00 eq.) in tetrahydrofuran (600 mL). The resulting solution was stirred for 5 hours at room temperature and it was then concentrated under vacuum. The residue was dissolved in 200 mL of water. The pH value of the solution was adjusted to 1-2 with hydrogen chloride aqueous (2Ν). The solid was collected by filtration and dried to give 31 g (92%) of 5-phenyl-N-[?ra«s-3-[5-[(lS)- l-hydroxyethyl]-l,3,4-oxadiazol-2-yl]cyclobutyl]isoxazole-3- carboxamide as a white solid. LC-MS (ES, m/z): [M+H] ⁺ = 355.0.

[0615] Step 3: (lS)-l-[5-[ir««s-3-(5-phenylisoxazole-3-amido)cyclobutyl]- l,3,4- oxadiazol-2-yl] ethyl methanesulfonate: MsCl (14.5 g, 126.58 mmol, 1.50 eq.) was added dropwise to a cold solution of 5-phenyl-N-[?ra«s-3-[5-[(lS)-l-hydroxyethyl]-l,3,4-oxadiazo l-2- yl]cyclobutyl]isoxazole-3-carboxamide (31 g, 87.48 mmol, 1.00 eq.) and TEA (26 g, 256.94 mmol, 3.00 eq.) in dichloromethane (500 mL) at 0°C. The resulting solution was stirred for 5 hours in a water/ice bath. The resulting mixture was washed with water (3x100 mL), CuS0 ₄ aqueous (2x100 mL) and brine (2x50 mL). The resulting mixture was concentrated under vacuum to give 40 g (crude) of (l S)-l-[5-[?raws-3-(5-phenylisoxazole-3-amido)cyclobutyl]- l,3,4-oxadiazol-2-yl]ethyl methanesulfonate as an off white solid. LC-MS (ES, m/z): [M+H] ⁺ = 433.0.

[0616] Step 4: 5-phenyl-7V-[ir««s-3-[5-[(lR)-l-(methylsulfanyl)ethyl]-l,3 ,4-oxadiazol-2- yl]cyclobutyl]isoxazole-3-carboxamide: sodium methanethiolate (13 g, 185.48 mmol, 2.00 eq.) was added to a solution of (lS)-l-[5-[?raws-3-(5-phenylisoxazole-3-amido)cyclobutyl]- l,3,4-oxadiazol-2-yl]ethyl methanesulfonate (40 g, 92.50 mmol, 1.00 eq.) in DMF (200 mL). The resulting solution was stirred for 5 hours at 100°C in an oil bath and it was then quenched by the addition of 100 mL of water. The resulting solution was extracted with ethyl acetate (3x100 mL) and the organic layers combined. The resulting mixture was washed with brine (2x20 mL) and concentrated under vacuum. This resulted in 32 g (crude) of 5-phenyl-N-[trans- 3-[5-[(lR)-l-(methylsulfanyl)ethyl]-l,3,4-oxadiazol-2-yl]cyc lobutyl]isoxazole-3-carboxamide as brown oil. LC-MS (ES, m/z): [M+H] ⁺ = 385.1.

[0617] Step 5: 5-phenyl-/V-[ir««s-3-[5-[(lR)-l-methanesulfonylethyl]-l,3, 4-oxadiazol-2- yl]cyclobutyl]isoxazole-3-carboxamide: m-CPBA (58 g, 336.10 mmol, 4.00 eq.) was added to a solution of 5-phenyl-N-[?ra«s-3-[5-[(lR)-l-(methylsulfanyl)ethyl]-l,3,4 -oxadiazol-2- yl]cyclobutyl]isoxazole-3-carboxamide (32 g, 83.24 mmol, 1.00 eq.) in dichloromethane (500 mL). The resulting solution was stirred for 4 hours at 0°C in a water/ice bath and it was then quenched with 300 mL of a ₂ S ₂ 03 aqueous. The separated organic layer was washed with aHC0 ₃ aqueous (2x300 mL) and concentrated under vacuum. The residue was applied onto a silica gel column with dichloromethane/MeOH(20: l) to give 14.16 g (41%) of 5-phenyl-N- [(?ra«s-3-[5-[(lR)-l-methanesulfonylethyl]-l,3,4-oxadiazol- 2-yl]cyclobutyl]isoxazole-3- carboxamide as a light yellow solid.

[0618] Analytical data:

[0619] LC-MS (ES, m/z): [M+H] ⁺ = 417.3

[0620] HPLC purity: 95.0% at 254 nm

'H NMR (DMSO-ifc, 400 MHz): δ 9.33-9.31 (d, J= 7.6 Hz, 1H), 7.96-7.93 (m, 2H), 7.59-7.54 (m, 3H), 7.38 (s, 1H), 5.18-5.13 (m, 1H), 4.73-4.67 (m, 1H), 3.77-3.73 (m, 1H), 3.16 (s, 3H), 2.75-2.60 (m, 4H), 1.74-1.72 (d, J= 7.2 Hz, 3H).

Example 61 : iV-(ir««s-3-(5-cyclobutyl-l,3,4-oxadiazol-2-yl)cyclobutyl) -5- phenylisoxazole-3-carboxamide:

[0621] The compound was prepared according to the procedure shown in example 50.

Appearance: white solid

[0622] Analytical data:

[0623] LC-MS (ES, m/z): [M+H] ⁺ 365.0

[0624] HPLC purity: 97.3% at 254 nm

[0625] 'H NMR (300 MHz, OMSO-d ₆ , ppm): δ 9.31-9.29 (m, 1H), 7.96-7.93 (m, 2H),

7.60-7.55 (m, 3H), 7.38 (s, 1H), 4.69-4.67 (m, 1H), 3.81-3.64 (m, 2H), 2.72-2.57 (m, 4H), 2.39-2.23 (m, 4H), 2.14-1.98 (m, 2H).

Example 62: iV-(ir««s-3-(lH-imidazol-l-yl)cyclobutyl)-5-phenylisoxazol e-3- carboxamide ^I -Boc 1. TEA.MsCI ^N -Boc N

HO MsO 2. Cs ₂ C0 ₃ , DMF, 80 °C

[0626] Step 1: tert-butyl iV-[ir««s-3-(methanesulfonyloxy)cyclobutyl]carbamate: MsCl (5.386 g, 46.83 mmol, 2.00 eq.) was added dropwise to a cold solution of tert-butyl N-[trans-3- hydroxycyclobutyl] carbamate (4.379 g, 23.39 mmol, 1.00 eq.) and TEA (7.095 g, 70.12 mmol, 3.00 eq.) in dichloromethane (25 mL at 0°C. The resulting solution was stirred for 3 hours at room temperature and it was then diluted with 200 mL of dichloromethane. The resulting mixture was washed with water (2x100 mL), dried over anhydrous sodium sulfate and concentrated under vacuum. The crude product was recrystallized from

dichloromethane/hexane in the ratio of 1 : 1 to give 5.548 g (89%) of tert-butyl N-[cis-3- (methanesulfonyloxy)cyclobutyl]carbamate as an off-white solid. [0627] Step 2: tert-butyl iV-[ir««s-3-(lH-imidazol-l-yl)cyclobutyl]carbamate: a solution of tert-butyl N-[czs-3-(methanesulfonyloxy)cyclobutyl]carbamate (530 mg, 2.00 mmol, 1.00 eq.), lH-imidazole (272 mg, 4.00 mmol, 2.00 eq.) and Cs ₂ C0 ₃ (1.956 g, 6.00 mmol, 3.01 eq.) in DMF (10 mL). was stirred overnight at 80 °C. The resulting mixture was concentrated under vacuum, diluted with 100 mL of ethyl acetate and the mixture was washed with water (2x50 mL), dried over anhydrous sodium sulfate and concentrated under vacuum to give 230 mg (crude) of tert-butyl N-[?ra«s-3-(lH-imidazol-l-yl)cyclobutyl]carbamate as yellow oil. LC- MS (ES, m/z): [M+H] ⁺ = 238.12.

[0628] Step 3: ir«ws-3-(lH-imidazol-l-yl)cyclobutan-l-amine hydrochloride: 2Ν hydrogen chloride aqueous (10 mL) was added to a solution of tert-butyl N-[trans-3-(lR- imidazol-l-yl)cyclobutyl]carbamate (230 mg, 0.97 mmol, 1.00 eq.) in tetrahydrofuran (10 mL). The resulting solution was stirred for 4 hours at room temperature, concentrated under vacuum to give 0.4 g (crude) of ?ra«s-3-(lH-imidazol-l-yl)cyclobutan-l -amine hydrochloride as yellow oil. LC-MS (ES, m/z): [M+H] ⁺ = 138.0.

[0629] Step 4: 5-phenyl-iV-[ir««s-3-(lH-imidazol-l-yl)cyclobutyl]isoxazol e-3- carboxamide: £raws-3-(lH-imidazol-l-yl)cyclobutan-l -amine hydrochloride (400 mg, 2.30 mmol, 0.70 eq.), HATU (1.507 g, 3.96 mmol, 1.20 eq.) and DIEA (1.279 g, 9.90 mmol, 3.00 eq.) were added to a solution of 5-phenylisoxazole-3-carboxylic acid (624 mg, 3.30 mmol, 1.00 eq.) in dichloromethane (30 mL). The resulting solution was stirred for 2 hours at room temperature and it was then concentrated under vacuum. The crude product was purified by Prep-HPLC with the following conditions (Waters): Column, XBridge BEH130 Prep C18 OBD Column, 19* 150mm 5um 13nm; mobile phase, water with 0.05%TFA and ACN (12.0% ACN up to 50.0% in 8 min); Detector, UV 254nm. This resulted in 58 mg (6%) of 5-phenyl-N- [£raws-3-(lH-imidazol-l-yl)cyclobutyl]isoxazole-3-carboxami de as a white solid.

[0630] Analytical data:

[0631] LC-MS (ES, m/z): [M+H] ⁺ = 309.2 [0632] HPLC purity: 99.4% at 254 nm

[0633] 'H NMR (300MHZ, OMSO-d ₆ , ppm): δ 9.28 (s, 1H), 7.98-7.93 (m, 3H), 7.51 (s,

1H), 7.60-7.56 (m, 3H), 7.37 (s, 1H), 5.20-5.1 1 (m, 1H), 4.69-4.60 (m, 1H), 2.91-2.45 (m, 4H).

Example 63: 7V-(3-(5-((R)-l-hydroxyethyl)-l,3,4-oxadiazol-2-yl)cyclohexy l)-5- phenylisoxazole-3-carboxamide

[0634] Step 1: 3-[[(tert-butoxy)carbonyl]amino]cyclohexane-l-carboxylic acid: sodium hydroxide (1.6 g, 40.00 mmol, 2.00 eq.) and B0C2O (5.232 g, 24.00 mmol, 1.20 eq.) were added to a solution of 3-aminocyclohexane-l-carboxylic acid (2.86 g, 19.97 mmol, 1.00 eq.) in water (50 mL) and the mixture was stirred for 3 hours at room temperature. The solids were collected by filtration to give 4.048 g (83%) of 3-[[(tert-butoxy)carbonyl]amino]cyclohexane-l- carboxylic acid as a white solid. LC-MS (ES, m/z): [M+H] ⁺ = 244.1.

[0635] Step 2: of tert-butyl 7V-(3-[N-[(2R)-2-[(tert-butyldimethylsilyl)oxy]propanoyl] hydrazinecarbonyl]cyclohexyl)carbamate: (2R)-2-[(tert- butyldimethylsilyl)oxy]propanehydrazide (637 mg, 2.92 mmol, 1.20 eq.), HATU (1.1 11 g, 2.92 mmol, 1.20 eq.) and DIEA (943 mg, 7.30 mmol, 3.00 eq.) were added to solution of 3-[[(tert- butoxy)carbonyl]amino]cyclohexane-l-carboxylic acid (592 mg, 2.43 mmol, 1.00 eq.) in dichloromethane (30 mL). The resulting solution was stirred for 2 hours at room temperature and it was then concentrated under vacuum. The residue was applied onto a silica gel column with ethyl acetate/petroleum ether (1 :5) to give 848 mg (79%) of tert-butyl N-(3-[N-[(2R)-2- [(tert-butyldimethylsilyl)oxy]propanoyl]hydrazinecarbonyl]cy clohexyl)carbamate as an off- white solid. LC-MS (ES, m/z): [M+H] ⁺ = 444.2. [0636] Step 3: 7V-(3-[5-[(lR)-l-[(tert-butyldimethylsilyl)oxy]ethyl]-l,3,4- oxadiazol-2- yl]cyclohexyl)carbamate: I ₂ (833 mg, 3.28 mmol, 2.00 eq.), TEA (993 mg, 9.81 mmol, 6.00 eq.) and tert-butyl N-(3-[N-[(2R)-2-[(tert- butyldimethylsilyl)oxy]propanoyl]hydrazinecarbonyl]cyclohexy l)carbamate (726 mg, 1.64 mmol, 1.00 eq.) were added slowly (in several batches) to a cold solution of PyPPh ₂ (862 mg, 3.28 mmol, 2.00 eq.) in dichloromethane (20 mL) at 0 °C. The resulting solution was stirred for 2 hours at room temperature and it was then concentrated under vacuum. The residue was applied onto a silica gel column with ethyl acetate/petroleum ether (1 : 10) to give 549 mg (79%) of tert-butyl N-(3-[5-[(lR)-l-[(tert-butyldimethylsilyl)oxy]ethyl]-l,3,4-o xadiazol-2- yl]cyclohexyl)carbamate as yellow oil. LC-MS (ES, m/z): [M+H] ⁺ = 426.2.

[0637] Step 4: (lR)-l-(5-(3-aminocyclohexyl)-l,3,4-oxadiazol-2-yl)ethan-l-o l: a solution of tert-butyl N-(3-[5-[(lR)-l-[(tert-butyldimethylsilyl)oxy]ethyl]-l,3,4-o xadiazol-2- yl]cyclohexyl)carbamate (549 mg, 1.29 mmol, 1.00 eq.) and trifluoroacetic acid (3 mL) in dichloromethane (10 mL) was stirred for 2 hours at room temperature. The resulting mixture was concentrated under vacuum to give 300 mg (crude) of (lR)-l-(5-(3-aminocyclohexyl)- l,3,4-oxadiazol-2-yl)ethan-l-ol as yellow oil. LC-MS (ES, m/z): [M-TFA+H] ⁺ = 212.3.

[0638] Step 5: (lR)-l-[5-[3-(5-phenylisoxazole-3-amido)cyclohexyl]-l,3,4-ox adiazol-2- yljethyl 5-phenylisoxazole-3-carboxylate: 5-phenylisoxazole-3-carboxylic acid (275 mg, 1.45 mmol, 1.50 eq.), HATU (553 mg, 1.45 mmol, 1.50 eq.) and DIEA (376 mg, 2.91 mmol, 3.00 eq.) were added to a solution of (lR)-l-(5-(3-aminocyclohexyl)-l,3,4-oxadiazol-2-yl)ethan-l-o l (300 mg, 0.97 mmol, 1.00 eq.) in dichloromethane (20 mL). The resulting solution was stirred for 2 hours at room temperature and it was then concentrated under vacuum. The residue was applied onto a silica gel column with ethyl acetate/petroleum ether (1 :5) to give 350 mg (65%) of (lR)-l-[5-[3-(5-phenylisoxazole-3-amido)cyclohexyl]-l,3,4-ox adiazol-2-yl]ethyl 5- phenylisoxazole-3-carboxylate as a white solid. LC-MS (ES, m/z): [M+Hf = 554.3.

[0639] Step 6: 7V-(3-[5-[(lR)-l-hydroxyethyl]-l,3,4-oxadiazol-2-yl]cyclohex yl)-5- phenylisoxazole-3-carboxamide: a solution of (lR)-l-[5-[3-(5-phenylisoxazole-3- amido)cyclohexyl]-l,3,4-oxadiazol-2-yl]ethyl 5-phenylisoxazole-3-carboxylate (350 mg, 0.63 mmol, 1.00 eq.) and LiOHLLO (133 mg, 3.17 mmol, 5.01 eq.) in methanol (20 mL)/water (3 mL) was stirred for 2 hours at 50°C. The resulting mixture was concentrated under vacuum, diluted with 50 mL of dichloromethane and it was then washed with brine (2x20 mL), dried over anhydrous sodium sulfate and concentrated under vacuum. The crude product was purified by Prep-HP LC with the following conditions (HPLC-10): Column, XBridge Shield RP18 OBD Column, 5 urn, 19* 150 mm; mobile phase, Water with 0.08% NH ₄ HCO ₃ and ACN (20.0% ACN up to 70.0% in 8 min); Detector, UV 254/220nm. This resulted in 86 mg (36%) of N-(3-[5-[(lR)-l-hydroxyethyl]-l,3,4-oxadiazol-2-yl]cyclohexy l)-5-phenylisoxazole-3- carboxamide as a white solid.

[0640] Analytical data:

[0641] LC-MS (ES, m/z): [M+H] ⁺ = 383.1

[0642] HPLC purity: 99.8% at 254 nm [0643] 'H NMR (400 MHz, OMSO-d ₆ , ppm): δ 8.83-8.81 (d, J= 8.4 Hz, 1H), 7.95-7.92

(m, 2H), 7.59-7.52 (m, 3H), 7.38 (s, 1H), 5.93-5.91 (d, J= 5.6 Hz, 1H), 4.92- 4.85 (m, 1H), 4.03-3.96 (m, 1H), 3.18-3.12 (m, 1H), 2.22-2.19 (m, 1H), 2.04- 2.01 (m, 1H), 1.88-1.86 (m, 2H), 1.68-1.46 (m, 7H).

Example 64: 7V-(3-(4-(hydroxymethyl)-lH-l,2,3-triazol-l-yl)cyclohexyl)-5 - phenylisoxazole-3-carboxamide and 7V-(3-(5-(hydroxymethyl)-lH-l,2,3-triazol-l- yl)cyclohexyl)-5-phenylisoxazole-3-carboxamide

[0644] Step 1: tert-butyl iV-(3-azidocyclohexyl)carbamate: DIAD (1.41 g, 6.97 mmol, 1.50 eq.), DPPA (1.53 g, 5.56 mmol, 1.20 eq.) and tert-butyl N-(3- hydroxycyclohexyl)carbamate (1 g, 4.64 mmol, 1.00 eq.) were added to a solution of PPI1 ₃ (1.82 g, 6.94 mmol, 1.50 eq.) in tetrahydrofuran (30 mL). The resulting solution was stirred for 2 hours at room temperature, diluted with 50 mL of ethyl acetate and it was then washed with brine (2x30 mL) and concentrated under vacuum. The residue was applied onto a silica gel column with ethyl acetate/petroleum ether (1 :20) to give 0.642 g (58%) of tert-butyl N-(3- azidocyclohexyl)carbamate as a light yellow solid.

[0645] Step 2: tert-butyl 7V-[3-[4/5-(hydroxymethyl)-lH-l,2,3-triazol-l- yljcyclohexyl] carbamate: a solution of tert-butyl N-(3-azidocyclohexyl)carbamate (642 mg, 2.67 mmol, 1.00 eq.) and prop-2-yn-l-ol (300 mg, 5.35 mmol, 2.00 eq.) in DMF (10 mL) was placed in a sealed tube and the solution was stirred for overnight at 100°C in an oil bath. The resulting mixture was concentrated under vacuum. The residue was applied onto a silica gel column with ethyl acetate/petroleum ether (3 : 1). This resulted in 582 mg (crude) mixture of tert-butyl N-[3-[4/5-(hydroxymethyl)- 1 H- 1 ,2,3 -triazol- 1 -yl]cyclohexyl]carbamate. LC-MS (ES, m/z): [M+H] ⁺ = 297.2. [0646] Step 3: [l-(3-aminocyclohexyl)-lH-l,2,3-triazol-4/5-yl]methanol: hydrogen chloride (3 mL) was added to a solution of mixture of tert-butyl N-[3-[4/5-(hydroxymethyl)- 1H- 1,2,3 -triazol- l-yl]cyclohexyl]carbamate (582 mg, 1.96 mmol, 1.00 eq., crude) in 1,4- dioxane (10 mL). The resulting solution was stirred for 4 hours at room temperature and then it was concentrated under vacuum. This resulted in 637 mg of mixture of [l-(3- aminocyclohexyl)-lH-l,2,3-triazol-4/5-yl]methanol as a brown oil. LC-MS (ES, m/z): [M+H] ⁺ = 197.1.

[0647] Step 4: 7V-[3-[5-(hydroxymethyl)-lH-l,2,3-triazol-l-yl]cyclohexyl]-5 - phenylisoxazole-3-carboxamide and 7V-[3-[4-(hydroxymethyl)-lH-l,2,3-triazol-l- yl]cyclohexyl]-5-phenylisoxazole-3-carboxamide: DIEA (1.26 g, 3.00 eq.), HATU (2.47 g, 2.00 eq.) and 5-phenylisoxazole-3-carboxylic acid (1.23 g, 6.5 mmol, 2.00 eq.) were added to a mixture of [l-(3-aminocyclohexyl)-lH-l,2,3-triazol-5-yl]methanol and [l-(3- aminocyclohexyl)-lH-l,2,3-triazol-4-yl]methanol (637 mg, 3.25 mmol, 1.00 eq.) in dichloromethane (100 mL). The resulting solution was stirred for 5 hours at room temperature and the reaction was then quenched by the addition of 40 mL of water. The resulting solution was extracted with dichloromethane (3x100 mL) and the combined organic layers were washed with brine (2x20 mL), dried over anhydrous sodium sulfate and concentrated under vacuum. The residue was applied onto a silica gel column with ethyl acetate (100%). This resulted in 25.9 mg (6%) of N-[3-[5-(hydroxymethyl)-lH-l,2,3-triazol-l-yl]cyclohexyl]-5- phenylisoxazole-3-carboxamide as an off-white solid and 36.4 mg (5%) of N-[3-[4- (hydroxymethyl)-lH-l,2,3-triazol-l-yl]cyclohexyl]-5-phenylis oxazole-3-carboxamide as an white solid.

[0648] 7V-[3-[4-(hydroxymethyl)-lH-l,2,3-triazol-l-yl]cyclohexyl]-5 -phenylisoxazole-3- carboxamide:

[0649] Analytical data:

[0650] LC-MS (ES, m/z): [M+H] ⁺ = 368.1 [0651] 'H NMR (DMSO-ifc, 400 MHz): δ 8.82-8.80 (d, J = 7.6 Hz, 1H), 8.05 (s, 1H), 7.95- 7.93 (m, 2H), 7.58-7.54 (m, 3H), 7.37 (s, 1H), 5.18-5.15 (m, 1H), 4.93 (br, 1H), 4.53-4.50 (m, 2H), 4.31-4.25 (m, 1H), 2.38-2.30 (m, 1H), 2.18-2.1 1 (m, 1H), 1.97-1.95 (m, 2H), 1.73-1.71 (m, 4H).

[0652] 7V-[3-[5-(hydroxymethyl)-lH-l,2,3-triazol-l-yl]cyclohexyl]-5 -phenylisoxazole-3- carboxamide:

[0653] Analytical data:

[0654] LC-MS (ES, m/z): [M+H] ⁺ = 368.1

[0655] ^X H NMR (DMSO-ifc, 400 MHz): δ 8.77-8.75 (d, J= 7.6 Hz, 1H), 7.94-7.93 (m, 2H),

7.60-7.55 (m, 4H), 7.37 (s, 1H), 5.50-5.43 (m, 1H), 4.92-4.91 (m, 1H), 4.60-4.52 (m, 3H), 2.37-2.12 (m, 2H), 2.03-1.82 (m, 2H), 1.75 (br, 3H), 1.60-1.45 (m, 1H),

1.82-1.75 (m, 4H).

Example 65: iV-[3-[5-(hydroxymethyl)-l,3,4-oxadiazol-2-yl]cyclopentyl]-5 - phenylisoxazole-3-carboxamide

[0656] Step 1: methyl 3-(5-phenylisoxazole-3-carboxamido)cyclopentane-l- carboxylate: into a 50-mL round-bottom flask, was placed a solution of methyl 3- aminocyclopentane-l-carboxylate (500 mg, 3.49 mmol, 1.00 eq.) in dichloromethane (10 mL). To the solution were added HATU (1.59 g, 4.18 mmol, 1.20 eq.), DIEA (1.6 g, 12.38 mmol, 3.50 eq.) and 5-phenylisoxazole-3-carboxylic acid (790 mg, 4.18 mmol, 1.20 eq.). The resulting solution was stirred for 2 hours at room temperature. The reaction was then quenched by the addition of water. The resulting solution was extracted with ethyl acetate and the combined organic layers were dried over anhydrous sodium sulfate and concentrated under vacuum. This resulted in 0.925 g (84%) of methyl 3-(5-phenylisoxazole-3- amido)cyclopentane-l-carboxylate as a light yellow solid. LC-MS (ES, m/z) [M+Hf = 315.1

[0657] Step 2: 3-(5-phenylisoxazole-3-amido)cyclopentane-l-carboxylic acid: into a 50- mL round-bottom flask, was placed a solution of methyl 3-(5-phenylisoxazole-3- amido)cyclopentane-l-carboxylate (925 mg, 2.94 mmol, 1.00 eq.) in tetrahydrofuran/H ₂ 0 (10/1 mL). To the solution was added LiOH (354 mg, 14.78 mmol, 5.00 eq.). The resulting solution was stirred for 1 hour at room temperature. The resulting mixture was diluted with 50mL of water. The resulting solution was washed with dichloromethane and the organic layers combined. The pH value of the aqueous layer was adjusted to 3 with hydrogen chloride aqueous (2 mol/L). The resulting solution was extracted with dichloromethane and the combined organic layers were dried over anhydrous sodium sulfate and concentrated under vacuum. This resulted in 0.7971 g (90%) of 3-(5-phenylisoxazole-3-amido)cyclopentane-l- carboxylic acid as a yellow solid. LC-MS (ES, m/z) [M+H] ⁺ = 301.1

[0658] Step 3: 7V-[3-([2-[(tert

butyldimethylsilyl)oxy]acetohydrazido]carbonyl)cyclopenty l]-5-phenylisoxazole-3- carboxamide: into a 250-mL round-bottom flask, was placed a solution of 3-(5- phenylisoxazole-3-amido)cyclopentane-l-carboxylic acid (2.8 g, 9.32 mmol, 1.00 eq.) in tetrahydrofuran (50 mL). To the solution were added T ₃ P (50%) (29.68 g, 5.00 eq.), TEA (4.71 g, 46.55 mmol, 5.00 eq.) and 2-[(tert-butyldimethylsilyl)oxy]acetohydrazide (2.4851 g, 12.16 mmol, 1.00 eq.). The resulting solution was stirred for 3 hours at 30°C. The reaction was then quenched by the addition of water. The resulting solution was extracted with dichloromethane and the combined organic layers were dried over anhydrous sodium sulfate. The solids were filtered out. The resulting mixture was concentrated under vacuum. The residue was applied onto a silica gel column with ethyl acetate/petroleum ether (10:9). This resulted in 1.12 g (25%) of N-[3-([2-[(tert-butyldimethylsilyl)oxy]acetohydrazido]carbon yl)cyclopentyl]-5- phenylisoxazole-3 -carboxamide as a yellow solid. LC-MS (ES, m/z) [M+Hf = 487.2

[0659] Step 4: 7V-(3-(5-((tert-butyldimethylsilyloxy)methyl)-l,3,4-oxadiazo l-2- yl)cyclopentyl)-5-phenylisoxazole-3-carboxamide: into a 100-mL round-bottom flask purged and maintained with an inert atmosphere of nitrogen, was placed a solution of Ρ1¾Ρ (2.83 g, 5.00 eq.) in dichloromethane (25 mL). To the solution were added I ₂ (2.72 g, 5.00 eq.), TEA (1.31 g, 12.95 mmol, 6.00 eq.) and N-[3-([2-[(tert- butyldimethylsilyl)oxy]acetohydrazido]carbonyl)cyclopentyl]- 5-phenylisoxazole-3- carboxamide (1.05 g, 2.16 mmol, 1.00 eq.). The resulting solution was stirred for 2 hours at 0°C. The reaction was then quenched by the addition of water. The resulting solution was extracted with dichloromethane and the combined organic layers were dried over anhydrous sodium sulfate and concentrated under vacuum. The residue was applied onto a silica gel column with ethyl acetate/petroleum ether (5: 1). This resulted in 0.2 g (20%) of N-(3-(5-((tert- butyldimethylsilyloxy)methyl)-l,3,4-oxadiazol-2-yl)cyclopent yl)-5-phenylisoxazole-3- carboxamide as a light yellow solid. LC-MS (ES, m/z) [M+H] ⁺ = 469.2

[0660] Step 5: iV-[3-[5-(hydroxymethyl)-l,3,4-oxadiazol-2-yl]cyclopentyl]-5 - phenylisoxazole-3-carboxamide: into a 25-mL round-bottom flask, was placed N-[3-(5-[[(tert- butyldimethylsilyl)oxy]methyl]-l,3,4-oxadiazol-2-yl)cyclopen tyl]-5-phenylisoxazole-3- carboxamide (468 mg, 1.00 mmol, 1.00 eq.), tetrahydrofuran (5 niL), TABF (0.27 g, 2.00 eq.). The resulting solution was stirred for 2 h at 0°C. The reaction was then quenched by the addition of water. The resulting solution was extracted with dichloromethane and the organic layers combined and dried over anhydrous sodium sulfate. The solids were filtered out. The resulting mixture was concentrated under vacuum. The residue was applied onto a silica gel column with dichloromethane/methanol (5: 1). The crude product was purified by Prep-HPLC with the following conditions: Column: XBridge Prep C18 OBD Column 19*250mm lOum; Mobile Phase A: Water with 0.5% NH ₄ HCO ₃ , Mobile Phase B: ACN; Flow rate: 25 mL/min; Gradient: 20% B to 60% B in 10 min; 254/220 nm. This resulted in 43 mg (12%) of N-[3-[5- (hydroxymethyl)-l,3,4-oxadiazol-2-yl]cyclopentyl]-5-phenylis oxazole-3-carboxamide as a white solid.

[0661] Yield: 12%

[0662] Appearance: white solid

[0663] Analytical data:

[0664] LC-MS (ES, M/Z): [M+l = 355.1

[0665] ^X H NMR: (DMSO-i¾, 300MHz, ppm): δ 8.89 (d, J

2H), 7.55-7.50 (m,3H),7.31 (s, 1H), 5.82-5.77 (m, 1H), 4.56 (d, J= 6.0 Hz, 2H), 4.42-4.35 (m, 1H), 3.48-3.37 (m, 1H), 2.41-2.35 (m, 1H), 2.10-1.88 (m, 4H), 1.81-1.71 (m, 1H).

Example 65: iV-(c s ir««s-4-(5-(hydroxymethyl)-l,3,4-oxadiazol-2-yl)cyclohexyl )-5- phenylisoxazole-3-carboxamide

[0666] A solution of N-[4-(5-[[(tert-butyldimethylsilyl)oxy]methyl]-l,3,4-oxadiaz ol-2- yl)cyclohexyl]-5-phenylisoxazole-3-carboxamide (170 mg, 0.35 mmol, 1.00 eq., prepared using similar methodology as in example 64) in tetrahydrofuran (6 mL) and pyridine hydrofluoride (0.5 mL) was stirred for 1 hour at room temperature. The reaction was then quenched by the addition of water. The solids were collected by filtration and washed with ethyl acetate. This resulted in 37.8 mg (29%) of N-(c«/?ra«s-4-(5-(hydroxymethyl)-l,3,4-oxadiazol-2- yl)cyclohexyl)-5-phenylisoxazole-3-carboxamide as a white solid. Then the resulting filtrate was extracted with ethyl acetate and the organic layers combined. The resulting mixture was washed with brine, dried over anhydrous sodium sulfate and concentrated under vacuum. The crude product was purified by Prep-HPLC with the following conditions (Waters): Column, X Bridge Prep C18 OBD Column, 19*250mm, lOum; mobile phase, Water with 0.05%

NH ₄ HCO ₃ and ACN (30.0% ACN up to 40.0% in 10 min); Detector, UV 254/220 nm. This resulted in 12 mg (10%) of 5-phenyl-N-[c s-4-[5-(hydroxymethyl)-l,3,4-oxadiazol-2- yl]cyclohexyl]-5-phenylisoxazole-3-carboxamide and 35 mg (29%) of 5-phenyl-N-[/ra¾s-4-[5- (hydroxymethyl)-l,3,4-oxadiazol-2-yl]cyclohexyl]-5-phenyliso xazole-3-carboxamide as a white solids.

[0667] 5-phenyl-/V-[ir««s-4-[5-(hydroxymethyl)-l,3,4-oxadiazol-2- yl]cyclohexyl]-5- phenylisoxazole-3-carboxamide:

[0668] Yield: 29% [0669] Appearance: white solid

[0670] Analytical data:

[0671] LC-MS (ES, m/z): [M+H] ⁺ = 369.1

[0672] ¾ NMR: (300MHz, OMSO-d ₆ , ppm): δ 8.76-8.73 (d, 1H, J= 8.1 Hz), 7.95-7.92

(m, 2H), 7.57-7.55 (m, 3H), 7.36 (s, 1H), 5.86-5.82 (t, 1H, J= 6.0 Hz), 4.61- 4.59 (d, 2H, J= 6.0 Hz), 3.85-3.83 (m, 1H) , 2.94-2.90 (m, 1H), 2.15-2.12 (m, 2H) , 1.98-1.95 (m, 2H), 1.69-1.50 (m, 4H).

[0673] 5-phenyl-/V-[c s-4-[5-(hydroxymethyl)-l,3,4-oxadiazol-2-yl]cyclohexyl]-5- phenylisoxazole-3-carboxamide:

[0674] Yield: 10% [0675] Appearance: white solid

[0676] Analytical data:

[0677] LC-MS (ES, m/z): [M+H] ⁺ = 369.1

[0678] ¾ NMR: (300MHz, OMSO-d ₆ , ppm): δ 8.65-8.63 (d, 1H, J= 7.5 Hz), 7.93-7.90

(m, 2H), 7.60-7.54 (m, 3H), 7.34 (s, 1H), 5.87-5.83 (t, 1H, J = 6.0 Hz), 4.63-

4.61 (d, 2H, J= 6.3 Hz), 3.98-3.94 (m, 1H) , 3.23-3.16 (m, 1H), 2.15-2.11 (m, 2H) , 1.90-1.82 (m, 2H), 1.78-1.62 (m, 4H).

Example 66: 5-(3,4-dihydroxyphenyl)-iV-(ir««s-3-(5-((R)-l-hydroxyethyl )-l,3,4- oxadiazol-2-yl)cyclobutyl)isoxazole-3-carboxamide

[0679] 5-(benzo[d][l,3]dioxol-5-yl)-N-(?ra«s-3-(5-((R)-l-hydroxyet hyl)-l,3,4-oxadiazol-2- yl)cyclobutyl)isoxazole-3-carboxamidewas prepared using the method methodology described in example 54. AICI ₃ (268 mg, 2.01 mmol, 4.00 eq.) was added slowly to a solution of 5-(2H- l,3-benzodioxol-5-yl)-N-[?ra«s-3-[5-[(lR)-l-hydroxyethyl]-l ,3,4-oxadiazol-2- yl]cyclobutyl]isoxazole-3-carboxamide (200 mg, 0.50 mmol, 1.00 eq.) in ethanethiol (5 mL) at 0°C. The resulting solution was stirred for 8 hours at room temperature, it was then quenched by the addition of 50 mL of water/ice. The solids were filtered and the mixture was concentrated under vacuum. The crude product was purified by Flash-Prep-HPLC with the following conditions (IntelFlash-1): Column, CI 8; mobile phase, H ₂ 0:CH ₃ CN = 100: 1 increasing to H ₂ 0:CH ₃ CN = 1 : 100 within 20 min; Detector, UV 254 nm. This resulted in 92 mg (47%) of 5-(3,4-dihydroxyphenyl)-N-[?ra«s-3-[5-[(lR)-l-hydroxyethyl] -l,3,4-oxadiazol-2- yl]cyclobutyl]isoxazole-3-carboxamide as a light yellow solid.

[0680] Analytical data: LC-MS (ES, m/z): [M+l] ⁺ = 387

[0681 ] HPLC purity: 96.9% at 254 nm [0682] ^X H NMR (400MHz, DMSO-i¾): δ 9.69 (s, 1H), 9.38 (s, 1H), 9.24-9.22 (d, J= 7.6

Hz, 1H), 7.26-7.24 (dd, J= 2.0 Hz, 2H), 7.1 (s, 1H), 6.75 (s, 1H), 5.95-5.94 (d, J = 5.2 Hz, 1H), 4.94-4.89 (m, 1H), 4.71-4.65 (m, 1H), 3.73-3.67 (m, 1H), 2.72- 2.57 (m, 4H), 1.49-1.48 (d, J= 6.4 Hz, 3H). Example 67: iV-(ir««s-3-(lH-benzo[d]imidazol-l-yl)cyclobutyl)-5-phenyl isoxazole-3- carboxamide

[0683] Step 1: tert-butyl iV-[ir««s-3-(l,3-dioxo-2,3-dihydro-lH-isoindol-2- yl)cyclobutyl] carbamate: triphenylphosphine (15.97 g, 60.89mmol, 1.50 eq.), 2,3-dihydro- lH-isoindole-l,3-dione (7.17 g, 48.73mmol, 1.20 eq.) and DIAD (12.31 g, 60.94mmol, 1.50 eq.) were added to a solution of tert-butyl N-[cz ^' s-3-hydroxycyclobutyl]carbamate (7.6 g, 40.59mmol, 1.00 eq.) in THF (100 mL). The solution was stirred for 2 hours at room temperature and it was then quenched by the addition of water. The resulting solution was extracted with ethyl acetate and the organic layers combined. The resulting mixture was washed with brine, dried over anhydrous sodium sulfate and concentrated under vacuum. The residue was applied onto a silica gel column with ethyl acetate/petroleum ether (1 : 15). This resulted in 3.5 g (27%) of tert-butyl N-[?raws-3-(l,3-dioxo-2,3-dihydro-lH-isoindol-2- yl)cyclobutyl]carbamate as a white solid. LC-MS (ES, m/z): [M+H] ⁺ = 317.0.

[0684] Step 2: 2-[ir««s-3-aminocyclobutyl]-2,3-dihydro-lH-isoindole-l,3-d ione:

concentrated hydrogen chloride (15mL) was added to a solution of tert-butyl N-[trans-3-(\,3- dioxo-2,3-dihydro-lH-isoindol-2-yl)cyclobutyl]carbamate (2.5 g, 7.90mmol, 1.00 eq.) in THF (20 mL) and the resulting solution was stirred overnight at room temperature. The resulting mixture was concentrated under vacuum. This resulted in 2.4 g (crude) of 2-[trans-3- aminocyclobutyl]-2,3-dihydro-lH-isoindole-l,3-dione as a white solid. LC-MS (ES, m/z): [M+H] ⁺ = 217.0.

[0685] Step 3: of 2-[ir««s-3-[(2-nitrophenyl)amino]cyclobutyl]-2,3-dihydro-l H- isoindole-l,3-dione: a solution of 2-[?ra«s-3-aminocyclobutyl]-2,3-dihydro-lH-isoindole-l,3- dione (600 mg, 2.77 mmol, 1.00 eq.), l-fluoro-2 -nitrobenzene (470 mg, 3.33 mmol, 1.20 eq.) and Cs ₂ C0 ₃ (2.72 g, 8.32 mmol, 3.00 eq.) in DMF (20 mL) was stirred for 3 hours at 90°C. The reaction was then quenched by the addition of water, extracted with ethyl acetate and the organic layers combined. The solution was dried over anhydrous sodium sulfate and concentrated under vacuum. The residue was applied onto a silica gel column with ethyl acetate/petroleum ether (1 :2) to give 680 mg (73%) of 2-[traws-3-[(2- nitrophenyl)amino]cyclobutyl]-2,3-dihydro-lH-isoindole-l,3-d ione as orange oil. LC-MS (ES, m/z): [M+H] ⁺ = 338.1.

[0686] Step 4: 2-[ir««s-3-[(2-aminophenyl)amino]cyclobutyl]-2,3-dihydro-l H- isoindole-l,3-dione: Pd/C (20 mgO was added to a solution of 2-[traws-3-[(2- nitrophenyl)amino]cyclobutyl]-2,3-dihydro-lH-isoindole-l,3-d ione (200 mg, 0.59mmol, 1.00 eq.) in methanol (30mL). The solution was degassed and back filled with hydrogen and it was stirred for 9 hours at room temperature. The solids were filtered out. The resulting mixture was concentrated under vacuum to give 230 mg (crude) of 2-[trans-3-[(2- aminophenyl)amino]cyclobutyl]-2,3-dihydro-lH-isoindole-l,3-d ione as brown oil. LC-MS (ES, m/z): [M+H] ⁺ = 308.1.

[0687] Step 5: 2-[ir««s-3-(lH-l,3-benzodiazol-l-yl)cyclobutyl]-2,3-dihydr o-lH- isoindole-l,3-dione: solution of 2-[?ra«s-3-[(2-aminophenyl)amino]cyclobutyl]-2,3-dihydro- lH-isoindole-l,3-dione (650 mg, 2.1 1 mmol, 1.00 eq.)), trimethoxymethane (450 mg, 4.24 mmol, 2.00 eq.) and 4-methylbenzene- 1 -sulfonic acid (73 mg, 0.42 mmol, 0.20 eq.) in toluene (4 mL) was irradiated with microwave radiation for 1 hour at 130°C. The reaction was then quenched by the addition of water, extracted with ethyl acetate and the organic layers combined. The resulting mixture was washed with brine, dried over anhydrous sodium sulfate and concentrated under vacuum to give 1.146 g (crude) of 2-[tra«s-3-(lH-l,3-benzodiazol-l- yl)cyclobutyl]-2,3-dihydro-lH-isoindole-l,3-dione as brown oil. LC-MS (ES, m/z): [M+H] ⁺ = 318.0. [0688] Step 6: ir«ws-3-(lH-l,3-benzodiazol-l-yl)cyclobutan-l-amine: solution of 2- [trans-3 -( 1H- 1 ,3-benzodiazol- 1 -yl)cyclobutyl]-2,3 -dihydro- 1 H-isoindole- 1 ,3 -dione (540 mg, 1.70mmol, 1.00 eq.) and NH ₂ NH ₂ .H ₂ 0 (320 mg, 6.40mmol, 3.00 eq.) in ethanol (15mL) was stirred overnight at room temperature. The solids were filtered out and then concentrated under vacuum. This resulted in 378 mg (crude) of ?ra¾s-3-(lH-l,3-benzodiazol-l-yl)cyclobutan-l- amine as a brown solid. LC-MS (ES, m/z): [M+H] ⁺ = 188.1.

[0689] Step 7: 5-phenyl-iV-[ir««s-3-(lH-l,3-benzodiazol-l-yl)cyclobutyl]i soxazole-3- carboxamide: 5-phenylisoxazole-3-carboxylic acid (374 mg, 1.98mmol, 1.00 eq.), HATU (902 mg, 2.37mmol, 1.20 eq.) and DIEA (766 mg, 5.93mmol, 3.00 eq.) were added to solution of ?raws-3-(lH-l,3-benzodiazol-l-yl)cyclobutan-l-amine (370 mg, 1.98mmol, 1.00 eq.) in dichloromethane (5mL) and the solution was stirred for overnight at room temperature. The reaction was then quenched by the addition of lOmL of water, extracted with dichloromethane (3x15mL) and the organic layers combined. The resulting mixture was washed with brine (3x25mL), dried over anhydrous sodium sulfate and concentrated under vacuum. The crude product was purified by Prep-HP LC with the following conditions (HPLC-10): Column, X Bridge BEH130 Prep C18 OBD Column, 19x150mm, 5um 13nm; mobile phase, Water with 0.05% NH ₄ HCO ₃ and ACN (37% ACN up to 52% in 8 min); Detector, UV 254 nm. This resulted in 37.2 mg (5%) of 5-phenyl-N-[?ra«s-3-(lH-l,3-benzodiazol-l- yl)cyclobutyl]isoxazole-3 -carboxamide as a light yellow solid. [0690] Analytical data:

[0691] LC-MS (ES, m/z): [M+H] ⁺ = 359.2

[0692] HPLC purity: 98.9% at 254 nm

[0693] ^X H NMR (CDC1 ₃ , 400 MHz): δ 8.39 (s, 1H), 7.89-7.81 (m, 3H), 7.52-7.50 (m, 3H),

7.48-7.43 (m, 1H), 7.39-7.35 (m, 2H), 7.00 (s, 1H), 5.25-5.21 (m, 1H), 4.81-4.79 (br, 1H), 3.17-3.10 (m, 2H), 2.98-2.95 (m, 2H).

Example 68: iV- ifr««s-3-(5-(l,l-dioxidothietan-3-yl)-l,3,4-oxadiazol-2-yl )cyclobutyl)-5- phenylisoxazole-3-carboxamide

[0694] A solution of N-trans-3 -(2-( 1 , 1 -dioxidothietane-3 -carbonyl)hydrazine- 1 - carbonyl)cyclobutyl)-5-phenylisoxazole-3-carboxamide (170 mg, 0.39 mmol, 1.00 eq., prepared using a similar procedure as shown in example 52) in POCI ₃ (5 mL, 1.00 eq.) was stirred for 3 hours at 100 °C. The reaction was then quenched by the addition of sodium bicarbonate/ice, extracted with ethyl acetate and the organic layers combined. The resulting mixture was washed with sodium bicarbonate aqueous (1x50 mL), dried over anhydrous sodium sulfate and concentrated under vacuum. The crude product was purified by Prep-HPLC with the following conditions (HPLC-10): Column, XBridge BEH130 Prep C18 OBD Column, 19* 150mm, 5um 13nm; mobile phase, Water with NH ₄ HCO ₃ (50 mmol/L) and ACN (40.0% ACN up to 55.0% in 12 min); Detector, UV 254 nm. This resulted in 54 mg (33%) oiN-(trans- 3 -(5 -( 1 , 1 -dioxidothietan-3 -yl)- 1 ,3 ,4-oxadiazol-2-yl)cyclobutyl)-5-phenylisoxazole-3 - carboxamide as a white solid.

[0695] Analytical data:

[0696] LC-MS (ES, m/z): [M+H] ⁺ = 415.1

[0697] HPLC purity: 98.3% at 254 nm

[0698] ^X H NMR (DMSO-ifc, 400 MHz): δ 9.32-9.30 (d, J= 7.6 Hz, 1H), 7.96-7.93 (m, 2H),

7.57-7.55 (m, 3H), 7.38 (s, 1H), 4.76-4.69 (m, 5H), 4.22-4.19 (m, 1H), 3.75-3.71 (m, 1H), 2.70-2.66 (m, 4H).

Example 69: 7V-(3-(4-(hydroxymethyl)-lH-l,2,3-triazol-l-yl)cyclopentyl)- 5- phenylisoxazole-3-carboxamide and 7V-(3-(5-(hydroxymethyl)-lH-l,2,3-triazol-l- yl)cyclopentyl)-5-phenylisoxazole-3-carboxamide

[0699] Step 1: tert-butyl 7V-(3-azidocyclopentyl)carbamate: DIAD (1.5 g, 7.43 mmol, 1.50 eq.) was added dropwise to a solution of triphenylphosphine (1.972 g, 7.52 mmol, 1.50 eq.) in tetrahydrofuran (50 mL) at 10°C in 5 min. The resulting solution was stirred for 20 min at 10°C and then added DPPA (1.65 g, 6.00 mmol, 1.20 eq.), and a solution of tert-butyl N-(3- hydroxycyclopentyl)carbamate (1 g, 4.97 mmol, 1.00 eq.) in tetrahydrofuran (20 mL). The mixture was stirred for 1 hour at 25°C, and then diluted with 100 mL of Ι¾0. The resulting solution was extracted with ethyl acetate (2x100 mL) and the organic layers combined, washed with brine (2x100 mL), dried over anhydrous sodium sulfate and concentrated under vacuum. The residue was applied onto a silica gel column with ethyl acetate/petroleum ether (1 :20) to give 785 mg (70%) of tert-butyl N-(3-azidocyclopentyl)carbamate as yellow oil.

[0700] Step 2: tert-butyl 7V-[3-[5-(hydroxymethyl)-lH-l,2,3-triazol-l- yl] c clop en tyl] carbamate and tert-butyl N-[3-[4-(hydroxymethyl)-lH-l,2,3-triazol-l- yl]cyclopentyl]carbamate: a solution oftert-butyl N-(3-azidocyclopentyl)carbamate (785 mg, 3.47 mmol, 1.00 eq.) and prop-2-yn-l-ol (387 mg, 6.90 mmol, 2.00 eq.) in DMF (5 mL) was stirred for 16 hours at 100°C. The resulting mixture was concentrated under vacuum. The residue was applied onto a silica gel column with ethyl acetate/petroleum ether (2: 1) to give 620 mg (63%) of a mixture oftert-butyl N-[3-[5-(hydroxymethyl)-lH-l,2,3-triazol-l- yl]cyclopentyl]carbamate and tert-butyl N-[3-[4-(hydroxymethyl)-lH-l,2,3-triazol-l- yl]cyclopentyl]carbamate as a yellow oil. LC-MS (ES, m/z): [M+H] ⁺ = 283.2

[0701] Step 3: [l-(3-aminocyclopentyl)-lH-l,2,3-triazol-5-yl]methanol and [l-(3- aminocyclopentyl)-lH-l,2,3-triazol-4-yl]methanol: concentrated hydrogen chloride (3 mL) was added to a solution of the mixture oftert-butyl N-[3-[5-(hydroxymethyl)-lH-l,2,3-triazol- l-yl]cyclopentyl]carbamate and tert-butyl N-[3-[4-(hydroxymethyl)-lH-l,2,3-triazol-l- yl]cyclopentyl]carbamate (620 mg, 2.20 mmol, 1.00 eq.) in 1,4-dioxane (10 mL) and the mixture was stirred for 3 hours at 25°C. The mixture was concentrated under vacuum. This resulted in 600 mg (crude) of a mixture of [l-(3-aminocyclopentyl)-lH-l,2,3-triazol-5- yljmethanol and [l-(3-aminocyclopentyl)-lH-l,2,3-triazol-4-yl]methanol as yellow oil. LC- MS (ES, m/z): [M+H] ⁺ = 183.1.

[0702] Step 4: 7V-[3-[5-(hydroxymethyl)-lH-l,2,3-triazol-l-yl]cyclopentyl]- 5- phenylisoxazole-3-carboxamide and 7V-[3-[4-(hydroxymethyl)-lH-l,2,3-triazol-l- yl]cyclopentyl]-5-phenylisoxazole-3-carboxamide: [ 1 -(3 -aminocyclopentyl)- 1 H- 1 ,2,3- triazol-5-yl]methanol and [l-(3-aminocyclopentyl)-lH-l,2,3-triazol-4-yl]methanol (327 mg, 1.8 mmol, 1.20 eq.) were added to a solution of 5-phenylisoxazole-3-carboxylic acid (285 mg, 1.50 mmol, 1.00 eq.), HATU (855 mg, 2.25 mmol, 1.50 eq.) and DIEA (580 mg, 4.49 mmol, 3.00 eq.) in dichloromethane (10 mL) and the mixture was stirred for 3 hours at 25°C. The resulting solution was diluted with 100 mL of Ι¾0, extracted with ethyl acetate (2x100 mL) and the organic layers combined. The resulting mixture was washed with brine (2x100 mL), dried over anhydrous sodium sulfate and concentrated under vacuum. The crude product was purified by Prep-TLC (petroleum ether/ethyl acetate=l :2). This resulted in 54.2 mg (10%) of N-[3-[5-(hydroxymethyl)-lH-l,2,3-triazol-l-yl]cyclopentyl]-5 -phenylisoxazole-3-carboxamide as a light yellow solid and 124.4 mg (23%) of N-[3-[4-(hydroxymethyl)-lH-l,2,3-triazol-l- yl]cyclopentyl]-5-phenylisoxazole-3-carboxamide as a white solid.

[0703] Analytical data:

[0704] 7V-[3-[5-(hydroxymethyl)-lH-l,2,3-triazol-l-yl]cyclopentyl]- 5-phenylisoxazole- 3-carboxamide

[0705] LC-MS (ES, m/z): [M+H = 354.3 [0706] ^X H NMR (400 MHz, DMSO-i¾) δ 9.03-9.02 (d, J= 7.6 Hz, 1H), 7.95-7.92 (m, 2H), 7.59-7.52 (m, 4H), 7.38 (s, 1H), 5.48-5.45 (t, J= 5.6 Hz, 1H), 5.03-4.96 (m, 1H), 4.62-4.60 (d, J= 5.6 Hz, 2H), 4.49-4.43 (q, J= 7.6 Hz, 1H), 2.60-2.57 (m, 1H), 2.26-2.21 (m, 3H), 2.14-2.04 (m, 1H), 2.00-1.93 (m, 1H).

[0707] iV-[3-[4-(hydroxymethyl)-lH-l,2,3-triazol-l-yl]cyclopentyl]- 5-phenylisoxazole- 3-carboxamide

[0708] LC-MS (ES, m/z): [M+H] ⁺ = 354.3 [0709] 'H NMR (400 MHz, DMSO-i/ ₆ ) δ 9.06 (d, J= 7.8 Hz, 1H), 8.10 (s, 1H), 7.97 - 7.92 (m, 2H), 7.63 - 7.52 (m, 3H), 7.39 (s, 1H), 5.19 (t, J= 5.6 Hz, 1H), 5.03 (q, J= 7.6 Hz, 1H), 4.53 (d, J= 5.7 Hz, 2H), 4.47 (q, J= 7.6 Hz, 1H), 2.64 (dd, J = 14.3, 6.7 Hz, 1H), 2.29 - 1.86 (m, 5H).

Example 70

Compounds A-T below are prepared using one or more of the above procedures"

Example 71; CFTR activity assays

i. Ussing measurements

[0730] As discussed above, Ussing measurements can be used to measure CFTR activity. In this method, primary lung epithelial cells (hBEs) homozygous for the Cystic Fibrosis-causing AF508 mutation were differentiated for a minimum of 4 weeks in an air-liquid interface on

SnapWell filter plates prior to the Ussing measurements. Cells were apically mucus-washed for 30 minutes prior to treatment with compounds. The basolateral media was removed and replaced with media containing the compound of interest diluted to its final concentration from DMSO stocks. Treated cells were incubated at 37°C and 5% CO2 for 24 hours. At the end of the treatment period, the cells on filters were transferred to the Ussing chamber and equilibrated for 30 minutes. The short-circuit current was measured in voltage clamp-mode ( h _o id = 0 mV), and the entire assay was conducted at a temperature of 36°C -36.5°C. Once the voltages stabilized, the chambers were clamped, and data was recorded by pulse readings every 5 seconds. Following baseline current stabilization, the following additions were applied and the changes in current and resistance of the cells was monitored:

1. Benzamil to the apical chamber to inhibit ENaC sodium channel.

2. Forskolin to both chambers to activate AF508-CFTR by phosphorylation.

3. Genistein to both chambers to potentiate AF508-CFTR channel opening.

4. CFTRinh-172 to the apical chamber to inhibit AF508-CFTR CI- conductance.

The inhibitable current (that current that is blocked by CFTRinh-172) is measured as the specific activity of the AF508-CFTR channel, and increases in response to compound in this activity over that observed in vehicle-treated samples are identified as the correction of AF508- CFTR function imparted by the compound tested.

11. hBE Equivalent Current (Ieq) Assay

[0731] Primary lung epithelial cells homozygous for the Cystic Fibrosis-causing AF508 mutation were differentiated for a minimum of 4 weeks in an air-liquid interface on Costar 24 well HTS filter plates prior to the equivalent current (Ieq) measurements. Cells were apically mucus-washed for 30 minutes 24h prior to treatment with compounds. The basolateral media was removed and replaced with media containing the compound of interest diluted to its final concentration from DMSO stocks. Treated cells were incubated at 37°C and 5% C0 ₂ for 24 hours. At the end of the treatment period, the media was changed to the Ieq experimental solution for 30 minutes before the experiment and plates are maintained in a C0 ₂ -free incubator during this period. The plates containing the cells were then placed in pre-warmed heating blocks at 36°C±0.5 for 15 minutes before measurements are taken. The transepithelial voltage (VT) and conductance (GT) were measured using a custom 24 channel current clamp (TECC- 24) with 24 well electrode manifold. The Ieq assay measurements were made following additions with standardized time periods: 1. The baseline VT and GT values were measured for approximately 20 minutes.

2. Benzamil was added to block ENaC for 15 minutes.

3 Forskolin plus VX-770 (ivacaftor) were added to maximally activate AF508-CFTR for

27 minutes.

4, Bumetanide was added to inhibit the NaK^Cl cotransporter and shut-off secretion of chloride. [0732] The activity data captured was the area under the curve (AUC) for the traces of the equivalent chloride current. The AUC was collected from the time of the forskolin/VX-770 addition until the inhibition by bumetanide addition. Correction in response to compound treatment was scored as the increase in the AUC for compound-treated samples over that of vehicle-treated samples.

[0733] The results are shown below in Table A. (** indicates activity >200% of VX-809 (1 uM) with compound at 10 uM and VX-809 at 1 uM; * indicates activity 100-200% of VX-809 (1 uM) with compound at 10 uM and VX-809 at 1 uM. ** indicates activity >200% of VX-809 (3 uM) with compound at 10 uM and VX-809 at 3 uM; indicates activity 100-200% of VX- 809 (3 uM) with compound at 10 uM and VX-809 at 3 uM.

Table A

- £61 - 096l/£10Z OAV

Example 72

i. Ussing measurements

[0734] As discussed above, Ussing measurements can be used to measure CFTR activity. In this method, primary lung epithelial cells (hBEs) with a Cystic fibrosis causing class I mutation are differentiated for a minimum of 4 weeks in an air-liquid interface on Snap Well™ filter plates prior to the Ussing measurements. Cells are apically mucus-washed for 30 minutes prior to treatment with compounds. The basolateral media is removed and replaced with media containing the compound of interest diluted to its final concentration from DMSO or aqueous stocks. Treated cells are incubated at 37°C and 5% CO2 for 24 hours. At the end of the treatment period, the cells on filters are transferred to the Ussing chamber and equilibrated for 30 minutes. The short-circuit current is measured in voltage clamp-mode (Vh _o id = 0 mV), and the entire assay is conducted at a temperature of 36°C -36.5°C. Once the voltages stabilize, the chambers are clamped, and data are recorded by pulse readings every 5 seconds. Following baseline current stabilization, the following additions are applied and the changes in current and resistance of the cells are monitored:

1. Benzamil to the apical chamber to inhibit E aC sodium channel.

2. Forskolin to both chambers to activate AF508-CFTR by phosphorylation.

3. Ivacaftor or Genistein to the apical chamber to potentiate AF508-CFTR channel opening. 4. CFTRinh- 172 to the apical chamber to inhibit AF508-CFTR CI- conductance.

[0735] The forskolin-sensitive current and inhibitable current (that potentiated current that is blocked by CFTRinh- 172) are measured as the specific activity of the AF508-CFTR channel, and increase in response to compound in this activity over that observed in vehicle-treated samples are identified as the correction of AF508-CFTR function imparted by the compound tested.

Example 73

i. Ussing measurements

[0736] As discussed above, Ussing measurements can be used to measure CFTR activity. In this method, primary lung epithelial cells (hBEs) with a Cystic Fibrosis-causing class III mutation are differentiated for a minimum of 4 weeks in an air-liquid interface on Snap Well filter plates prior to the Ussing measurements. Cells are apically mucus-washed for 30 minutes prior to treatment with compounds. The basolateral media is removed and replaced with media containing the compound of interest diluted to its final concentration from DMSO stocks. Treated cells are incubated at 37°C and 5% CO2 for 24 hours. At the end of the treatment period, the cells on filters are transferred to the Ussing chamber and equilibrated for 30 minutes. The short-circuit current is measured in voltage clamp-mode (Vh _o id = 0 mV), and the entire assay is conducted at a temperature of 36°C -36.5°C. Once the voltages stabilize, the chambers are clamped, and data is recorded by pulse readings every 5 seconds. Following baseline current stabilization, the following additions are applied and the changes in current and resistance of the cells is monitored:

1. Benzamil to the apical chamber to inhibit ENaC sodium channel.

2. Forskolin to both chambers to activate AF508-CFTR by phosphorylation.

3. VX-770 or Genistein to the apical chamber to potentiate AF508-CFTR channel opening.

4. CFTRinh-172 to the apical chamber to inhibit AF508-CFTR CI- conductance.

[0737] The forskolin-sensitive current and inhibitable current (that potentiated current that is blocked by CFTRinh-172) are measured as the specific activity of the AF508-CFTR channel, and increase in response to compound in this activity over that observed in vehicle-treated samples are identified as the correction of AF508-CFTR function imparted by the compound tested.

Example 74

i. Ussing measurements

[0738] As discussed above, Ussing measurements can be used to measure CFTR activity. In this method, primary lung epithelial cells (hBEs) with a Cystic Fibrosis-causing class V mutation are differentiated for a minimum of 4 weeks in an air-liquid interface on Snap Well™ filter plates prior to the Ussing measurements. Cells are apically mucus-washed for 30 minutes prior to treatment with compounds. The basolateral media is removed and replaced with media containing the compound of interest diluted to its final concentration from DMSO stocks. Treated cells are incubated at 37°C and 5% CO2 for 24 hours. At the end of the treatment period, the cells on filters are transferred to the Ussing chamber and equilibrated for 30 minutes. The short-circuit current is measured in voltage clamp-mode (V _ho i _d = 0 mV), and the entire assay is conducted at a temperature of 36°C -36.5°C. Once the voltages stabilize, the chambers are clamped, and data is recorded by pulse readings every 5 seconds. Following baseline current stabilization, the following additions are applied and the changes in current and resistance of the cells is monitored:

1. Benzamil to the apical chamber to inhibit E aC sodium channel.

2. Forskolin to both chambers to activate AF508-CFTR by phosphorylation.

3. VX-770 or Genistiein to the apical chamber to potentiate AF508-CFTR channel opening. 4. CFTRinh- 172 to the apical chamber to inhibit AF508-CFTR CI- conductance.

[0739] The forskolin-sensitive current and inhibitable current (that potentiated current that is blocked by CFTRinh- 172) are measured as the specific activity of the AF508-CFTR channel, and increases in response to compound in this activity over that observed in vehicle-treated samples are identified as the correction of AF508-CFTR function imparted by the compound tested. ii. hBE Equivalent Current (Ieq) Assay

[0740] Primary lung epithelial cells homozygous for the Cystic Fibrosis-causing AF508 mutation are differentiated for a minimum of 4 weeks in an air-liquid interface on Costar 24 well HTS filter plates prior to the equivalent current (Ieq) measurements. Cells are apically mucus-washed for 30 minutes 24h prior to treatment with compounds. The basolateral media is removed and replaced with media containing the compound of interest diluted to its final concentration from DMSO stocks. Treated cells are incubated at 37°C and 5% CO ₂ for 24 hours. At the end of the treatment period, the media is changed to the Ieq experimental solution for 30 minutes before the experiment and plates are maintained in a C0 ₂ -free incubator during this period. The plates containing the cells are then placed in pre-warmed heating blocks at 36°C±0.5 for 15 minutes before measurements are taken. The transepithelial voltage (VT) and conductance (GT) are measured using a custom 24 channel current clamp (TECC-24) with 24 well electrode manifold. The Ieq assay measurements are made following additions with standardized time periods: 1. The baseline VT and GT values are measured for approximately 20 minutes.

2. Benzamil is added to block ENaC for 15 minutes.

3. Forskolin plus VX-770 (ivacaftor) are added to maximally activate AF508-CFTR for 27 minutes.

4. Bumetanide is added to inhibit the NaK^Cl cotransporter and shut-off secretion of chloride.

[0741] The activity data captured is the area under the curve (AUC) for the traces of the equivalent chloride current. The AUC is collected from the time of the forskolin/VX-770 addition until the inhibition by bumetanide addition. Correction in response to compound treatment is scored as the increase in the AUC for compound-treated samples over that of vehicle-treated samples.

[0742] While this invention has been particularly shown and described with references to preferred embodiments thereof, it will be understood by those skilled in the art that various changes in form and details may be made therein without departing from the scope of the invention encompassed by the appended claims.

INCORPORATION BY REFERENCE

[0743] All publications and patents mentioned herein, including those items listed below, are hereby incorporated by reference in their entirety for all purposes as if each individual publication or patent was specifically and individually incorporated by reference. In case of conflict, the present application, including any definitions herein, will control.

EQUIVALENTS

[0744] While specific embodiments of the subject invention have been discussed, the above specification is illustrative and not restrictive. Many variations of the invention will become apparent to those skilled in the art upon review of this specification. The full scope of the invention should be determined by reference to the claims, along with their full scope of equivalents, and the specification, along with such variations. [0745] Unless otherwise indicated, all numbers expressing quantities of ingredients, reaction conditions, and so forth used in the specification and claims are to be understood as being modified in all instances by the term "about." Accordingly, unless indicated to the contrary, the numerical parameters set forth in this specification and attached claims are approximations that may vary depending upon the desired properties sought to be obtained by the present disclosure.