CROSS-REFERENCE TO RELATED APPLICATIONS

This application claims priority to U.S. Provisional Application No. 62/580,734, filed November 2, 2017 and U.S. Provisional Application No. 62/643,061 , filed March 14, 2018, which are incorporated herein by reference in their entirety.

BACKGROUND

In metazoa, diverse stress signals converge at a single phosphorylation event at serine 51 of a common effector, the translation initiation factor eIF2a. This step is carried out by four eIF2a kinases in mammalian cells: PERK, which responds to an accumulation of unfolded proteins in the endoplasmic reticulum (ER), GCN2 to amino acid starvation and UV light, PKR to viral infection and metabolic stress, and HRI to heme deficiency. This collection of signaling pathways has been termed the "integrated stress response" (ISR), as they converge on the same molecular event. eIF2a phosphorylation results in an attenuation of translation with

consequences that allow cells to cope with the varied stresses (Wek, R.C. et al, Biochem Soc Trans (2006) 34(Pt 1):7- 11).

eIF2 (which is comprised of three subunits, α, β and γ) binds GTP and the initiator Met- tRNA to form the ternary complex (eIF2-GTP-Met-tRNA;), which, in turn, associates with the 40S ribosomal subunit scanning the 5'UTR of mRNAs to select the initiating AUG codon. Upon phosphorylation of its a-subunit, eIF2 becomes a competitive inhibitor of its GTP- exchange factor (GEF), eIF2B (Hinnebusch, A.G. and Lorsch, J.R. Cold Spring Harbor Perspect Biol (2012) 4(10)). The tight and nonproductive binding of phosphorylated eIF2 to eIF2B prevents loading of the eIF2 complex with GTP, thus blocking ternary complex formation and reducing translation initiation (Krishnamoorthy, T. et al, Mol Cell Biol (2001) 21(15):5018-

5030). Because eIF2B is less abundant than eIF2, phosphorylation of only a small fraction of the total eIF2 has a dramatic impact on eIF2B activity in cells.

eIF2B is a complex molecular machine, composed of five different subunits, eIF2B l through eIF2B5. eIF2B5 catalyzes the GDP/GTP exchange reaction and, together with a partially homologous subunit eIF2B3, constitutes the "catalytic core" (Williams, D.D. et al, / Biol Chem (2001) 276:24697-24703). The three remaining subunits (eIF2B l , eIF2B2, and eIF2B4) are also highly homologous to one another and form a "regulatory sub-complex" that provides binding sites for eIF2B 's substrate eIF2 (Dev, K. et al, Mol Cell Biol (2010) 30:5218- 5233). The exchange of GDP with GTP in eIF2 is catalyzed by its dedicated guanine nucleotide exchange factor (GEF) eIF2B. eIF2B exists as a decamer (B I2 B22 B32 B42 B52) or dimer of two pentamers in cells (Gordiyenko, Y. et al, Nat Commun (2014) 5:3902; Wortham, N.C. et al,

FASEB J (2014) 28:2225-2237). Molecules such as ISRIB interact with and stabilize the eIF2B dimer conformation, thereby enhancing intrinsic GEF activity and making cells less sensitive to the cellular effects of phosphorylation of eIF2D (Sidrauski, C. et al, eLife (2015) e07314;

Sekine, Y. et al, Science (2015) 348: 1027-1030). As such, small molecule therapeutics that can modulate eIF2B activity may have the potential to attenuate the PERK branch of the UPR and the overall ISR, and therefore may be used in the prevention and/or treatment of various diseases, such as a neurodegenerative disease, a leukodystrophy, cancer, an inflammatory disease, a musculoskeletal disease, or a metabolic disease. SUMMARY OF THE INVENTION

The present invention features compounds, compositions, and methods for the modulation of eIF2B (e.g., activation of eIF2B) and the attenuation of the ISR signaling pathway. In some embodiments, the present invention features an eIF2B modulator (e.g., an eIF2B activator) comprising a compound of Formula (I) or Formula (II), or a pharmaceutically acceptable salt, solvate, hydrate, tautomer, or stereoisomer thereof. In other embodiments, the present invention features methods of using a compound of Formula (I) or Formula (II), or a pharmaceutically acceptable salt, solvate, hydrate, tautomer, or stereoisomer thereof for the treatment of a disease or disorder, e.g., a neurodegenerative disease, a leukodystrophy, cancer, an inflammatory disease, a musculoskeletal disease, a metabolic disease, or a disease or disorder associated with impaired function of eIF2B or components in the ISR pathway (e.g., eIF2 pathway).

In one aspect, the present invention features a com ound of Formula (I):

Formula (I) or a pharmaceutically acceptable salt, solvate, hydrate, tautomer, or stereoisomer thereof, wherein:

D is a bridged bicyclic cycloalkyl, bridged bicyclic heterocyclyl, or cubanyl, wherein each bridged bicyclic cycloalkyl, bridged bicyclic heterocyclyl, or cubanyl is optionally substituted with 1-4 R ^x groups; and wherein if the bridged bicyclic heterocyclyl contains a substitutable nitrogen moiety, the substitutable nitrogen moiety may be optionally substituted by R ^N1 ;

L ¹ is C C alkylene or 2-7-membered heteroalkylene, wherein each Cj-C alkylene or 2- 7-membered heteroalkylene is optionally substituted with 1-5 R ^x ;

L is C C alkylene or 2-7-membered heteroalkylene, wherein each C C alkylene or 2-

7-membered heteroalkylene is optionally substituted with 1-5 R ^x ;

1 2

R andR" are each independently hydrogen, C C alkyl, C C alkoxy-C2-C6 alkyl, hydroxy-C ₂ -C ₆ alkyl, silyloxy-C ₂ -C ₆ alkyl, and d-C ₆ alkyl-C(0)NR ^B R ^c ;

R ^N1 is selected from the group consisting of hydrogen, C -Ce alkyl, hydroxy-C2-C6 alkyl, halo-C ₂ -C ₆ alkyl, amino-C ₂ -C ₆ alkyl, cyano-C ₂ -C ₆ alkyl, -C(0)NR ^B R ^c , -C(0)R ^D , -C(0)OR ^D , and -S(0) ₂ R ^D ;

A and W are each independently phenyl or 5-6 membered heteroaryl, wherein each phenyl or 5-6-membered heteroaryl is optionally substituted with 1-5 R ^Y ;

each R ^x is independently selected from the group consisting of C C alkyl, hydroxy-Ci- Ce alkyl, halo-Q-Ce alkyl, amino-Q-Ce alkyl, cyano-Q-C ₆ alkyl, oxo, halo, cyano, -OR ^A , - NR ^B R ^C ,— NR ^B C(0)R ^D , -C(0)NR ^B R ^c , -C(0)R ^D , -C(0)OH, -C(0)OR ^D , -SR ^E , -S(0)R ^D , and - S(0) ₂ R ^D ;

each R ^Y is independently selected from the group consisting of hydrogen, Ci-Ce alkyl, hydroxy-Ci-C6 alkyl, C C alkoxy-Ci-C6 alkyl, halo-Ci-C6 alkyl, halo-Ci-C6 alkoxy, amino-Ci- C ₆ alkyl, cyano-Ci-Ce alkyl, H0 ₂ C- Ci-C ₆ alkyl, oxo, halo, cyano, -OR ^A , -NR ^B R ^C , -

NR ^B C(0)R ^D , -C(0)NR ^B R ^c , -C(0)R ^D , -C(0)OH, -C(0)OR ^D , -S(R ^F ) _m , -S(0)R ^D , -S(0) ₂ R ^D , and G^ or

2 R ^Y groups on adjacent atoms, together with the atoms to which they are attached form a 3-7-membered fused cycloalkyl, 3-7 membered heterocyclyl, aryl, or 5-6 membered heteroaryl, optionally substituted with 1-5 R ^x ;

each G ¹ is independently C3-C6 cycloalkyl, 4-7-membered heterocyclyl, aryl, or 5-6- membered heteroaryl, wherein each C3-C6 cycloalkyl, 4-7-membered heterocyclyl, aryl, or 5-6- membered heteroaryl is optionally substituted with 1-3 R ^z ; each R ^z is independently selected from the group consisting of C ₁ -C6 alkyl, hydroxy-Ci- C ₆ alkyl, halo-Ci-Q alkyl, halo, cyano, -OR ^A , -NR ^B R ^C ,— NR ^B C(0)R ^D , -C(0)NR ^B R ^c , -C(0)R ^D , -C(0)OH, -C(0)OR ^D , and -S(0) ₂ R ^D ;

R ^A is, at each occurrence, independently hydrogen, C ₁ -C6 alkyl, halo-Ci-C6 alkyl, - C(0)NR ^B R ^c , -C(0)R ^D , or -C(0)OR ^D ;

each of R B and R C is independently hydrogen or C ₁ -C6 alkyl; or

R B and R C together with the atom to which they are attached form a 3-7-membered heterocyclyl optionally substituted with 1-3 R ^z ;

each R ^D is independently C ₁ -C6 alkyl, or halo-Ci-C6 alkyl;

each R ^E is independently hydrogen, C ₁ -C6 alkyl, or halo-Ci-C6 alkyl;

each R ^F is independently hydrogen, C ₁ -C6 alkyl, halo, or halo-Ci-C6 alkyl;

m is 1 when R ^F is hydrogen or Q-C6 alkyl, 3 when R ^F is C ₁ -C6 alkyl, or 5 when R ^F is halo.

In some embodiments, D is a bridged bicyclic cycloalkyl or bridged bicyclic

heterocyclyl, each of which is optionally substituted with 1-4 R ^x .

In some embodiments, D is a bridged 5-8 membered bicyclic cycloalkyl or heterocyclyl, each of which is optionally substituted with 1-4 R ^x . bicyclo[l.l. l]pentane, bicyclo[2.2.2]octane, bicyclo[2.1.1]hexane, bicyclo[3.1.1]heptane, bicyclo[2.2.1]heptane, bicyclo[3.2.1]octane, 2- azabicyclo[2.2.2]octane, or 2-oxabicyclo[2.2.2]octane, each of which is optionally substituted with 1-4 R ^x groups.

ituted with 1-4 R ^x . In

some embodiments, D is

In some embodiments, D is substituted with O R . In some embodiments, D is

In some embodiments, D is substituted with 1 or 2 R . In some embodiments, D is

In some embodiments, each R is independently selected from the group consisting of oxo, -OH, -C(0)OH, -C(0)OR ^D , halo, and hydroxy-Q-Ce alkyl.

o or -OR ^A (e.g., oxo or OH). In some embodiments, D is

In spome embodiments, L is CH ₂ 0-* or CH ₂ CH ₂ 0-*, wherein "-*" indicates the attachment point to A. In some embodiments, L is selected from the group consisting of -CH ₂ -*, -CH2CH2-*, CH ₂ CH ₂ CH ₂ -*, -CH(CH ₃ )-*, -CH ₂ (CH ₃ )CH ₂ -*,

-CH ₂ C(0)*, -CH ₂ 0-*, -N(CH ₂ CONH ₂ )CH ₂ -* and -CH ₂ CH ₂ 0-*, wherein "-*" indicates the attachment point to W.

In some embodiments, R 1 and R 2 are each hydrogen or C1-C6 alkyl. In some embodiments, R 1 andR2 are each hydrogen or 1 2

-CH ₃ . In some embodiments, R andR are each hydrogen.

In some embodiments, A is phenyl and W is independently phenyl or 5-6-membered heteroaryl. In some embodiments, each A and W is independently phenyl. In some embodiments, A is phenyl and W is 5-6-membered heteroaryl.

In some embodiments, W is a monocyclic 5-6-membered heteroaryl. In some embodiments, 2 R ^Y groups on adjacent atoms of W, together with the atoms to which they are attached form a 3-7-membered fused cycloalkyl or heterocyclyl optionally substituted with 1-5 R ^x forming a bicyclic heteroaryl. In some embodiments, W is a 10-membered heteroaryl, a 9- membered heteroaryl, a 6-membered heteroaryl, or a 5-membered heteroaryl. In some embodiments, W is a heteroaryl containing nitrogen, oxygen or sulfur as allowed by valence. some embodiments, each A and W is selected from:

and

R . \ N>H . *- R _Y , and a ^N ~N ^ ^r

In some embodiments, each R is independently Ci-C alkyl, C(¾H-Ci-C6 alkyl, Ci-C alkoxy-d-Ce alkyl, halo-C C ₆ alkyl, halo-d-C ₆ alkoxy, halo, cyano, -OR ^A , -NR ^B R ^C , - C(0)NR ^B R ^c , -S(0) ₂ R ^D , -S(R ^F ) _m , or G ¹ , or 2 R ^Y groups on adjacent atoms, together with the atoms to which they are attached form a 3-7-membered fused cycloalkyl, 3-7 membered heterocyclyl, aryl, or 5-6 membered heteroaryl, optionally substituted with 1-5 R ^x .

In some embodiments, R ^Y is chloro, fluoro, -CH ₃ , -CH ₂ CH ₃ , -CH ₂ CH ₂ CH ₃ , - CH ₂ CH ₂ CH ₂ CH ₃ , -CH(CH ₃ ) ₂ , -CH ₂ CH(CH ₃ ) ₂ , -C(CH ₃ ) ₃ , -CF ₃ , -CHF _2, -CH ₂ C0 ₂ H, - CH ₂ OCH ₃ , CH ₂ C0 ₂ H, -OCH ₃ , -OCH ₂ CH ₃ , -OCH(CH ₃ ) ₂ , -OCHF ₂ , -OCF ₃ , -OCH ₂ CHF ₃ - C(0)NH ₂ , -N(CH ₃ ) ₂ , -S(0) ₂ CH ₃ , -S(0) ₂ NH ₂ , or -SCF ₃ .

In some embodiments, each A and W is optionally substituted with 1-5 R ^Y . In some embodiments, R ^Y is Cj-C alkyl, Cj-C alkoxy-Ci-C6 alkyl, halo-Ci-C6 alkyl, halo-Ci-C6 alkoxy, halo, cyano, -OR ^A , -NR ^B R ^C , -S(0) ₂ R ^D , -S(R ^F ) _m , or G ¹ . In some embodiments, R ^Y is chloro, fluoro, -CH ₃ , -CH ₂ CH ₃ , CH ₂ CH ₂ CH ₃ , -CH ₂ CH ₂ CH ₂ CH ₃ , -CH(CH ₃ ) ₂ , -CH ₂ CH(CH ₃ ) ₂ , -C(CH ₃ ) ₃ , -CF ₃ , -CH ₂ OCH ₃ , -OCH ₃ , -OCH ₂ CH ₃ , -OCH(CH ₃ ) ₂ , -OCHF ₂ , -OCF ₃ , -OCH ₂ CHF ₂ , N(CH ₃ ) ₂ , - S(0) ₂ CH ₃ , -S(0) ₂ NH ₂ , or SCF ₃ .

In some embodiments, G ¹ is phenyl optionally substituted with 1-3 R ^z . In some embodiments, each R is C ₁ -C6 alkyl (e.g., CH ₃ ).

In some embodiments, each A and W is independently a phenyl optionally substituted

some embodiments, each R ^Y is independently chloro, fluoro, or CH ₃ . In some embodiments,

In some embodiments, G ¹ is phenyl optionally substituted with 1-3 R ^z . In some embodiments, each R ^z is Cj-C alkyl (e.g., (¾).

In some embodiments the compound of Formula (I) is a compound of Formula (I-a):

Formula (I-a)

or a pharmaceutically acceptable salt, solvate, hydrate, tautomer, or stereoisomer thereof, wherein D is a bridged bicyclic cycloalkyl, bridged bicyclic heterocyclyl, or cubanyl, wherein each bridged bicyclic cycloalkyl, bridged bicyclic heterocyclyl, or cubanyl is optionally substituted with 1-4 R ^x ; L ¹ and L ² are each independently Q-Ce aikylene or 2-7-membered heteroalkylene, wherein each C _\ -C alkylene or 2-7-membered heteroalkylene is optionally substituted with 1-5 R ^x ; R ¹ and R ² are each independently hydrogen, C -Ce alkyl, C -Ce alkoxy- C2-C6 alkyl, hydroxy-C2-C6 alkyl, silyloxy-C2-C6 alkyl; A and W are each independently phenyl or 5-6-membered heteroaryl, wherein each phenyl or 5-6-membered heteroaryl is optionally substituted with 1-5 R ^Y ; each R ^x is independently selected from the group consisting of C Ce alkyl, hydroxy-Ci-C6 alkyl, halo-Ci-C6 alkyl, amino-Ci-C6 alkyl, cyano-Ci-C6 alkyl, oxo, halo, cyano, -OR ^A , -NR ^B R ^C ,— NR ^B C(0)R ^D , -C(0)NR ^B R ^c , -C(0)R ^D , -C(0)OH, -C(0)OR ^D , -SR ^E , - S(0)R ^D , and -S(0)2R ^D ; each R ^Y is independently selected from the group consisting of hydrogen, C ₁ -C6 alkyl, hydroxy-Ci-C6 alkyl, halo-Ci-C6 alkyl, halo-Ci-C6 alkoxy, amino-Ci-C6 alkyl, cyano-Ci-Ce alkyl, oxo, halo, cyano, -OR ^A , -NR ^B R ^C ,— NR ^B C(0)R ^D , -C(0)NR ^B R ^c , - C(0)R ^D , -C(0)OH, -C(0)OR ^D , -S(R ^F ) _m , -S(0)R ^D , -S(0) ₂ R ^D , and G ¹ ; or 2 R ^Y groups on adjacent atoms, together with the atoms to which they are attached form a 3-7-membered fused cycloalkyl or heterocyclyl optionally substituted with 1-5 R ^x ; each G ¹ is independently C3-C6 cycloalkyl, 4-7-membered heterocyclyl, aryl, or 5-6-membered heteroaryl, wherein each C3-C6 cycloalkyl, 4-7-membered heterocyclyl, aryl, or 5-6-membered heteroaryl is optionally

z z

substituted with 1-3 R ; each R is independently selected from the group consisting of C ₁ -C6 alkyl, hydroxy-d-C ₆ alkyl, halo-d-Ce alkyl, halo, cyano, -OR ^A , -NR ^B R ^C ,— NR ^B C(0)R ^D , - C(0)NR ^B R ^c , -C(0)R ^D , -C(0)OH, -C(0)OR ^D , and -S(0) ₂ R ^D ; R ^A is, at each occurrence, independently hydrogen, C C ₆ alkyl, halo-Q-Ce alkyl, -C(0)NR ^B R ^c , -C(0)R ^D , -C(0)OH, or -

D B C B C

C(0)OR ; each of R and R is independently hydrogen or C ₁ -C6 alkyl; or R and R together with the atom to which they are attached form a 3-7-membered heterocyclyl optionally substituted with 1-3 R ^z ; each R ^D is independently Cj-C alkyl or halo-Ci-C6 alkyl; each R ^E is independently hydrogen Cj-C alkyl, or halo-Ci-C6 alkyl; each R ^F is independently hydrogen, C C alkyl, halo-Ci-C6 alkyl, or halo; and m is 1 when R ^F is hydrogen or Cj-C alkyl, 3 when R ^F is C C alkyl, or 5 when R ^F is halo.

In some embodiments, the compound of Formula (I) is a compound of Formula (I-b):

Formula (I-b)

or a pharmaceutically acceptable salt, solvate, hydrate, tautomer, or stereoisomer thereof,

1 2

wherein at least one of L and L is independently 2-7-membered heteroalkylene optionally

X 1 substituted by 1-5 R , wherein "-*" indicates the attachment point to A and W, respectively; R

2 Y

and R are each hydrogen or C C alkyl; A is phenyl substituted with 1-2 R ; W is phenyl or 5-6 membered heteroaryl, each of which is optionally substituted with 1-5 R ^Y ; each R ^x is oxo or - OR ^A ; and each R ^Y is independently selected from the group consisting of C C alkyl, C C alkoxy-d-Ce alkyl, halo-C C ₆ alkyl, halo-Q-Ce alkoxy, halo, cyano, -OR ^A , -NR ^B R ^C , -

C(0)NR ^B R ^c , -S(0) ₂ R ^D , -S(R ^F ) _m , or G ¹ ; or 2 R ^Y groups on adjacent atoms, together with the atoms to which they are attached form a 3-7-membered fused cycloalkyl, 3-7 membered heterocyclyl, aryl, or 5-6 membered heteroaryl, optionally substituted with 1-5 R ^x ; G ¹ is phenyl optionally substituted with 1-3 R ^z ; each R ^z is independently C ₁ -C6 alkyl; R ^A is, at each

B C

occurrence, independently hydrogen, C ₁ -C6 alkyl, or halo-Ci-C6 alkyl; each of R and R is independently hydrogen or C ₁ -C6 alkyl; each R ^D is independently C ₁ -C6 alkyl, halo-Ci-C6 alkyl, or -NR ^B1 R ^C1 ; each R ^F is independently hydrogen, C ₁ -C6 alkyl, halo-Ci-C6 alkyl, or halo; each of R ^B1 and R ^cl is independently hydrogen or C ₁ -C6 alkyl; and m is 1 when R ^F is hydrogen or C ₁ -C6 alkyl, 3 when R ^F is C ₁ -C6 alkyl, or 5 when R ^F is halo.

1 2

In some embodiments, at least one of L and L is independently 2-7-membered heteroalkylene optionally substituted by 1-5 R ^x . In some embodiments, both of L ¹ and L ² are independently 2-7-membered heteroalkylene optionally substituted by 1-5 R ^x . In some

1 2

embodiments, L is 2-7-membered heteroalkylene and L is independently selected from C ₁ -C6 alkylene or 2-7-membered heteroalkylene, wherein each alkylene and heteroalkylene is

X 1 2

optionally substituted by 1-5 R . In some embodiments, both of L and L are independently 2- 7-membered heteroalkylene substituted by 0 R . In some embodiments, L is independently selected from CH2O-* or CH2CH2O-*, L is independently selected from -CH ₂ -*, -CH2CH2-*, CH2CH2CH2-*, -CH ₂ (CH ₃ )-*, -CH ₂ (CH ₃ )CH ₂ -*, CH ₂ 0-* or CH ₂ CH ₂ 0-*, and "-*" indicates the attachment point to A and W, respectively. In some embodiments, each L 1 and L 2 is independently selected from CH2O-* or CH2CH2O-*, and "-*" indicates the attachment point to

A and W, respectively. In some embodiments, L 1 is CH2O-* and L 2 is CH2CH2O-*, and "-*" indicates the attachment point to A and W, respectively.

In some embodiments, R 1 and R 2 are each hydrogen or C ₁ -C6 alkyl. In some

embodiments, R 1 andR2 are each hydrogen or some embodiments, R 1 andR2

-CH ₃ . In are each hydrogen.

In some embodiments, each A and W is independently phenyl or 5-6 membered heteroaryl, optionally substituted with 1-5 R . In some embodiments, A is phenyl and W is independently phenyl or 5-6 membered heteroaryl. In some embodiments, each A and W is independently phenyl. In some embodiments, A is phenyl and W is 5-6 membered heteroaryl.

In some embodiments, W is a monocyclic heteroaryl. In some embodiments, W is a bicyclic heteroaryl. In some embodiments, W is a 10-membered heteroaryl, a 9-membered heteroaryl, a 6-membered heteroaryl, or a 5-membered heteroaryl. In some embodiments, W is a heteroaryl containing nitrogen, oxygen or sulfur as allowed by valence.

In some embodiments, each A and W is selected from:

In some embodiments, each A and W is optionally substituted with 1-5 R ^Y . In some embodiments, R ^Y is Cj-C alkyl, Cj-C alkoxy-Ci-C6 alkyl, halo-Ci-C6 alkyl, halo-Ci-C6 alkoxy, halo, cyano, -OR^,— NR R , -S(0) ₂ R or -S(R ^r ) _m . In some embodiments, R is chloro, fluoro, -CH ₃ , -CH ₂ CH ₃ , CH ₂ CH ₂ CH ₃ , -CH ₂ CH ₂ CH ₂ CH ₃ , -CH(CH ₃ ) ₂ , -CH ₂ CH(CH ₃ ) ₂ , -C(CH ₃ ) ₃ , -CF ₃ , -CH ₂ OCH ₃ , -OCH ₃ , -OCH ₂ CH ₃ , -OCH(CH ₃ ) ₂ , -OCHF ₂ , -OCF ₃ , -OCH ₂ CHF ₂ , N(CH ₃ ) ₂ , - S(0) ₂ CH ₃ , -S(0) ₂ NH ₂ , or SCF ₃ .

In some embodiments, G ¹ is phenyl optionally substituted with 1-3 R ^z . In some embodiments, each R ^z is Cj-C alkyl (e.g., CH ₃ ).

In some embodiments, the compound of Formula (I) is a compound of Formula (I-c):

Formula (I-c)

or a pharmaceutically acceptable salt, solvate, hydrate, tautomer, or stereoisomer thereof, wherein L ¹ and L ² are each independently CH ₂ -*, -CH ₂ CH ₂ -*, CH ₂ CH ₂ CH ₂ -*, -CH ₂ (CH ₃ )-*, - CH ₂ (CH ₃ )CH ₂ -*, CH ₂ 0-* or CH ₂ CH ₂ 0-*, wherein "-*" indicates the attachment point to A and

1 2

W, respectively; R and R are each hydrogen; A and W are each independently phenyl substituted with 1-2 R ^Y ; and each R ^Y is independently selected from the group consisting of chloro, fluoro, and CH ₃ .

1 2

In some embodiments, at least one of L and L is independently 2-7-membered heteroalkylene optionally substituted by 1-5 R ^x . In some embodiments, both of L ¹ and L ² are independently 2-7-membered heteroalkylene optionally substituted by 1-5 R ^x . In some

1 2

embodiments, both of L and L are independently 2-7-membered heteroalkylene substituted by 0 R ^X . In some embodiments, at least one of L ¹ and L ² is independently Cj-C alkylene optionally substituted by 1-5 R ^x . In some embodiments, each L ¹ and L ² is independently selected from CH ₂ -*, CH(CH ₃ )-*, CH2CH2-*, CH(CH ₃ )CH ₂ -*, CH2CH ₂ CH2-*,CH ₂ 0-* or CH ₂ CH ₂ 0-*, and "- *" indicates the attachment point to A and W, respectively. In some embodiments, each L ¹ and L is independently selected from CH2O-* or CH2CH2O-*, and "-*" indicates the attachment point to A and W, respectively. In some embodiments, L 1 is CH2O-* and L 2 is CH2CH2O-*, and "-*" indicates the attachment point to A and W, respectively.

In some embodiments, R 1 and R 2 are each hydrogen.

In some embodiments, each A and W is independently a phenyl optionally substituted wit

and s,

A is and W is selected from ,

some embodiments, each R is inde endently chloro fluoro, or CH ₃ . In some embodiments,

each of A and W is selected from In some embodime ome

embodiments, A is and W is selected from:

f Formula (I-d)

Formula (I-d)

or a pharmaceutically acceptable salt, solvate, hydrate, tautomer, or stereoisomer thereof, wherein each of A and W is defined as for Formula (I).

In some embodiments, the compound of Formula (I) is a compound of Formula (I-e):

Formula (I-e)

or a pharmaceutically acceptable salt, solvate, hydrate, tautomer, or stereoisomer thereof, wherein each of D, W and R ^Y is defined as for Formula (I).

In some emb la (I-f):

Formula (I-f)

or a pharmaceutically acceptable salt, solvate, hydrate, tautomer, or stereoisomer thereof, wherein each of W and R ^Y is defined as for Formula (I).

In some embodiments, the compound of Formula (I) is a compound of Formula (I-g):

Formula (I-g)

or a pharmaceutically acceptable salt, solvate, hydrate, tautomer, or stereoisomer thereof, wherein each of W and R ^Y is defined as for Formula (I).

In some embodiments, the compound of Formula (I) (e.g., a compound of Formula (I-a), (I-b), (I-c), (I-d), (I-e), (I-f), or (I-g)) is selected from a compound set forth in Table 1 or a pharmaceutically acceptable salt, solvate, hydrate, tautomer, or stereoisomer thereof.

In some embodiments, the compound of Formula (I) (e.g., a compound of Formula (I-a), (I-b), (I-c), (I-d), (I-e), (I-f), or (I-g)) or a pharmaceutically acceptable salt thereof is formulated as a pharmaceutically acceptable composition comprising a disclosed compound and a pharmaceutically acceptable carrier. Also disclosed herein is a compound of Formula (II):

Formula (II)

or a pharmaceutically acceptable salt, solvate, hydrate, tautomer, or stereoisomer thereof, wherein:

D is a bridged bicyclic cycloalkyl, bridged bicyclic heterocyclyl, or cubanyl, wherein each bridged bicyclic cycloalkyl, bridged bicyclic heterocyclyl, or cubanyl is optionally substituted with 1-4 R groups; and wherein if the bridged bicyclic heterocyclyl contains a substitutable nitrogen moiety, the substitutable nitrogen moiety may be optionally substituted by R ^N1 ;

L ¹ is C C alkylene or 2-7-membered heteroalkylene, wherein Cj-C alkylene or 2-7- membered heteroalkylene is optionally substituted with 1-5 R ^x ;

1 2

R and R" are each independently hydrogen, C C alkyl, C C alkoxy-C2-C6 alkyl, hydroxy-C2-C6 alkyl, or silyloxy-C2-C6 alkyl;

R ^N1 is selected from the group consisting of hydrogen, C C alkyl, hydroxy-C2-C6 alkyl, halo-C ₂ -C ₆ alkyl, amino-C ₂ -C ₆ alkyl, cyano-C ₂ -C ₆ alkyl, -C(0)NR ^B R ^c , -C(0)R ^D , -C(0)OR ^D , and -S(0) ₂ R ^D ;

A and W are each independently phenyl or 5-6 membered heteroaryl, wherein each phenyl or 5-6-membered heteroaryl is optionally substituted with 1-5 R ^Y ;

each R ^x is independently selected from the group consisting of Ci-Ce alkyl, hydroxy-Ci- C alkyl, halo-Ci-C6 alkyl, amino-Ci-C6 alkyl, cyano-Ci-C6 alkyl, oxo, halo, cyano, -OR ^A , - NR ^B R ^C ,— NR ^B C(0)R ^D , -C(0)NR ^B R ^c , -C(0)R ^D , -C(0)OH, -C(0)OR ^D , -SR ^E , -S(0)R ^D , and - S(0) ₂ R ^D ;

each R is independently selected from the group consisting of hydrogen, Ci-Ce alkyl, hydroxy-Ci-C6 alkyl, C _\ -C alkoxy-Ci-C6 alkyl, halo-Ci-C6 alkyl, halo-Ci-C6 alkoxy, amino-Ci- C ₆ alkyl, cyano-Ci-Ce alkyl, oxo, halo, cyano, -OR ^A , -NR ^B R ^C ,— NR ^B C(0)R ^D , -C(0)NR ^B R ^c , - C(0)R ^D , -C(0)OH, -C(0)OR ^D , -S(R ^F ) _m , -S(0)R ^D , -S(0) ₂ R ^D , and G ¹ ; or 2 R ^Y groups on adjacent atoms, together with the atoms to which they are attached form a 3-7-membered fused cycloalkyl, 3-7 membered heterocyclyl, aryl, or 5-6 membered heteroaryl, optionally substituted with 1-5 R ^x ;

each G ¹ is independently C3-C6 cycloalkyl, 4-7-membered heterocyclyl, aryl, or 5-6- membered heteroaryl, wherein each C3-C6 cycloalkyl, 4-7-membered heterocyclyl, aryl, or 5-6- membered heteroaryl is optionally substituted with 1-3 R ^z ;

each R ^z is independently selected from the group consisting of C ₁ -C6 alkyl, hydroxy-Ci- C ₆ alkyl, halo-Ci-Q alkyl, halo, cyano, -OR ^A , -NR ^B R ^C ,— NR ^B C(0)R ^D , -C(0)NR ^B R ^c , -C(0)R ^D , -C(0)OH, -C(0)OR ^D , and -S(0) ₂ R ^D ;

R ^A is, at each occurrence, independently hydrogen, C ₁ -C6 alkyl, halo-Ci-C6 alkyl, - C(0)NR ^B R ^c , -C(0)R ^D , or -C(0)OR ^D ;

B C

each of R and R is independently hydrogen or C ₁ -C6 alkyl; or

B C

R and R together with the atom to which they are attached form a 3-7-membered heterocyclyl optionally substituted with 1-3 R ;

each R ^D is independently C ₁ -C6 alkyl, or halo-Ci-C6 alkyl;

each R ^E is independently hydrogen, C ₁ -C6 alkyl, or halo-Ci-C6 alkyl;

each R ^F is independently hydrogen, C ₁ -C6 alkyl, halo, or halo-Ci-C6 alkyl;

B 1 CI

each of R and R is independently hydrogen or C Ce alkyl; and

m is 1 when R ^F is hydrogen or Q-C6 alkyl, 3 when R ^F is C ₁ -C6 alkyl, or 5 when R ^F is halo.

In some embodiments, D is selected from the group consisting of

In some embodiments, each R is independently selected from the group consisting of oxo, -OR ^A (e.g., OH or OCH ₃ ), -C(0)OH, -C(0)OR ^D (e.g., -C(0)OCH ₃ ), halo, and hydroxy- C ₁ -C6 alkyl. In some embodiments, each of R ¹ and R ² is hydrogen or CH ₃ . each R ^x is independently selected from the group consisting of oxo, -OH, -OCH ₃ , -C(0)OH, -C(0)OCH ₃ , halo, and hydroxy-Ci-C6 alkyl.

In some embodiments, L ¹ is C¾0-* or CH2CH2O-*, wherein "-*" indicates the attachment point to A. In some embodiments A is selected from the group consisting of:

In some embodiments W is selected from the group consisting of:

wherein R is hydrogen or CH ₃ .

In some embodiments, each R ^Y is independently hydrogen, bromo, chloro, fluoro, iodo, CF ₃ , CHF ₂ , CH2CF ₃ , CH ₃ , CH2CH ₃ , OH, CH ₂ OH, C(CH ₃ ) ₂ OH, OCH ₃ , OCH ₂ CH _3, OCF ₃ , OCH ₂ CF ₃ , S(0) ₂ CH ₃ , S(0) ₂ CH ₂ CH ₂ CH ₃ , CN, N(CH ₃ ) ₂ , SF ₅ , SCH ₃ , NH ₂ , C(CH) ₃ , CH(CH ₃ ) ₂ , CH ₂ CN, CH ₂ NH ₂ , CH(OH)CH ₃ , C(OH)(CH ₃ )CF ₃ , S(0) ₂ CH ₃ , C(0)CH ₃ , C(0)OCH ₃ , C(0)OH, OCHF ₂ or G ¹ .

In some embodiments the compound of Formula (II) is a compound of Formula (Il-a):

Formula (Il-a)

or a pharmaceutically acceptable salt, solvate, hydrate, tautomer, or stereoisomer thereof, wherein: D is bicyclo[l.l. l]pentanyl, bicyclo[2.2.2]octanyl, or 2-oxabicyclo[2.2.2]octane, each of which is optionally substituted with 1-4 R ^x groups;

A is phenyl or pyridyl, each of which is optionally substituted with 1-5 R ^Y groups;

W is phenyl, pyridyl, pyrazinyl, pyrimidinyl, thiazolyl, isoxazolyl, or pyrazolyl, each of which is optionally substituted on one or more available carbons with 1-5 R ^Y groups; and wherein pyrazolyl may be optionally substituted on an available nitrogen with hydrogen or CH ₃ ;

L ¹ is CH2O-* or CH2CH2O-*, wherein "-*" indicates the attachment point to A;

each R ^x is independently fluoro, oxo, OH, OCH ₃ , C(0)OH, or C(0)OCH ₃ ;

each R ^Y is independently hydrogen, bromo, chloro, fluoro, iodo, CF ₃ , CHF2, CH2CF ₃ , CH ₃ , CH2CH ₃ , OH, CH ₂ OH, C(CH ₃ ) ₂ OH, OCH ₃ , OCH ₂ CH _3, OCF ₃ , OCH ₂ CF ₃ , S(0) ₂ CH ₃ , S(0)2CH ₂ CH ₂ CH3, CN, N(CH ₃ ) ₂ , SF ₅ , SCH ₃ , NH ₂ , C(CH) ₃ , CH(CH ₃ ) ₂ , CH ₂ CN, CH ₂ NH ₂ , CH(OH)CH ₃ , C(OH)(CH ₃ )CF ₃ , S(0) ₂ CH ₃ , C(0)CH ₃ , C(0)OCH ₃ , C(0)OH, OCHF ₂ or G ¹ ;

2 R ^Y groups on adjacent atoms, together with the atoms to which they are attached form a furanyl, pyrrolyl, or dioxolanyl ring, each of which is optionally substituted with 1-2 R ; and each of R 1 and R 2 is hydrogen or CH ₃ .

In some embodiments, the compound of Formula (II) (e.g., a compound of Formula (Il-a) or a pharmaceutically acceptable salt thereof is formulated as a pharmaceutically acceptable composition comprising a disclosed compound and a pharmaceutically acceptable carrier.

In some embodiments, the compound of Formula (II) (e.g., a compound of Formula (Il-a) is selected from a compound set forth in Table 1 or a pharmaceutically acceptable salt, solvate, hydrate, tautomer, or stereoisomer thereof.

In another aspect, the present invention features a method of treating a neurodegenerative disease, a leukodystrophy, cancer, an inflammatory disease, a musculoskeletal disease, a metabolic disease, a mitochondrial disease, or a disease or disorder associated with impaired function of eIF2B or components in the ISR pathway (e.g., eIF2 pathway) in a subject, wherein the method comprises administering a compound of Formula (I) or Formula (II), or a pharmaceutically acceptable salt, solvate, hydrate, tautomer, or stereoisomer thereof, or a composition thereof, to a subject.

In some embodiments, the method comprises the treatment of a neurodegenerative disease. In some embodiments, the neurodegenerative disease comprises vanishing white matter disease, childhood ataxia with CNS hypo-myelination, a leukodystrophy, a

leukoencephalopathy, hypomyelinating or demyelinating disease, an intellectual disability syndrome, progressive supranuclear palsy, corticobasal degeneration, adrenoleukodystrophy, X- linked adrenoleukodystrophy, cerebral adrenoleukodystrophy, Pelizaeus-Merzbacher Disease, Krabbe disease, leukodystrophy due to mutation in DARS2 gene (sometimes known as lukoencephalopathy with brainstem and spinal cord involvement and lactate elevation (LBSL), DARS2-related spectrum disorders, Alzheimer's disease, amyotrophic lateral sclerosis,

Creutzfeldt-Jakob disease, frontotemporal dementia, Gerstmann-Straussler-Scheinker disease, Huntington's disease, dementia (e.g., HIV-associated dementia or Lewy body dementia), kuru, Parkinson's disease, progressive nuclear palsy, a tauopathy, or a prion disease. In some embodiments, the neurodegenerative disease comprises vanishing white matter disease. In some embodiments, the neurodegenerative disease comprises a psychiatric disease such as agoraphobia, Alzheimer's disease, anorexia nervosa, amnesia, anxiety disorder, bipolar disorder, body dysmorphic disorder, bulimia nervosa, claustrophobia, depression, delusions, Diogenes syndrome, dyspraxia, insomnia, Munchausen's syndrome, narcolepsy, narcissistic personality disorder, obsessive-compulsive disorder, psychosis, phobic disorder, schizophrenia, seasonal affective disorder, schizoid personality disorder, sleepwalking, social phobia, substance abuse, tardive dyskinesia, Tourette syndrome, or trichotillomania. In some embodiments, the neurodegenerative disease comprises a disease or disorder with symptoms of cognitive impairment or cognitive decline such as Alzheimer's disease, Parkinson's disease, Huntington's disease, schizophrenia, autism, frontotemporal dementia, dementia (e.g., HIV-associated dementia or Lewy body dementia), age related dementia, chronic traumatic encephalopathy, HIV-induced neurocognitive impairment, a HIV-associated neurocognitive disorder, a hypoxic injury (e.g., premature brain injury, chronic perinatal hypoxia), traumatic brain injury, stroke, or postoperative cognitive dysfunction. In some embodiments, the neurodegenerative disease comprises an intellectual disability syndrome. In some embodiments, the neurodegenerative disease comprises mild cognitive impairment.

In some embodiments, the method comprises the treatment of cancer. In some embodiments, the cancer comprises pancreatic cancer, breast cancer, multiple myeloma, or a cancer of the secretory cells. In some embodiments, the method comprises the treatment of cancer in combination with a chemotherapeutic agent for the enhancement of memory (e.g., long term memory).

In some embodiments, the method comprises the treatment of an inflammatory disease.

In some embodiments, the inflammatory disease comprises postoperative cognitive dysfunction, traumatic brain injury, arthritis (e.g., rheumatoid arthritis, psoriatic arthritis, or juvenile idiopathic arthritis), systemic lupus erythematosus (SLE), myasthenia gravis, diabetes (e.g., juvenile onset diabetes or diabetes mellitus type 1), Guillain-Barre syndrome, Hashimoto's encephalitis, Hashimoto's thyroiditis, ankylosing spondylitis, psoriasis, Sjogren's syndrome, vasculitis, glomerulonephritis, auto-immune thyroiditis, Behcet's disease, Crohn's disease, ulcerative colitis, bullous pemphigoid, sarcoidosis, ichthyosis, Graves' ophthalmopathy, inflammatory bowel disease, Addison's disease, vitiligo, asthma (e.g., allergic asthma), acne vulgaris, celiac disease, chronic prostatitis, pelvic inflammatory disease, reperfusion injury, sarcoidosis, transplant rejection, interstitial cystitis, or atopic dermatitis.

In some embodiments, the method comprises the treatment of a musculoskeletal disease. In some embodiments, the musculoskeletal disease comprises muscular dystrophy, multiple sclerosis, Freidrich's ataxia, a muscle wasting disorder (e.g., muscle atrophy, sarcopenia, cachexia), inclusion body myopathy, progressive muscular atrophy, motor neuron disease, carpal tunnel syndrome, epicondylitis, tendinitis, back pain, muscle pain, muscle soreness, repetitive strain disorders, or paralysis.

In some embodiments, the method comprises the treatment of a metabolic disease. In some embodiments, the metabolic disease comprises non-alcoholic steatohepatitis (NASH), nonalcoholic fatty liver disease (NAFLD), liver fibrosis, obesity, heart disease, atherosclerosis, arthritis, cystinosis, phenylketonuria, proliferative retinopathy, or Kearns-Sayre disease.

In some embodiments, the method comprises the treatment of a mitochondrial disease. In some embodiments, the mitochondrial disease is associated with, or is a result of, or is caused by mitochondrial dysfunction, one or more mitochondrial protein mutations, or one or more mitochondrial DNA mutations. In some embodiments, the mitochondrial disease is a mitochondrial myopathy. In some embodiments, the mitochondrial disease, e.g., the mitochondrial myopathy, is selected from the group consisting of Barth syndrome, chronic progressive external ophthalmoplegia (cPEO), Kearns-Sayre syndrome (KSS), Leigh syndrome (e.g., MILS, or maternally inherited Leigh syndrome), mitochondrial DNA depletion syndromes (MDDS, e.g., Alpers syndrome), mitochondrial encephalomyopathy (e.g., mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS)), mitochondrial neurogastrointestinal encephalomyopathy (MNGIE), myoclonus epilepsy with ragged red fibers (MERRF), neuropathy, ataxia, retinitis pigmentosa (NARP), Leber's hereditary optic neuropathy (LHON), and Pearson syndrome.

In another aspect, the present invention features a method of treating a disease or disorder related to modulation (e.g., a decrease) in eIF2B activity or level, modulation (e.g., a decrease) of eIF2a activity or level, modulation (e.g., an increase) in eIF2a phosphorylation, modulation (e.g., an increase) of phosphorylated eIF2a pathway activity, or modulation (e.g., an increase) of ISR activity in a subject, wherein the method comprises administering a compound of Formula (I) or Formula (II), or a pharmaceutically acceptable salt, solvate, hydrate, tautomer, or stereoisomer thereof, or a composition thereof, to a subject. In some embodiments, the disease may be caused by a mutation to a gene or protein sequence related to a member of the eIF2 pathway (e.g., the eIF2a signaling pathway or ISR pathway).

In another aspect, the present invention features a method of treating a leukodystrophy such as vanishing white matter disease (VWMD) or childhood ataxia with central nervous system hypomyelination. In some embodiments, the leukodystrophy is characterized by an amino acid mutation (e.g., an amino acid deletion, amino acid addition, or amino acid substitution) in a tRNA synthetase. In some embodiments, administration of a compound of Formula (I) or Formula (II) enhances eIF2B activity in a subject with a leukodystrophy, such as vanishing white matter disease (VWMD) or childhood ataxia with central nervous system hypomyelination.

In another aspect, the present invention features a method of treating a disease or disorder related to an amino acid mutation (e.g., an amino acid deletion, amino acid addition, or amino acid substitution) in a gene or gene product (e.g., RNA or protein) that modulates (e.g., reduces) protein synthesis. In some embodiments, administration of a compound of Formula (I) or Formula (II) enhances residual GEF activity of a mutant GEF complex in a subject.

In another aspect, the present invention features a composition for use in treating a neurodegenerative disease, a leukodystrophy, cancer, an inflammatory disease, a

musculoskeletal disease, a metabolic disease, or a mitochondrial disease in a subject, wherein the composition comprises a compound of Formula (I) or Formula (II), or a pharmaceutically acceptable salt, solvate, hydrate, tautomer, or stereoisomer thereof.

In some embodiments, the neurodegenerative disease comprises vanishing white matter disease, childhood ataxia with CNS hypo-myelination, a leukodystrophy, a

leukoencephalopathy, hypomyelinating or demyelinating disease, an intellectual disability syndrome, progressive supranuclear palsy, corticobasal degeneration, adrenoleukodystrophy, X- linked adrenoleukodystrophy, cerebral adrenoleukodystrophy, Pelizaeus-Merzbacher Disease, Krabbe disease, leukodystrophy due to mutation in DARS2 gene (sometimes known as lukoencephalopathy with brainstem and spinal cord involvement and lactate elevation (LBSL), DARS2-related spectrum disorders, Alzheimer's disease, amyotrophic lateral sclerosis,

Creutzfeldt-Jakob disease, frontotemporal dementia, Gerstmann-Straussler-Scheinker disease, Huntington's disease, dementia (e.g., HIV-associated dementia or Lewy body dementia), kuru, Parkinson's disease, progressive nuclear palsy, a tauopathy, or a prion disease. In some embodiments, the neurodegenerative disease comprises vanishing white matter disease. In some embodiments, the neurodegenerative disease comprises a psychiatric disease such as agoraphobia, Alzheimer's disease, anorexia nervosa, amnesia, anxiety disorder, bipolar disorder, body dysmorphic disorder, bulimia nervosa, claustrophobia, depression, delusions, Diogenes syndrome, dyspraxia, insomnia, Munchausen's syndrome, narcolepsy, narcissistic personality disorder, obsessive-compulsive disorder, psychosis, phobic disorder, schizophrenia, seasonal affective disorder, schizoid personality disorder, sleepwalking, social phobia, substance abuse, tardive dyskinesia, Tourette syndrome, or trichotillomania. In some embodiments, the neurodegenerative disease comprises a disease or disorder with symptoms of cognitive impairment or cognitive decline such as Alzheimer's disease, Parkinson's disease, Huntington's disease, schizophrenia, autism, frontotemporal dementia, dementia (e.g., HIV-associated dementia or Lewy body dementia), age related dementia, chronic traumatic encephalopathy, HIV-induced neurocognitive impairment, a HIV-associated neurocognitive disorder, a hypoxic injury (e.g., premature brain injury, chronic perinatal hypoxia), traumatic brain injury, stroke, or postoperative cognitive dysfunction. In some embodiments, the neurodegenerative disease comprises an intellectual disability syndrome. In some embodiments, the neurodegenerative disease comprises mild cognitive impairment.

In some embodiments, the cancer comprises pancreatic cancer, breast cancer, multiple myeloma, or a cancer of the secretory cells. In some embodiments, the method comprises the treatment of cancer in combination with a chemotherapeutic agent for the enhancement of memory (e.g., long term memory).

In some embodiments, the inflammatory disease comprises postoperative cognitive dysfunction, traumatic brain injury, arthritis (e.g., rheumatoid arthritis, psoriatic arthritis, or juvenile idiopathic arthritis), systemic lupus erythematosus (SLE), myasthenia gravis, diabetes (e.g., juvenile onset diabetes or diabetes mellitus type 1), Guillain-Barre syndrome, Hashimoto's encephalitis, Hashimoto's thyroiditis, ankylosing spondylitis, psoriasis, Sjogren's syndrome, vasculitis, glomerulonephritis, auto-immune thyroiditis, Behcet's disease, Crohn's disease, ulcerative colitis, bullous pemphigoid, sarcoidosis, ichthyosis, Graves' ophthalmopathy, inflammatory bowel disease, Addison's disease, vitiligo, asthma (e.g., allergic asthma), acne vulgaris, celiac disease, chronic prostatitis, pelvic inflammatory disease, reperfusion injury, sarcoidosis, transplant rejection, interstitial cystitis, or atopic dermatitis. In some embodiments, the musculoskeletal disease comprises muscular dystrophy, multiple sclerosis, Freidrich's ataxia, a muscle wasting disorder (e.g., muscle atrophy, sarcopenia, cachexia), inclusion body myopathy, progressive muscular atrophy, motor neuron disease, carpal tunnel syndrome, epicondylitis, tendinitis, back pain, muscle pain, muscle soreness, repetitive strain disorders, or paralysis.

In some embodiments, the metabolic disease comprises non-alcoholic steatohepatitis (NASH), non-alcoholic fatty liver disease (NAFLD), liver fibrosis, obesity, heart disease, atherosclerosis, arthritis, cystinosis, phenylketonuria, proliferative retinopathy, or Kearns-Sayre disease.

In some embodiments, the mitochondrial disease is associated with, or is a result of, or is caused by mitochondrial dysfunction, one or more mitochondrial protein mutations, or one or more mitochondrial DNA mutations. In some embodiments, the mitochondrial disease is a mitochondrial myopathy. In some embodiments, the mitochondrial disease, e.g., the

mitochondrial myopathy, is selected from the group consisting of Barth syndrome, chronic progressive external ophthalmoplegia (cPEO), Kearns-Sayre syndrome (KSS), Leigh syndrome (e.g., MILS, or maternally inherited Leigh syndrome), mitochondrial DNA depletion syndromes (MDDS, e.g., Alpers syndrome), mitochondrial encephalomyopathy (e.g., mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS)), mitochondrial neurogastrointestinal encephalomyopathy (MNGIE), myoclonus epilepsy with ragged red fibers (MERRF), neuropathy, ataxia, retinitis pigmentosa (NARP), Leber's hereditary optic neuropathy (LHON), and Pearson syndrome.

In another aspect, the present invention features a composition for use in treating a disease or disorder related to modulation (e.g., a decrease) in eIF2B activity or level, modulation (e.g., a decrease) of eIF2a activity or level, modulation (e.g., an increase) in eIF2a

phosphorylation, modulation (e.g., an increase) of phosphorylated eIF2a pathway activity, or modulation (e.g., an increase) of ISR activity in a subject, wherein the composition comprises a compound of Formula (I) or Formula (II), or a pharmaceutically acceptable salt, solvate, hydrate, tautomer, or stereoisomer thereof. In some embodiments, the disease may be caused by a mutation to a gene or protein sequence related to a member of the eIF2 pathway (e.g., the eIF2a signaling pathway or ISR pathway).

In another aspect, the present invention features a composition for use in treating a leukodystrophy such as vanishing white matter disease (VWMD) or childhood ataxia with central nervous system hypomyelination. In some embodiments, the leukodystrophy is characterized by an amino acid mutation (e.g., an amino acid deletion, amino acid addition, or amino acid substitution) in a tRNA synthetase. In some embodiments, the composition comprising a compound of Formula (I) or Formula (II) enhances eIF2B activity in a subject with a leukodystrophy, such as vanishing white matter disease (VWMD) or childhood ataxia with central nervous system hypomyelination.

In another aspect, the present invention features a composition for use in treating a disease or disorder related to an amino acid mutation (e.g., an amino acid deletion, amino acid addition, or amino acid substitution) in a gene or gene product (e.g., RNA or protein) that modulates (e.g., reduces) protein synthesis. In some embodiments, the composition comprising a compound of Formula (I) or Formula (II) enhances residual GEF activity of a mutant GEF complex in a subject.

DETAILED DESCRIPTION OF THE INVENTION

The present invention features compounds, compositions, and methods comprising a compound of Formula (I) or Formula (II), or a pharmaceutically acceptable salt, solvate, hydrate, tautomer, or stereoisomer thereof for use, e.g., in the modulation (e.g., activation) of eIF2B and the attenuation of the ISR signaling pathway.

Definitions

Chemical Definitions

Definitions of specific functional groups and chemical terms are described in more detail below. The chemical elements are identified in accordance with the Periodic Table of the Elements, CAS version, Handbook of Chemistry and Physics, 75 ^th Ed., inside cover, and specific functional groups are generally defined as described therein. Additionally, general principles of organic chemistry, as well as specific functional moieties and reactivity, are described in Thomas Sorrell, Organic Chemistry, University Science Books, Sausalito, 1999; Smith and March, March's Advanced Organic Chemistry, 5 ^th Edition, John Wiley & Sons, Inc., New York, 2001 ; Larock, Comprehensive Organic Transformations, VCH Publishers, Inc., New York, 1989; and

Carruthers, Some Modern Methods of Organic Synthesis, 3 rd Edition, Cambridge University Press, Cambridge, 1987.

The abbreviations used herein have their conventional meaning within the chemical and biological arts. The chemical structures and formulae set forth herein are constructed according to the standard rules of chemical valency known in the chemical arts. Compounds described herein can comprise one or more asymmetric centers, and thus can exist in various isomeric forms, e.g., enantiomers and/or diastereomers. For example, the compounds described herein can be in the form of an individual enantiomer, diastereomer or geometric isomer, or can be in the form of a mixture of stereoisomers, including racemic mixtures and mixtures enriched in one or more stereoisomer. Isomers can be isolated from mixtures by methods known to those skilled in the art, including chiral high pressure liquid chromatography (HPLC) and the formation and crystallization of chiral salts; or preferred isomers can be prepared by asymmetric syntheses. See, for example, Jacques et al. ,

Enantiomers, Racemates and Resolutions (Wiley Interscience, New York, 1981); Wilen et al. , Tetrahedron 33:2725 (1977); Eliel, Stereochemistry of Carbon Compounds (McGraw-Hill, NY, 1962); and Wilen, Tables of Resolving Agents and Optical Resolutions p. 268 (E.L. Eliel, Ed., Univ. of Notre Dame Press, Notre Dame, IN 1972). The invention additionally encompasses compounds described herein as individual isomers substantially free of other isomers, and alternatively, as mixtures of various isomers.

As used herein a pure enantiomeric compound is substantially free from other enantiomers or stereoisomers of the compound (i.e., in enantiomeric excess). In other words, an "S" form of the compound is substantially free from the "R" form of the compound and is, thus, in enantiomeric excess of the "R" form. The term "enantiomerically pure" or "pure enantiomer" denotes that the compound comprises more than 75% by weight, more than 80% by weight, more than 85% by weight, more than 90% by weight, more than 91 % by weight, more than 92% by weight, more than 93% by weight, more than 94% by weight, more than 95% by weight, more than 96% by weight, more than 97% by weight, more than 98% by weight, more than 99% by weight, more than 99.5% by weight, or more than 99.9% by weight, of the enantiomer. In certain embodiments, the weights are based upon total weight of all enantiomers or

stereoisomers of the compound.

In the compositions provided herein, an enantiomerically pure compound can be present with other active or inactive ingredients. For example, a pharmaceutical composition comprising enantiomerically pure R-compound can comprise, for example, about 90% excipient and about 10% enantiomerically pure R-compound. In certain embodiments, the enantiomerically pure R- compound in such compositions can, for example, comprise, at least about 95% by weight R- compound and at most about 5% by weight S-compound, by total weight of the compound. For example, a pharmaceutical composition comprising enantiomerically pure S-compound can comprise, for example, about 90% excipient and about 10% enantiomerically pure S-compound. In certain embodiments, the enantiomerically pure S-compound in such compositions can, for example, comprise, at least about 95% by weight S-compound and at most about 5% by weight R-compound, by total weight of the compound. In certain embodiments, the active ingredient can be formulated with little or no excipient or carrier.

Compound described herein may also comprise one or more isotopic substitutions. For example, H may be in any isotopic form, including 1 H, 2 H (D or deuterium), and 3 H (T or tritium); C may be in any isotopic form, including ¹² C, ¹³ C, and ¹⁴ C; O may be in any isotopic form, including ¹⁶ 0 and ¹⁸ 0; and the like.

The articles "a" and "an" may be used herein to refer to one or to more than one (i.e. at least one) of the grammatical objects of the article. By way of example "an analogue" means one analogue or more than one analogue.

When a range of values is listed, it is intended to encompass each value and sub-range within the range. For example "C ₁ -C ₆ alkyl" is intended to encompass, Q, C2, C ₃ , C4, C5, C ₆ , Ci-C ₆ , C ₁ -C5, C ₁ -C4, C ₁ -C3, C ₁ -C2, C2-C6, C2-C5, C2-C4, C2-C3, C3-C6, C3-C5, C3-C4, C4-C6, C4- C ₅ , and C ₅ -C ₆ alkyl.

The following terms are intended to have the meanings presented therewith below and are useful in understanding the description and intended scope of the present invention.

"Alkyl" refers to a radical of a straight-chain or branched saturated hydrocarbon group having from 1 to 20 carbon atoms ("C ₁ -C2 ₀ alkyl"). In some embodiments, an alkyl group has 1 to 12 carbon atoms alkyl"). In some embodiments, an alkyl group has 1 to 8 carbon atoms ("Ci-C ₈ alkyl"). In some embodiments, an alkyl group has 1 to 6 carbon atoms ("C ₁ -C6 alkyl"). In some embodiments, an alkyl group has 1 to 5 carbon atoms ("C ₁ -C5 alkyl"). In some embodiments, an alkyl group has 1 to 4 carbon atoms ("C ₁ -C4 alkyl"). In some embodiments, an alkyl group has 1 to 3 carbon atoms ("C ₁ -C ₃ alkyl"). In some embodiments, an alkyl group has 1 to 2 carbon atoms ("C ₁ -C2 alkyl"). In some embodiments, an alkyl group has 1 carbon atom ("Ci alkyl"). In some embodiments, an alkyl group has 2 to 6 carbon atoms ("C2-C6 alkyl"). Examples of Ci-C ₆ alkyl groups include methyl (Q), ethyl (C ₂ ), n-propyl (C ₃ ), isopropyl (C ₃ ), n-butyl (C4), tert-butyl (C4), sec-butyl (C4), iso-butyl (C4), n-pentyl (C _¾ ), 3-pentanyl (C _¾ ), amyl (C _¾ ), neopentyl (C _¾ ), 3-methyl-2-butanyl (C _¾ ), tertiary amyl (C _¾ ), and n-hexyl (C ₆ ). Additional examples of alkyl groups include n-heptyl (C ₇ ), n-octyl (C ₈ ) and the like. Each instance of an alkyl group may be independently optionally substituted, i.e., unsubstituted (an "unsubstituted alkyl") or substituted (a "substituted alkyl") with one or more substituents; e.g., for instance from 1 to 5 substituents, 1 to 3 substituents, or 1 substituent. In certain embodiments, the alkyl group is unsubstituted Ci_io alkyl (e.g., -CH ₃ ). In certain embodiments, the alkyl group is substituted Ci_6 alkyl. Common alkyl abbreviations include Me (-CH ₃ ), Et (- CH2CH3), iPr (-CH(CH ₃ ) ₂ ), nPr (-CH ₂ CH ₂ CH ₃ ), n-Bu (-CH2CH2CH2CH3), or i-Bu (- CH ₂ CH(CH ₃ ) ₂ ).

The term "alkylene," by itself or as part of another substituent, means, unless otherwise stated, a divalent radical derived from an alkyl, as exemplified, but not limited by, - CH2CH2CH2CH2-. Typically, an alkyl (or alkylene) group will have from 1 to 24 carbon atoms, with those groups having 10 or fewer carbon atoms being preferred in the present invention. The term "alkenylene," by itself or as part of another substituent, means, unless otherwise stated, a divalent radical derived from an alkene. An alkylene group may be described as, e.g., a Ci-C ₆ - membered alkylene, wherein the term "membered" refers to the non-hydrogen atoms within the moiety.

"Alkenyl" refers to a radical of a straight-chain or branched hydrocarbon group having from 2 to 20 carbon atoms, one or more carbon-carbon double bonds, and no triple bonds ("C ₂ - C2 ₀ alkenyl"). In some embodiments, an alkenyl group has 2 to 10 carbon atoms ("C ₂ -Cio alkenyl"). In some embodiments, an alkenyl group has 2 to 8 carbon atoms ("C2-C8 alkenyl"). In some embodiments, an alkenyl group has 2 to 6 carbon atoms ("C2-C6 alkenyl"). In some embodiments, an alkenyl group has 2 to 5 carbon atoms ("C2-C5 alkenyl"). In some

embodiments, an alkenyl group has 2 to 4 carbon atoms ("C2-C4 alkenyl"). In some

embodiments, an alkenyl group has 2 to 3 carbon atoms ("C2-C ₃ alkenyl"). In some embodiments, an alkenyl group has 2 carbon atoms ("C ₂ alkenyl"). The one or more carbon- carbon double bonds can be internal (such as in 2-butenyl) or terminal (such as in 1-butenyl). Examples of C2-C4 alkenyl groups include ethenyl (C ₂ ), 1-propenyl (C ₃ ), 2-propenyl (C ₃ ), 1- butenyl (C4), 2-butenyl (C4), butadienyl (C4), and the like. Examples of C2-C6 alkenyl groups include the aforementioned C2-4 alkenyl groups as well as pentenyl (C5), pentadienyl (C5), hexenyl (C ₆ ), and the like. Additional examples of alkenyl include heptenyl (C ₇ ), octenyl (C ₈ ), octatrienyl (C ₈ ), and the like. Each instance of an alkenyl group may be independently optionally substituted, i.e. , unsubstituted (an "unsubstituted alkenyl") or substituted (a

"substituted alkenyl") with one or more substituents e.g., for instance from 1 to 5 substituents, 1 to 3 substituents, or 1 substituent. In certain embodiments, the alkenyl group is unsubstituted C2- ₁₀ alkenyl. In certain embodiments, the alkenyl group is substituted C2-6 alkenyl.

"Aryl" refers to a radical of a monocyclic or polycyclic (e.g., bicyclic or tricyclic) 4n+2 aromatic ring system (e.g., having 6, 10, or 14 π electrons shared in a cyclic array) having 6-14 ring carbon atoms and zero heteroatoms provided in the aromatic ring system ("C6-C14 aryl"). In some embodiments, an aryl group has six ring carbon atoms ("C ₆ aryl"; e.g., phenyl). In some embodiments, an aryl group has ten ring carbon atoms ("Cio aryl"; e.g., naphthyl such as 1- naphthyl and 2-naphthyl). In some embodiments, an aryl group has fourteen ring carbon atoms ("CM aryl"; e.g., anthracyl). An aryl group may be described as, e.g., a C6-Cio-membered aryl, wherein the term "membered" refers to the non-hydrogen ring atoms within the moiety. Aryl groups include, but are not limited to, phenyl, naphthyl, indenyl, and tetrahydronaphthyl. Each instance of an aryl group may be independently optionally substituted, i.e., unsubstituted (an "unsubstituted aryl") or substituted (a "substituted aryl") with one or more substituents. In certain embodiments, the aryl group is unsubstituted C6-C14 aryl. In certain embodiments, the aryl group is substituted C6-C14 aryl.

In certain embodiments, an aryl group is substituted with one or more of groups selected from halo, Ci-C ₈ alkyl, halo-Ci-Cs alkyl, haloxy-Ci-Cs alkyl, cyano, hydroxy, alkoxy Ci-C ₈ alkyl, and amino.

Exam les of representative substituted aryls include the following

wherein one of R and R may be hydrogen and at least one of R and R is each independently selected from Q-Cg alkyl, halo-Q-Cg alkyl, 4-10 membered heterocyclyl, alkanoyl, alkoxy-Ci-Cs alkyl, heteroaryloxy, alkylamino, arylamino, heteroarylamino,

NR ⁵⁸ COR ⁵⁹ , NR ⁵⁸ SOR ⁵⁹ NR ⁵⁸ S0 ₂ R ⁵⁹ , C(0)Oalkyl, C(0)Oaryl, CONR ⁵⁸ R ⁵⁹ , CONR ⁵⁸ OR ⁵⁹ , NR ⁵⁸ R ⁵⁹ , S0 ₂ NR ⁵⁸ R ⁵⁹ , S-alkyl, S(0)-alkyl, S(0) ₂ -alkyl, S-aryl, S(0)-aryl, S(0 ₂ )-aryl; or R ⁵⁶ and R ⁵⁷ may be joined to form a cyclic ring (saturated or unsaturated) from 5 to 8 atoms, optionally containing one or more heteroatoms selected from the group N, O, or S.

yclyl group include the following:

wherein each W is selected from C(R ) ₂ , NR , O, and S; and each Y' is selected from carbonyl, NR ⁶⁶ , O and S; and R ⁶⁶ is independently hydrogen, Ci-C ₈ alkyl, C3-C10 cycloalkyl, 4- 10 membered heterocyclyl, C6-C10 aryl, and 5-10 membered heteroaryl. An "arylene" and a "heteroarylene," alone or as part of another substituent, mean a divalent radical derived from an aryl and heteroaryl, respectively. Non-limiting examples of heteroaryl groups include pyridinyl, pyrimidinyl, thiophenyl, thienyl, furanyl, indolyl, benzoxadiazolyl, benzodioxolyl, benzodioxanyl, thianaphthanyl, pyrrolopyridinyl, indazolyl, quinolinyl, quinoxalinyl, pyridopyrazinyl, quinazolinonyl, benzoisoxazolyl, imidazopyridinyl, benzofuranyl, benzothienyl, benzothiophenyl, phenyl, naphthyl, biphenyl, pyrrolyl, pyrazolyl, imidazolyl, pyrazinyl, oxazolyl, isoxazolyl, thiazolyl, furylthienyl, pyridyl, pyrimidyl, benzothiazolyl, purinyl, benzimidazolyl, isoquinolyl, thiadiazolyl, oxadiazolyl, pyrrolyl, diazolyl, triazolyl, tetrazolyl, benzothiadiazolyl, isothiazolyl, pyrazolopyrimidinyl,

pyrrolopyrimidinyl, benzotriazolyl, benzoxazolyl, or quinolyl. The examples above may be substituted or unsubstituted and divalent radicals of each heteroaryl example above are non- limiting examples of heteroarylene.

"Halo" or "halogen," independently or as part of another substituent, mean, unless otherwise stated, a fluorine (F), chlorine (CI), bromine (Br), or iodine (I) atom. The term "halide" by itself or as part of another substituent, refers to a fluoride, chloride, bromide, or iodide atom. In certain embodiments, the halo group is either fluorine or chlorine.

Additionally, terms such as "haloalkyl" are meant to include monohaloalkyl and polyhaloalkyl. For example, the term "halo-Cj-Ce alkyl" includes, but is not limited to, fluoromethyl, difluoromethyl, trifluoromethyl, 2,2,2-trifluoroethyl, 4-chlorobutyl, 3- bromopropyl, and the like.

The term "heteroalkyl," by itself or in combination with another term, means, unless otherwise stated, a non-cyclic stable straight or branched chain, or combinations thereof, including at least one carbon atom and at least one heteroatom selected from the group consisting of O, N, P, Si, and S, and wherein the nitrogen and sulfur atoms may optionally be oxidized, and the nitrogen heteroatom may optionally be quaternized. The heteroatom(s) O, N, P, S, and Si may be placed at any interior position of the heteroalkyl group or at the position at which the alkyl group is attached to the remainder of the molecule. Exemplary heteroalkyl groups include, but are not limited to: -CH ₂ -CH ₂ -0-CH ₃ , -CH ₂ -CH ₂ -NH-CH ₃ , -CH ₂ -CH ₂ - N(CH ₃ )-CH ₃ , -CH ₂ -S-CH ₂ -CH ₃ , -CH ₂ -CH ₂ , -S(0) ₂ , -S(0)-CH ₃ , -S(0) ₂ -CH _3, -CH ₂ -CH ₂ -S(0) ₂ - CH ₃ , -CH=CH-0-CH ₃ , -Si(CH ₃ ) ₃ , -CH ₂ -CH=N-OCH ₃ , -CH=CH-N(CH ₃ )-CH ₃ , -0-CH ₃ , and -O- CH ₂ -CH ₃ . Up to two or three heteroatoms may be consecutive, such as, for example, -CH ₂ -NH- OCH ₃ and -CH ₂ -0-Si(CH ₃ ) ₃ . Where "heteroalkyl" is recited, followed by recitations of specific heteroalkyl groups, such as -CH ₂ 0, -NR B R C , or the like, it will be understood that the terms B C

heteroalkyl and -CH2O or -NR R are not redundant or mutually exclusive. Rather, the specific heteroalkyl groups are recited to add clarity. Thus, the term "heteroalkyl" should not be

B C

interpreted herein as excluding specific heteroalkyl groups, such as -CH2O, -NR R , or the like.

Similarly, the term "heteroalkylene," by itself or as part of another substituent, means, unless otherwise stated, a divalent radical derived from heteroalkyl, as exemplified, but not limited by, -CH2O- and -CH2CH2O-. A heteroalkylene group may be described as, e.g., a 2-7- membered heteroalkylene, wherein the term "membered" refers to the non-hydrogen atoms within the moiety. For heteroalkylene groups, heteroatoms can also occupy either or both of the chain termini (e.g., alkyleneoxy, alkylenedioxy, alkyleneamino, alkylenediamino, and the like). Still further, for alkylene and heteroalkylene linking groups, no orientation of the linking group is implied by the direction in which the formula of the linking group is written. For example, the formula -C(0) ₂ R'- may represent both -C(0) ₂ R'- and -R'C(0) ₂ -.

"Heteroaryl" refers to a radical of a 5-10 membered monocyclic or bicyclic 4n+2 aromatic ring system (e.g., having 6 or 10 π electrons shared in a cyclic array) having ring carbon atoms and 1-4 ring heteroatoms provided in the aromatic ring system, wherein each heteroatom is independently selected from nitrogen, oxygen and sulfur ("5-10 membered heteroaryl"). In heteroaryl groups that contain one or more nitrogen atoms, the point of attachment can be a carbon or nitrogen atom, as valency permits. Heteroaryl bicyclic ring systems can include one or more heteroatoms in one or both rings. "Heteroaryl" also includes ring systems wherein the heteroaryl ring, as defined above, is fused with one or more aryl groups wherein the point of attachment is either on the aryl or heteroaryl ring, and in such instances, the number of ring members designates the number of ring members in the fused (aryl/heteroaryl) ring system. Bicyclic heteroaryl groups wherein one ring does not contain a heteroatom (e.g., indolyl, quinolinyl, carbazolyl, and the like) the point of attachment can be on either ring, i.e., either the ring bearing a heteroatom (e.g., 2-indolyl) or the ring that does not contain a heteroatom (e.g., 5-indolyl). A heteroaryl group may be described as, e.g., a 6-10-membered heteroaryl, wherein the term "membered" refers to the non-hydrogen ring atoms within the moiety.

In some embodiments, a heteroaryl group is a 5-10 membered aromatic ring system having ring carbon atoms and 1-4 ring heteroatoms provided in the aromatic ring system, wherein each heteroatom is independently selected from nitrogen, oxygen, and sulfur ("5-10 membered heteroaryl"). In some embodiments, a heteroaryl group is a 5-8 membered aromatic ring system having ring carbon atoms and 1-4 ring heteroatoms provided in the aromatic ring system, wherein each heteroatom is independently selected from nitrogen, oxygen, and sulfur ("5-8 membered heteroaryl"). In some embodiments, a heteroaryl group is a 5-6 membered aromatic ring system having ring carbon atoms and 1-4 ring heteroatoms provided in the aromatic ring system, wherein each heteroatom is independently selected from nitrogen, oxygen, and sulfur ("5-6 membered heteroaryl"). In some embodiments, the 5-6 membered heteroaryl has 1-3 ring heteroatoms selected from nitrogen, oxygen, and sulfur. In some embodiments, the 5-6 membered heteroaryl has 1-2 ring heteroatoms selected from nitrogen, oxygen, and sulfur. In some embodiments, the 5-6 membered heteroaryl has 1 ring heteroatom selected from nitrogen, oxygen, and sulfur. Each instance of a heteroaryl group may be independently optionally substituted, i.e. , unsubstituted (an "unsubstituted heteroaryl") or substituted (a

"substituted heteroaryl") with one or more substituents. In certain embodiments, the heteroaryl group is unsubstituted 5-14 membered heteroaryl. In certain embodiments, the heteroaryl group is substituted 5-14 membered heteroaryl.

Exemplary 5-membered heteroaryl groups containing one heteroatom include, without limitation, pyrrolyl, furanyl and thiophenyl. Exemplary 5-membered heteroaryl groups containing two heteroatoms include, without limitation, imidazolyl, pyrazolyl, oxazolyl, isoxazolyl, thiazolyl, and isothiazolyl. Exemplary 5-membered heteroaryl groups containing three heteroatoms include, without limitation, triazolyl, oxadiazolyl, and thiadiazolyl.

Exemplary 5-membered heteroaryl groups containing four heteroatoms include, without limitation, tetrazolyl. Exemplary 6-membered heteroaryl groups containing one heteroatom include, without limitation, pyridinyl. Exemplary 6-membered heteroaryl groups containing two heteroatoms include, without limitation, pyridazinyl, pyrimidinyl, and pyrazinyl. Exemplary 6- membered heteroaryl groups containing three or four heteroatoms include, without limitation, triazinyl and tetrazinyl, respectively. Exemplary 7-membered heteroaryl groups containing one heteroatom include, without limitation, azepinyl, oxepinyl, and thiepinyl. Exemplary 5,6- bicyclic heteroaryl groups include, without limitation, indolyl, isoindolyl, indazolyl, benzotriazolyl, benzothiophenyl, isobenzothiophenyl, benzofuranyl, benzoisofuranyl, benzimidazolyl, benzoxazolyl, benzisoxazolyl, benzoxadiazolyl, benzthiazolyl, benzisothiazolyl, benzthiadiazolyl, indolizinyl, and purinyl. Exemplary 6,6-bicyclic heteroaryl groups include, without limitation, naphthyridinyl, pteridinyl, quinolinyl, isoquinolinyl, cinnolinyl, quinoxalinyl, phthalazinyl, and quinazolinyl.

Examples of representative heteroaryls include the following formulae:

wherein each Y is selected from carbonyl, N, NR , O, and S; and R is independently hydrogen, Ci-C ₈ alkyl, C3-C ₁₀ cycloalkyl, 4-10 membered heterocyclyl, C6-C ₁₀ aryl, and 5-10 membered heteroaryl.

"Cycloalkyl" refers to a radical of a non-aromatic cyclic hydrocarbon group having from

3 to 10 ring carbon atoms ("C ₃ -C ₁₀ cycloalkyl") and zero heteroatoms in the non-aromatic ring system. In some embodiments, a cycloalkyl group has 3 to 8 ring carbon atoms ("C ₃ -C8 cycloalkyl"). In some embodiments, a cycloalkyl group has 3 to 6 ring carbon atoms ("C ₃ -C6 cycloalkyl"). In some embodiments, a cycloalkyl group has 3 to 6 ring carbon atoms ("C ₃ -C6 cycloalkyl"). In some embodiments, a cycloalkyl group has 5 to 10 ring carbon atoms ("C5-C ₁₀ cycloalkyl"). A cycloalkyl group may be described as, e.g., a C4-C ₇ -membered cycloalkyl, wherein the term "membered" refers to the non-hydrogen ring atoms within the moiety.

Exemplary C ₃ -C6 cycloalkyl groups include, without limitation, cyclopropyl (C ₃ ), cyclopropenyl (C ₃ ), cyclobutyl (C4), cyclobutenyl (C4), cyclopentyl (C _¾ ), cyclopentenyl (C _¾ ), cyclohexyl (C ₆ ), cyclohexenyl (C ₆ ), cyclohexadienyl (C ₆ ), and the like. Exemplary C ₃ -C ₈ cycloalkyl groups include, without limitation, the aforementioned C ₃ -C6 cycloalkyl groups as well as cycloheptyl (C ₇ ), cycloheptenyl (C ₇ ), cycloheptadienyl (C ₇ ), cycloheptatrienyl (C ₇ ), cyclooctyl (C ₈ ), cyclooctenyl (C ₈ ), cubanyl (C ₈ ), bicyclo[l . l . l]pentanyl (C5), bicyclo[2.2.2]octanyl (C ₈ ), bicyclo[2.1.1]hexanyl (C ₆ ), bicyclo[3.1.1]heptanyl (C ₇ ), and the like. Exemplary C ₃ -C ₁₀ cycloalkyl groups include, without limitation, the aforementioned C ₃ -C ₈ cycloalkyl groups as well as cyclononyl (C9), cyclononenyl (C9), cyclodecyl, (C ₁₀ ), cyclodecenyl (C ₁₀ ), octahydro- lH-indenyl (C9), decahydronaphthalenyl (C ₁₀ ), spiro[4.5]decanyl (C ₁₀ ), and the like. As the foregoing examples illustrate, in certain embodiments, the cycloalkyl group is either monocyclic ("monocyclic cycloalkyl") or contain a fused, bridged or spiro ring system such as a bicyclic system ("tricyclic cycloalkyl") and can be saturated or can be partially unsaturated. "Cycloalkyl" also includes ring systems wherein the cycloalkyl ring, as defined above, is fused with one or more aryl groups wherein the point of attachment is on the cycloalkyl ring, and in such instances, the number of carbons continue to designate the number of carbons in the cycloalkyl ring system. Each instance of a cycloalkyl group may be independently optionally substituted, i.e., unsubstituted (an "unsubstituted cycloalkyl") or substituted (a "substituted cycloalkyl") with one or more substituents. In certain embodiments, the cycloalkyl group is unsubstituted C3-C10 cycloalkyl. In certain embodiments, the cycloalkyl group is a substituted C3-C10 cycloalkyl.

In some embodiments, "cycloalkyl" is a monocyclic, saturated cycloalkyl group having from 3 to 10 ring carbon atoms ("C3-C10 cycloalkyl"). In some embodiments, a cycloalkyl group has 3 to 8 ring carbon atoms ("C3-C8 cycloalkyl"). In some embodiments, a cycloalkyl group has 3 to 6 ring carbon atoms ("C3-C6 cycloalkyl"). In some embodiments, a cycloalkyl group has 5 to 6 ring carbon atoms ("C5-C6 cycloalkyl"). In some embodiments, a cycloalkyl group has 5 to 10 ring carbon atoms ("C5-C10 cycloalkyl"). Examples of C5-C6 cycloalkyl groups include cyclopentyl (C _¾ ) and cyclohexyl (C _¾ ). Examples of C3-C6 cycloalkyl groups include the aforementioned C5-C6 cycloalkyl groups as well as cyclopropyl (C3) and cyclobutyl (C ₄ ).

Examples of C3-C8 cycloalkyl groups include the aforementioned C3-C6 cycloalkyl groups as well as cycloheptyl (C ) and cyclooctyl (Cg). Unless otherwise specified, each instance of a cycloalkyl group is independently unsubstituted (an "unsubstituted cycloalkyl") or substituted (a "substituted cycloalkyl") with one or more substituents. In certain embodiments, the cycloalkyl group is unsubstituted C3-C10 cycloalkyl. In certain embodiments, the cycloalkyl group is substituted C3-C10 cycloalkyl.

"Heterocyclyl" or "heterocyclic" refers to a radical of a 3- to 10-membered non- aromatic ring system having ring carbon atoms and 1 to 4 ring heteroatoms, wherein each heteroatom is independently selected from nitrogen, oxygen, sulfur, boron, phosphorus, and silicon ("3-10 membered heterocyclyl"). In heterocyclyl groups that contain one or more nitrogen atoms, the point of attachment can be a carbon or nitrogen atom, as valency permits. A heterocyclyl group can either be monocyclic ("monocyclic heterocyclyl") or a fused, bridged or spiro ring system such as a bicyclic system ("bicyclic heterocyclyl"), and can be saturated or can be partially unsaturated. Heterocyclyl bicyclic ring systems can include one or more

heteroatoms in one or both rings. "Heterocyclyl" also includes ring systems wherein the heterocyclyl ring, as defined above, is fused with one or more cycloalkyl groups wherein the point of attachment is either on the cycloalkyl or heterocyclyl ring, or ring systems wherein the heterocyclyl ring, as defined above, is fused with one or more aryl or heteroaryl groups, wherein the point of attachment is on the heterocyclyl ring, and in such instances, the number of ring members continue to designate the number of ring members in the heterocyclyl ring system. A heterocyclyl group may be described as, e.g., a 3-7-membered heterocyclyl, wherein the term "membered" refers to the non-hydrogen ring atoms, i.e., carbon, nitrogen, oxygen, sulfur, boron, phosphorus, and silicon, within the moiety. Each instance of heterocyclyl may be independently optionally substituted, i.e. , unsubstituted (an "unsubstituted heterocyclyl") or substituted (a "substituted heterocyclyl") with one or more substituents. In certain embodiments, the heterocyclyl group is unsubstituted 3-10 membered heterocyclyl. In certain embodiments, the heterocyclyl group is substituted 3-10 membered heterocyclyl.

In some embodiments, a heterocyclyl group is a 5-10 membered non-aromatic ring system having ring carbon atoms and 1-4 ring heteroatoms, wherein each heteroatom is independently selected from nitrogen, oxygen, sulfur, boron, phosphorus, and silicon ("5-10 membered heterocyclyl"). In some embodiments, a heterocyclyl group is a 5-8 membered non- aromatic ring system having ring carbon atoms and 1-4 ring heteroatoms, wherein each heteroatom is independently selected from nitrogen, oxygen, and sulfur ("5-8 membered heterocyclyl"). In some embodiments, a heterocyclyl group is a 5-6 membered non-aromatic ring system having ring carbon atoms and 1-4 ring heteroatoms, wherein each heteroatom is independently selected from nitrogen, oxygen, and sulfur ("5-6 membered heterocyclyl"). In some embodiments, the 5-6 membered heterocyclyl has 1-3 ring heteroatoms selected from nitrogen, oxygen, and sulfur. In some embodiments, the 5-6 membered heterocyclyl has 1-2 ring heteroatoms selected from nitrogen, oxygen, and sulfur. In some embodiments, the 5-6 membered heterocyclyl has one ring heteroatom selected from nitrogen, oxygen, and sulfur.

Exemplary 3-membered heterocyclyl groups containing one heteroatom include, without limitation, azirdinyl, oxiranyl, thiorenyl. Exemplary 4-membered heterocyclyl groups containing one heteroatom include, without limitation, azetidinyl, oxetanyl and thietanyl.

Exemplary 5-membered heterocyclyl groups containing one heteroatom include, without limitation, tetrahydrofuranyl, dihydrofuranyl, tetrahydrothiophenyl, dihydrothiophenyl, pyrrolidinyl, dihydropyrrolyl and pyrrolyl-2,5-dione. Exemplary 5-membered heterocyclyl groups containing two heteroatoms include, without limitation, dioxolanyl, oxasulfuranyl, disulfuranyl, and oxazolidin-2-one. Exemplary 5-membered heterocyclyl groups containing three heteroatoms include, without limitation, triazolinyl, oxadiazolinyl, and thiadiazolinyl. Exemplary 6-membered heterocyclyl groups containing one heteroatom include, without limitation, piperidinyl, tetrahydropyranyl, dihydropyridinyl, and thianyl. Exemplary 6- membered heterocyclyl groups containing two heteroatoms include, without limitation, piperazinyl, morpholinyl, dithianyl, dioxanyl. Exemplary 6-membered heterocyclyl groups containing two heteroatoms include, without limitation, triazinanyl. Exemplary 7-membered heterocyclyl groups containing one heteroatom include, without limitation, azepanyl, oxepanyl and thiepanyl. Exemplary 8-membered heterocyclyl groups containing one heteroatom include, without limitation, azocanyl, oxecanyl and thiocanyl. Exemplary 5-membered heterocyclyl groups fused to a aryl ring (also referred to herein as a 5,6-bicyclic heterocyclic ring) include, without limitation, indolinyl, isoindolinyl, dihydrobenzofuranyl, dihydrobenzothienyl, benzoxazolinonyl, and the like. Exemplary 6-membered heterocyclyl groups fused to an aryl ring (also referred to herein as a 6,6-bicyclic heterocyclic ring) include, without limitation, tetrahydroquinolinyl, tetrahydroisoquinolinyl, and the like.

Particular examples of heterocyclyl groups are shown in the following illustrative exampl

wherein each W" is selected from CR , C(R ) ₂ , NR , O, and S; and each Y" is selected from NR ⁶⁷ , O, and S; and R ⁶⁷ is independently hydrogen, Ci-C ₈ alkyl, C3-C10 cycloalkyl, 4-10 membered heterocyclyl, C6-C10 aryl, and 5-10-membered heteroaryl. These heterocyclyl rings may be optionally substituted with one or more groups selected from the group consisting of acyl, acylamino, acyloxy, alkoxy, alkoxycarbonyl, alkoxycarbonylamino, amino, substituted amino, aminocarbonyl (e.g., amido), aminocarbonylamino, aminosulfonyl, sulfonylamino, aryl, aryloxy, azido, carboxyl, cyano, cycloalkyl, halogen, hydroxy, keto, nitro, thiol, -S-alkyl, -S- aryl, -S(0)-alkyl, -S(0)-aryl, -S(0)2-alkyl, and -S(0)2-aryl. Substituting groups include carbonyl or thiocarbonyl which provide, for example, lactam and urea derivatives.

"Nitrogen-containing heterocyclyl" group means a 4- to 7- membered non-aromatic cyclic group containing at least one nitrogen atom, for example, but without limitation, morpholine, piperidine (e.g. 2-piperidinyl, 3-piperidinyl and 4-piperidinyl), pyrrolidine (e.g. 2- pyrrolidinyl and 3-pyrrolidinyl), azetidine, pyrrolidone, imidazoline, imidazolidinone, 2- pyrazoline, pyrazolidine, piperazine, and N-alkyl piperazines such as N-methyl piperazine. Particular examples include azetidine, piperidone and piperazone.

70 71 70 71

"Amino" refers to the radical -NR R , wherein R and R are each independently hydrogen, Ci-C ₈ alkyl, C3-C10 cycloalkyl, 4-10 membered heterocyclyl, C6-C10 aryl, and 5-10- membered heteroaryl. In some embodiments, amino refers to NH2.

"Cyano" refers to the radical -CN.

"Hydroxy" refers to the radical -OH.

Alkyl, alkenyl, alkynyl, cycloalkyl, heterocyclyl, aryl, and heteroaryl groups, as defined herein, are optionally substituted (e.g., "substituted" or "unsubstituted" alkyl, "substituted" or "unsubstituted" alkenyl, "substituted" or "unsubstituted" alkynyl, "substituted" or

"unsubstituted" cycloalkyl, "substituted" or "unsubstituted" heterocyclyl, "substituted" or "unsubstituted" aryl or "substituted" or "unsubstituted" heteroaryl group). In general, the term "substituted", whether preceded by the term "optionally" or not, means that at least one hydrogen present on a group (e.g., a carbon or nitrogen atom) is replaced with a permissible substituent, e.g., a substituent which upon substitution results in a stable compound, e.g., a compound which does not spontaneously undergo transformation such as by rearrangement, cyclization, elimination, or other reaction. Unless otherwise indicated, a "substituted" group has a substituent at one or more substitutable positions of the group, and when more than one position in any given structure is substituted, the substituent is either the same or different at each position. The term "substituted" is contemplated to include substitution with all permissible substituents of organic compounds, such as any of the substituents described herein that result in the formation of a stable compound. The present invention contemplates any and all such combinations in order to arrive at a stable compound. For purposes of this invention, heteroatoms such as nitrogen may have hydrogen substituents and/or any suitable substituent as described herein which satisfy the valencies of the heteroatoms and results in the formation of a stable moiety.

Two or more substituents may optionally be joined to form aryl, heteroaryl, cycloalkyl, or heterocycloalkyl groups. Such so-called ring-forming substituents are typically, though not necessarily, found attached to a cyclic base structure. In one embodiment, the ring-forming substituents are attached to adjacent members of the base structure. For example, two ring- forming substituents attached to adjacent members of a cyclic base structure create a fused ring structure. In another embodiment, the ring-forming substituents are attached to a single member of the base structure. For example, two ring-forming substituents attached to a single member of a cyclic base structure create a spirocyclic structure. In yet another embodiment, the ring- forming substituents are attached to non-adjacent members of the base structure.

A "counterion" or "anionic counterion" is a negatively charged group associated with a cationic quaternary amino group in order to maintain electronic neutrality. Exemplary counterions include halide ions (e.g., F ^~ , CI ^" , Br ^" , Γ), N0 ₃ ^" , C10 ₄ ^" , OH ^" , H ₂ P0 ₄ ^" , HS0 ₄ ^" , sulfonate ions (e.g., methansulfonate, trifluoromethanesulfonate, p-toluenesulfonate, benzenesulfonate, 10-camphor sulfonate, naphthalene-2-sulfonate, naphthalene- 1 -sulfonic acid-5-sulfonate, ethan-l-sulfonic acid-2-sulfonate, and the like), and carboxylate ions (e.g., acetate, ethanoate, propanoate, benzoate, glycerate, lactate, tartrate, glycolate, and the like).

The term "pharmaceutically acceptable salts" is meant to include salts of the active compounds that are prepared with relatively nontoxic acids or bases, depending on the particular substituents found on the compounds described herein. When compounds of the present invention contain relatively acidic functionalities, base addition salts can be obtained by contacting the neutral form of such compounds with a sufficient amount of the desired base, either neat or in a suitable inert solvent. Examples of pharmaceutically acceptable base addition salts include sodium, potassium, calcium, ammonium, organic amino, or magnesium salt, or a similar salt. When compounds of the present invention contain relatively basic functionalities, acid addition salts can be obtained by contacting the neutral form of such compounds with a sufficient amount of the desired acid, either neat or in a suitable inert solvent. Examples of pharmaceutically acceptable acid addition salts include those derived from inorganic acids like hydrochloric, hydrobromic, nitric, carbonic, monohydrogencarbonic, phosphoric,

monohydrogenphosphoric, dihydrogenphosphoric, sulfuric, monohydrogensulfuric, hydriodic, or phosphorous acids and the like, as well as the salts derived from relatively nontoxic organic acids like acetic, propionic, isobutyric, maleic, malonic, benzoic, succinic, suberic, fumaric, lactic, mandelic, phthalic, benzenesulfonic, p-tolylsulfonic, citric, tartaric, methanesulfonic, and the like. Also included are salts of amino acids such as arginate and the like, and salts of organic acids like glucuronic or galactunoric acids and the like (see, e.g., Berge et al, Journal of Pharmaceutical Science 66: 1 -19 (1977)). Certain specific compounds of the present invention contain both basic and acidic functionalities that allow the compounds to be converted into either base or acid addition salts. Other pharmaceutically acceptable carriers known to those of skill in the art are suitable for the present invention. Salts tend to be more soluble in aqueous or other protonic solvents that are the corresponding free base forms. In other cases, the preparation may be a lyophilized powder in a first buffer, e.g., in 1 mM-50 mM histidine, 0. l%-2% sucrose, 2%- 7% mannitol at a pH range of 4.5 to 5.5, that is combined with a second buffer prior to use.

Thus, the compounds of the present invention may exist as salts, such as with pharmaceutically acceptable acids. The present invention includes such salts. Examples of such salts include hydrochlorides, hydrobromides, sulfates, methanesulfonates, nitrates, maleates, acetates, citrates, fumarates, tartrates (e.g., (+) -tartrates, (-)-tartrates, or mixtures thereof including racemic mixtures), succinates, benzoates, and salts with amino acids such as glutamic acid. These salts may be prepared by methods known to those skilled in the art.

The neutral forms of the compounds are preferably regenerated by contacting the salt with a base or acid and isolating the parent compound in the conventional manner. The parent form of the compound differs from the various salt forms in certain physical properties, such as solubility in polar solvents.

In addition to salt forms, the present invention provides compounds, which are in a prodrug form. Prodrugs of the compounds described herein are those compounds that readily undergo chemical changes under physiological conditions to provide the compounds of the present invention. Additionally, prodrugs can be converted to the compounds of the present invention by chemical or biochemical methods in an ex vivo environment. For example, prodrugs can be slowly converted to the compounds of the present invention when placed in a transdermal patch reservoir with a suitable enzyme or chemical reagent.

Certain compounds of the present invention can exist in unsolvated forms as well as solvated forms, including hydrated forms. In general, the solvated forms are equivalent to unsolvated forms and are encompassed within the scope of the present invention. Certain compounds of the present invention may exist in multiple crystalline or amorphous forms. In general, all physical forms are equivalent for the uses contemplated by the present invention and are intended to be within the scope of the present invention.

As used herein, the term "salt" refers to acid or base salts of the compounds used in the methods of the present invention. Illustrative examples of acceptable salts are mineral acid (hydrochloric acid, hydrobromic acid, phosphoric acid, and the like) salts, organic acid (acetic acid, propionic acid, glutamic acid, citric acid and the like) salts, quaternary ammonium (methyl iodide, ethyl iodide, and the like) salts.

Certain compounds of the present invention possess asymmetric carbon atoms (optical or chiral centers) or double bonds; the enantiomers, racemates, diastereomers, tautomers, geometric isomers, stereoisometric forms that may be defined, in terms of absolute stereochemistry, as (R)- or (S)- or, as (D)- or (L)- for amino acids, and individual isomers are encompassed within the scope of the present invention. The compounds of the present invention do not include those which are known in art to be too unstable to synthesize and/or isolate. The present invention is meant to include compounds in racemic and optically pure forms. Optically active (R)- and (S)-, or (D)- and (L)-isomers may be prepared using chiral synthons or chiral reagents, or resolved using conventional techniques. When the compounds described herein contain olefinic bonds or other centers of geometric asymmetry, and unless specified otherwise, it is intended that the compounds include both E and Z geometric isomers.

As used herein, the term "isomers" refers to compounds having the same number and kind of atoms, and hence the same molecular weight, but differing in respect to the structural arrangement or configuration of the atoms.

The term "tautomer," as used herein, refers to one of two or more structural isomers which exist in equilibrium and which are readily converted from one isomeric form to another.

It will be apparent to one skilled in the art that certain compounds of this invention may exist in tautomeric forms, all such tautomeric forms of the compounds being within the scope of the invention.

The terms "treating" or "treatment" refers to any indicia of success in the treatment or amelioration of an injury, disease, pathology or condition, including any objective or subjective parameter such as abatement; remission; diminishing of symptoms or making the injury, pathology or condition more tolerable to the patient; slowing in the rate of degeneration or decline; making the final point of degeneration less debilitating; improving a patient's physical or mental well-being. The treatment or amelioration of symptoms can be based on objective or subjective parameters; including the results of a physical examination, neuropsychiatric exams, and/or a psychiatric evaluation. For example, certain methods herein treat cancer (e.g.

pancreatic cancer, breast cancer, multiple myeloma, cancers of secretory cells),

neurodegenerative diseases (e.g. Alzheimer's disease, Parkinson's disease, frontotemporal dementia), leukodystrophies (e.g., vanishing white matter disease, childhood ataxia with CNS hypo-myelination), postsurgical cognitive dysfunction, traumatic brain injury, stroke, spinal cord injury, intellectual disability syndromes, inflammatory diseases, musculoskeletal diseases, metabolic diseases, or diseases or disorders associated with impaired function of eIF2B or components in a signal transduction or signaling pathway including the ISR and decreased eIF2 pathway activity). For example certain methods herein treat cancer by decreasing or reducing or preventing the occurrence, growth, metastasis, or progression of cancer or decreasing a symptom of cancer; treat neurodegeneration by improving mental wellbeing, increasing mental function, slowing the decrease of mental function, decreasing dementia, delaying the onset of dementia, improving cognitive skills, decreasing the loss of cognitive skills, improving memory, decreasing the degradation of memory, decreasing a symptom of neurodegeneration or extending survival; treat vanishing white matter disease by reducing a symptom of vanishing white matter disease or reducing the loss of white matter or reducing the loss of myelin or increasing the amount of myelin or increasing the amount of white matter; treat childhood ataxia with CNS hypo-myelination by decreasing a symptom of childhood ataxia with CNS hypo-myelination or increasing the level of myelin or decreasing the loss of myelin; treat an intellectual disability syndrome by decreasing a symptom of an intellectual disability syndrome, treat an inflammatory disease by treating a symptom of the inflammatory disease; treat a musculoskeletal disease by treating a symptom of the musculoskeletal disease; or treat a metabolic disease by treating a symptom of the metabolic disease. Symptoms of a disease, disorder, or condition described herein (e.g., cancer, a neurodegenerative disease, a leukodystrophy, an inflammatory disease, a musculoskeletal disease, a metabolic disease, or a condition or disease associated with impaired function of eIF2B or components in a signal transduction pathway including the eIF2 pathway, eIF2D phosphorylation, or ISR pathway) would be known or may be determined by a person of ordinary skill in the art. The term "treating" and conjugations thereof, include prevention of an injury, pathology, condition, or disease (e.g. preventing the development of one or more symptoms of a disease, disorder, or condition described herein).

An "effective amount" is an amount sufficient to accomplish a stated purpose (e.g. achieve the effect for which it is administered, treat a disease, reduce enzyme activity, increase enzyme activity, or reduce one or more symptoms of a disease or condition). An example of an "effective amount" is an amount sufficient to contribute to the treatment, prevention, or reduction of a symptom or symptoms of a disease, which could also be referred to as a

"therapeutically effective amount. A "prophylactically effective amount" of a drug is an amount of a drug that, when administered to a subject, will have the intended prophylactic effect, e.g., preventing or delaying the onset (or reoccurrence) of an injury, disease, pathology or condition, or reducing the likelihood of the onset (or reoccurrence) of an injury, disease, pathology, or condition, or their symptoms. The full prophylactic effect does not necessarily occur by administration of one dose, and may occur only after administration of a series of doses. Thus, a prophylactically effective amount may be administered in one or more administrations. The exact amounts will depend on the purpose of the treatment, and will be ascertainable by one skilled in the art using known techniques (see, e.g., Lieberman, Pharmaceutical Dosage Forms (vols. 1-3, 1992); Lloyd, The Art, Science and Technology of Pharmaceutical Compounding (1999); Pickar, Dosage Calculations (1999); and Remington: The Science and Practice of Pharmacy, 20th Edition, 2003, Gennaro, Ed., Lippincott, Williams & Wilkins).

A "reduction" of a symptom or symptoms (and grammatical equivalents of this phrase) means decreasing of the severity or frequency of the symptom(s), or elimination of the symptom(s).

The term "associated" or "associated with" in the context of a substance or substance activity or function associated with a disease (e.g., a disease or disorder described herein, e.g., cancer, a neurodegenerative disease, a leukodystrophy, an inflammatory disease, a

musculoskeletal disease, a metabolic disease, or a disease or disorder associated with impaired function of eIF2B or components in a signal transduction pathway including the eIF2 pathway, eIF2D phosphorylation, or ISR pathway) means that the disease is caused by (in whole or in part), or a symptom of the disease is caused by (in whole or in part) the substance or substance activity or function. For example, a symptom of a disease or condition associated with an impaired function of the eIF2B may be a symptom that results (entirely or partially) from a decrease in eIF2B activity (e.g. decrease in eIF2B activity or levels, increase in eIF2a phosphorylation or activity of phosphorylated eIF2a or reduced eIF2 activity or increase in activity of phosphorylated eIF2a signal transduction or the ISR signalling pathway). As used herein, what is described as being associated with a disease, if a causative agent, could be a target for treatment of the disease. For example, a disease associated with decreased eIF2 activity or eIF2 pathway activity, may be treated with an agent (e.g., compound as described herein) effective for increasing the level or activity of eIF2 or eIF2 pathway or a decrease in phosphorylated eIF2a activity or the ISR pathway. For example, a disease associated with phosphorylated eIF2a may be treated with an agent (e.g., compound as described herein) effective for decreasing the level of activity of phosphorylated eIF2a or a downstream component or effector of phosphorylated eIF2a. For example, a disease associated with eIF2a, may be treated with an agent (e.g., compound as described herein) effective for increasing the level of activity of eIF2 or a downstream component or effector of eIF2.

"Control" or "control experiment" is used in accordance with its plain ordinary meaning and refers to an experiment in which the subjects or reagents of the experiment are treated as in a parallel experiment except for omission of a procedure, reagent, or variable of the experiment. In some instances, the control is used as a standard of comparison in evaluating experimental effects.

"Contacting" is used in accordance with its plain ordinary meaning and refers to the process of allowing at least two distinct species (e.g. chemical compounds including biomolecules, or cells) to become sufficiently proximal to react, interact or physically touch. It should be appreciated, however, that the resulting reaction product can be produced directly from a reaction between the added reagents or from an intermediate from one or more of the added reagents which can be produced in the reaction mixture. The term "contacting" may include allowing two species to react, interact, or physically touch, wherein the two species may be a compound as described herein and a protein or enzyme (e.g. eIF2B, eIF2a, or a component of the eIF2 pathway or ISR pathway). In some embodiments contacting includes allowing a compound described herein to interact with a protein or enzyme that is involved in a signaling pathway (e.g. eIF2B, eIF2a, or a component of the eIF2 pathway or ISR pathway).

As defined herein, the term "inhibition", "inhibit", "inhibiting" and the like in reference to a protein-inhibitor (e.g., antagonist) interaction means negatively affecting (e.g., decreasing) the activity or function of the protein relative to the activity or function of the protein in the absence of the inhibitor. In some embodiments, inhibition refers to reduction of a disease or symptoms of disease. In some embodiments, inhibition refers to a reduction in the activity of a signal transduction pathway or signaling pathway. Thus, inhibition includes, at least in part, partially or totally blocking stimulation, decreasing, preventing, or delaying activation, or inactivating, desensitizing, or down-regulating signal transduction or enzymatic activity or the amount of a protein. In some embodiments, inhibition refers to a decrease in the activity of a signal transduction pathway or signaling pathway (e.g., eIF2B, eIF2a, or a component of the eIF2 pathway, pathway activated by eIF2a phosphorylation, or ISR pathway). Thus, inhibition may include, at least in part, partially or totally decreasing stimulation, decreasing or reducing activation, or inactivating, desensitizing, or down-regulating signal transduction or enzymatic activity or the amount of a protein increased in a disease (e.g. eIF2B, eIF2a, or a component of the eIF2 pathway or ISR pathway, wherein each is associated with cancer, a neurodegenerative disease, a leukodystrophy, an inflammatory disease, a musculoskeletal disease, or a metabolic disease). Inhibition may include, at least in part, partially or totally decreasing stimulation, decreasing or reducing activation, or deactivating, desensitizing, or down-regulating signal transduction or enzymatic activity or the amount of a protein (e.g. eIF2B, eIF2a, or component of the eIF2 pathway or ISR pathway) that may modulate the level of another protein or increase cell survival (e.g., decrease in phosphorylated eIF2a pathway activity may increase cell survival in cells that may or may not have an increase in phosphorylated eIF2a pathway activity relative to a non-disease control or decrease in eIF2a pathway activity may increase cell survival in cells that may or may not have an increase in eIF2a pathway activity relative to a non-disease control).

As defined herein, the term "activation", "activate", "activating" and the like in reference to a protein-activator (e.g. agonist) interaction means positively affecting (e.g., increasing) the activity or function of the protein (e.g. eIF2B, eIF2a, or component of the eIF2 pathway or ISR pathway) relative to the activity or function of the protein in the absence of the activator (e.g. compound described herein). In some embodiments, activation refers to an increase in the activity of a signal transduction pathway or signaling pathway (e.g. eIF2B, eIF2a, or component of the eIF2 pathway or ISR pathway). Thus, activation may include, at least in part, partially or totally increasing stimulation, increasing or enabling activation, or activating, sensitizing, or up- regulating signal transduction or enzymatic activity or the amount of a protein decreased in a disease (e.g. level of eIF2B, eIF2a, or component of the eIF2 pathway or ISR pathway associated with cancer, a neurodegenerative disease, a leukodystrophy, an inflammatory disease, a musculoskeletal disease, or a metabolic disease). Activation may include, at least in part, partially or totally increasing stimulation, increasing or enabling activation, or activating, sensitizing, or up-regulating signal transduction or enzymatic activity or the amount of a protein (e.g., eIF2B, eIF2a, or component of the eIF2 pathway or ISR pathway) that may modulate the level of another protein or increase cell survival (e.g., increase in eIF2a activity may increase cell survival in cells that may or may not have a reduction in eIF2a activity relative to a non- disease control).

The term "modulation" refers to an increase or decrease in the level of a target molecule or the function of a target molecule. In some embodiments, modulation of eIF2B, eIF2a, or a component of the eIF2 pathway or ISR pathway may result in reduction of the severity of one or more symptoms of a disease associated with eIF2B, eIF2a, or a component of the eIF2 pathway or ISR pathway (e.g., cancer, a neurodegenerative disease, a leukodystrophy, an inflammatory disease, a musculoskeletal disease, or a metabolic disease) or a disease that is not caused by eIF2B, eIF2a, or a component of the eIF2 pathway or ISR pathway but may benefit from modulation of eIF2B, eIF2a, or a component of the eIF2 pathway or ISR pathway (e.g., decreasing in level or level of activity of eIF2B, eIF2a or a component of the eIF2 pathway). The term "modulator" as used herein refers to modulation of (e.g., an increase or decrease in) the level of a target molecule or the function of a target molecule. In embodiments, a modulator of eIF2B, eIF2a, or component of the eIF2 pathway or ISR pathway is an anticancer agent. In embodiments, a modulator of eIF2B, eIF2a, or component of the eIF2 pathway or ISR pathway is a neuroprotectant. In embodiments, a modulator of eIF2B, eIF2a, or component of the eIF2 pathway or ISR pathway is a memory enhancing agent. In embodiments, a modulator of eIF2B, eIF2a, or component of the eIF2 pathway or ISR pathway is a memory enhancing agent (e.g., a long term memory enhancing agent). In embodiments, a modulator of eIF2B, eIF2a, or component of the eIF2 pathway or ISR pathway is an anti-inflammatory agent. In some embodiments, a modulator of eIF2B, eIF2a, or component of the eIF2 pathway or ISR pathway is a pain-relieving agent.

"Patient" or "subject in need thereof refers to a living organism suffering from or prone to a disease or condition that can be treated by administration of a compound or pharmaceutical composition, as provided herein. Non-limiting examples include humans, other mammals, bovines, rats, mice, dogs, monkeys, goat, sheep, cows, deer, and other non-mammalian animals. In some embodiments, a patient is human. In some embodiments, a patient is a domesticated animal. In some embodiments, a patient is a dog. In some embodiments, a patient is a parrot. In some embodiments, a patient is livestock animal. In some embodiments, a patient is a mammal. In some embodiments, a patient is a cat. In some embodiments, a patient is a horse. In some embodiments, a patient is bovine. In some embodiments, a patient is a canine. In some embodiments, a patient is a feline. In some embodiments, a patient is an ape. In some embodiments, a patient is a monkey. In some embodiments, a patient is a mouse. In some embodiments, a patient is an experimental animal. In some embodiments, a patient is a rat. In some embodiments, a patient is a hamster. In some embodiments, a patient is a test animal. In some embodiments, a patient is a newborn animal. In some embodiments, a patient is a newborn human. In some embodiments, a patient is a newborn mammal. In some embodiments, a patient is an elderly animal. In some embodiments, a patient is an elderly human. In some

embodiments, a patient is an elderly mammal. In some embodiments, a patient is a geriatric patient.

"Disease", "disorder" or "condition" refers to a state of being or health status of a patient or subject capable of being treated with a compound, pharmaceutical composition, or method provided herein. In some embodiments, the compounds and methods described herein comprise reduction or elimination of one or more symptoms of the disease, disorder, or condition, e.g., through administration of a compound of Formula (I) or Formula (II), or a pharmaceutically acceptable salt thereof.

The term "signaling pathway" as used herein refers to a series of interactions between cellular and optionally extra-cellular components (e.g. proteins, nucleic acids, small molecules, ions, lipids) that conveys a change in one component to one or more other components, which in turn may convey a change to additional components, which is optionally propagated to other signaling pathway components.

"Pharmaceutically acceptable excipient" and "pharmaceutically acceptable carrier" refer to a substance that aids the administration of an active agent to and absorption by a subject and can be included in the compositions of the present invention without causing a significant adverse toxicological effect on the patient. Non-limiting examples of pharmaceutically acceptable excipients include water, NaCl, normal saline solutions, lactated Ringer's, normal sucrose, normal glucose, binders, fillers, disintegrants, lubricants, coatings, sweeteners, flavors, salt solutions (such as Ringer's solution), alcohols, oils, gelatins, carbohydrates such as lactose, amylose or starch, fatty acid esters, hydroxymethycellulose, polyvinyl pyrrolidine, and colors, and the like. Such preparations can be sterilized and, if desired, mixed with auxiliary agents such as lubricants, preservatives, stabilizers, wetting agents, emulsifiers, salts for influencing osmotic pressure, buffers, coloring, and/or aromatic substances and the like that do not deleteriously react with the compounds of the invention. One of skill in the art will recognize that other pharmaceutical excipients are useful in the present invention.

The term "preparation" is intended to include the formulation of the active compound with encapsulating material as a carrier providing a capsule in which the active component with or without other carriers, is surrounded by a carrier, which is thus in association with it.

Similarly, cachets and lozenges are included. Tablets, powders, capsules, pills, cachets, and lozenges can be used as solid dosage forms suitable for oral administration.

As used herein, the term "administering" means oral administration, administration as a suppository, topical contact, intravenous, parenteral, intraperitoneal, intramuscular, intralesional, intrathecal, intracranial, intranasal or subcutaneous administration, or the implantation of a slow- release device, e.g., a mini-osmotic pump, to a subject. Administration is by any route, including parenteral and transmucosal (e.g., buccal, sublingual, palatal, gingival, nasal, vaginal, rectal, or transdermal). Parenteral administration includes, e.g., intravenous, intramuscular, intra-arterial, intradermal, subcutaneous, intraperitoneal, intraventricular, and intracranial. Other modes of delivery include, but are not limited to, the use of liposomal formulations, intravenous infusion, transdermal patches, etc. By "co-administer" it is meant that a composition described herein is administered at the same time, just prior to, or just after the administration of one or more additional therapies (e.g., anti-cancer agent, chemotherapeutic, or treatment for a

neurodegenerative disease). The compound of the invention can be administered alone or can be coadministered to the patient. Coadministration is meant to include simultaneous or sequential administration of the compound individually or in combination (more than one compound or agent). Thus, the preparations can also be combined, when desired, with other active substances (e.g. to reduce metabolic degradation).

The term "eIF2B" as used herein refers to the heteropentameric eukaryotic translation initiation factor 2B. eIF2B is composed of five subunits: eIF2B l, eIF2B2, eIF2B3, eIF2B4 and eIF2B5. eIF2B l refers to the protein associated with Entrez gene 1967, OMIM 606686, Uniprot Q14232, and/or RefSeq (protein) NP _. 001405. eIF2B2 refers to the protein associated with Entrez gene 8892, OMIM 606454, Uniprot P49770, and/or RefSeq (protein) NP_055054.

eIF2B3 refers to the protein associated with Entrez gene 8891, OMIM 606273, Uniprot Q9NR50, and/or RefSeq (protein) NP_065098. eIF2B4 refers to the protein associated with Entrez gene 8890, OMIM 606687, Uniprot Q9UI10, and/or RefSeq (protein) NP_751945.

eIF2B5 refers to the protein associated with Entrez gene 8893, OMIM 603945, Uniprot Q13144, and/or RefSeq (protein) NP_003898.

The terms "eIF2alpha", "eIF2a"or "eIF2a" are interchangeable and refer to the protein "eukaryotic translation initiation factor 2 alpha subunit eIF2Sl ". In embodiments, "eIF2alpha", "eIF2a"or "eIF2a" refer to the human protein. Included in the terms eIF2alpha", "eIF2a"or "eIF2a" are the wildtype and mutant forms of the protein. In embodiments, " eIF2alpha", "eIF2a"or "eIF2a" refer to the protein associated with Entrez Gene 1965, OMIM 603907, UniProt P05198, and/or RefSeq (protein) NP_004085. In embodiments, the reference numbers immediately above refer to the protein and associated nucleic acids known as of the date of filing of this application.

Compounds

In one aspect, the present invention features a com ound of Formula (I):

Formula (I) or a pharmaceutically acceptable salt, solvate, hydrate, tautomer, or stereoisomer thereof, wherein:

D is a bridged bicyclic cycloalkyl, bridged bicyclic heterocyclyl, or cubanyl, wherein each bridged bicyclic cycloalkyl, bridged bicyclic heterocyclyl, or cubanyl is optionally substituted with 1-4 R ^x groups; and wherein if the bridged bicyclic heterocyclyl contains a substitutable nitrogen moiety, the substitutable nitrogen moiety may be optionally substituted by R ^N1 ;

L ¹ is C C alkylene or 2-7-membered heteroalkylene, wherein each Cj-C alkylene or 2- 7-membered heteroalkylene is optionally substituted with 1-5 R ^x ;

L is C C alkylene or 2-7-membered heteroalkylene, wherein each C C alkylene or 2-

7-membered heteroalkylene is optionally substituted with 1-5 R ^x ;

1 2

R andR" are each independently hydrogen, C C alkyl, C C alkoxy-C2-C6 alkyl, hydroxy-C ₂ -C ₆ alkyl, silyloxy-C ₂ -C ₆ alkyl, and d-C ₆ alkyl-C(0)NR ^B R ^c ;

R ^N1 is selected from the group consisting of hydrogen, C -Ce alkyl, hydroxy-C2-C6 alkyl, halo-C ₂ -C ₆ alkyl, amino-C ₂ -C ₆ alkyl, cyano-C ₂ -C ₆ alkyl, -C(0)NR ^B R ^c , -C(0)R ^D , -C(0)OR ^D , and -S(0) ₂ R ^D ;

A and W are each independently phenyl or 5-6 membered heteroaryl, wherein each phenyl or 5-6-membered heteroaryl is optionally substituted with 1-5 R ^Y ;

each R ^x is independently selected from the group consisting of C C alkyl, hydroxy-Ci- Ce alkyl, halo-Q-Ce alkyl, amino-Q-Ce alkyl, cyano-Q-C ₆ alkyl, oxo, halo, cyano, -OR ^A , - NR ^B R ^C ,— NR ^B C(0)R ^D , -C(0)NR ^B R ^c , -C(0)R ^D , -C(0)OH, -C(0)OR ^D , -SR ^E , -S(0)R ^D , and - S(0) ₂ R ^D ;

each R ^Y is independently selected from the group consisting of hydrogen, Ci-Ce alkyl, hydroxy-Ci-C6 alkyl, C C alkoxy-Ci-C6 alkyl, halo-Ci-C6 alkyl, halo-Ci-C6 alkoxy, amino-Ci- C ₆ alkyl, cyano-Ci-Ce alkyl, H0 ₂ C- Ci-C ₆ alkyl, oxo, halo, cyano, -OR ^A , -NR ^B R ^C , -

NR ^B C(0)R ^D , -C(0)NR ^B R ^c , -C(0)R ^D , -C(0)OH, -C(0)OR ^D , -S(R ^F ) _m , -S(0)R ^D , -S(0) ₂ R ^D , and G^ or

2 R ^Y groups on adjacent atoms, together with the atoms to which they are attached form a 3-7-membered fused cycloalkyl, 3-7 membered heterocyclyl, aryl, or 5-6 membered heteroaryl, optionally substituted with 1-5 R ^x ;

each G ¹ is independently C3-C6 cycloalkyl, 4-7-membered heterocyclyl, aryl, or 5-6- membered heteroaryl, wherein each C3-C6 cycloalkyl, 4-7-membered heterocyclyl, aryl, or 5-6- membered heteroaryl is optionally substituted with 1-3 R ^z ; each R ^z is independently selected from the group consisting of C ₁ -C6 alkyl, hydroxy-Ci- C ₆ alkyl, halo-Ci-Q alkyl, halo, cyano, -OR ^A , -NR ^B R ^C ,— NR ^B C(0)R ^D , -C(0)NR ^B R ^c , -C(0)R ^D , -C(0)OH, -C(0)OR ^D , and -S(0) ₂ R ^D ;

R ^A is, at each occurrence, independently hydrogen, C ₁ -C6 alkyl, halo-Ci-C6 alkyl, - C(0)NR ^B R ^c , -C(0)R ^D , or -C(0)OR ^D ;

each of R B and R C is independently hydrogen or C ₁ -C6 alkyl; or

R B and R C together with the atom to which they are attached form a 3-7-membered heterocyclyl optionally substituted with 1-3 R ^z ;

each R ^D is independently C ₁ -C6 alkyl, or halo-Ci-C6 alkyl;

each R ^E is independently hydrogen, C ₁ -C6 alkyl, or halo-Ci-C6 alkyl;

each R ^F is independently hydrogen, C ₁ -C6 alkyl, halo, or halo-Ci-C6 alkyl;

m is 1 when R ^F is hydrogen or Q-C6 alkyl, 3 when R ^F is C ₁ -C6 alkyl, or 5 when R ^F is halo.

In some embodiments, D is a bridged bicyclic cycloalkyl or bridged bicyclic

heterocyclyl, each of which is optionally substituted with 1-4 R ^x .

In some embodiments, D is a bridged 5-8 membered bicyclic cycloalkyl or heterocyclyl, each of which is optionally substituted with 1-4 R ^x . bicyclo[l.l. l]pentane, bicyclo[2.2.2]octane, bicyclo[2.1.1]hexane, bicyclo[3.1.1]heptane, bicyclo[2.2.1]heptane, bicyclo[3.2.1]octane, 2- azabicyclo[2.2.2]octane, or 2-oxabicyclo[2.2.2]octane, each of which is optionally substituted with 1-4 R ^x groups.

ituted with 1-4 R ^x . In

some embodiments, D is

In some embodiments, D is substituted with O R . In some embodiments, D is

In some embodiments, D is substituted with 1 or 2 R . In some embodiments, D is

In some embodiments, each R is independently selected from the group consisting of oxo, -OH, -C(0)OH, -C(0)OR ^D , halo, and hydroxy-Q-Ce alkyl.

o or -OR ^A (e.g., oxo or OH). In some embodiments, D is

In spome embodiments, L is CH ₂ 0-* or CH ₂ CH ₂ 0-*, wherein "-*" indicates the attachment point to A. In some embodiments, L is selected from the group consisting of -CH ₂ -*, -CH2CH2-*, CH ₂ CH ₂ CH ₂ -*, -CH(CH ₃ )-*, -CH ₂ (CH ₃ )CH ₂ -*,

-CH ₂ C(0)*, -CH ₂ 0-*, -N(CH ₂ CONH ₂ )CH ₂ -* and -CH ₂ CH ₂ 0-*, wherein "-*" indicates the attachment point to W.

In some embodiments, R 1 and R 2 are each hydrogen or C1-C6 alkyl. In some embodiments, R 1 andR2 are each hydrogen or -CH ₃ . In some embodiments, R 1 andR2 are each hydrogen.

In some embodiments, A is phenyl and W is independently phenyl or 5-6-membered heteroaryl. In some embodiments, each A and W is independently phenyl. In some embodiments, A is phenyl and W is 5-6-membered heteroaryl.

In some embodiments, W is a monocyclic 5-6-membered heteroaryl. In some embodiments, 2 R ^Y groups on adjacent atoms of W, together with the atoms to which they are attached form a 3-7-membered fused cycloalkyl or heterocyclyl optionally substituted with 1-5 R ^x forming a bicyclic heteroaryl. In some embodiments, W is a 10-membered heteroaryl, a 9- membered heteroaryl, a 6-membered heteroaryl, or a 5-membered heteroaryl. In some embodiments, W is a heteroaryl containing nitrogen, oxygen or sulfur as allowed by valence. some embodiments, each A and W is selected from:

and

In some embodiments, each R is independently Ci-C alkyl, C(¾H-Ci-C6 alkyl, Ci-C alkoxy-d-Ce alkyl, halo-C C ₆ alkyl, halo-d-C ₆ alkoxy, halo, cyano, -OR ^A , -NR ^B R ^C , - C(0)NR ^B R ^c , -S(0) ₂ R ^D , -S(R ^F ) _m , or G ¹ , or 2 R ^Y groups on adjacent atoms, together with the atoms to which they are attached form a 3-7-membered fused cycloalkyl, 3-7 membered heterocyclyl, aryl, or 5-6 membered heteroaryl, optionally substituted with 1-5 R ^x .

In some embodiments, R ^Y is chloro, fluoro, -CH ₃ , -CH ₂ CH ₃ , -CH ₂ CH ₂ CH ₃ , - CH ₂ CH ₂ CH ₂ CH ₃ , -CH(CH ₃ ) ₂ , -CH ₂ CH(CH ₃ ) ₂ , -C(CH ₃ ) ₃ , -CF ₃ , -CHF _2, -CH ₂ C0 ₂ H, - CH ₂ OCH ₃ , CH ₂ C0 ₂ H, -OCH ₃ , -OCH ₂ CH ₃ , -OCH(CH ₃ ) ₂ , -OCHF ₂ , -OCF ₃ , -OCH ₂ CHF ₃ - C(0)NH ₂ , -N(CH ₃ ) ₂ , -S(0) ₂ CH ₃ , -S(0) ₂ NH ₂ , or -SCF ₃ .

In some embodiments, each A and W is optionally substituted with 1-5 R ^Y . In some embodiments, R ^Y is Cj-C alkyl, Cj-C alkoxy-Ci-C6 alkyl, halo-Ci-C6 alkyl, halo-Ci-C6 alkoxy, halo, cyano, -OR ^A , -NR ^B R ^C , -S(0) ₂ R ^D , -S(R ^F ) _m , or G ¹ . In some embodiments, R ^Y is chloro, fluoro, -CH ₃ , -CH ₂ CH ₃ , CH ₂ CH ₂ CH ₃ , -CH ₂ CH ₂ CH ₂ CH ₃ , -CH(CH ₃ ) ₂ , -CH ₂ CH(CH ₃ ) ₂ , -C(CH ₃ ) ₃ , -CF ₃ , -CH ₂ OCH ₃ , -OCH ₃ , -OCH ₂ CH ₃ , -OCH(CH ₃ ) ₂ , -OCHF ₂ , -OCF ₃ , -OCH ₂ CHF ₂ , N(CH ₃ ) ₂ , - S(0) ₂ CH ₃ , -S(0) ₂ NH ₂ , or SCF ₃ .

In some embodiments, G ¹ is phenyl optionally substituted with 1-3 R ^z . In some embodiments, each R is C ₁ -C6 alkyl (e.g., CH ₃ ).

In some embodiments, each A and W is independently a phenyl optionally substituted

some embodiments, each R ^Y is independently chloro, fluoro, or CH ₃ . In some embodiments,

In some embodiments, G ¹ is phenyl optionally substituted with 1-3 R ^z . In some embodiments, each R ^z is Cj-C alkyl (e.g., (¾).

In some embodiments the compound of Formula (I) is a compound of Formula (I-a):

Formula (I-a)

or a pharmaceutically acceptable salt, solvate, hydrate, tautomer, or stereoisomer thereof, wherein D is a bridged bicyclic cycloalkyl, bridged bicyclic heterocyclyl, or cubanyl, wherein each bridged bicyclic cycloalkyl, bridged bicyclic heterocyclyl, or cubanyl is optionally substituted with 1-4 R ^x ; L ¹ and L ² are each independently Q-Ce aikylene or 2-7-membered heteroalkylene, wherein each C _\ -C alkylene or 2-7-membered heteroalkylene is optionally substituted with 1-5 R ^x ; R ¹ and R ² are each independently hydrogen, C -Ce alkyl, C -Ce alkoxy- C2-C6 alkyl, hydroxy-C2-C6 alkyl, silyloxy-C2-C6 alkyl; A and W are each independently phenyl or 5-6-membered heteroaryl, wherein each phenyl or 5-6-membered heteroaryl is optionally substituted with 1-5 R ^Y ; each R ^x is independently selected from the group consisting of C Ce alkyl, hydroxy-Ci-C6 alkyl, halo-Ci-C6 alkyl, amino-Ci-C6 alkyl, cyano-Ci-C6 alkyl, oxo, halo, cyano, -OR ^A , -NR ^B R ^C ,— NR ^B C(0)R ^D , -C(0)NR ^B R ^c , -C(0)R ^D , -C(0)OH, -C(0)OR ^D , -SR ^E , - S(0)R ^D , and -S(0)2R ^D ; each R ^Y is independently selected from the group consisting of hydrogen, C ₁ -C6 alkyl, hydroxy-Ci-C6 alkyl, halo-Ci-C6 alkyl, halo-Ci-C6 alkoxy, amino-Ci-C6 alkyl, cyano-Ci-Ce alkyl, oxo, halo, cyano, -OR ^A , -NR ^B R ^C ,— NR ^B C(0)R ^D , -C(0)NR ^B R ^c , - C(0)R ^D , -C(0)OH, -C(0)OR ^D , -S(R ^F ) _m , -S(0)R ^D , -S(0) ₂ R ^D , and G ¹ ; or 2 R ^Y groups on adjacent atoms, together with the atoms to which they are attached form a 3-7-membered fused cycloalkyl or heterocyclyl optionally substituted with 1-5 R ^x ; each G ¹ is independently C3-C6 cycloalkyl, 4-7-membered heterocyclyl, aryl, or 5-6-membered heteroaryl, wherein each C3-C6 cycloalkyl, 4-7-membered heterocyclyl, aryl, or 5-6-membered heteroaryl is optionally

z z

substituted with 1-3 R ; each R is independently selected from the group consisting of C ₁ -C6 alkyl, hydroxy-d-C ₆ alkyl, halo-d-Ce alkyl, halo, cyano, -OR ^A , -NR ^B R ^C ,— NR ^B C(0)R ^D , - C(0)NR ^B R ^c , -C(0)R ^D , -C(0)OH, -C(0)OR ^D , and -S(0) ₂ R ^D ; R ^A is, at each occurrence, independently hydrogen, C C ₆ alkyl, halo-Q-Ce alkyl, -C(0)NR ^B R ^c , -C(0)R ^D , -C(0)OH, or -

D B C B C

C(0)OR ; each of R and R is independently hydrogen or C ₁ -C6 alkyl; or R and R together with the atom to which they are attached form a 3-7-membered heterocyclyl optionally substituted with 1-3 R ^z ; each R ^D is independently Cj-C alkyl or halo-Ci-C6 alkyl; each R ^E is independently hydrogen Cj-C alkyl, or halo-Ci-C6 alkyl; each R ^F is independently hydrogen, C C alkyl, halo-Ci-C6 alkyl, or halo; and m is 1 when R ^F is hydrogen or Cj-C alkyl, 3 when R ^F is C C alkyl, or 5 when R ^F is halo.

In some embodiments, the compound of Formula (I) is a compound of Formula (I-b):

Formula (I-b)

or a pharmaceutically acceptable salt, solvate, hydrate, tautomer, or stereoisomer thereof,

1 2

wherein at least one of L and L is independently 2-7-membered heteroalkylene optionally

X 1 substituted by 1-5 R , wherein "-*" indicates the attachment point to A and W, respectively; R

2 Y

and R are each hydrogen or C C alkyl; A is phenyl substituted with 1-2 R ; W is phenyl or 5-6 membered heteroaryl, each of which is optionally substituted with 1-5 R ^Y ; each R ^x is oxo or - OR ^A ; and each R ^Y is independently selected from the group consisting of C C alkyl, C C alkoxy-d-Ce alkyl, halo-C C ₆ alkyl, halo-Q-Ce alkoxy, halo, cyano, -OR ^A , -NR ^B R ^C , -

C(0)NR ^B R ^c , -S(0) ₂ R ^D , -S(R ^F ) _m , or G ¹ ; or 2 R ^Y groups on adjacent atoms, together with the atoms to which they are attached form a 3-7-membered fused cycloalkyl, 3-7 membered heterocyclyl, aryl, or 5-6 membered heteroaryl, optionally substituted with 1-5 R ^x ; G ¹ is phenyl optionally substituted with 1-3 R ^z ; each R ^z is independently C ₁ -C6 alkyl; R ^A is, at each

B C

occurrence, independently hydrogen, C ₁ -C6 alkyl, or halo-Ci-C6 alkyl; each of R and R is independently hydrogen or C ₁ -C6 alkyl; each R ^D is independently C ₁ -C6 alkyl, halo-Ci-C6 alkyl, or -NR ^B1 R ^C1 ; each R ^F is independently hydrogen, C ₁ -C6 alkyl, halo-Ci-C6 alkyl, or halo; each of R ^B1 and R ^cl is independently hydrogen or C ₁ -C6 alkyl; and m is 1 when R ^F is hydrogen or C ₁ -C6 alkyl, 3 when R ^F is C ₁ -C6 alkyl, or 5 when R ^F is halo.

1 2

In some embodiments, at least one of L and L is independently 2-7-membered heteroalkylene optionally substituted by 1-5 R ^x . In some embodiments, both of L ¹ and L ² are independently 2-7-membered heteroalkylene optionally substituted by 1-5 R ^x . In some

1 2

embodiments, L is 2-7-membered heteroalkylene and L is independently selected from C ₁ -C6 alkylene or 2-7-membered heteroalkylene, wherein each alkylene and heteroalkylene is

X 1 2

optionally substituted by 1-5 R . In some embodiments, both of L and L are independently 2- 7-membered heteroalkylene substituted by 0 R . In some embodiments, L is independently selected from CH2O-* or CH2CH2O-*, L is independently selected from -CH ₂ -*, -CH2CH2-*, CH2CH2CH2-*, -CH ₂ (CH ₃ )-*, -CH ₂ (CH ₃ )CH ₂ -*, CH ₂ 0-* or CH ₂ CH ₂ 0-*, and "-*" indicates the attachment point to A and W, respectively. In some embodiments, each L 1 and L 2 is independently selected from CH2O-* or CH2CH2O-*, and "-*" indicates the attachment point to

A and W, respectively. In some embodiments, L 1 is CH2O-* and L 2 is CH2CH2O-*, and "-*" indicates the attachment point to A and W, respectively.

In some embodiments, R 1 and R 2 are each hydrogen or C ₁ -C6 alkyl. In some

embodiments, R 1 andR2 are each hydrogen or some embodiments, R 1 andR2

-CH ₃ . In are each hydrogen.

In some embodiments, each A and W is independently phenyl or 5-6 membered heteroaryl, optionally substituted with 1-5 R . In some embodiments, A is phenyl and W is independently phenyl or 5-6 membered heteroaryl. In some embodiments, each A and W is independently phenyl. In some embodiments, A is phenyl and W is 5-6 membered heteroaryl.

In some embodiments, W is a monocyclic heteroaryl. In some embodiments, W is a bicyclic heteroaryl. In some embodiments, W is a 10-membered heteroaryl, a 9-membered heteroaryl, a 6-membered heteroaryl, or a 5-membered heteroaryl. In some embodiments, W is a heteroaryl containing nitrogen, oxygen or sulfur as allowed by valence.

In some embodiments, each A and W is selected from:

In some embodiments, each A and W is optionally substituted with 1-5 R ^Y . In some embodiments, R ^Y is Cj-C alkyl, Cj-C alkoxy-Ci-C6 alkyl, halo-Ci-C6 alkyl, halo-Ci-C6 alkoxy, halo, cyano, -OR^,— NR R , -S(0) ₂ R or -S(R ^r ) _m . In some embodiments, R is chloro, fluoro, -CH ₃ , -CH ₂ CH ₃ , CH ₂ CH ₂ CH ₃ , -CH ₂ CH ₂ CH ₂ CH ₃ , -CH(CH ₃ ) ₂ , -CH ₂ CH(CH ₃ ) ₂ , -C(CH ₃ ) ₃ , -CF ₃ , -CH ₂ OCH ₃ , -OCH ₃ , -OCH ₂ CH ₃ , -OCH(CH ₃ ) ₂ , -OCHF ₂ , -OCF ₃ , -OCH ₂ CHF ₂ , N(CH ₃ ) ₂ , - S(0) ₂ CH ₃ , -S(0) ₂ NH ₂ , or SCF ₃ .

In some embodiments, G ¹ is phenyl optionally substituted with 1-3 R ^z . In some embodiments, each R ^z is Cj-C alkyl (e.g., CH ₃ ).

In some embodiments, the compound of Formula (I) is a compound of Formula (I-c):

Formula (I-c)

or a pharmaceutically acceptable salt, solvate, hydrate, tautomer, or stereoisomer thereof, wherein L ¹ and L ² are each independently CH ₂ -*, -CH ₂ CH ₂ -*, CH ₂ CH ₂ CH ₂ -*, -CH ₂ (CH ₃ )-*, - CH ₂ (CH ₃ )CH ₂ -*, CH ₂ 0-* or CH ₂ CH ₂ 0-*, wherein "-*" indicates the attachment point to A and

1 2

W, respectively; R and R are each hydrogen; A and W are each independently phenyl substituted with 1-2 R ^Y ; and each R ^Y is independently selected from the group consisting of chloro, fluoro, and CH ₃ .

1 2

In some embodiments, at least one of L and L is independently 2-7-membered heteroalkylene optionally substituted by 1-5 R ^x . In some embodiments, both of L ¹ and L ² are independently 2-7-membered heteroalkylene optionally substituted by 1-5 R ^x . In some

1 2

embodiments, both of L and L are independently 2-7-membered heteroalkylene substituted by 0 R ^X . In some embodiments, at least one of L ¹ and L ² is independently Cj-C alkylene optionally substituted by 1-5 R ^x . In some embodiments, each L ¹ and L ² is independently selected from CH ₂ -*, CH(CH ₃ )-*, CH2CH2-*, CH(CH ₃ )CH ₂ -*, CH2CH ₂ CH2-*,CH ₂ 0-* or CH ₂ CH ₂ 0-*, and "- *" indicates the attachment point to A and W, respectively. In some embodiments, each L ¹ and L is independently selected from CH2O-* or CH2CH2O-*, and "-*" indicates the attachment point to A and W, respectively. In some embodiments, L 1 is CH2O-* and L 2 is CH2CH2O-*, and "-*" indicates the attachment point to A and W, respectively.

In some embodiments, R 1 and R 2 are each hydrogen.

In some embodiments, each A and W is independently a phenyl optionally substituted wit

and s,

A is and W is selected from ,

some embodiments, each R is inde endently chloro fluoro, or CH ₃ . In some embodiments,

each of A and W is selected from In some embodime ome

embodiments, A is and W is selected from:

f Formula (I-d)

Formula (I-d)

or a pharmaceutically acceptable salt, solvate, hydrate, tautomer, or stereoisomer thereof, wherein each of A and W is defined as for Formula (I).

In some embodiments, the compound of Formula (I) is a compound of Formula (I-e):

Formula (I-e)

or a pharmaceutically acceptable salt, solvate, hydrate, tautomer, or stereoisomer thereof, wherein each of D, W and R ^Y is defined as for Formula (I).

In some emb la (I-f):

Formula (I-f)

or a pharmaceutically acceptable salt, solvate, hydrate, tautomer, or stereoisomer thereof, wherein each of W and R ^Y is defined as for Formula (I).

In some embodiments, the compound of Formula (I) is a compound of Formula (I-g):

Formula (I-g)

or a pharmaceutically acceptable salt, solvate, hydrate, tautomer, or stereoisomer thereof, wherein each of W and R ^Y is defined as for Formula (I).

In some embodiments, the compound of Formula (I) (e.g., a compound of Formula (I-a), (I-b), (I-c), (I-d), (I-e), (I-f), or (I-g)) is selected from a compound set forth in Table 1 or a pharmaceutically acceptable salt, solvate, hydrate, tautomer, or stereoisomer thereof.

In some embodiments, the compound of Formula (I) (e.g., a compound of Formula (I-a), (I-b), (I-c), (I-d), (I-e), (I-f), or (I-g)) or a pharmaceutically acceptable salt thereof is formulated as a pharmaceutically acceptable composition comprising a disclosed compound and a pharmaceutically acceptable carrier. Also disclosed herein is a compound of Formula (II):

Formula (II)

or a pharmaceutically acceptable salt, solvate, hydrate, tautomer, or stereoisomer thereof, wherein:

D is a bridged bicyclic cycloalkyl, bridged bicyclic heterocyclyl, or cubanyl, wherein each bridged bicyclic cycloalkyl, bridged bicyclic heterocyclyl, or cubanyl is optionally substituted with 1-4 R groups; and wherein if the bridged bicyclic heterocyclyl contains a substitutable nitrogen moiety, the substitutable nitrogen moiety may be optionally substituted by R ^N1 ;

L ¹ is C C alkylene or 2-7-membered heteroalkylene, wherein Cj-C alkylene or 2-7- membered heteroalkylene is optionally substituted with 1 -5 R ^x ;

1 2

R and R" are each independently hydrogen, C C alkyl, C C alkoxy-C2-C6 alkyl, hydroxy-C2-C6 alkyl, or silyloxy-C2-C6 alkyl;

R ^N1 is selected from the group consisting of hydrogen, C C alkyl, hydroxy-C2-C6 alkyl, halo-C ₂ -C ₆ alkyl, amino-C ₂ -C ₆ alkyl, cyano-C ₂ -C ₆ alkyl, -C(0)NR ^B R ^c , -C(0)R ^D , -C(0)OR ^D , and -S(0) ₂ R ^D ;

A and W are each independently phenyl or 5-6 membered heteroaryl, wherein each phenyl or 5-6-membered heteroaryl is optionally substituted with 1-5 R ^Y ;

each R ^x is independently selected from the group consisting of Ci-Ce alkyl, hydroxy-Ci- C alkyl, halo-Ci-C6 alkyl, amino-Ci-C6 alkyl, cyano-Ci-C6 alkyl, oxo, halo, cyano, -OR ^A , - NR ^B R ^C ,— NR ^B C(0)R ^D , -C(0)NR ^B R ^c , -C(0)R ^D , -C(0)OH, -C(0)OR ^D , -SR ^E , -S(0)R ^D , and - S(0) ₂ R ^D ;

each R is independently selected from the group consisting of hydrogen, Ci-Ce alkyl, hydroxy-Ci-C6 alkyl, C _\ -C alkoxy-Ci-C6 alkyl, halo-Ci-C6 alkyl, halo-Ci-C6 alkoxy, amino-Ci- C ₆ alkyl, cyano-Ci-Ce alkyl, oxo, halo, cyano, -OR ^A , -NR ^B R ^C ,— NR ^B C(0)R ^D , -C(0)NR ^B R ^c , - C(0)R ^D , -C(0)OH, -C(0)OR ^D , -S(R ^F ) _m , -S(0)R ^D , -S(0) ₂ R ^D , and G ¹ ; or 2 R ^Y groups on adjacent atoms, together with the atoms to which they are attached form a 3-7-membered fused cycloalkyl, 3-7 membered heterocyclyl, aryl, or 5-6 membered heteroaryl, optionally substituted with 1-5 R ^x ;

each G ¹ is independently C3-C6 cycloalkyl, 4-7-membered heterocyclyl, aryl, or 5-6- membered heteroaryl, wherein each C3-C6 cycloalkyl, 4-7-membered heterocyclyl, aryl, or 5-6- membered heteroaryl is optionally substituted with 1-3 R ^z ;

each R ^z is independently selected from the group consisting of C ₁ -C6 alkyl, hydroxy-Ci- C ₆ alkyl, halo-Ci-Q alkyl, halo, cyano, -OR ^A , -NR ^B R ^C ,— NR ^B C(0)R ^D , -C(0)NR ^B R ^c , -C(0)R ^D , -C(0)OH, -C(0)OR ^D , and -S(0) ₂ R ^D ;

R ^A is, at each occurrence, independently hydrogen, C ₁ -C6 alkyl, halo-Ci-C6 alkyl, - C(0)NR ^B R ^c , -C(0)R ^D , or -C(0)OR ^D ;

B C

each of R and R is independently hydrogen or C ₁ -C6 alkyl; or

B C

R and R together with the atom to which they are attached form a 3-7-membered heterocyclyl optionally substituted with 1-3 R ;

each R ^D is independently C ₁ -C6 alkyl, or halo-Ci-C6 alkyl;

each R ^E is independently hydrogen, C ₁ -C6 alkyl, or halo-Ci-C6 alkyl;

each R ^F is independently hydrogen, C ₁ -C6 alkyl, halo, or halo-Ci-C6 alkyl;

B 1 CI

each of R and R is independently hydrogen or C Ce alkyl; and

m is 1 when R ^F is hydrogen or Q-C6 alkyl, 3 when R ^F is C ₁ -C6 alkyl, or 5 when R ^F is halo.

In some embodiments, D is selected from the group consisting of

In some embodiments, each R is independently selected from the group consisting of oxo, -OR ^A (e.g., OH or OCH ₃ ), -C(0)OH, -C(0)OR ^D (e.g., -C(0)OCH ₃ ), halo, and hydroxy- C ₁ -C6 alkyl. In some embodiments, each of R ¹ and R ² is hydrogen or CH ₃ . each R ^x is independently selected from the group consisting of oxo, -OH, -OCH ₃ , -C(0)OH, -C(0)OCH ₃ , halo, and hydroxy-Ci-C6 alkyl.

In some embodiments, L ¹ is C¾0-* or CH2CH2O-*, wherein "-*" indicates the attachment point to A. In some embodiments A is selected from the group consisting of:

In some embodiments W is selected from the group consisting of:

wherein R is hydrogen or CH ₃ .

In some embodiments, each R ^Y is independently hydrogen, bromo, chloro, fluoro, iodo, CF ₃ , CHF ₂ , CH2CF ₃ , CH ₃ , CH2CH ₃ , OH, CH ₂ OH, C(CH ₃ ) ₂ OH, OCH ₃ , OCH ₂ CH _3, OCF ₃ , OCH ₂ CF ₃ , S(0) ₂ CH ₃ , S(0) ₂ CH ₂ CH ₂ CH ₃ , CN, N(CH ₃ ) ₂ , SF ₅ , SCH ₃ , NH ₂ , C(CH) ₃ , CH(CH ₃ ) ₂ , CH ₂ CN, CH ₂ NH ₂ , CH(OH)CH ₃ , C(OH)(CH ₃ )CF ₃ , S(0) ₂ CH ₃ , C(0)CH ₃ , C(0)OCH ₃ , C(0)OH, OCHF ₂ or G ¹ .

In some embodiments the compound of Formula (II) is a compound of Formula (Il-a):

Formula (Il-a)

or a pharmaceutically acceptable salt, solvate, hydrate, tautomer, or stereoisomer thereof, wherein: D is bicyclo[l.l. l]pentanyl, bicyclo[2.2.2]octanyl, or 2-oxabicyclo[2.2.2]octane, each of which is optionally substituted with 1-4 R ^x groups;

A is phenyl or pyridyl, each of which is optionally substituted with 1-5 R ^Y groups;

W is phenyl, pyridyl, pyrazinyl, pyrimidinyl, thiazolyl, isoxazolyl, or pyrazolyl, each of which is optionally substituted on one or more available carbons with 1-5 R ^Y groups; and wherein pyrazolyl may be optionally substituted on an available nitrogen with hydrogen or CH ₃ ;

L ¹ is CH2O-* or CH2CH2O-*, wherein "-*" indicates the attachment point to A;

each R ^x is independently fluoro, oxo, OH, OCH ₃ , C(0)OH, or C(0)OCH ₃ ;

each R ^Y is independently hydrogen, bromo, chloro, fluoro, iodo, CF ₃ , CHF2, CH2CF ₃ , CH ₃ , CH2CH ₃ , OH, CH ₂ OH, C(CH ₃ ) ₂ OH, OCH ₃ , OCH ₂ CH _3, OCF ₃ , OCH ₂ CF ₃ , S(0) ₂ CH ₃ , S(0)2CH ₂ CH ₂ CH3, CN, N(CH ₃ ) ₂ , SF ₅ , SCH ₃ , NH ₂ , C(CH) ₃ , CH(CH ₃ ) ₂ , CH ₂ CN, CH ₂ NH ₂ , CH(OH)CH ₃ , C(OH)(CH ₃ )CF ₃ , S(0) ₂ CH ₃ , C(0)CH ₃ , C(0)OCH ₃ , C(0)OH, OCHF ₂ or G ¹ ;

2 R ^Y groups on adjacent atoms, together with the atoms to which they are attached form a furanyl, pyrrolyl, or dioxolanyl ring, each of which is optionally substituted with 1-2 R ; and each of R 1 and R 2 is hydrogen or CH ₃ .

In some embodiments, a compound disclosed herein or a pharmaceutically acceptable salt thereof is formulated as a pharmaceutically acceptable composition comprising a disclosed compound and a pharmaceutically acceptable carrier.

In some embodiments, a compound disclosed herein is selected from a compound set forth in Table 1 or a pharmaceutically acceptable salt, solvate, hydrate, tautomer, or stereoisomer thereof.

Table 1 : Exemplary compounds of the invention

Compound Structure Compound Structure

Number Number

100 224

Methods of Making Exemplary Compounds

The compounds of the invention may be better understood in connection with the following synthetic schemes and methods which illustrate a means by which the compounds can be prepared. The compounds of this invention can be prepared by a variety of synthetic procedures. A representative synthetic procedure is illustrated in, but is not limited to, that

1 2 1 2

shown in Schemes 1-4. The variables A, D, W, L , L , R , and R are defined as detailed herein, e.g., in the Summary. Scheme 1 : Representative scheme for synthesis of exemplary compounds of the invention.

As shown in Scheme 1, compounds of Formula (1-6) can be prepared from compounds of Formula (1-1). Compounds of Formula (1-1) can be coupled with carboxylic acids of Formula (1-2) under amide bond forming conditions to give compounds of Formula (1-3). Examples of conditions known to generate amides from a mixture of a carboxylic acid and an amine include but are not limited to adding a coupling reagent such as but not limited to N-(3- dimethylaminopropyl)-N-ethylcarbodiimide or 1 -(3-dimethylaminopropyl)-3-ethylcarbodiirnide (EDC, EDAC or EDCI), 1,3-dicyclohexylcarbodiimide (DCC), bis(2-oxo-3-oxazolidinyl)- phosphinic chloride (BOPC1), N-[(dimethylamino)-lH-l,2,3-triazolo-[4,5-¾]pyridin-l- ylmethylene] -N-methylmethanaminium hexafluorophosphate N-oxide or 2-(7-azabenzotriazol- 1 - yl)-NNN,N-tetramethyluronium hexafluorophosphate or l-[bis(dimethylamino)methylene]- lH-l,2,3-triazolo[4,5- ?]pyridinium 3-oxid hexafluorophosphate or 2-(3H-[l,2,3]triazolo[4,5- Z?]pyridin-3-yl)-l,l,3,3-tetramethylisouronium hexafluorophosphate(V) or 2-(7-aza-lH- benzotriazole-l-yl)-l,l,3,3-tetramethyluronium hexafluorophosphate (HATU), 0-(benzotriazol- l-yl)-NNN',N-tetramethyluronium tetrafluoroborate (TBTU), 2-(lH-benzo[ ][l,2,3]triazol-l- yl)-l,l,3,3-tetramethylisouronium hexafluorophosphate(V) (HBTU), 2,4,6-tripropyl-l,3, 5,2,4,6- trioxatriphosphinane 2,4,6-trioxide (T3P®), (l-cyano-2-ethoxy-2-oxoethylidenaminooxy)- dimethylamino-mo holino-carbenium hexafluorophosphate (COMU®), and fluoro-N,N,N,N- tetramethylformamidinium hexafluorophosphate. The coupling reagents may be added as a solid, a solution, or as the reagent bound to a solid support resin. In addition to the coupling reagents, auxiliary-coupling reagents may facilitate the coupling reaction. Auxiliary coupling reagents that are often used in the coupling reactions include but are not limited to

(dimethylamino)pyridine (DMAP), l-hydroxy-7-azabenzotriazole (HOAT), and 1- hydroxybenzotriazole (HOBT). The coupling reaction may be carried out optionally in the presence of a base such as triethylamine or diisopropylethylamine. The coupling reaction may be carried out in solvents such as but not limited to tetrahydrofuran, NN-dimethylformamide, N,N-dimethylacetamide, dimethyl sulfoxide, dichlorome thane, or ethyl acetate. Alternatively, carboxylic acids of Formula (1-2) may be converted to the corresponding acid chlorides by reaction with thionyl chloride, PCI ₃ , PCI ₅ , cyanuric chloride, or oxalyl chloride. The reactions with thionyl chloride and oxalyl chloride can be catalyzed with N,N-dimethylformamide at ambient temperature in a solvent such as dichlorome thane. The resultant acid chlorides can then reacted with amines of Formula (1-1) optionally in the presence of a base such as a tertiary amine base such as but not limited to triethylamine or diisopropylethylamine or an aromatic base such as pyridine, at room temperature in a solvent such as dichloromethane to give amides of Formula (1-3). Esters of Formula (1-3) can be hydrolyzed to compounds of Formula (1-4). For example, esters of Formula (1 -3) can be treated with a base such as lithium hydroxide, sodium hydroxide, or potassium hydroxide in a solvent such as methanol, ethanol, tetrahydrofuran or a with a mixture of tetrahydrofuran and water at ambient temperature or heated from 0.5 to 8 hours to give compounds of Formula (1-4). Carboxylic acids of Formula (14) can be coupled to amines of Formula (1-5) under the amide bond coupling conditions described above to give compounds of Formula (1-6). The carboxylic acids of Formula (1-4) can be converted to the corresponding acid chlorides again as described above. The carboxylic acid chlorides derived from carboxylic acids of Formula (1-4) can be reacted with amines of Formula (1-5) to also give compounds of Formula (1-6). Compounds of Formula (1-6) are representative of compounds of Formula (I).

Scheme 2: Representative scheme for synthesis of exemplary compounds of the invention.

H

®-L ² -N

R

\ hydrolysis R^ (1-5)

N-C ^D y-C0 ₂ C C ₄ alkyl * ^" N-( D )— C0 ₂ H '

J, amide bond

(2-1) P (2-2) coupling

(1 -6)

As shown in Scheme 2, compounds of Formula (1-6) can also be prepared from compounds of Formula (2-1). N-Protected amino esters of Formula (2-1), wherein P ¹ is an amine protecting group known in the literature or to one of skill in the art, can be hydrolyzed to compounds of Formula (2-2). For example, N-protected amino esters of Formula (2-1) can be treated with a base such as lithium hydroxide, sodium hydroxide, or potassium hydroxide in a solvent such as methanol, ethanol, tetrahydrofuran or a with a mixture of tetrahydrofuran and water at ambient temperature or heated from 0.5 to 8 hours to give compounds of Formula (2-2). Alternatively, when (2- 1) is a teri-butyl ester, treatment under acidic conditions such as hydrochloric acid in dioxane or trifluoroacetic acid in dichloromethane can provide compounds of formula (2-2). Compounds of Formula (2-2) can be coupled with amines of Formula (1-5) under amide bond forming conditions to give compounds of Formula (2-3). Examples of conditions known to generate amides from a mixture of a carboxylic acid and an amine include but are not limited to adding a coupling reagent such as but not limited to N-(3- dimethylaminopropyl)-N-ethylcarbodiimide or l-(3-dimethylaminopropyl)-3-ethylcarbodiirnide (EDC, EDAC or EDCI), 1,3-dicyclohexylcarbodiimide (DCC), bis(2-oxo-3-oxazolidinyl)- phosphinic chloride (BOPC1), N-[(dimethylamino)-lH-l ,2,3-triazolo-[4,5-¾]pyridin- l- ylmethylene]-N-methylmethanaminium hexafluorophosphate N-oxide or 2-(7-azabenzotriazol-l- yl)-N,N,N,N-tetramethyluronium hexafluorophosphate or l-[bis(dimethylamino)methylene]- lH-l ,2,3-triazolo[4,5-¾]pyridinium 3-oxid hexafluorophosphate or 2-(3H-[l,2,3]triazolo[4,5- Z?]pyridin-3-yl)- l ,l ,3,3-tetramethylisouronium hexafluorophosphate(V) or 2-(7-aza-lH- benzotriazole-l-yl)-l ,l ,3,3-tetramethyluronium hexafluorophosphate (HATU), 0-(benzotriazol- l-yl)-NNN' N-tetramethyluronium tetrafluoroborate (TBTU), 2-(lH-benzo[ ] [l ,2,3]triazol-l- yl)-l ,l ,3,3-tetramethylisouronium hexafluorophosphate(V) (HBTU), 2,4,6-tripropyl-l ,3, 5,2,4,6- trioxatriphosphinane 2,4,6-trioxide (T3P®), (l-cyano-2-ethoxy-2-oxoethylidenaminooxy)- dimethylamino-mo holino-carbenium hexafluorophosphate (COMU®), and fluoro-N,N,N,N- tetramethylformamidinium hexafluorophosphate. The coupling reagents may be added as a solid, a solution, or as the reagent bound to a solid support resin. In addition to the coupling reagents, auxiliary-coupling reagents may facilitate the coupling reaction. Auxiliary coupling reagents that are often used in the coupling reactions include but are not limited to

(dimethylamino)pyridine (DMAP), l-hydroxy-7-azabenzotriazole (HOAT), and 1- hydroxybenzotriazole (HOBT). The coupling reaction may be carried out optionally in the presence of a base such as triethylamine or diisopropylethylamine. The coupling reaction may be carried out in solvents such as but not limited to tetrahydrofuran, NN-dimethylformamide, N,N-dimethylacetamide, dimethyl sulfoxide, dichlorome thane, or ethyl acetate. Alternatively, carboxylic acids of Formula (2-2) may be converted to the corresponding acid chlorides by reaction with thionyl chloride, PCI ₃ , PCI5, cyanuric chloride, or oxalyl chloride. The reactions with thionyl chloride and oxalyl chloride can be catalyzed with N,N-dimethylformamide at ambient temperature in a solvent such as dichlorome thane. The resultant acid chlorides can then reacted with amines of Formula (1-5) optionally in the presence of a base such as a tertiary amine base such as but not limited to triethylamine or diisopropylethylamine or an aromatic base such as pyridine, at room temperature in a solvent such as dichloromethane to give amides of Formula (2-3). The amine protecting group, P ¹ , of compounds of formula (2-3) can be removed under conditions known in the literature or to one of skill to give amines of formula (2-4).

Amines of Formula (2-4) can be coupled to carboxylic acids of Formula (1-2) under the amide bond coupling conditions described above to give compounds of Formula (2-3). The carboxylic acids of Formula (1-2) can be converted to the corresponding acid chlorides again as described above. The carboxylic acid chlorides derived from carboxylic acids of Formula (1-2) can be reacted with amines of Formula (2-4) to also give compounds of Formula (1-6). Compounds of Formula (1-6) are representative of compounds of Formula (I).

Scheme 3: Representative scheme for synthesis of exemplary compounds of the invention.

(3-1)

(3-4)

(3-3)

As shown in Scheme 3, compounds of Formula (3-4) can be prepared from the compound of Formula (3-1). The compound of Formula (3-1) can be coupled with compounds of Formula (1-5) using the amide bond forming conditions described in Schemes 1 and 2 to give compounds of Formula (3-2). Compounds of Formula (3-2) can be reacted with ammonia in a solvent such as but not limited to methanol to give compounds of Formula (3-3). Compounds of Formula (3-3) can be coupled with carboxylic acids of Formula (1-2) under amide bond forming conditions described in Schemes 1 and 2 to give compounds of Formula (3-4). Compounds of Formula (3-4) are representative of compounds of Formula (I). cheme 4: Representative scheme for synthesis of exemplary compounds of the invention.

(4-3) coupling

As shown in Scheme 4, compounds of Formula (1-4) can be prepared from compounds of Formula (4-1). Aldehydes of Formula (4-1), wherein P ¹ is an amine protecting group known in the literature or to one of skill in the art, can be oxidized with an oxidant such as but not limited to a mixture of sodium chlorite, sodium dihydrogen phosphate, 2-methyl-2-butene in a solvent mixture such as but not limited to teri-butanol, tetrahydrofuran and water at or near ambient temperature to give carboxylic acids of Formula (4-2). Compounds of Formula (4-2) can be converted to compounds of Formula (4-3) in a two-step process. In the first step, the carboxylic acid of compounds of Formula (4-2) can be treated with (diazomethyl)trimethylsilane in solvent such as methanol to give the corresponding methyl ester. Subsequently in the next step, the amine protecting group can be removed under conditions known to one of skill in the art and dependent on the particular protecting group. For example, when the amine protecting group is teri-butoxycarbonyl, treatment with an acid such as trifluoroacetic acid or hydrogen chloride in a solvent such as dichloromethane or dioxane removes the amine protecting group. Compounds of Formula (4-3) can be coupled with carboxylic acids of Formula (1-2) under amide bond forming conditions described in Schemes 1 and 2 to give compounds of Formula (4- 4). Esters of formula (4-4) can be hydrolyzed with a base such as but not limited to lithium hydroxide, sodium hydroxide or potassium hydroxide in an optionally warmed solvent or solvent mixture such as methanol and tetrahydrofuran to give compounds of formula (1-4). Compounds of formula (1-4) can then be taken forward as shown in Scheme 1.

Pharmaceutical Compositions

The present invention features pharmaceutical compositions comprising a compound of Formula (I) or Formula (II), or a pharmaceutically acceptable salt, solvate, hydrate, tautomer, or stereoisomer thereof. In some embodiments, the pharmaceutical composition further comprises a pharmaceutically acceptable excipient. In some embodiments, the compound of Formula (I) or Formula (II), or a pharmaceutically acceptable salt, solvate, hydrate, tautomer, stereoisomer thereof is provided in an effective amount in the pharmaceutical composition. In some embodiments, the effective amount is a therapeutically effective amount. In certain

embodiments, the effective amount is a prophylactically effective amount.

Pharmaceutical compositions described herein can be prepared by any method known in the art of pharmacology. In general, such preparatory methods include the steps of bringing the compound of Formula (I) or Formula (II) (the "active ingredient") into association with a carrier and/or one or more other accessory ingredients, and then, if necessary and/or desirable, shaping and/or packaging the product into a desired single- or multi-dose unit. Pharmaceutical compositions can be prepared, packaged, and/or sold in bulk, as a single unit dose, and/or as a plurality of single unit doses. As used herein, a "unit dose" is a discrete amount of the pharmaceutical composition comprising a predetermined amount of the active ingredient. The amount of the active ingredient is generally equal to the dosage of the active ingredient which would be administered to a subject and/or a convenient fraction of such a dosage such as, for example, one -half or one-third of such a dosage.

Relative amounts of a compound of Formula (I) or Formula (II), the pharmaceutically acceptable excipient, and/or any additional ingredients in a pharmaceutical composition of the invention will vary, depending upon the identity, size, and/or condition of the subject treated and further depending upon the route by which the composition is to be administered. By way of example, the composition may comprise between 0.1% and 100% (w/w) of a compound of Formula (I) or Formula (II).

The term "pharmaceutically acceptable excipient" refers to a non-toxic carrier, adjuvant, diluent, or vehicle that does not destroy the pharmacological activity of the compound with which it is formulated. Pharmaceutically acceptable excipients useful in the manufacture of the pharmaceutical compositions of the invention are any of those that are well known in the art of pharmaceutical formulation and include inert diluents, dispersing and/or granulating agents, surface active agents and/or emulsifiers, disintegrating agents, binding agents, preservatives, buffering agents, lubricating agents, and/or oils. Pharmaceutically acceptable excipients useful in the manufacture of the pharmaceutical compositions of the invention include, but are not limited to, ion exchangers, alumina, aluminum stearate, lecithin, serum proteins, such as human serum albumin, buffer substances such as phosphates, glycine, sorbic acid, potassium sorbate, partial glyceride mixtures of saturated vegetable fatty acids, water, salts or electrolytes, such as protamine sulfate, disodium hydrogen phosphate, potassium hydrogen phosphate, sodium chloride, zinc salts, colloidal silica, magnesium trisilicate, polyvinyl pyrrolidone, cellulose-based substances, polyethylene glycol, sodium carboxymethylcellulose, polyacrylates, waxes, polyethylene-polyoxypropylene-block polymers, polyethylene glycol and wool fat.

Compositions of the present invention may be administered orally, parenterally

(including subcutaneous, intramuscular, intravenous and intradermal), by inhalation spray, topically, rectally, nasally, buccally, vaginally or via an implanted reservoir. In some embodiments, provided compounds or compositions are administrable intravenously and/or orally.

The term "parenteral" as used herein includes subcutaneous, intravenous, intramuscular, intraocular, intravitreal, intra-articular, intra-synovial, intrasternal, intrathecal, intrahepatic, intraperitoneal intralesional and intracranial injection or infusion techniques. Preferably, the compositions are administered orally, subcutaneously, intraperitoneally or intravenously. Sterile injectable forms of the compositions of this invention may be aqueous or oleaginous suspension. These suspensions may be formulated according to techniques known in the art using suitable dispersing or wetting agents and suspending agents. The sterile injectable preparation may also be a sterile injectable solution or suspension in a non-toxic parenterally acceptable diluent or solvent, for example as a solution in 1 ,3-butanediol. Among the acceptable vehicles and solvents that may be employed are water, Ringer's solution and isotonic sodium chloride solution. In addition, sterile, fixed oils are conventionally employed as a solvent or suspending medium.

Pharmaceutically acceptable compositions of this invention may be orally administered in any orally acceptable dosage form including, but not limited to, capsules, tablets, aqueous suspensions or solutions. In the case of tablets for oral use, carriers commonly used include lactose and corn starch. Lubricating agents, such as magnesium stearate, are also typically added. For oral administration in a capsule form, useful diluents include lactose and dried cornstarch. When aqueous suspensions are required for oral use, the active ingredient is combined with emulsifying and suspending agents. If desired, certain sweetening, flavoring or coloring agents may also be added. In some embodiments, a provided oral formulation is formulated for immediate release or sustained/delayed release. In some embodiments, the composition is suitable for buccal or sublingual administration, including tablets, lozenges and pastilles. A compound of Formula (I) or Formula (II) may also be in micro-encapsulated form.

The compositions of the present invention can be delivered by transdermally, by a topical route, formulated as applicator sticks, solutions, suspensions, emulsions, gels, creams, ointments, pastes, jellies, paints, powders, and aerosols. Oral preparations include tablets, pills, powder, dragees, capsules, liquids, lozenges, cachets, gels, syrups, slurries, suspensions, etc., suitable for ingestion by the patient. Solid form preparations include powders, tablets, pills, capsules, cachets, suppositories, and dispersible granules. Liquid form preparations include solutions, suspensions, and emulsions, for example, water or water/propylene glycol solutions. The compositions of the present invention may additionally include components to provide sustained release and/or comfort. Such components include high molecular weight, anionic mucomimetic polymers, gelling polysaccharides and finely-divided drug carrier substrates. These components are discussed in greater detail in U.S. Patent Nos. 4,911 ,920; 5,403,841 ; 5,212, 162; and 4,861 ,760. The entire contents of these patents are incorporated herein by reference in their entirety for all purposes. The compositions of the present invention can also be delivered as microspheres for slow release in the body. For example, microspheres can be administered via intradermal injection of drug-containing microspheres, which slowly release subcutaneously (see Rao, J. Biomater Sci. Polym. Ed. 7:623-645, 1995; as biodegradable and injectable gel formulations (see, e.g., Gao Pharm. Res.12:857-863, 1995); or, as microspheres for oral administration (see, e.g., Eyles, J. Pharm. Pharmacol. 49:669-674, 1997). In another embodiment, the formulations of the compositions of the present invention can be delivered by the use of liposomes which fuse with the cellular membrane or are endocytosed, i.e., by employing receptor ligands attached to the liposome, that bind to surface membrane protein receptors of the cell resulting in endocytosis. By using liposomes, particularly where the liposome surface carries receptor ligands specific for target cells, or are otherwise preferentially directed to a specific organ, one can focus the delivery of the compositions of the present invention into the target cells in vivo. (See, e.g., Al-Muhammed, J. Microencapsul. 13:293-306, 1996; Chonn, Curr. Opin. Biotechnol. 6:698-708, 1995; Ostro, J. Hosp. Pharm. 46: 1576-1587, 1989). The compositions of the present invention can also be delivered as nanoparticles.

Alternatively, pharmaceutically acceptable compositions of this invention may be administered in the form of suppositories for rectal administration. Pharmaceutically acceptable compositions of this invention may also be administered topically, especially when the target of treatment includes areas or organs readily accessible by topical application, including diseases of the eye, the skin, or the lower intestinal tract. Suitable topical formulations are readily prepared for each of these areas or organs.

In some embodiments, in order to prolong the effect of a drug, it is often desirable to slow the absorption of the drug from subcutaneous or intramuscular injection. This can be accomplished by the use of a liquid suspension of crystalline or amorphous material with poor water solubility. The rate of absorption of the drug then depends upon its rate of dissolution which, in turn, may depend upon crystal size and crystalline form. Alternatively, delayed absorption of a parenterally administered drug form is accomplished by dissolving or suspending the drug in an oil vehicle.

Although the descriptions of pharmaceutical compositions provided herein are principally directed to pharmaceutical compositions which are suitable for administration to humans, it will be understood by the skilled artisan that such compositions are generally suitable for administration to animals of all sorts. Modification of pharmaceutical compositions suitable for administration to humans in order to render the compositions suitable for administration to various animals is well understood, and the ordinarily skilled veterinary pharmacologist can design and/or perform such modification with ordinary experimentation.

Compounds provided herein, e.g., a compound of Formula (I) or Formula (II), or a pharmaceutically acceptable salt, solvate, hydrate, tautomer, or stereoisomer thereof are typically formulated in dosage unit form, e.g., single unit dosage form, for ease of administration and uniformity of dosage. It will be understood, however, that the total daily usage of the compositions of the present invention will be decided by the attending physician within the scope of sound medical judgment. The specific therapeutically effective dose level for any particular subject or organism will depend upon a variety of factors including the disease being treated and the severity of the disorder; the activity of the specific active ingredient employed; the specific composition employed; the age, body weight, general health, sex and diet of the subject; the time of administration, route of administration, and rate of excretion of the specific active ingredient employed; the duration of the treatment; drugs used in combination or coincidental with the specific active ingredient employed; and like factors well known in the medical arts.

The exact amount of a compound required to achieve an effective amount will vary from subject to subject, depending, for example, on species, age, and general condition of a subject, severity of the side effects or disorder, identity of the particular compound(s), mode of administration, and the like. The desired dosage can be delivered three times a day, two times a day, once a day, every other day, every third day, every week, every two weeks, every three weeks, or every four weeks. In certain embodiments, the desired dosage can be delivered using multiple administrations (e.g. , two, three, four, five, six, seven, eight, nine, ten, eleven, twelve, thirteen, fourteen, or more administrations).

In certain embodiments, an effective amount of a compound of Formula (I) or Formula (II), or a pharmaceutically acceptable salt, solvate, hydrate, tautomer, or stereoisomer thereof for administration one or more times a day may comprise about 0.0001 mg to about 5000 mg, e.g., from about 0.0001 mg to about 4000 mg, about 0.0001 mg to about 2000 mg, about 0.0001 mg to about 1000 mg, about 0.001 mg to about 1000 mg, about 0.01 mg to about 1000 mg, about 0.1 mg to about 1000 mg, about 1 mg to about 1000 mg, about 1 mg to about 100 mg, about 10 mg to about 1000 mg, or about 100 mg to about 1000 mg, of a compound per unit dosage form.

In certain embodiments, a compound of Formula (I) or Formula (II), or a

pharmaceutically acceptable salt, solvate, hydrate, tautomer, or stereoisomer thereof may be at dosage levels sufficient to deliver from about 0.001 mg/kg to about 1000 mg/kg, e.g., about 0.001 mg/kg to about 500 mg/kg, about 0.01 mg/kg to about 250 mg/kg, about 0.1 mg/kg to about 100 mg/kg, about 0.1 mg/kg to about 50 mg/kg, about 0.1 mg/kg to about 40 mg/kg, about 0.1 mg/kg to about 25 mg/kg, about 0.01 mg/kg to about 10 mg/kg, about 0.1 mg/kg to about 10 mg/kg, or about 1 mg/kg to about 50 mg/kg, of subject body weight per day, one or more times a day, to obtain the desired therapeutic effect.

It will be appreciated that dose ranges as described herein provide guidance for the administration of provided pharmaceutical compositions to an adult. The amount to be administered to, for example, a child or an adolescent can be determined by a medical practitioner or person skilled in the art and can be lower or the same as that administered to an adult.

It will be also appreciated that a compound or composition, e.g., a compound of Formula (I) or Formula (II), or a pharmaceutically acceptable salt, solvate, hydrate, tautomer, or stereoisomer thereof as described herein, can be administered in combination with one or more additional pharmaceutical agents. The compounds or compositions can be administered in combination with additional pharmaceutical agents that improve their bioavailability, reduce and/or modify their metabolism, inhibit their excretion, and/or modify their distribution within the body. It will also be appreciated that the therapy employed may achieve a desired effect for the same disorder, and/or it may achieve different effects.

The compound or composition can be administered concurrently with, prior to, or subsequent to, one or more additional pharmaceutical agents, which may be useful as, e.g. , combination therapies. Pharmaceutical agents include therapeutically active agents.

Pharmaceutical agents also include prophylactically active agents. Each additional

pharmaceutical agent may be administered at a dose and/or on a time schedule determined for that pharmaceutical agent. The additional pharmaceutical agents may also be administered together with each other and/or with the compound or composition described herein in a single dose or administered separately in different doses. The particular combination to employ in a regimen will take into account compatibility of the inventive compound with the additional pharmaceutical agents and/or the desired therapeutic and/or prophylactic effect to be achieved. In general, it is expected that the additional pharmaceutical agents utilized in combination be utilized at levels that do not exceed the levels at which they are utilized individually. In some embodiments, the levels utilized in combination will be lower than those utilized individually.

Exemplary additional pharmaceutical agents include, but are not limited to, antiproliferative agents, anti-cancer agents, anti-diabetic agents, anti-inflammatory agents, immunosuppressant agents, and pain-relieving agents. Pharmaceutical agents include small organic molecules such as drug compounds (e.g., compounds approved by the U.S. Food and Drug Administration as provided in the Code of Federal Regulations (CFR)), peptides, proteins, carbohydrates, monosaccharides, oligosaccharides, polysaccharides, nucleoproteins, mucoproteins, lipoproteins, synthetic polypeptides or proteins, small molecules linked to proteins, glycoproteins, steroids, nucleic acids, DNAs, RNAs, nucleotides, nucleosides, oligonucleotides, antisense oligonucleotides, lipids, hormones, vitamins, and cells.

Pharmaceutical compositions provided by the present invention include compositions wherein the active ingredient (e.g., compounds described herein, including embodiments or examples) is contained in a therapeutically effective amount, i.e., in an amount effective to achieve its intended purpose. The actual amount effective for a particular application will depend, inter alia, on the condition being treated. When administered in methods to treat a disease, such compositions will contain an amount of active ingredient effective to achieve the desired result, e.g., modulating the activity of a target molecule (e.g. eIF2B, eIF2 or component of eIF2a signal transduction pathway or component of phosphorylated eIF2a pathway or the ISR pathway), and/or reducing, eliminating, or slowing the progression of disease symptoms (e.g. symptoms of cancer, a neurodegenerative disease, a leukodystrophy, an inflammatory disease, a musculoskeletal disease, a metabolic disease, or a disease or disorder associated with impaired function of eIF2B, eIF2a or a component of the eIF2 pathway or ISR pathway). Determination of a therapeutically effective amount of a compound of the invention is well within the capabilities of those skilled in the art, especially in light of the detailed disclosure herein.

The dosage and frequency (single or multiple doses) administered to a mammal can vary depending upon a variety of factors, for example, whether the mammal suffers from another disease, and its route of administration; size, age, sex, health, body weight, body mass index, and diet of the recipient; nature and extent of symptoms of the disease being treated (e.g. a symptom of cancer, a neurodegenerative disease, a leukodystrophy, an inflammatory disease, a musculoskeletal disease, a metabolic disease, or a disease or disorder associated with impaired function of eIF2B, eIF2 a, or a component of the eIF2 pathway or ISR pathway), kind of concurrent treatment, complications from the disease being treated or other health-related problems. Other therapeutic regimens or agents can be used in conjunction with the methods and compounds of Applicants' invention. Adjustment and manipulation of established dosages (e.g., frequency and duration) are well within the ability of those skilled in the art. For any compound described herein, the therapeutically effective amount can be initially determined from cell culture assays. Target concentrations will be those concentrations of active compound(s) that are capable of achieving the methods described herein, as measured using the methods described herein or known in the art.

As is well known in the art, therapeutically effective amounts for use in humans can also be determined from animal models. For example, a dose for humans can be formulated to achieve a concentration that has been found to be effective in animals. The dosage in humans can be adjusted by monitoring compounds effectiveness and adjusting the dosage upwards or downwards, as described above. Adjusting the dose to achieve maximal efficacy in humans based on the methods described above and other methods is well within the capabilities of the ordinarily skilled artisan.

Dosages may be varied depending upon the requirements of the patient and the compound being employed. The dose administered to a patient, in the context of the present invention should be sufficient to affect a beneficial therapeutic response in the patient over time. The size of the dose also will be determined by the existence, nature, and extent of any adverse side-effects. Determination of the proper dosage for a particular situation is within the skill of the practitioner. Generally, treatment is initiated with smaller dosages which are less than the optimum dose of the compound. Thereafter, the dosage is increased by small increments until the optimum effect under circumstances is reached. Dosage amounts and intervals can be adjusted individually to provide levels of the administered compound effective for the particular clinical indication being treated. This will provide a therapeutic regimen that is commensurate with the severity of the individual's disease state.

Utilizing the teachings provided herein, an effective prophylactic or therapeutic treatment regimen can be planned that does not cause substantial toxicity and yet is effective to treat the clinical symptoms demonstrated by the particular patient. This planning should involve the careful choice of active compound by considering factors such as compound potency, relative bioavailability, patient body weight, presence and severity of adverse side effects, preferred mode of administration and the toxicity profile of the selected agent.

Also encompassed by the invention are kits (e.g. , pharmaceutical packs). The inventive kits may be useful for preventing and/or treating a disease (e.g. , cancer, a neurodegenerative disease, a leukodystrophy, an inflammatory disease, a musculoskeletal disease, a metabolic disease, or other disease or condition described herein).

The kits provided may comprise an inventive pharmaceutical composition or compound and a container (e.g. , a vial, ampule, bottle, syringe, and/or dispenser package, or other suitable container). In some embodiments, provided kits may optionally further include a second container comprising a pharmaceutical excipient for dilution or suspension of an inventive pharmaceutical composition or compound. In some embodiments, the inventive pharmaceutical composition or compound provided in the container and the second container are combined to form one unit dosage form.

Thus, in one aspect, provided are kits including a first container comprising a compound of Formula (I) or Formula (II), or a pharmaceutically acceptable salt, solvate, hydrate, tautomer, or stereoisomer thereof, or a pharmaceutical composition thereof. In certain embodiments, the kits are useful in preventing and/or treating a proliferative disease in a subject. In certain embodiments, the kits further include instructions for administering a compound of Formula (I) or Formula (II), or a pharmaceutically acceptable salt, solvate, hydrate, tautomer, or stereoisomer thereof, or a pharmaceutical composition thereof, to a subject to prevent and/or treat a disease described herein.

Methods of Treatment

The present invention features compounds, compositions, and methods comprising a compound of Formula (I) or Formula (II), or a pharmaceutically acceptable salt, co-crystal, solvate, hydrate, tautomer, ester, N-oxide or stereoisomer thereof. In some embodiments, the compounds, compositions, and methods are used in the prevention or treatment of a disease, disorder, or condition. Exemplary diseases, disorders, or conditions include, but are not limited to a neurodegenerative disease, a leukodystrophy, a cancer, an inflammatory disease, an autoimmune disease, a viral infection, a skin disease, a fibrotic disease, a hemoglobin disease, a kidney disease, a hearing loss condition, an ocular disease, a disease with mutations that leads to UPR induction, a malaria infection, a musculoskeletal disease, a metabolic disease, or a mitochondrial disease.

In some embodiments, the disease, disorder, or condition is related to (e.g., caused by) modulation of (e.g., a decrease in) eIF2B activity or level, eIF2a activity or level, or a component of the eIF2 pathway or ISR pathway. In some embodiments, the disease, disorder, or condition is related to modulation of a signaling pathway related to a component of the eIF2 pathway or ISR pathway (e.g., phosphorylation of a component of the eIF2 pathway or ISR pathway). In some embodiments, the disease, disorder, or condition is related to (e.g., caused by) neurodegeneration. In some embodiments, the disease, disorder, or condition is related to (e.g., caused by) neural cell death or dysfunction. In some embodiments, the disease, disorder, or condition is related to (e.g., caused by) glial cell death or dysfunction. In some embodiments, the disease, disorder, or condition is related to (e.g., caused by) an increase in the level or activity of eIF2B, eIF2a, or a component of the eIF2 pathway or ISR pathway. In some embodiments, the disease, disorder, or condition is related to (e.g., caused by) a decrease in the level or activity of eIF2B, eIF2a, or a component of the eIF2 pathway or ISR pathway.

In some embodiments, the disease may be caused by a mutation to a gene or protein sequence related to a member of the eIF2 pathway (e.g., eIF2B, eIF2a, or other component). Exemplary mutations include an amino acid mutation in the eIF2B l , eIF2B2, eIF2B3, eIF2B4, eIF2B5 subunits. In some embodiments, an amino acid mutation (e.g., an amino acid substitution, addition, or deletion) in a particular protein that may result in a structural change, e.g., a conformational or steric change, that affects the function of the protein. For example, in some embodiments, amino acids in and around the active site or close to a binding site (e.g., a phosphorylation site, small molecule binding site, or protein-binding site) may be mutated such that the activity of the protein is impacted. In some instances, the amino acid mutation (e.g., an amino acid substitution, addition, or deletion) may be conservative and may not substantially impact the structure or function of a protein. For example, in certain cases, the substitution of a serine residue with a threonine residue may not significantly impact the function of a protein. In other cases, the amino acid mutation may be more dramatic, such as the substitution of a charged amino acid (e.g., aspartic acid or lysine) with a large, nonpolar amino acid (e.g., phenylalanine or tryptophan) and therefore may have a substantial impact on protein function. The nature of the mutations that affect the structure of function of a gene or protein may be readily identified using standard sequencing techniques, e.g., deep sequencing techniques that are well known in the art. In some embodiments, a mutation in a member of the eIF2 pathway may affect binding or activity of a compound of Formula (I) or Formula (II), or a pharmaceutically acceptable salt, co- crystal, solvate, hydrate, tautomer, ester, N-oxide or stereoisomer thereof and thereby modulate treatment of a particular disease, disorder, or condition, or a symptom thereof. In some embodiments, an eIF2 protein may comprise an amino acid mutation (e.g., an amino acid substitution, addition, or deletion) at an alanine, arginine, asparagine, aspartic acid, cysteine, glutamic acid, glutamine, glycine, histidine, isoleucine, leucine, lysine, methionine, phenylalanine, proline, serine, threonine, tryptophan, tyrosine, or valine residue. In some embodiments, an eIF2 protein may comprise an amino acid substitution at an alanine, arginine, asparagine, aspartic acid, cysteine, glutamic acid, glutamine, glycine, histidine, isoleucine, leucine, lysine, methionine, phenylalanine, proline, serine, threonine, tryptophan, tyrosine, or valine residue. In some embodiments, an eIF2 protein may comprise an amino acid addition at an alanine, arginine, asparagine, aspartic acid, cysteine, glutamic acid, glutamine, glycine, histidine, isoleucine, leucine, lysine, methionine, phenylalanine, proline, serine, threonine, tryptophan, tyrosine, or valine residue. In some embodiments, an eIF2 protein may comprise an amino acid deletion at an alanine, arginine, asparagine, aspartic acid, cysteine, glutamic acid, glutamine, glycine, histidine, isoleucine, leucine, lysine, methionine, phenylalanine, proline, serine, threonine, tryptophan, tyrosine, or valine residue.

In some embodiments, the eIF2 protein may comprise an amino acid mutation (e.g., an amino acid substitution, addition, or deletion) at an alanine, arginine, asparagine, aspartic acid, cysteine, glutamic acid, glutamine, glycine, histidine, isoleucine, leucine, lysine, methionine, phenylalanine, proline, serine, threonine, tryptophan, tyrosine, or valine residue in the eIF2B l , eIF2B2, eIF2B3, eIF2B4, eIF2B5 subunits. In some embodiments, the eIF2 protein may comprise an amino acid substitution at an alanine, arginine, asparagine, aspartic acid, cysteine, glutamic acid, glutamine, glycine, histidine, isoleucine, leucine, lysine, methionine, phenylalanine, proline, serine, threonine, tryptophan, tyrosine, or valine residue in the eIF2B l , eIF2B2, eIF2B3, eIF2B4, eIF2B5 subunits. In some embodiments, the eIF2 protein may comprise an amino acid addition at an alanine, arginine, asparagine, aspartic acid, cysteine, glutamic acid, glutamine, glycine, histidine, isoleucine, leucine, lysine, methionine, phenylalanine, proline, serine, threonine, tryptophan, tyrosine, or valine residue in the eIF2B l , eIF2B2, eIF2B3, eIF2B4, eIF2B5 subunits. In some embodiments, the eIF2 protein may comprise an amino acid deletion at an alanine, arginine, asparagine, aspartic acid, cysteine, glutamic acid, glutamine, glycine, histidine, isoleucine, leucine, lysine, methionine, phenylalanine, proline, serine, threonine, tryptophan, tyrosine, or valine residue in the eIF2B l , eIF2B2, eIF2B3, eIF2B4, eIF2B5 subunits. Exemplary mutations include V183F (eIF2B l subunit), H341Q (eIF2B3), I346T (eIF2B3), R483W (eIF2B4), Rl 13H (eIF2B5), and R195H (eIF2B5). In some embodiments, an amino acid mutation (e.g., an amino acid substitution, addition, or deletion) in a member of the eIF2 pathway (e.g., an eIF2B protein subunit) may affect binding or activity of a compound of Formula (I) or Formula (II), or a pharmaceutically acceptable salt, co-crystal, solvate, hydrate, tautomer, ester, N-oxide or stereoisomer thereof and thereby modulate treatment of a particular disease, disorder, or condition, or a symptom thereof.

Neurodegenerative Disease

In some embodiments, the compound of Formula (I) or Formula (II), or a

pharmaceutically acceptable salt, co-crystal, solvate, hydrate, tautomer, ester, N-oxide or stereoisomer thereof is used to treat a neurodegenerative disease. As used herein, the term "neurodegenerative disease" refers to a disease or condition in which the function of a subject's nervous system becomes impaired. Examples of a neurodegenerative disease that may be treated with a compound, pharmaceutical composition, or method described herein include Alexander's disease, Alper's disease, Alzheimer's disease, Amyotrophic lateral sclerosis (ALS), Ataxia telangiectasia, Batten disease (also known as Spielmeyer-Vogt-Sjogren-Batten disease), Bovine spongiform encephalopathy (BSE), Canavan disease, Cockayne syndrome, Corticobasal degeneration, Creutzfeldt- Jakob disease, Dystonia, frontotemporal dementia (FTD), Gerstmann- Straussler-Scheinker syndrome, Huntington's disease, HIV-associated dementia, Kennedy's disease, Krabbe disease, kuru, Lewy body dementia, Machado-Joseph disease (Spinocerebellar ataxia type 3), Multiple system atrophy, Multisystem proteinopathy, Narcolepsy,

Neuroborreliosis, Parkinson's disease, Pelizaeus-Merzbacher Disease, Pick's disease, Primary lateral sclerosis, Prion diseases, Refsum's disease, Sandhoff disease, Schilder's disease, Subacute combined degeneration of spinal cord secondary to Pernicious Anaemia, Schizophrenia, Spinocerebellar ataxia (multiple types with varying characteristics, e.g., Spinocerebellar ataxia type 2 or Spinocerebellar ataxia type 8), Spinal muscular atrophy, Steele-Richardson-Olszewski disease, progressive supranuclear palsy, corticobasal degeneration, adrenoleukodystrophy, X- linked adrenoleukodystrophy, cerebral adrenoleukodystrophy, Pelizaeus-Merzbacher Disease, Krabbe disease, leukodystrophy due to mutation in DARS2 gene (sometimes known as lukoencephalopathy with brainstem and spinal cord involvement and lactate elevation

(LBSL), DARS2-related spectrum disorders, or Tabes dorsalis. In some embodiments, the neurodegenerative disease comprises vanishing white matter disease, childhood ataxia with CNS hypo-myelination, a leukodystrophy, a leukoencephalopathy, a hypomyelinating or demyelinating disease, an intellectual disability syndrome (e.g., Fragile X syndrome), Alzheimer's disease, amyotrophic lateral sclerosis (ALS), Creutzfeldt-Jakob disease, frontotemporal dementia (FTD), Gerstmann-Straussler-Scheinker disease, Huntington's disease, dementia (e.g., HIV-associated dementia or Lewy body dementia), kuru, multiple sclerosis, Parkinson's disease, or a prion disease.

In some embodiments, the neurodegenerative disease comprises vanishing white matter disease, childhood ataxia with CNS hypo-myelination, a leukodystrophy, a

leukoencephalopathy, a hypomyelinating or demyelinating disease, or an intellectual disability syndrome (e.g., Fragile X syndrome). In some embodiments, the neurodegenerative disease comprises a psychiatric disease such as agoraphobia, Alzheimer's disease, anorexia nervosa, amnesia, anxiety disorder, attention deficit disorder, bipolar disorder, body dysmorphic disorder, bulimia nervosa, claustrophobia, depression, delusions, Diogenes syndrome, dyspraxia, insomnia, Munchausen's syndrome, narcolepsy, narcissistic personality disorder, obsessive-compulsive disorder, psychosis, phobic disorder, schizophrenia, seasonal affective disorder, schizoid personality disorder, sleepwalking, social phobia, substance abuse, tardive dyskinesia, Tourette syndrome, or trichotillomania.

In some embodiments, the compound of Formula (I) or Formula (II), or a

pharmaceutically acceptable salt, co-crystal, solvate, hydrate, tautomer, ester, N-oxide or stereoisomer thereof is used to treat vanishing white matter disease. Exemplary methods of treating vanishing white matter disease include, but are not limited to, reducing or eliminating a symptom of vanishing white matter disease, reducing the loss of white matter, reducing the loss of myelin, increasing the amount of myelin, or increasing the amount of white matter in a subject.

In some embodiments, the compound of Formula (I) or Formula (II), or a

pharmaceutically acceptable salt, co-crystal, solvate, hydrate, tautomer, ester, N-oxide or stereoisomer thereof is used to treat childhood ataxia with CNS hypo-myelination. Exemplary methods of treating childhood ataxia with CNS hypo-myelination include, but are not limited to, reducing or eliminating a symptom of childhood ataxia with CNS hypo-myelination, increasing the level of myelin, or decreasing the loss of myelin in a subject. In some embodiments, the compound of Formula (I) or Formula (II), or a

pharmaceutically acceptable salt, co-crystal, solvate, hydrate, tautomer, ester, N-oxide or stereoisomer thereof is used to treat an intellectual disability syndrome (e.g., Fragile X syndrome). Exemplary methods of treating an intellectual disability syndrome include, but are not limited to, reducing or eliminating a symptom of an intellectual disability syndrome.

In some embodiments, the compound of Formula (I) or Formula (II), or a

pharmaceutically acceptable salt, co-crystal, solvate, hydrate, tautomer, ester, N-oxide or stereoisomer thereof is used to treat neurodegeneration. Exemplary methods of treating neurodegeneration include, but are not limited to, improvement of mental wellbeing, increasing mental function, slowing the decrease of mental function, decreasing dementia, delaying the onset of dementia, improving cognitive skills, decreasing the loss of cognitive skills, improving memory, decreasing the degradation of memory, or extending survival.

In some embodiments, the compound of Formula (I) or Formula (II), or a

pharmaceutically acceptable salt, co-crystal, solvate, hydrate, tautomer, ester, N-oxide or stereoisomer thereof is used to treat a leukoencephalopathy or demyelinating disease. Exemplary leukoencephalopathies include, but are not limited to, progressive multifocal

leukoencephalopathy, toxic leukoencephalopathy, leukoencephalopathy with vanishing white matter, leukoencephalopathy with neuroaxonal spheroids, reversible posterior

leukoencephalopathy syndrome, hypertensive leukoencephalopathy, megalencephalic leukoencephalopathy with subcortical cysts, Charcot-Marie-Tooth disorder, and Devic' s disease. A leukoencephalopathy may comprise a demyelinating disease, which may be inherited or acquired. In some embodiments, an acquired demyelinating disease may be an inflammatory demyelinating disease (e.g., an infectious inflammatory demyelinating disease or a noninfectious inflammatory demyelinating disease), a toxic demyelinating disease, a metabolic demyelinating disease, a hypoxic demyelinating disease, a traumatic demyelinating disease, or an ischemic demyelinating disease (e.g., Binswanger's disease). Exemplary methods of treating a leukoencephalopathy or demyelinating disease include, but are not limited to, reducing or eliminating a symptom of a leukoencephalopathy or demyelinating disease, reducing the loss of myelin, increasing the amount of myelin, reducing the loss of white matter in a subject, or increasing the amount of white matter in a subject. In some embodiments, the compound of Formula (I) or Formula (II), or a

pharmaceutically acceptable salt, co-crystal, solvate, hydrate, tautomer, ester, N-oxide or stereoisomer thereof is used to treat a traumatic injury or a toxin-induced injury to the nervous system (e.g., the brain). Exemplary traumatic brain injuries include, but are not limited to, a brain abscess, concussion, ischemia, brain bleeding, cranial fracture, diffuse axonal injury, locked-in syndrome, or injury relating to a traumatic force or blow to the nervous system or brain that causes damage to an organ or tissue. Exemplary toxin-induced brain injuries include, but are not limited to, toxic encephalopathy, meningitis (e.g. bacterial meningitis or viral meningitis), meningoencephalitis, encephalitis (e.g., Japanese encephalitis, eastern equine encephalitis, West Nile encephalitis), Guillan-Barre syndrome, Sydenham's chorea, rabies, leprosy, neurosyphilis, a prion disease, or exposure to a chemical (e.g., arsenic, lead, toluene, ethanol, manganese, fluoride, dichlorodiphenyltrichloroethane (DDT),

dichlorodiphenyldichloroethylene (DDE), tetrachloroethylene, a polybrominated diphenyl ether, a pesticide, a sodium channel inhibitor, a potassium channel inhibitor, a chloride channel inhibitor, a calcium channel inhibitor, or a blood brain barrier inhibitor).

In other embodiments, the compound of Formula (I) or Formula (II), or a

pharmaceutically acceptable salt, co-crystal, solvate, hydrate, tautomer, ester, N-oxide or stereoisomer thereof is used to improve memory in a subject. Induction of memory has been shown to be facilitated by decreased and impaired by increased eIF2a phosphorylation.

Regulators of translation, such as compounds disclosed herein (e.g. a compound of Formula (I) or Formula (II)), could serve as therapeutic agents that improve memory in human disorders associated with memory loss such as Alzheimer's disease and in other neurological disorders that activate the UPR or ISR in neurons and thus could have negative effects on memory

consolidation such as Parkinson's disease, schizophrenia, amyotrophic lateral sclerosis (ALS) and prion diseases. In addition, a mutation in eIF2y that disrupts complex integrity linked intellectual disability (intellectual disability syndrome or ID) to impaired translation initiation in humans. Hence, two diseases with impaired eIF2 function, ID and VWM, display distinct phenotypes but both affect mainly the brain and impair learning. In some embodiments, the disease or condition is unsatisfactory memory (e.g., working memory, long term memory, short term memory, or memory consolidation). In still other embodiments, the compound of Formula (I) or Formula (II), or a pharmaceutically acceptable salt, co-crystal, solvate, hydrate, tautomer, ester, N-oxide or stereoisomer thereof is used in a method to improve memory in a subject (e.g., working memory, long term memory, short term memory, or memory consolidation). In some embodiments, the subject is human. In some embodiments, the subject is a non-human mammal. In some embodiments, the subject is a domesticated animal. In some embodiments, the subject is a dog. In some embodiments, the subject is a bird. In some embodiments, the subject is a horse. In embodiments, the patient is a bovine. In some embodiments, the subject is a primate.

Cancer In some embodiments, the compound of Formula (I) or Formula (II), or a

pharmaceutically acceptable salt, co-crystal, solvate, hydrate, tautomer, or stereoisomer thereof is used to treat cancer. As used herein, "cancer" refers to human cancers and carcinomas, sarcomas, adenocarcinomas, lymphomas, leukemias, melanomas, etc., including solid and lymphoid cancers, kidney, breast, lung, bladder, colon, ovarian, prostate, pancreas, stomach, brain, head and neck, skin, uterine, testicular, glioma, esophagus, liver cancer, including hepatocarcinoma, lymphoma, including B -acute lymphoblastic lymphoma, non-Hodgkin's lymphomas (e.g., Burkitt's, Small Cell, and Large Cell lymphomas), Hodgkin's lymphoma, leukemia (including AML, ALL, and CML), and/or multiple myeloma. In some further instances, "cancer" refers to lung cancer, breast cancer, ovarian cancer, leukemia, lymphoma, melanoma, pancreatic cancer, sarcoma, bladder cancer, bone cancer, brain cancer, cervical cancer, colon cancer, esophageal cancer, gastric cancer, liver cancer, head and neck cancer, kidney cancer, myeloma, thyroid cancer, prostate cancer, metastatic cancer, or carcinoma.

As used herein, the term "cancer" refers to all types of cancer, neoplasm or malignant tumors found in mammals, including leukemia, lymphoma, carcinomas and sarcomas.

Exemplary cancers that may be treated with a compound, pharmaceutical composition, or method provided herein include lymphoma, sarcoma, bladder cancer, bone cancer, brain tumor, cervical cancer, colon cancer, esophageal cancer, gastric cancer, head and neck cancer, kidney cancer, myeloma, thyroid cancer, leukemia, prostate cancer, breast cancer (e.g., ER positive, ER negative, chemotherapy resistant, herceptin resistant, HER2 positive, doxorubicin resistant, tamoxifen resistant, ductal carcinoma, lobular carcinoma, primary, metastatic), ovarian cancer, pancreatic cancer, liver cancer (e.g., hepatocellular carcinoma), lung cancer (e.g., non-small cell lung carcinoma, squamous cell lung carcinoma, adenocarcinoma, large cell lung carcinoma, small cell lung carcinoma, carcinoid, sarcoma), glioblastoma multiforme, glioma, or melanoma. Additional examples include, cancer of the thyroid, endocrine system, brain, breast, cervix, colon, head & neck, liver, kidney, lung, non-small cell lung, melanoma, mesothelioma, ovary, sarcoma, stomach, uterus or Medulloblastoma (e.g., WNT-dependent pediatric

medulloblastoma), Hodgkin's Disease, Non-Hodgkin's Lymphoma, multiple myeloma, neuroblastoma, glioma, glioblastoma multiforme, ovarian cancer, rhabdomyosarcoma, primary thrombocytosis, primary macroglobulinemia, primary brain tumors, cancer, malignant pancreatic insulanoma, malignant carcinoid, urinary bladder cancer, premalignant skin lesions, testicular cancer, lymphomas, thyroid cancer, neuroblastoma, esophageal cancer, genitourinary tract cancer, malignant hypercalcemia, endometrial cancer, adrenal cortical cancer, neoplasms of the endocrine or exocrine pancreas, medullary thyroid cancer, medullary thyroid carcinoma, melanoma, colorectal cancer, papillary thyroid cancer, hepatocellular carcinoma, Paget' s Disease of the Nipple, Phyllodes Tumors, Lobular Carcinoma, Ductal Carcinoma, cancer of the pancreatic stellate cells, cancer of the hepatic stellate cells, or prostate cancer.

The term "leukemia" refers broadly to progressive, malignant diseases of the blood- forming organs and is generally characterized by a distorted proliferation and development of leukocytes and their precursors in the blood and bone marrow. Leukemia is generally clinically classified on the basis of (1) the duration and character of the disease-acute or chronic; (2) the type of cell involved; myeloid (myelogenous), lymphoid (lymphogenous), or monocytic; and (3) the increase or non-increase in the number abnormal cells in the blood-leukemic or aleukemic (subleukemic). Exemplary leukemias that may be treated with a compound, pharmaceutical composition, or method provided herein include, for example, acute nonlymphocytic leukemia, chronic lymphocytic leukemia, acute granulocytic leukemia, chronic granulocytic leukemia, acute promyelocytic leukemia, adult T-cell leukemia, aleukemic leukemia, a leukocythemic leukemia, basophylic leukemia, blast cell leukemia, bovine leukemia, chronic myelocytic leukemia, leukemia cutis, embryonal leukemia, eosinophilic leukemia, Gross' leukemia, hairy- cell leukemia, hemoblastic leukemia, hemocytoblastic leukemia, histiocytic leukemia, stem cell leukemia, acute monocytic leukemia, leukopenic leukemia, lymphatic leukemia, lymphoblastic leukemia, lymphocytic leukemia, lymphogenous leukemia, lymphoid leukemia, lymphosarcoma cell leukemia, mast cell leukemia, megakaryocyte leukemia, micromyeloblastic leukemia, monocytic leukemia, myeloblasts leukemia, myelocytic leukemia, myeloid granulocytic leukemia, myelomonocytic leukemia, Naegeli leukemia, plasma cell leukemia, multiple myeloma, plasmacytic leukemia, promyelocytic leukemia, Rieder cell leukemia, Schilling's leukemia, stem cell leukemia, subleukemic leukemia, or undifferentiated cell leukemia.

The term "sarcoma" generally refers to a tumor which is made up of a substance like the embryonic connective tissue and is generally composed of closely packed cells embedded in a fibrillar or homogeneous substance. Sarcomas that may be treated with a compound, pharmaceutical composition, or method provided herein include a chondrosarcoma, fibrosarcoma, lymphosarcoma, melanosarcoma, myxosarcoma, osteosarcoma, Abemethy's sarcoma, adipose sarcoma, liposarcoma, alveolar soft part sarcoma, ameloblastic sarcoma, botryoid sarcoma, chloroma sarcoma, chorio carcinoma, embryonal sarcoma, Wilms' tumor sarcoma, endometrial sarcoma, stromal sarcoma, Ewing's sarcoma, fascial sarcoma, fibroblastic sarcoma, giant cell sarcoma, granulocytic sarcoma, Hodgkin's sarcoma, idiopathic multiple pigmented hemorrhagic sarcoma, immunoblastic sarcoma of B cells, lymphoma, immunoblastic sarcoma of T-cells, Jensen's sarcoma, Kaposi's sarcoma, Kupffer cell sarcoma, angiosarcoma, leukosarcoma, malignant mesenchymoma sarcoma, parosteal sarcoma, reticulocytic sarcoma, Rous sarcoma, serocystic sarcoma, synovial sarcoma, or telangiectaltic sarcoma.

The term "melanoma" is taken to mean a tumor arising from the melanocytic system of the skin and other organs. Melanomas that may be treated with a compound, pharmaceutical composition, or method provided herein include, for example, acral-lentiginous melanoma, amelanotic melanoma, benign juvenile melanoma, Cloudman's melanoma, S91 melanoma, Harding- Passey melanoma, juvenile melanoma, lentigo maligna melanoma, malignant melanoma, nodular melanoma, subungal melanoma, or superficial spreading melanoma.

The term "carcinoma" refers to a malignant new growth made up of epithelial cells tending to infiltrate the surrounding tissues and give rise to metastases. Exemplary carcinomas that may be treated with a compound, pharmaceutical composition, or method provided herein include, for example, medullary thyroid carcinoma, familial medullary thyroid carcinoma, acinar carcinoma, acinous carcinoma, adenocystic carcinoma, adenoid cystic carcinoma, carcinoma adenomatosum, carcinoma of adrenal cortex, alveolar carcinoma, alveolar cell carcinoma, basal cell carcinoma, basaloid carcinoma, basosquamous cell carcinoma, bronchioalveolar carcinoma, bronchiolar carcinoma, bronchogenic carcinoma, cerebriform carcinoma, cholangiocellular carcinoma, chorionic carcinoma, colloid carcinoma, comedo carcinoma, corpus carcinoma, cribriform carcinoma, carcinoma en cuirasse, carcinoma cutaneum, cylindrical carcinoma, cylindrical cell carcinoma, duct carcinoma, ductal carcinoma, carcinoma durum, embryonal carcinoma, encephaloid carcinoma, epidermoid carcinoma, carcinoma epitheliale adenoides, exophytic carcinoma, carcinoma ex ulcere, carcinoma fibrosum, gelatiniforni carcinoma, gelatinous carcinoma, giant cell carcinoma, carcinoma gigantocellulare, glandular carcinoma, granulosa cell carcinoma, hair-matrix carcinoma, hematoid carcinoma, hepatocellular carcinoma, Hurthle cell carcinoma, hyaline carcinoma, hypernephroid carcinoma, infantile embryonal carcinoma, carcinoma in situ, intraepidermal carcinoma, intraepithelial carcinoma, Krompecher's carcinoma, Kulchitzky-cell carcinoma, large-cell carcinoma, lenticular carcinoma, carcinoma lenticulare, lipomatous carcinoma, lobular carcinoma, lymphoepithelial carcinoma, carcinoma medullare, medullary carcinoma, melanotic carcinoma, carcinoma molle, mucinous carcinoma, carcinoma muciparum, carcinoma mucocellulare, mucoepidermoid carcinoma, carcinoma mucosum, mucous carcinoma, carcinoma myxomatodes, nasopharyngeal carcinoma, oat cell carcinoma, carcinoma ossificans, osteoid carcinoma, papillary carcinoma, periportal carcinoma, preinvasive carcinoma, prickle cell carcinoma, pultaceous carcinoma, renal cell carcinoma of kidney, reserve cell carcinoma, carcinoma sarcomatodes, schneiderian carcinoma, scirrhous carcinoma, carcinoma scroti, signet-ring cell carcinoma, carcinoma simplex, small-cell carcinoma, solanoid carcinoma, spheroidal cell carcinoma, spindle cell carcinoma, carcinoma spongiosum, squamous carcinoma, squamous cell carcinoma, string carcinoma, carcinoma telangiectaticum, carcinoma telangiectodes, transitional cell carcinoma, carcinoma tuberosum, tubular carcinoma, tuberous carcinoma, verrucous carcinoma, or carcinoma villosum.

In some embodiments, the compound of Formula (I) or Formula (II) or a

pharmaceutically acceptable salt, solvate, hydrate, tautomer, or stereoisomer thereof is used to treat pancreatic cancer, breast cancer, multiple myeloma, cancers of secretory cells. For example certain methods herein treat cancer by decreasing or reducing or preventing the occurrence, growth, metastasis, or progression of cancer. In some embodiments, the methods described herein may be used to treat cancer by decreasing or eliminating a symptom of cancer. In some embodiments, the compound of Formula (I) or Formula (II) or a pharmaceutically acceptable salt, solvate, hydrate, tautomer, or stereoisomer thereof may be used as a single agent in a composition or in combination with another agent in a composition to treat a cancer described herein (e.g., pancreatic cancer, breast cancer, multiple myeloma, cancers of secretory cells).

In some embodiments, the compounds (compounds described herein, e.g. , a compound of Formula (I) or Formula (II)) and compositions (e.g. , compositions comprising a compound described herein, e.g. , a compound of Formula (I) or Formula (II))) are used with a cancer immunotherapy (e.g. , a checkpoint blocking antibody) to treat a subject (e.g. , a human subject), e.g. , suffering from a disease or disorder described herein (e.g. , abnormal cell growth, e.g. , cancer (e.g. , a cancer described herein)). The methods described herein comprise administering a compound described herein, e.g., a compound of Formula (I) or Formula (II) and an

immunotherapy to a subject having abnormal cell growth such as cancer. Exemplary immunotherapies include, but are not limited to the following.

In some embodiments, the immunotherapeutic agent is a compound (e.g., a ligand, an antibody) that inhibits the immune checkpoint blockade pathway. In some embodiments, the immunotherapeutic agent is a compound that inhibits the indoleamine 2,3-dioxygenase (IDO) pathway. In some embodiments, the immunotherapeutic agent is a compound that agonizes the STING pathway. Cancer immunotherapy refers to the use of the immune system to treat cancer. Three groups of immunotherapy used to treat cancer include cell-based, antibody-based, and cytokine therapies. All groups exploit cancer cells' display of subtly different structures (e.g. , molecular structure; antigens, proteins, molecules, carbohydrates) on their surface that can be detected by the immune system. Cancer immunotherapy (i.e., anti-tumor immunotherapy or antitumor immunotherapeutics) includes but is not limited to, immune checkpoint antibodies (e.g. , PD-1 antibodies, PD-L1 antibodies, PD-L2 antibodies, CTLA-4 antibodies, TIM3 antibodies, LAG3 antibodies, TIGIT antibodies); and cancer vaccines (i.e., anti-tumor vaccines or vaccines based on neoantigens such as a peptide or RNA vaccine).

Cell-based therapies (e.g. , cancer vaccines), usually involve the removal of immune cells from a subject suffering from cancer, either from the blood or from a tumor. Immune cells specific for the tumor will be activated, grown, and returned to a subject suffering from cancer where the immune cells provide an immune response against the cancer. Cell types that can be used in this way are e.g. , natural killer cells, lymphokine-activated killer cells, cytotoxic T-cells, dendritic cells, CAR-T therapies (i.e., chimeric antigen receptor T-cells which are T-cells engineered to target specific antigens), TIL therapy (i.e., administration of tumor-infiltrating lymphocytes), TCR gene therapy, protein vaccines, and nucleic acid vaccines. An exemplary cell-based therapy is Provenge. In some embodiments, the cell-based therapy is a CAR-T therapy. Interleukin-2 and interferon-alpha are examples of cytokines, proteins that regulate and coordinate the behavior of the immune system.

Cancer Vaccines with Neoantigens

Neoantigens are antigens encoded by tumor-specific mutated genes. Technological innovations have made it possible to dissect the immune response to patient-specific neoantigens that arise as a consequence of tumor-specific mutations, and emerging data suggest that recognition of such neoantigens is a major factor in the activity of clinical immunotherapies. These observations indicate that neoantigen load may form a biomarker in cancer

immunotherapy. Many novel therapeutic approaches are being developed that selectively enhance T cell reactivity against this class of antigens. One approach to target neoantigens is via cancer vaccine. These vaccines can be developed using peptides or RNA, e.g., synthetic peptides or synthetic RNA.

Antibody therapies are antibody proteins produced by the immune system and that bind to a target antigen on the surface of a cell. Antibodies are typically encoded by an

immunoglobulin gene or genes, or fragments thereof. In normal physiology antibodies are used by the immune system to fight pathogens. Each antibody is specific to one or a few proteins, and those that bind to cancer antigens are used, e.g., for the treatment of cancer. Antibodies are capable of specifically binding an antigen or epitope. (Fundamental Immunology, 3 rd Edition, W.E., Paul, ed., Raven Press, N.Y. (1993). Specific binding occurs to the corresponding antigen or epitope even in the presence of a heterogeneous population of proteins and other biologies. Specific binding of an antibody indicates that it binds to its target antigen or epitope with an affinity that is substantially greater than binding to irrelevant antigens. The relative difference in affinity is often at least 25% greater, more often at least 50% greater, most often at least 100% greater. The relative difference can be at least 2-fold, at least 5-fold, at least 10-fold, at least 25- fold, at least 50-fold, at least 100-fold, or at least 1000-fold, for example.

Exemplary types of antibodies include without limitation human, humanized, chimeric, monoclonal, polyclonal, single chain, antibody binding fragments, and diabodies. Once bound to a cancer antigen, antibodies can induce antibody-dependent cell-mediated cytotoxicity, activate the complement system, prevent a receptor interacting with its ligand or deliver a payload of chemotherapy or radiation, all of which can lead to cell death. Exemplary antibodies for the treatment of cancer include but are not limited to, Alemtuzumab, Bevacizumab, Bretuximab vedotin, Cetuximab, Gemtuzumab ozogamicin, Ibritumomab tiuxetan, Ipilimumab,

Ofatumumab, Panitumumab, Rituximab, Tositumomab, Trastuzumab, Nivolumab,

Pembrolizumab, Avelumab, durvalumab and pidilizumab.

Checkpoint blocking antibodies

The methods described herein comprise, in some embodiments, treating a human subject suffering from a disease or disorder described herein, the method comprising administering a composition comprising a cancer immunotherapy (e.g., an immunotherapeutic agent). In some embodiments, the immunotherapeutic agent is a compound (e.g., an inhibitor or antibody) that inhibits the immune checkpoint blockade pathway. Immune checkpoint proteins, under normal physiological conditions, maintain self-tolerance (e.g. , prevent autoimmunity) and protect tissues from damage when the immune system is responding to e.g. , pathogenic infection. Immune checkpoint proteins can be dysregulated by tumors as an important immune resistance mechanism. (Pardoll, Nature Rev. Cancer, 2012, 12, 252-264). Agonists of co- stimulatory receptors or antagonists of inhibitory signals (e.g., immune checkpoint proteins), provide an amplification of antigen-specific T-cell responses. Antibodies that block immune checkpoints do not target tumor cells directly but typically target lymphocyte receptors or their ligands to enhance endogenous antitumor activity.

Exemplary checkpoint blocking antibodies include but are not limited to, anti-CTLA-4, anti-PD-1, anti-LAG3 (i.e., antibodies against lymphocyte activation gene 3), and anti-TIM3 (i.e., antibodies against T-cell membrane protein 3). Exemplary anti-CTLA-4 antibodies include but are not limited to, ipilimumab and tremelimumab. Exemplary anti-PD-1 ligands include but are not limited to, PD-L1 (i.e., B7-H1 and CD274) and PD-L2 (i.e., B7-DC and CD273).

Exemplary anti-PD-1 antibodies include but are not limited to, nivolumab (i.e., MDX-1106, BMS-936558, or ONO-4538)), CT-011, AMP-224, pembrolizumab (trade name Keytruda), and MK-3475. Exemplary PD-L1 -specific antibodies include but are not limited to, BMS936559 (i.e., MDX-1105), MEDI4736 and MPDL-3280A. Exemplary checkpoint blocking antibodies also include but are not limited to, IMP321 and MGA271.

T-regulatory ceils (e.g., CD4+, CD25+, or T-reg) are also involved in policing the distinction between self and non-self (e.g., foreign) antigens, and may represent an important mechanism in suppression of immune response in many cancers. T-reg ceils can either emerge from the thymus (i.e., "natural T-reg") or can differentiate from mature T-celis under circumstances of peripheral tolerance induction (i.e., '"induced T-reg"), Strategies that minimize the action of T-reg ceils would therefore be expected to facilitate the immune response to tumors. (Sutmuller, van Duivemvoorde et al., 2001).

IDO pathway inhibitors The IDO pathway regulates immune response by suppressing T cell function and enabling local tumor immune escape. IDO expression by antigen-presenting cells (APCs) can lead to tryptophan depletion, and resulting antigen-specific T cell energy and regulatory T cell recruitment. Some tumors even express IDO to shield themselves from the immune system. A compound that inhibits IDO or the IDO pathway thereby activating the immune system to attack the cancer (e.g., tumor in a subject). Exemplary IDO pathway inhibitors include indoximod, epacadostat and EOS200271.

STING pathway agonists

Stimulator of interferon genes (STING) is an adaptor protein that plays an important role in the activation of type I interferons in response to cytosolic nucleic acid ligands. Evidence indicates involvement of the STING pathway in the induction of antitumor immune response. It has been shown that activation of the STING-dependent pathway in cancer cells can result in tumor infiltration with immune cells and modulation of the anticancer immune response. STING agonists are being developed as a class of cancer therapeutics. Exemplary STING agonists include MK-1454 and ADU-S100. Co-stimulatory antibodies

The methods described herein comprise, in some embodiments, treating a human subject suffering from a disease or disorder described herein, the method comprising administering a composition comprising a cancer immunotherapy (e.g. , an immunotherapeutic agent). In some embodiments, the immunotherapeutic agent is a co-stimulatory inhibitor or antibody. In some embodiments, the methods described herein comprise depleting or activating anti-4-lBB, anti- OX40, anti-GITR, anti-CD27 and anti-CD40, and variants thereof.

Inventive methods of the present invention contemplate single as well as multiple administrations of a therapeutically effective amount of a compound as described herein. Compounds, e.g., a compound as described herein, can be administered at regular intervals, depending on the nature, severity and extent of the subject's condition. In some embodiments, a compound described herein is administered in a single dose. In some embodiments, a compound described herein is administered in multiple doses.

Inflammatory Disease

In some embodiments, the compound of Formula (I) or Formula (II), or a

pharmaceutically acceptable salt, co-crystal, solvate, hydrate, tautomer, ester, N-oxide or stereoisomer thereof is used to treat an inflammatory disease. As used herein, the term

"inflammatory disease" refers to a disease or condition characterized by aberrant inflammation (e.g. an increased level of inflammation compared to a control such as a healthy person not suffering from a disease). Examples of inflammatory diseases include postoperative cognitive dysfunction, arthritis (e.g., rheumatoid arthritis, psoriatic arthritis, juvenile idiopathic arthritis), systemic lupus erythematosus (SLE), myasthenia gravis, juvenile onset diabetes, diabetes mellitus type 1 , Guillain-Barre syndrome, Hashimoto's encephalitis, Hashimoto's thyroiditis, ankylosing spondylitis, psoriasis, Sjogren's syndrome, vasculitis, glomerulonephritis, autoimmune thyroiditis, Behcet's disease, Crohn's disease, ulcerative colitis, bullous pemphigoid, sarcoidosis, ichthyosis, Graves' ophthalmopathy, inflammatory bowel disease, Addison's disease, Vitiligo, asthma (e.g., allergic asthma), acne vulgaris, celiac disease, chronic prostatitis, inflammatory bowel disease, pelvic inflammatory disease, reperfusion injury, sarcoidosis, transplant rejection, interstitial cystitis, atherosclerosis, and atopic dermatitis. Proteins associated with inflammation and inflammatory diseases (e.g. aberrant expression being a symptom or cause or marker of the disease) include interleukin-6 (IL-6), interleukin-8 (IL-8), interleukin- 18 (IL-18), TNF-a (tumor necrosis factor-alpha), and C-reactive protein (CRP). In some embodiments, the inflammatory disease comprises postoperative cognitive dysfunction, arthritis (e.g., rheumatoid arthritis, psoriatic arthritis, or juvenile idiopathic arthritis), systemic lupus erythematosus (SLE), myasthenia gravis, diabetes (e.g., juvenile onset diabetes or diabetes mellitus type 1), Guillain-Barre syndrome, Hashimoto's encephalitis, Hashimoto's thyroiditis, ankylosing spondylitis, psoriasis, Sjogren's syndrome, vasculitis, glomerulonephritis, auto-immune thyroiditis, Behcet's disease, Crohn's disease, ulcerative colitis, bullous pemphigoid, sarcoidosis, ichthyosis, Graves' ophthalmopathy, inflammatory bowel disease, Addison's disease, vitiligo, asthma (e.g., allergic asthma), acne vulgaris, celiac disease, chronic prostatitis, pelvic inflammatory disease, reperfusion injury, sarcoidosis, transplant rejection, interstitial cystitis, atherosclerosis, or atopic dermatitis.

In some embodiments, the inflammatory disease comprises postoperative cognitive dysfunction, which refers to a decline in cognitive function (e.g. memory or executive function (e.g. working memory, reasoning, task flexibility, speed of processing, or problem solving)) following surgery.

In other embodiments, the method of treatment is a method of prevention. For example, a method of treating postsurgical cognitive dysfunction may include preventing postsurgical cognitive dysfunction or a symptom of postsurgical cognitive dysfunction or reducing the severity of a symptom of postsurgical cognitive dysfunction by administering a compound described herein prior to surgery.

In some embodiments, the compound of Formula (I) or Formula (II), or a

pharmaceutically acceptable salt, co-crystal, solvate, hydrate, tautomer, ester, N-oxide or stereoisomer thereof is used to treat an inflammatory disease (e.g., an inflammatory disease described herein) by decreasing or eliminating a symptom of the disease. In some embodiments, the compound of Formula (I) or Formula (II), or a pharmaceutically acceptable salt, co-crystal, solvate, hydrate, tautomer, ester, N-oxide or stereoisomer thereof may be used as a single agent in a composition or in combination with another agent in a composition to treat an inflammatory disease (e.g., an inflammatory disease described herein).

Musculoskeletal Diseases

In some embodiments, the compound of Formula (I) or Formula (II), or a

pharmaceutically acceptable salt, co-crystal, solvate, hydrate, tautomer, ester, N-oxide or stereoisomer thereof is used to treat a musculoskeletal disease. As used herein, the term

"musculoskeletal disease" refers to a disease or condition in which the function of a subject's musculoskeletal system (e.g., muscles, ligaments, tendons, cartilage, or bones) becomes impaired. Exemplary musculoskeletal diseases that may be treated with a compound of Formula (I) or Formula (II), or a pharmaceutically acceptable salt, co-crystal, solvate, hydrate, tautomer, ester, N-oxide or stereoisomer thereof include muscular dystrophy (e.g., Duchenne muscular dystrophy, Becker muscular dystrophy, distal muscular dystrophy, congenital muscular dystrophy, Emery-Dreifuss muscular dystrophy, facioscapulohumeral muscular dystrophy, myotonic muscular dystrophy type 1, or myotonic muscular dystrophy type 2), limb girdle muscular dystrophy, multisystem proteinopathy, rhizomelic chondrodysplasia punctata, X-linked recessive chondrodysplasia punctata, Conradi-Hunermann syndrome, Autosomal dominant chondrodysplasia punctata, stress induced skeletal disorders (e.g., stress induced osteoporosis), multiple sclerosis, amyotrophic lateral sclerosis (ALS), primary lateral sclerosis, progressive muscular atrophy, progressive bulbar palsy, pseudobulbar palsy, spinal muscular atrophy, progressive spinobulbar muscular atrophy, spinal cord spasticity, spinal muscle atrophy, myasthenia gravis, neuralgia, fibromyalgia, Machado-Joseph disease, Paget's disease of bone, cramp fasciculation syndrome, Freidrich's ataxia, a muscle wasting disorder (e.g., muscle atrophy, sarcopenia, cachexia), an inclusion body myopathy, motor neuron disease, or paralysis.

In some embodiments, the compound of Formula (I) or Formula (II), or a

pharmaceutically acceptable salt, co-crystal, solvate, hydrate, tautomer, ester, N-oxide or stereoisomer thereof is used to treat a musculoskeletal disease (e.g., a musculoskeletal disease described herein) by decreasing or eliminating a symptom of the disease. In some embodiments, the method of treatment comprises treatment of muscle pain or muscle stiffness associated with a musculoskeletal disease. In some embodiments, the compound of Formula (I) or Formula (II), or a pharmaceutically acceptable salt, co-crystal, solvate, hydrate, tautomer, ester, N-oxide or stereoisomer thereof may be used as a single agent in a composition or in combination with another agent in a composition to treat a musculoskeletal disease (e.g., a musculoskeletal disease described herein).

Metabolic Diseases

In some embodiments, the compound of Formula (I) or Formula (II), or a

pharmaceutically acceptable salt, co-crystal, solvate, hydrate, tautomer, ester, N-oxide or stereoisomer thereof is used to treat metabolic disease. As used herein, the term "metabolic disease" refers to a disease or condition affecting a metabolic process in a subject. Exemplary metabolic diseases that may be treated with a compound of Formula (I) or Formula (II), or a pharmaceutically acceptable salt, co-crystal, solvate, hydrate, tautomer, ester, N-oxide or stereoisomer thereof include non-alcoholic steatohepatitis (NASH), non-alcoholic fatty liver disease (NAFLD), liver fibrosis, obesity, heart disease, atherosclerosis, arthritis, cystinosis, diabetes (e.g., Type I diabetes, Type II diabetes, or gestational diabetes), phenylketonuria, proliferative retinopathy, or Kearns-Sayre disease.

In some embodiments, the compound of Formula (I) or Formula (II), or a

pharmaceutically acceptable salt, co-crystal, solvate, hydrate, tautomer, ester, N-oxide or stereoisomer thereof is used to treat a metabolic disease (e.g., a metabolic disease described herein) by decreasing or eliminating a symptom of the disease. In some embodiments, the method of treatment comprises decreasing or eliminating a symptom comprising elevated blood pressure, elevated blood sugar level, weight gain, fatigue, blurred vision, abdominal pain, flatulence, constipation, diarrhea, jaundice, and the like. In some embodiments, the compound of Formula (I) or Formula (II), or a pharmaceutically acceptable salt, solvate, hydrate, tautomer, or stereoisomer thereof may be used as a single agent in a composition or in combination with another agent in a composition to treat a metabolic disease (e.g., a musculoskeletal disease described herein).

Mitochondrial Diseases

In some embodiments, the compound of Formula (I) or Formula (II) or a

pharmaceutically acceptable salt, co-crystal, solvate, hydrate, tautomer, ester, N-oxide or stereoisomer thereof is used to treat mitochondrial disease. As used herein, the term

"mitochondrial disease" refers to a disease or condition affecting the mitochondria in a subject. In some embodiments, the mitochondrial disease is associated with, or is a result of, or is caused by mitochondrial dysfunction, one or more mitochondrial protein mutations, or one or more mitochondrial DNA mutations. In some embodiments, the mitochondrial disease is a mitochondrial myopathy. In some embodiments, mitochondrial diseases, e.g., the mitochondrial myopathy, that may be treated with a compound of Formula (I) or Formula (II) or a

pharmaceutically acceptable salt, co-crystal, solvate, hydrate, tautomer, ester, N-oxide or stereoisomer thereof include, e.g., Barth syndrome, chronic progressive external

ophthalmoplegia (cPEO), Kearns-Sayre syndrome (KSS), Leigh syndrome (e.g., MILS, or maternally inherited Leigh syndrome), mitochondrial DNA depletion syndromes (MDDS, e.g., Alpers syndrome), mitochondrial encephalomyopathy (e.g., mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS)), mitochondrial neurogastrointestinal encephalomyopathy (MNGIE), myoclonus epilepsy with ragged red fibers (MERRF), neuropathy, ataxia, retinitis pigmentosa (NARP), Leber's hereditary optic neuropathy (LHON), and Pearson syndrome.

In some embodiments, the compound of Formula (I) or Formula (II) or a

pharmaceutically acceptable salt, co-crystal, solvate, hydrate, tautomer, ester, N-oxide or stereoisomer thereof is used to treat a mitochondrial disease described herein by decreasing or eliminating a symptom of the disease. In some embodiments, the compound of Formula (I) or Formula (II) or a pharmaceutically acceptable salt, co-crystal, solvate, hydrate, tautomer, ester, N-oxide or stereoisomer thereof may be used as a single agent in a composition or in combination with another agent in a composition to treat a mitochondrial disease described herein.

Hearing Loss

In some embodiments, the compound of Formula (I) or Formula (II) or a

pharmaceutically acceptable salt, co-crystal, solvate, hydrate, tautomer, ester, N-oxide or stereoisomer thereof is used to treat hearing loss. As used herein, the term "hearing loss" or "hearing loss condition" may broadly encompass any damage to the auditory systems, organs, and cells or any impairment of an animal subject's ability to hear sound, as measured by standard methods and assessments known in the art, for example otoacoustic emission testing, pure tone testing, and auditory brainstem response testing. Exemplary hearing loss conditions that may be treated with a compound of Formula (I) or Formula (II), or a pharmaceutically acceptable salt, co-crystal, solvate, hydrate, tautomer, ester, N-oxide or stereoisomer thereof include, but are not limited to, mitochondrial nonsyndromic hearing loss and deafness, hair cell death, age-related hearing loss, noise-induced hearing loss, genetic or inherited hearing loss, hearing loss experienced as a result of ototoxic exposure, hearing loss resulting from disease, and hearing loss resulting from trauma. In some embodiments, mitochondrial nonsyndromic hearing loss and deafness is a MT-RNR1 -related hearing loss. In some embodiments, the MT-RNR1 -related hearing loss is the result of amino glycoside ototoxicity. In some embodiments, mitochondrial nonsyndromic hearing loss and deafness is a MT-TS1 -related hearing loss. In some

embodiments, mitochondrial nonsyndromic hearing loss and deafness is characterized by sensorineural hearing loss. In some embodiments, the compound of Formula (I) or Formula (II) or a

pharmaceutically acceptable salt, co-crystal, solvate, hydrate, tautomer, ester, N-oxide or stereoisomer thereof is used to treat a hearing loss condition described herein by decreasing or eliminating a symptom of the disease. In some embodiments, the compound of Formula (I) or Formula (II) or a pharmaceutically acceptable salt, co-crystal, solvate, hydrate, tautomer, ester, N-oxide or stereoisomer thereof may be used as a single agent in a composition or in combination with another agent in a composition to treat a hearing loss condition described herein.

Ocular Disease In some embodiments, the compound of Formula (I) or Formula (II) or a

pharmaceutically acceptable salt, co-crystal, solvate, hydrate, tautomer, ester, N-oxide or stereoisomer thereof is used to treat eye disease. As used herein, the term "ocular disease" may refer to a disease or condition in which the function of a subject's eye becomes impaired.

Exemplary ocular diseases and conditions that may be treated with a compound of Formula (I) or Formula (II), or a pharmaceutically acceptable salt, co-crystal, solvate, hydrate, tautomer, ester, N-oxide or stereoisomer thereof include cataracts, glaucoma, endoplasmic reticulum (ER) stress, autophagy deficiency, age-related macular degeneration (AMD), or diabetic retinopathy.

In some embodiments, the compound of Formula (I) or Formula (II) or a

pharmaceutically acceptable salt, co-crystal, solvate, hydrate, tautomer, ester, N-oxide or stereoisomer thereof is used to treat an ocular disease or condition described herein by decreasing or eliminating a symptom of the disease. In some embodiments, the compound of Formula (I) or Formula (II) or a pharmaceutically acceptable salt, co-crystal, solvate, hydrate, tautomer, ester, N-oxide or stereoisomer thereof may be used as a single agent in a composition or in combination with another agent in a composition to treat an ocular disease or condition described herein.

Kidney Diseases

In some embodiments, the compound of Formula (I) or Formula (II) or a

pharmaceutically acceptable salt, co-crystal, solvate, hydrate, tautomer, ester, N-oxide or stereoisomer thereof is used to treat kidney disease. As used herein, the term "kidney disease" may refer to a disease or condition in which the function of a subject's kidneys becomes impaired. Exemplary kidney diseases that may be treated with a compound of Formula (I) or Formula (II), or a pharmaceutically acceptable salt, co-crystal, solvate, hydrate, tautomer, ester, N-oxide or stereoisomer thereof include Abderhalden-Kaufmann-Lignac syndrome

(Nephropathic Cystinosis), Abdominal Compartment Syndrome, Acetaminophen-induced Nephrotoxicity, Acute Kidney Failure/ Acute Kidney Injury, Acute Lobar Nephronia, Acute Phosphate Nephropathy, Acute Tubular Necrosis, Adenine Phosphoribosyltransferase

Deficiency, Adenovirus Nephritis, Alagille Syndrome, Alport Syndrome, Amyloidosis, ANCA Vasculitis Related to Endocarditis and Other Infections, Angiomyolipoma, Analgesic

Nephropathy, Anorexia Nervosa and Kidney Disease, Angiotensin Antibodies and Focal Segmental Glomerulosclerosis, Antiphospholipid Syndrome, Anti-TNF-a Therapy-related Glomerulonephritis, APOL1 Mutations, Apparent Mineralocorticoid Excess Syndrome, Aristolochic Acid Nephropathy, Chinese Herbal Nephropathy, Balkan Endemic Nephropathy, Arteriovenous Malformations and Fistulas of the Urologic Tract, Autosomal Dominant Hypocalcemia, Bardet-Biedl Syndrome, Bartter Syndrome, Bath Salts and Acute Kidney Injury, Beer Potomania, Beeturia, β-Thalassemia Renal Disease, Bile Cast Nephropathy, BK Polyoma Virus Nephropathy in the Native Kidney, Bladder Rupture, Bladder Sphincter Dyssynergia, Bladder Tamponade, Border-Crossers' Nephropathy, Bourbon Virus and Acute Kidney Injury, Burnt Sugarcane Harvesting and Acute Renal Dysfunction, Byetta and Renal Failure, Clq Nephropathy, C3 Glomerulopathy, C3 Glomerulopathy with Monoclonal Gammopathy, C4 Glomerulopathy, Calcineurin Inhibitor Nephrotoxicity, Callilepsis Laureola Poisoning, Cannabinoid Hyperemesis Acute Renal Failure, Cardiorenal syndrome, Carfilzomib-Indiced Renal Injury, CFHR5 nephropathy, Charcot-Marie-Tooth Disease with Glomerulopathy, Chinese Herbal Medicines and Nephrotoxicity, Cherry Concentrate and Acute Kidney Injury, Cholesterol Emboli, Churg-Strauss syndrome, Chyluria, Ciliopathy, Cocaine and the Kidney, Cold Diuresis, Colistin Nephrotoxicity, Collagenofibrotic Glomerulopathy, Collapsing

Glomerulopathy, Collapsing Glomerulopathy Related to CMV, Combination Antiretroviral (cART) Related-Nephropathy, Congenital Anomalies of the Kidney and Urinary Tract

(CAKUT), Congenital Nephrotic Syndrome, Congestive Renal Failure, Conorenal syndrome (Mainzer-Saldino Syndrome or Saldino-Mainzer Disease), Contrast Nephropathy, Copper Sulphate Intoxication, Cortical Necrosis, Crizotinib-related Acute Kidney Injury,

Cryocrystalglobulinemia, Cryoglobuinemia, Crystalglobulin-Induced Nephropathy, Crystal- Induced Acute Kidney injury, Crystal-Storing Histiocytosis, Cystic Kidney Disease, Acquired, Cystinuria, Dasatinib-Induced Nephrotic-Range Proteinuria, Dense Deposit Disease (MPGN Type 2), Dent Disease (X-linked Recessive Nephrolithiasis), DHA Crystalline Nephropathy, Dialysis Disequilibrium Syndrome, Diabetes and Diabetic Kidney Disease, Diabetes Insipidus, Dietary Supplements and Renal Failure, Diffuse Mesangial Sclerosis, Diuresis, Djenkol Bean Poisoning (Djenkolism), Down Syndrome and Kidney Disease, Drugs of Abuse and Kidney Disease, Duplicated Ureter, EAST syndrome, Ebola and the Kidney, Ectopic Kidney, Ectopic Ureter, Edema, Swelling, Erdheim-Chester Disease, Fabry's Disease, Familial Hypocalciuric Hypercalcemia, Fanconi Syndrome, Fraser syndrome, Fibronectin Glomerulopathy, Fibrillary Glomerulonephritis and Immunotactoid Glomerulopathy, Fraley syndrome, Fluid Overload, Hypervolemia, Focal Segmental Glomerulosclerosis, Focal Sclerosis, Focal Glomerulosclerosis, Galloway Mowat syndrome, Giant Cell (Temporal) Arteritis with Kidney Involvement, Gestational Hypertension, Gitelman Syndrome, Glomerular Diseases, Glomerular Tubular Reflux, Glycosuria, Goodpasture Syndrome, Green Smoothie Cleanse Nephropathy, HANAC Syndrome, Harvoni (Ledipasvir with Sofosbuvir)-Induced Renal Injury, Hair Dye Ingestion and Acute Kidney Injury, Hantavirus Infection Podocytopathy, Heat Stress Nephropathy, Hematuria (Blood in Urine), Hemolytic Uremic Syndrome (HUS), Atypical Hemolytic Uremic Syndrome (aHUS), Hemophagocytic Syndrome, Hemorrhagic Cystitis, Hemorrhagic Fever with Renal Syndrome (HFRS, Hantavirus Renal Disease, Korean Hemorrhagic Fever, Epidemic

Hemorrhagic Fever, Nephropathis Epidemica), Hemosiderinuria, Hemosiderosis related to Paroxysmal Nocturnal Hemoglobinuria and Hemolytic Anemia, Hepatic Glomerulopathy, Hepatic Veno-Occlusive Disease, Sinusoidal Obstruction Syndrome, Hepatitis C-Associated Renal Disease, Hepatocyte Nuclear Factor Ιβ-Associated Kidney Disease, Hepatorenal Syndrome, Herbal Supplements and Kidney Disease, High Altitude Renal Syndrome, High Blood Pressure and Kidney Disease, HIV-Associated Immune Complex Kidney Disease (HIVICK), HIV-Associated Nephropathy (HIVAN), HNFlB-related Autosomal Dominant Tubulointerstitial Kidney Disease, Horseshoe Kidney (Renal Fusion), Hunner's Ulcer,

Hydroxychloroquine-induced Renal Phospholipidosis, Hyperaldosteronism, Hypercalcemia, Hyperkalemia, Hypermagnesemia, Hypernatremia, Hyperoxaluria, Hyperphosphatemia, Hypocalcemia, Hypocomplementemic Urticarial Vasculitic Syndrome, Hypokalemia,

Hypokalemia-induced renal dysfunction, Hypokalemic Periodic Paralysis, Hypomagnesemia, Hyponatremia, Hypophosphatemia, Hypophosphatemia in Users of Cannabis, Hypertension, Hypertension, Monogenic, Iced Tea Nephropathy, Ifosfamide Nephrotoxicity, IgA Nephropathy, IgG4 Nephropathy, Immersion Diuresis, Immune-Checkpoint Therapy-Related Interstitial Nephritis, Infliximab-Related Renal Disease, Interstitial Cystitis, Painful Bladder Syndrome (Questionnaire), Interstitial Nephritis, Interstitial Nephritis, Karyomegalic, Ivemark's syndrome, JC Virus Nephropathy, Joubert Syndrome, Ketamine-Associated Bladder Dysfunction, Kidney Stones, Nephrolithiasis, Kombucha Tea Toxicity, Lead Nephropathy and Lead-Related

Nephrotoxicity, Lecithin Cholesterol Acyltransferase Deficiency (LCAT Deficiency),

Leptospirosis Renal Disease, Light Chain Deposition Disease, Monoclonal Immunoglobulin Deposition Disease, Light Chain Proximal Tubulopathy, Liddle Syndrome, Lightwood-Albright Syndrome, Lipoprotein Glomerulopathy, Lithium Nephrotoxicity, LMX1B Mutations Cause Hereditary FSGS, Loin Pain Hematuria, Lupus, Systemic Lupus Erythematosis, Lupus Kidney Disease, Lupus Nephritis, Lupus Nephritis with Antineutrophil Cytoplasmic Antibody

Seropositivity, Lupus Podocytopathy, Lyme Disease-Associated Glomerulonephritis, Lysinuric Protein Intolerance, Lysozyme Nephropathy, Malarial Nephropathy, Malignancy-Associated Renal Disease, Malignant Hypertension, Malakoplakia, McKittrick-Wheelock Syndrome, MDMA (Molly; Ecstacy; 3,4-Methylenedioxymethamphetamine) and Kidney Failure, Meatal Stenosis, Medullary Cystic Kidney Disease, Urolodulin-Associated Nephropathy, Juvenile

Hyperuricemic Nephropathy Type 1 , Medullary Sponge Kidney, Megaureter, Melamine Toxicity and the Kidney, MELAS Syndrome, Membranoproliferative Glomerulonephritis, Membranous Nephropathy, Membranous-like Glomerulopathy with Masked IgG Kappa Deposits,

MesoAmerican Nephropathy, Metabolic Acidosis, Metabolic Alkalosis, Methotrexate-related Renal Failure, Microscopic Polyangiitis, Milk-alkalai syndrome, Minimal Change Disease,

Monoclonal Gammopathy of Renal Significance, Dysproteinemia, Mouthwash Toxicity, MUCl Nephropathy, Multicystic dysplastic kidney, Multiple Myeloma, Myeloproliferative Neoplasms and Glomerulopathy, Nail-patella Syndrome, NARP Syndrome, Nephrocalcinosis, Nephrogenic Systemic Fibrosis, Nephroptosis (Floating Kidney, Renal Ptosis), Nephrotic Syndrome, Neurogenic Bladder, 9/11 and Kidney Disease, Nodular Glomerulosclerosis, Non-Gonococcal Urethritis, Nutcracker syndrome, Oligomeganephronia, Orofaciodigital Syndrome, Orotic Aciduria, Orthostatic Hypotension, Orthostatic Proteinuria, Osmotic Diuresis, Osmotic

Nephrosis, Ovarian Hyperstimulation Syndrome, Oxalate Nephropathy, Page Kidney, Papillary Necrosis, Papillorenal Syndrome (Renal-Coloboma Syndrome, Isolated Renal Hypoplasia), PARN Mutations and Kidney Disease, Parvovirus B 19 and the Kidney, The Peritoneal-Renal Syndrome, POEMS Syndrome, Posterior Urethral Valve, Podocyte Infolding Glomerulopathy, Post-infectious Glomerulonephritis, Post-streptococcal Glomerulonephritis, Post-infectious Glomerulonephritis, Atypical, Post-Infectious Glomerulonephritis (IgA-Dominant), Mimicking IgA Nephropathy, Polyarteritis Nodosa, Polycystic Kidney Disease, Posterior Urethral Valves, Post-Obstructive Diuresis, Preeclampsia, Propofol infusion syndrome, Proliferative

Glomerulonephritis with Monoclonal IgG Deposits (Nasr Disease), Propolis (Honeybee Resin) Related Renal Failure, Proteinuria (Protein in Urine), Pseudohyperaldosteronism,

Pseudohypobicarbonatemia, Pseudohypoparathyroidism, Pulmonary-Renal Syndrome,

Pyelonephritis (Kidney Infection), Pyonephrosis, Pyridium and Kidney Failure, Radiation Nephropathy, Ranolazine and the Kidney, Refeeding syndrome, Reflux Nephropathy, Rapidly Progressive Glomerulonephritis, Renal Abscess, Peripnephric Abscess, Renal Agenesis, Renal Arcuate Vein Microthrombi- Associated Acute Kidney Injury, Renal Artery Aneurysm, Renal Artery Dissection, Spontaneous, Renal Artery Stenosis, Renal Cell Cancer, Renal Cyst, Renal Hypouricemia with Exercise-induced Acute Renal Failure, Renal Infarction, Renal

Osteodystrophy, Renal Tubular Acidosis, Renin Mutations and Autosomal Dominant

Tubulointerstitial Kidney Disease, Renin Secreting Tumors (Juxtaglomerular Cell Tumor), Reset Osmostat, Retrocaval Ureter, Retroperitoneal Fibrosis, Rhabdomyolysis, Rhabdomyolysis related to Bariatric Sugery, Rheumatoid Arthritis-Associated Renal Disease, Sarcoidosis Renal Disease, Salt Wasting, Renal and Cerebral, Schistosomiasis and Glomerular Disease, Schimke immuno-osseous dysplasia, Scleroderma Renal Crisis, Serpentine Fibula-Polycystic Kidney Syndrome, Exner Syndrome, Sickle Cell Nephropathy, Silica Exposure and Chronic Kidney Disease, Sri Lankan Farmers' Kidney Disease, Sjogren's Syndrome and Renal Disease, Synthetic Cannabinoid Use and Acute Kidney Injury, Kidney Disease Following Hematopoietic Cell

Transplantation, Kidney Disease Related to Stem Cell Transplantation, TAFRO Syndrome, Tea and Toast Hyponatremia, Tenofovir-Induced Nephrotoxicity, Thin Basement Membrane Disease, Benign Familial Hematuria, Thrombotic Microangiopathy Associated with Monoclonal Gammopathy, Trench Nephritis, Trigonitis, Tuberculosis, Genitourinary, Tuberous Sclerosis, Tubular Dysgenesis, Immune Complex Tubulointerstitial Nephritis Due to Autoantibodies to the Proximal Tubule Brush Border, Tumor Lysis Syndrome, Uremia, Uremic Optic Neuropathy, Ureteritis Cystica, Ureterocele, Urethral Caruncle, Urethral Stricture, Urinary Incontinence, Urinary Tract Infection, Urinary Tract Obstruction, Urogenital Fistula, Uromodulin-Associated Kidney Disease, Vancomycin- Associated Cast Nephropathy, Vasomotor Nephropathy,

Vesicointestinal Fistula, Vesicoureteral Reflux, VGEF Inhibition and Renal Thrombotic

Microangiopathy, Volatile Anesthetics and Acute Kidney Injury, Von Hippel-Lindau Disease, Waldenstrom's Macroglobulinemic Glomerulonephritis, Warfarin-Related Nephropathy, Wasp Stings and Acute Kidney Injury, Wegener's Granulomatosis, Granulomatosis with Polyangiitis, West Nile Virus and Chronic Kidney Disease, Wunderlich syndrome, Zellweger Syndrome, or Cerebrohepatorenal Syndrome.

In some embodiments, the compound of Formula (I) or Formula (II) or a

pharmaceutically acceptable salt, co-crystal, solvate, hydrate, tautomer, ester, N-oxide or stereoisomer thereof is used to treat a kidney disease described herein by decreasing or eliminating a symptom of the disease. In some embodiments, the compound of Formula (I) or Formula (II) or a pharmaceutically acceptable salt, co-crystal, solvate, hydrate, tautomer, ester, N-oxide or stereoisomer thereof may be used as a single agent in a composition or in combination with another agent in a composition to treat a kidney disease described herein.

Skin Diseases

In some embodiments, the compound of Formula (I) or Formula (II) or a

pharmaceutically acceptable salt, co-crystal, solvate, hydrate, tautomer, ester, N-oxide or stereoisomer thereof is used to treat a skin disease. As used herein, the term "skin disease" may refer to a disease or condition affecting the skin. Exemplary skin diseases that may be treated with a compound of Formula (I) or Formula (II), or a pharmaceutically acceptable salt, co- crystal, solvate, hydrate, tautomer, ester, N-oxide or stereoisomer thereof include acne, alopecia areata, basal cell carcinoma, Bowen's disease, congenital erythropoietic porphyria, contact dermatitis, Darier's disease, disseminated superficial actinic porokeratosis, dystrophic epidermolysis bullosa, eczema (atopic eczema), extra-mammary Paget's disease, epidermolysis bullosa simplex, erythropoietic protoporphyria, fungal infections of nails, Hailey-Hailey disease, herpes simplex, hidradenitis suppurativa, hirsutism, hyperhidrosis, ichthyosis, impetigo, keloids, keratosis pilaris, lichen planus, lichen sclerosus, melanoma, melasma, mucous membrane pemphigoid, pemphigoid, pemphigus vulgaris, pityriasis lichenoides, pityriasis rubra pilaris, plantar warts (verrucas), polymorphic light eruption, psoriasis, plaque psoriasis, pyoderma gangrenosum, rosacea, scabies, scleroderma, shingles, squamous cell carcinoma, sweet's syndrome, urticaria and angioedema and vitiligo.

In some embodiments, the compound of Formula (I) or Formula (II) or a

pharmaceutically acceptable salt, co-crystal, solvate, hydrate, tautomer, ester, N-oxide or stereoisomer thereof is used to treat a skin disease described herein by decreasing or eliminating a symptom of the disease. In some embodiments, the compound of Formula (I) or Formula (II) or a pharmaceutically acceptable salt, co-crystal, solvate, hydrate, tautomer, ester, N-oxide or stereoisomer thereof may be used as a single agent in a composition or in combination with another agent in a composition to treat a skin disease described herein.

Fibrotic Diseases In some embodiments, the compound of Formula (I) or Formula (II) or a

pharmaceutically acceptable salt, co-crystal, solvate, hydrate, tautomer, ester, N-oxide or stereoisomer thereof is used to treat a fibrotic disease. As used herein, the term "fibrotic disease" may refer to a disease or condition that is defined by the accumulation of excess extracellular matrix components. Exemplary fibrotic diseases that may be treated with a compound of Formula (I) or Formula (II), or a pharmaceutically acceptable salt, co-crystal, solvate, hydrate, tautomer, ester, N-oxide or stereoisomer thereof include adhesive capsulitis, arterial stiffness, arthrofibrosis, atrial fibrosis, cardiac fibrosis, cirrhosis, congenital hepatic fibrosis, Crohn's disease, cystic fibrosis, Dupuytren's contracture, endomyocardial fibrosis, glial scar, hepatitis C, hypertrophic cardiomyopathy, hypersensitivity pneumonitis, idiopathic pulmonary fibrosis, idiopathic interstitial pneumonia, interstitial lung disease, keloid, mediastinal fibrosis, myelofibrosis, nephrogenic systemic fibrosis, non-alcoholic fatty liver disease, old myocardial infarction, Peyronie's disease, pneumoconiosis, pneumonitis, progressive massive fibrosis, pulmonary fibrosis, radiation-induced lung injury, retroperitoneal fibrosis, scleroderma/systemic sclerosis, silicosis and ventricular remodeling. In some embodiments, the compound of Formula (I) or Formula (II) or a

pharmaceutically acceptable salt, co-crystal, solvate, hydrate, tautomer, ester, N-oxide or stereoisomer thereof is used to treat a fibrotic disease described herein by decreasing or eliminating a symptom of the disease. In some embodiments, the compound of Formula (I) or Formula (II) or a pharmaceutically acceptable salt, co-crystal, solvate, hydrate, tautomer, ester, N-oxide or stereoisomer thereof may be used as a single agent in a composition or in combination with another agent in a composition to treat a fibrotic disease described herein.

Hemoglobin Disorders

In some embodiments, the compound of Formula (I) or Formula (II) or a

pharmaceutically acceptable salt, co-crystal, solvate, hydrate, tautomer, ester, N-oxide or stereoisomer thereof is used to treat a hemoglobin disease. As used herein, the terms

"hemoglobin disease" or "hemoglobin disorder" may refer to a disease or condition characterized by an abnormal production or structure of the hemoglobin protein. Exemplary hemoglobin diseases that may be treated with a compound of Formula (I) or Formula (II), or a

pharmaceutically acceptable salt, co-crystal, solvate, hydrate, tautomer, ester, N-oxide or stereoisomer thereof include "dominant" β-thalassemia, acquired (toxic) methemoglobinemia, carboxyhemoglobinemia, congenital Heinz body hemolytic anemia, HbH disease, HbS/β- thalassemia, HbE^-thalassemia, HbSC disease, homozygous a ⁺ -thalassemia (phenotype of a°- thalassemia), Hydrops fetalis with Hb Bart's, sickle cell anemia/disease, sickle cell trait, sickle β- thalassemia disease, a ⁺ -thalassemia, a°-thalassemia, a- Thalassemia associated with

myelodysplastic syndromes, a-Thalassemia with mental retardation syndrome (ATR), β°- Thalassemia, ⁺ -Thalassemia, δ-Thalassemia, γ-Thalassemia, β-Thalassemia major, β- Thalassemia intermedia, δβ-Thalassemia, and εγδβ-Thalassemia.

In some embodiments, the compound of Formula (I) or Formula (II) or a

pharmaceutically acceptable salt, co-crystal, solvate, hydrate, tautomer, ester, N-oxide or stereoisomer thereof is used to treat a hemoglobin disease described herein by decreasing or eliminating a symptom of the disease. In some embodiments, the compound of Formula (I) or Formula (II) or a pharmaceutically acceptable salt, co-crystal, solvate, hydrate, tautomer, ester, N-oxide or stereoisomer thereof may be used as a single agent in a composition or in combination with another agent in a composition to treat a hemoglobin disease described herein.

Autoimmune Diseases

In some embodiments, the compound of Formula (I) or Formula (II) or a

pharmaceutically acceptable salt, co-crystal, solvate, hydrate, tautomer, ester, N-oxide or stereoisomer thereof is used to treat an autoimmune disease. As used herein, the term

"autoimmune disease" may refer to a disease or condition in which the immune system of a subject attacks and damages the tissues of said subject. Exemplary kidney diseases that may be treated with a compound of Formula (I) or Formula (II), or a pharmaceutically acceptable salt, co-crystal, solvate, hydrate, tautomer, ester, N-oxide or stereoisomer thereof include Achalasia, Addison's disease, Adult Still's disease, Agammaglobulinemia, Alopecia areata, Amyloidosis, Ankylosing spondylitis, Anti-GBM/Anti-TBM nephritis, Antiphospholipid syndrome,

Autoimmune angioedema, Autoimmune dysautonomia, Autoimmune encephalomyelitis, Autoimmune hepatitis, Autoimmune inner ear disease (AIED), Autoimmune myocarditis, Autoimmune oophoritis, Autoimmune orchitis, Autoimmune pancreatitis, Autoimmune retinopathy, Autoimmune urticaria, Axonal & neuronal neuropathy (AMAN), Balo disease, Behcet's disease, Benign mucosal pemphigoid, Bullous pemphigoid, Castleman disease (CD), Celiac disease, Chagas disease, Chronic inflammatory demyelinating polyneuropathy (CIDP), Chronic recurrent multifocal osteomyelitis (CRMO), Churg-Strauss Syndrome (CSS) or Eosinophilic Granulomatosis (EGPA), Cicatricial pemphigoid, Cogan's syndrome, Cold agglutinin disease, Congenital heart block, Coxsackie myocarditis, CREST syndrome, Crohn's disease, Dermatitis herpetiformis, Dermatomyositis, Devic's disease (neuromyelitis optica), Discoid lupus, Dressier' s syndrome, Endometriosis, Eosinophilic esophagitis (EoE),

Eosinophilic fasciitis, Erythema nodosum, Essential mixed cryoglobulinemia, Evans syndrome, Fibromyalgia, Fibrosing alveolitis, Giant cell arteritis (temporal arteritis), Giant cell myocarditis, Glomerulonephritis, Goodpasture's syndrome, Granulomatosis with Polyangiitis, Graves' disease, Guillain-Barre syndrome, Hashimoto's thyroiditis, Hemolytic anemia, Henoch- Schonlein purpura (HSP), Herpes gestationis or pemphigoid gestationis (PG), Hidradenitis

Suppurativa (HS) (Acne Inversa), Hypogammaglobulinemia, IgA Nephropathy, IgG4-related sclerosing disease, Immune thrombocytopenic purpura (ITP), Inclusion body myositis (IBM), Interstitial cystitis (IC), Juvenile arthritis, Juvenile diabetes (Type 1 diabetes), Juvenile myositis (JM), Kawasaki disease, Lambert-Eaton syndrome, Leukocytoclastic vasculitis, Lichen planus, Lichen sclerosus, Ligneous conjunctivitis, Linear IgA disease (LAD), Lupus, Lyme disease chronic, Meniere's disease, Microscopic polyangiitis (MP A), Mixed connective tissue disease (MCTD), Mooren's ulcer, Mucha-Habermann disease, Multifocal Motor Neuropathy (MMN) or MMNCB, Multiple sclerosis, Myasthenia gravis, Myositis, Narcolepsy, Neonatal Lupus, Neuromyelitis optica, Neutropenia, Ocular cicatricial pemphigoid, Optic neuritis, Palindromic rheumatism (PR), PANDAS, Paraneoplastic cerebellar degeneration (PCD), Paroxysmal nocturnal hemoglobinuria (PNH), Parry Romberg syndrome, Pars planitis (peripheral uveitis), Parsonnage-Turner syndrome,, Pemphigus, Peripheral neuropathy, Perivenous

encephalomyelitis, Pernicious anemia (PA), POEMS syndrome, Polyarteritis nodosa,

Polyglandular syndrome type I, Polyglandular syndrome type II, Polyglandular syndrome type III, Polymyalgia rheumatica, Polymyositis, Postmyocardial infarction syndrome,

Postpericardiotomy syndrome, Primary biliary cirrhosis, Primary sclerosing cholangitis, Progesterone dermatitis, Psoriasis, Psoriatic arthritis, Pure red cell aplasia (PRCA), Pyoderma gangrenosum, Raynaud's phenomenon, Reactive Arthritis, Reflex sympathetic dystrophy, Relapsing polychondritis, Restless legs syndrome (RLS), Retroperitoneal fibrosis, Rheumatic fever, Rheumatoid arthritis, Sarcoidosis, Schmidt syndrome, Scleritis, Scleroderma, Sjogren's syndrome, Sperm & testicular autoimmunity, Stiff person syndrome (SPS), Subacute bacterial endocarditis (SBE), Susac's syndrome, Sympathetic ophthalmia (SO), Takayasu's arteritis, Temporal arteritis/Giant cell arteritis, Thrombocytopenic purpura (TTP), Tolosa-Hunt syndrome (THS), Transverse myelitis, Type 1 diabetes, Ulcerative colitis (UC), Undifferentiated connective tissue disease (UCTD), Uveitis, Vasculitis, Vitiligo, Vogt-Koyanagi-Harada Disease, and Wegener's granulomatosis (or Granulomatosis with Polyangiitis (GPA)).

In some embodiments, the compound of Formula (I) or Formula (II) or a

pharmaceutically acceptable salt, co-crystal, solvate, hydrate, tautomer, ester, N-oxide or stereoisomer thereof is used to treat an autoimmune disease described herein by decreasing or eliminating a symptom of the disease. In some embodiments, the compound of Formula (I) or Formula (II) or a pharmaceutically acceptable salt, co-crystal, solvate, hydrate, tautomer, ester, N-oxide or stereoisomer thereof may be used as a single agent in a composition or in combination with another agent in a composition to treat an autoimmune disease described herein.

Viral Infections

In some embodiments, the compound of Formula (I) or Formula (II) or a

pharmaceutically acceptable salt, co-crystal, solvate, hydrate, tautomer, ester, N-oxide or stereoisomer thereof is used to treat a viral infection. Exemplary viral infections that may be treated with a compound of Formula (I) or Formula (II), or a pharmaceutically acceptable salt, co-crystal, solvate, hydrate, tautomer, ester, N-oxide or stereoisomer thereof include influenza, human immunodeficiency virus (HIV) and herpes.

In some embodiments, the compound of Formula (I) or Formula (II) or a

pharmaceutically acceptable salt, co-crystal, solvate, hydrate, tautomer, ester, N-oxide or stereoisomer thereof is used to treat a viral infection described herein by decreasing or eliminating a symptom of the disease. In some embodiments, the compound of Formula (I) or Formula (II) or a pharmaceutically acceptable salt, co-crystal, solvate, hydrate, tautomer, ester, N-oxide or stereoisomer thereof may be used as a single agent in a composition or in combination with another agent in a composition to treat a viral infection described herein. Malaria Infection

In some embodiments, the compound of Formula (I) or Formula (II) or a

pharmaceutically acceptable salt, co-crystal, solvate, hydrate, tautomer, ester, N-oxide or stereoisomer thereof is used to treat a malaria. As used herein, the term "malaria" may refer to a parasitic disease of protozoan of the Plasmodium genus that causes infection of red blood cells (RBCs). Exemplary forms of malaria infection that may be treated with a compound of Formula (I) or Formula (II), or a pharmaceutically acceptable salt, co-crystal, solvate, hydrate, tautomer, ester, N-oxide or stereoisomer thereof include infection caused by Plasmodium vivax,

Plasmodium ovale, Plasmodium malariae and Plasmodium falciparum. In some embodiments, the malaria infection that may be treated with a compound of Formula (I) or Formula (II), or a pharmaceutically acceptable salt, co-crystal, solvate, hydrate, tautomer, ester, N-oxide or stereoisomer thereof is resistant/recrudescent malaria.

In some embodiments, the compound of Formula (I) or Formula (II) or a

pharmaceutically acceptable salt, co-crystal, solvate, hydrate, tautomer, ester, N-oxide or stereoisomer thereof is used to treat a malaria infection described herein by decreasing or eliminating a symptom of the disease. In some embodiments, the compound of Formula (I) or Formula (II) or a pharmaceutically acceptable salt, co-crystal, solvate, hydrate, tautomer, ester, ^V-oxide or stereoisomer thereof may be used as a single agent in a composition or in combination with another agent in a composition to treat a malaria infection described herein. Diseases with Mutations Leading to Unfolded Protein Response (UPR) Induction

In some embodiments, the compound of Formula (I) or Formula (II) or a

pharmaceutically acceptable salt, co-crystal, solvate, hydrate, tautomer, ester, N-oxide or stereoisomer thereof is used to treat a disease with mutations that leads to UPR induction.

Exemplary disease with mutations that lead to UPR induction include Marinesco-Sjogren syndrome, neuropathic pain, diabetic neuropathic pain, noise induced hearing loss, non- syndromic sensorineural hearing loss, age-related hearing loss, Wolfram syndrome, Darier White disease, Usher syndrome, collagenopathies, Thin basement nephropathy, Alport syndrome, skeletal chondrodysplasia, metaphyseal chondrodysplasia type Schmid, and

Pseudochondrodysplasia. In some embodiments, the compound of Formula (I) or Formula (II) or a

pharmaceutically acceptable salt, co-crystal, solvate, hydrate, tautomer, ester, N-oxide or stereoisomer thereof is used to treat a disease with mutations that leads to UPR induction described herein by decreasing or eliminating a symptom of the disease. In some embodiments, the compound of Formula (I) or Formula (II) or a pharmaceutically acceptable salt, co-crystal, solvate, hydrate, tautomer, ester, N-oxide or stereoisomer thereof may be used as a single agent in a composition or in combination with another agent in a composition to treat a disease with mutations that leads to UPR induction described herein.

Methods of Modulating Protein Production In another aspect, disclosed herein is a method of modulating the expression of eIF2B, eIF2a, a component of the eIF2 pathway, component of the ISR pathway or any combination thereof in a cell, the method comprising contacting the cell with an effective amount of a compound of Formula (I) or Formula (II), or a pharmaceutically acceptable salt, co-crystal, solvate, hydrate, tautomer, ester, N-oxide or stereoisomer thereof, thereby modulating the expression of eIF2B, eIF2a, a component of the eIF2 pathway, component of the ISR pathway or any combination thereof in the cell. In some embodiments, contacting the compound of Formula (I) or Formula (II), or a pharmaceutically acceptable salt, co-crystal, solvate, hydrate, tautomer, ester, N-oxide or stereoisomer thereof with the cell increases the expression of eIF2B, eIF2a, a component of the eIF2 pathway, component of the ISR pathway or any combination thereof in the cell. In some embodiments, contacting the compound of Formula (I) or Formula (II), or a pharmaceutically acceptable salt, co-crystal, solvate, hydrate, tautomer, ester, N-oxide or stereoisomer thereof with the cell decreases the expression of eIF2B, eIF2a, a component of the eIF2 pathway, component of the ISR pathway or any combination thereof in the cell.

In another aspect, disclosed herein is a method of preventing or treating a condition, disease or disorder described herein in a patient in need thereof, the method comprising administering to the patient an effective amount of a compound of Formula (I) or Formula (II), or a pharmaceutically acceptable salt, co-crystal, solvate, hydrate, tautomer, ester, N-oxide or stereoisomer thereof, wherein the compound of Formula (I) or Formula (II), or a

pharmaceutically acceptable salt, co-crystal, solvate, hydrate, tautomer, ester, N-oxide or stereoisomer thereof modulates the expression of eIF2B, eIF2a, a component of the eIF2 pathway, component of the ISR pathway or any combination thereof by the patient's cells, thereby treating the condition, disease or disorder. In some embodiments, the condition, disease or disorder is characterized by aberrant expression of eIF2B, eIF2a, a component of the eIF2 pathway, component of the ISR pathway or any combination thereof by the patient's cells. In some embodiments, the compound of Formula (I) or Formula (II), or a pharmaceutically acceptable salt, co-crystal, solvate, hydrate, tautomer, ester, N-oxide or stereoisomer thereof increases the expression of eIF2B, eIF2a, a component of the eIF2 pathway, component of the ISR pathway or any combination thereof by the patient's cells, thereby treating the condition, disease or disorder. In some embodiments, the compound of Formula (I) or Formula (II), or a pharmaceutically acceptable salt, co-crystal, solvate, hydrate, tautomer, ester, N-oxide or stereoisomer thereof decreases the expression of eIF2B, eIF2a, a component of the eIF2 pathway, component of the ISR pathway or any combination thereof by the patient's cells, thereby treating the condition, disease or disorder.

In another aspect, disclosed herein is a method of modulating the activity of eIF2B, eIF2a, a component of the eIF2 pathway, component of the ISR pathway or any combination thereof in a cell, the method comprising contacting the cell with an effective amount of a compound of Formula (I) or Formula (II), or a pharmaceutically acceptable salt, co-crystal, solvate, hydrate, tautomer, ester, N-oxide or stereoisomer thereof, thereby modulating the activity of eIF2B, eIF2a, a component of the eIF2 pathway, component of the ISR pathway or any combination thereof in the cell. In some embodiments, contacting the compound of Formula (I) or Formula (II), or a pharmaceutically acceptable salt, co-crystal, solvate, hydrate, tautomer, ester, N-oxide or stereoisomer thereof with the cell increases the activity of eIF2B, eIF2a, a component of the eIF2 pathway, component of the ISR pathway or any combination thereof in the cell. In some embodiments, contacting the compound of Formula (I) or Formula (II), or a pharmaceutically acceptable salt, co-crystal, solvate, hydrate, tautomer, ester, N-oxide or stereoisomer thereof with the cell decreases the activity of eIF2B, eIF2a, a component of the eIF2 pathway, component of the ISR pathway or any combination thereof in the cell.

In another aspect, disclosed herein is a method of preventing or treating a condition, disease or disorder described herein in a patient in need thereof, the method comprising administering to the patient an effective amount of a compound of Formula (I) or Formula (II), or a pharmaceutically acceptable salt, co-crystal, solvate, hydrate, tautomer, ester, N-oxide or stereoisomer thereof, wherein the compound of Formula (I) or Formula (II), or a pharmaceutically acceptable salt, co-crystal, solvate, hydrate, tautomer, ester, N-oxide or stereoisomer thereof modulates the activity of eIF2B, eIF2a, a component of the eIF2 pathway, component of the ISR pathway or any combination thereof by the patients cells, thereby treating the condition, disease or disorder. In some embodiments, the condition, disease or disorder is characterized by aberrant activity of eIF2B, eIF2a, a component of the eIF2 pathway, component of the ISR pathway or any combination thereof in the patient's cells. In some embodiments, the compound of Formula (I) or Formula (II), or a pharmaceutically acceptable salt, co-crystal, solvate, hydrate, tautomer, ester, N-oxide or stereoisomer thereof increases the activity of eIF2B, eIF2a, a component of the eIF2 pathway, component of the ISR pathway or any combination thereof in the patient's cells, thereby treating the condition, disease or disorder. In some embodiments, the compound of Formula (I) or Formula (II), or a pharmaceutically acceptable salt, co-crystal, solvate, hydrate, tautomer, ester, N-oxide or stereoisomer thereof decreases the activity of eIF2B, eIF2a, a component of the eIF2 pathway, component of the ISR pathway or any combination thereof in the patient's cells, thereby treating the condition, disease or disorder. In some embodiments, administering an effective amount of a compound of Formula (I) or Formula (II), or a pharmaceutically acceptable salt, co-crystal, solvate, hydrate, tautomer, ester, N-oxide or stereoisomer thereof, wherein the compound of Formula (I) or Formula (II), or a pharmaceutically acceptable salt, co-crystal, solvate, hydrate, tautomer, ester, N-oxide or stereoisomer thereof modulates both the expression and the activity of eIF2B, eIF2a, a component of the eIF2 pathway, component of the ISR pathway or any combination thereof in the patients cells, thereby treating the condition, disease or disorder.

In some embodiments, the compound of Formula (I) or Formula (II) is chemically modified, prior to (ex vivo) or after (in vivo) contacting with a cell, forming a biologically active compound that modulates the expression and/or activity of eIF2B, eIF2a, a component of the eIF2 pathway, component of the ISR pathway or any combination thereof in the cell. In some embodiments, the compound of Formula (I) or Formula (II) is metabolized by the patient forming a biologically active compound that modulates the expression and/or activity of eIF2B, eIF2a, a component of the eIF2 pathway, component of the ISR pathway or any combination thereof in the patients cells, thereby treating a condition, disease or disorder disclosed herein. In some embodiments, the biologically active compound is the compound of formula (II). In one aspect, disclosed herein is a method of treating a disease related to a modulation of eIF2B activity or levels, eIF2a activity or levels, or the activity or levels of a component of the eIF2 pathway or the ISR pathway in a patient in need thereof, comprising administering to the patient an effective amount of a compound of Formula (I) or Formula (II). In some

embodiments, the modulation comprises an increase in eIF2B activity or levels, increase in eIF2a activity or levels, or increase in activity or levels of a component of the eIF2 pathway or the ISR pathway. In some embodiments, the disease may be caused by a mutation to a gene or protein sequence related to a member of the eIF2 pathway (e.g., the eIF2a signaling pathway).

Methods of Increasing Protein Activity and Production In another aspect, the compound of Formula (I) or Formula (II), or a pharmaceutically acceptable salt, co-crystal, solvate, hydrate, tautomer, ester, N-oxide or stereoisomer thereof may be useful in applications where increasing production output of eIF2B, eIF2a, a component of the eIF2 pathway, a component of the ISR pathway or any combination thereof is desirable, such as in vitro cell free systems for protein production. In some embodiments, the present invention features a method of increasing expression of eIF2B, eIF2a, a component of the eIF2 pathway, a component of the ISR pathway or any combination thereof by a cell or in vitro expression system, the method comprising contacting the cell or in vitro expression system with an effective amount of a compound of Formula (I) or Formula (II), or a pharmaceutically acceptable salt, co-crystal, solvate, hydrate, tautomer, ester, N-oxide or stereoisomer thereof. In some embodiments, the method is a method of increasing the expression of eIF2B, eIF2a, a component of the eIF2 pathway, a component of the ISR pathway or any combination thereof by a cell comprising contacting the cell with an effective amount of a compound described herein (e.g., the compound of Formula (I) or Formula (II), or a

pharmaceutically acceptable salt, co-crystal, solvate, hydrate, tautomer, ester, N-oxide or stereoisomer thereof). In other embodiments, the method is a method of increasing the expression of eIF2B, eIF2a, a component of the eIF2 pathway, a component of the ISR pathway or any combination thereof by an in vitro protein expression system comprising contacting the in vitro expression system with a compound described herein (e.g. the compound of Formula (I) or Formula (II), or a pharmaceutically acceptable salt, co-crystal, solvate, hydrate, tautomer, ester, N-oxide or stereoisomer thereof). In some embodiments, contacting the cell or in vitro expression system with an effective amount of a compound of Formula (I) or Formula (II), or a pharmaceutically acceptable salt, co-crystal, solvate, hydrate, tautomer, ester, N-oxide or stereoisomer thereof increases expression of eIF2B, eIF2a, a component of the eIF2 pathway, a component of the ISR pathway or any combination thereof in the cell or in vitro expression system by about 1%, about 2%, about 3%, about 4%, about 5%, about 6%, about 7%, about 8%, about 9%, about 10%, about 15%, about 20%, about 25%, about 30%, about 40%, about 45%, about 50%, about 60%, about 65%, about 70%, about 75%, about 80%, about 85%, about 90%, about 95%, or about 100%. In some embodiments, contacting the cell or in vitro expression system with an effective amount of a compound of Formula (I) or Formula (II), or a

pharmaceutically acceptable salt, co-crystal, solvate, hydrate, tautomer, ester, N-oxide or stereoisomer thereof increases expression of eIF2B, eIF2a, a component of the eIF2 pathway, a component of the ISR pathway or any combination thereof in the cell or in vitro expression system by about 1-fold, about 2-fold, about 3-fold, about 4-fold, about 5-fold, about 6-fold, about 7-fold, about 8-fold, about 9-fold, about 10-fold, about 20-fold, about 30-fold, about 40- fold, about 50-fold, about 60-fold, about 70-fold, about 80-fold, about 90-fold, about 100-fold, about 200-fold, about 300-fold, about 400-fold, about 500-fold, about 600-fold about 700-fold, about 800-fold, about 900-fold, about 1000-fold, about 10000-fold, about 100000-fold, or about 1000000-fold.

In some embodiments, the present invention features a method of increasing the expression of eIF2B, eIF2a, a component of the eIF2 pathway, a component of the ISR pathway or any combination thereof by a patient cells, the method comprising administering to the patient an effective amount of a compound of Formula (I) or Formula (II), or a pharmaceutically acceptable salt, co-crystal, solvate, hydrate, tautomer, ester, N-oxide or stereoisomer thereof, wherein the patient has been diagnosed with a disease, disorder, or condition disclosed herein and wherein the disease, disorder or condition is characterized by aberrant expression of eIF2B, eIF2a, a component of the eIF2 pathway, a component of the ISR pathway or any combination thereof (e.g., a leukodystrophy, a leukoencephalopathy, a hypomyelinating or demyelinating disease, muscle-wasting disease, or sarcopenia). In some embodiments, administering to the patient in need thereof an effective amount of a compound of Formula (I) or Formula (II), or a pharmaceutically acceptable salt, co-crystal, solvate, hydrate, tautomer, ester, N-oxide or stereoisomer thereof increases the expression of eIF2B, eIF2a, a component of the eIF2 pathway, a component of the ISR pathway or any combination thereof by the patients cells about 1%, about 2%, about 3%, about 4%, about 5%, about 6%, about 7%, about 8%, about 9%, about 10%, about 15%, about 20%, about 25%, about 30%, about 40%, about 45%, about 50%, about 60%, about 65%, about 70%, about 75%, about 80%, about 85%, about 90%, about 95%, or about 100%, thereby treating the disease, disorder or condition. In some embodiments, administering to the patient in need thereof an effective amount of a compound of Formula (I) or Formula (II), or a pharmaceutically acceptable salt, co-crystal, solvate, hydrate, tautomer, ester, N-oxide or stereoisomer thereof increases expression of eIF2B, eIF2a, a component of the eIF2 pathway, a component of the ISR pathway or any combination thereof by the patients cells about 1-fold, about 2-fold, about 3-fold, about 4-fold, about 5-fold, about 6-fold, about 7-fold, about 8- fold, about 9-fold, about 10-fold, about 20-fold, about 30-fold, about 40-fold, about 50-fold, about 60-fold, about 70-fold, about 80-fold, about 90-fold, about 100-fold, about 200-fold, about 300-fold, about 400-fold, about 500-fold, about 600-fold about 700-fold, about 800-fold, about 900-fold, about 1000-fold, about 10000-fold, about 100000-fold, or about 1000000-fold, thereby treating the disease, disorder or condition.

In another aspect, the compound of Formula (I) or Formula (II), or a pharmaceutically acceptable salt, co-crystal, solvate, hydrate, tautomer, ester, N-oxide or stereoisomer thereof may be useful in applications where increasing the activity of eIF2B, eIF2a, a component of the eIF2 pathway, a component of the ISR pathway or any combination thereof is desirable.

In some embodiments, the present invention features a method of increasing the activity of eIF2B, eIF2a, a component of the eIF2 pathway, a component of the ISR pathway or any combination thereof in a cell, the method comprising contacting the cell with an effective amount of a compound of Formula (I) or Formula (II), or a pharmaceutically acceptable salt, co- crystal, solvate, hydrate, tautomer, ester, N-oxide or stereoisomer thereof. In some embodiments, contacting the cell with an effective amount of a compound of Formula (I) or Formula (II), or a pharmaceutically acceptable salt, co-crystal, solvate, hydrate, tautomer, ester, N-oxide or stereoisomer thereof increases the activity of eIF2B, eIF2a, a component of the eIF2 pathway, a component of the ISR pathway or any combination thereof in the cell by about 1%, about 2%, about 3%, about 4%, about 5%, about 6%, about 7%, about 8%, about 9%, about 10%, about 15%, about 20%, about 25%, about 30%, about 40%, about 45%, about 50%, about 60%, about 65%, about 70%, about 75%, about 80%, about 85%, about 90%, about 95%, or about 100%. In some embodiments, contacting the cell with an effective amount of a compound of Formula (I) or Formula (II), or a pharmaceutically acceptable salt, co-crystal, solvate, hydrate, tautomer, ester, N-oxide or stereoisomer thereof increases the activity of eIF2B, eIF2a, a component of the eIF2 pathway, a component of the ISR pathway or any combination thereof in the cell by about 1-fold, about 2-fold, about 3-fold, about 4-fold, about 5-fold, about 6-fold, about 7-fold, about 8- fold, about 9-fold, about 10-fold, about 20-fold, about 30-fold, about 40-fold, about 50-fold, about 60-fold, about 70-fold, about 80-fold, about 90-fold, about 100-fold, about 200-fold, about 300-fold, about 400-fold, about 500-fold, about 600-fold about 700-fold, about 800-fold, about 900-fold, about 1000-fold, about 10000-fold, about 100000-fold, or about 1000000-fold.

In some embodiments, the present invention features a method of increasing the activity of eIF2B, eIF2a, a component of the eIF2 pathway, a component of the ISR pathway or any combination thereof in a patient in need thereof, the method comprising administering to the patient an effective amount of a compound of Formula (I) or Formula (II), or a pharmaceutically acceptable salt, co-crystal, solvate, hydrate, tautomer, ester, N-oxide or stereoisomer thereof, wherein the patient has been diagnosed with a disease, disorder, or condition disclosed herein and wherein the disease, disorder or condition is characterized by lowered levels of protein activity. In some embodiments, administering to the patient in need thereof an effective amount of a compound of Formula (I) or Formula (II), or a pharmaceutically acceptable salt, co-crystal, solvate, hydrate, tautomer, ester, N-oxide or stereoisomer thereof increases the activity of eIF2B, eIF2a, a component of the eIF2 pathway, a component of the ISR pathway or any combination thereof in the patient by about 1%, about 2%, about 3%, about 4%, about 5%, about 6%, about 7%, about 8%, about 9%, about 10%, about 15%, about 20%, about 25%, about 30%, about

40%, about 45%, about 50%, about 60%, about 65%, about 70%, about 75%, about 80%, about 85%, about 90%, about 95%, or about 100%, thereby treating the disease, disorder or condition. In some embodiments, administering to the patient in need thereof an effective amount of a compound of Formula (I) or Formula (II), or a pharmaceutically acceptable salt, co-crystal, solvate, hydrate, tautomer, ester, N-oxide or stereoisomer thereof increases the activity of eIF2B, eIF2a, a component of the eIF2 pathway, a component of the ISR pathway or any combination thereof in the patient by about 1-fold, about 2-fold, about 3-fold, about 4-fold, about 5-fold, about 6-fold, about 7-fold, about 8-fold, about 9-fold, about 10-fold, about 20-fold, about 30- fold, about 40-fold, about 50-fold, about 60-fold, about 70-fold, about 80-fold, about 90-fold, about 100-fold, about 200-fold, about 300-fold, about 400-fold, about 500-fold, about 600-fold about 700-fold, about 800-fold, about 900-fold, about 1000-fold, about 10000-fold, about 100000-fold, or about 1000000-fold, thereby treating the disease, disorder or condition. In some embodiments, the compound of Formula (I) or Formula (II) is chemically modified, prior to (ex vivo) or after (in vivo) contacting with the cell or in vitro expression system, forming a biologically active compound that increases the expression and/or activity of eIF2B, eIF2a, a component of the eIF2 pathway, component of the ISR pathway or any combination thereof in the cells and/or in vitro expression system. In some embodiments, the compound of Formula (I) or Formula (II) is metabolized by the patient forming a biologically active compound that increases the expression and/or activity of eIF2B, eIF2a, a component of the eIF2 pathway, component of the ISR pathway or any combination thereof in the patients cells, thereby treating a condition, disease or disorder disclosed herein. In some embodiments, the biologically active compound is the compound of formula (II).

Methods of Decreasing Protein Activity and Production

In another aspect, the compound of Formula (I) or Formula (II), or a pharmaceutically acceptable salt, co-crystal, solvate, hydrate, tautomer, ester, N-oxide or stereoisomer thereof may be useful in applications where decreasing production output of eIF2B, eIF2a, a component of the eIF2 pathway, a component of the ISR pathway or any combination thereof is desirable.

In some embodiments, the present invention features a method of decreasing expression of eIF2B, eIF2a, a component of the eIF2 pathway, a component of the ISR pathway or any combination thereof in a cell, the method comprising contacting the cells with an effective amount of a compound of Formula (I) or Formula (II), or a pharmaceutically acceptable salt, co- crystal, solvate, hydrate, tautomer, ester, N-oxide or stereoisomer thereof. In some embodiments, contacting the cells with an effective amount of a compound of Formula (I) or Formula (II), or a pharmaceutically acceptable salt, co-crystal, solvate, hydrate, tautomer, ester, N-oxide or stereoisomer thereof decreases expression of eIF2B, eIF2a, a component of the eIF2 pathway, a component of the ISR pathway or any combination thereof in the cell by about 1 %, about 2%, about 3%, about 4%, about 5%, about 6%, about 7%, about 8%, about 9%, about 10%, about 15%, about 20%, about 25%, about 30%, about 40%, about 45%, about 50%, about 60%, about 65%, about 70%, about 75%, about 80%, about 85%, about 90%, about 95%, or about 100%.

In some embodiments, the present invention features a method of decreasing the expression of eIF2B, eIF2a, a component of the eIF2 pathway, a component of the ISR pathway or any combination thereof in a patient in need thereof, the method comprising administering to the patient an effective amount of a compound of Formula (I) or Formula (II), or a

pharmaceutically acceptable salt, co-crystal, solvate, hydrate, tautomer, ester, N-oxide or stereoisomer thereof, wherein the patient has been diagnosed with a disease, disorder, or condition described herein and wherein the disease, disorder or condition is characterized by increased levels of protein production. In some embodiments, administering to the patient in need thereof an effective amount of a compound of Formula (I) or Formula (II), or a

pharmaceutically acceptable salt, co-crystal, solvate, hydrate, tautomer, ester, N-oxide or stereoisomer thereof decreases the expression of eIF2B, eIF2a, a component of the eIF2 pathway, a component of the ISR pathway or any combination thereof in the patient by about 1 %, about 2%, about 3%, about 4%, about 5%, about 6%, about 7%, about 8%, about 9%, about 10%, about 15 , about 20%, about 25%, about 30%, about 40%, about 45%, about 50%, about 60%, about 65%, about 70%, about 75%, about 80%, about 85%, about 90%, about 95%, or about 100%, thereby treating the disease, disorder or condition.

In another aspect, the compound of Formula (I) or Formula (II), or a pharmaceutically acceptable salt, co-crystal, solvate, hydrate, tautomer, ester, N-oxide or stereoisomer thereof may be useful in applications where decreasing the activity of eIF2B, eIF2a, a component of the eIF2 pathway, a component of the ISR pathway or any combination thereof is desirable.

In some embodiments, the present invention features a method of decreasing the activity of eIF2B, eIF2a, a component of the eIF2 pathway, a component of the ISR pathway or any combination thereof in a cell, the method comprising contacting the cell with an effective amount of a compound of Formula (I) or Formula (II), or a pharmaceutically acceptable salt, co- crystal, solvate, hydrate, tautomer, ester, N-oxide or stereoisomer thereof. In some embodiments, contacting the cell with an effective amount of a compound of Formula (I) or Formula (II), or a pharmaceutically acceptable salt, co-crystal, solvate, hydrate, tautomer, ester, N-oxide or stereoisomer thereof decreases the activity of eIF2B, eIF2a, a component of the eIF2 pathway, a component of the ISR pathway or any combination thereof in the cell by about 1 %, about 2%, about 3%, about 4%, about 5%, about 6%, about 7%, about 8%, about 9%, about 10%, about 15%, about 20%, about 25%, about 30%, about 40%, about 45%, about 50%, about 60%, about 65%, about 70%, about 75%, about 80%, about 85%, about 90%, about 95%, or about 100%, thereby treating the disease, disorder or condition. In some embodiments, the present invention features a method of decreasing the activity of eIF2B, eIF2a, a component of the eIF2 pathway, a component of the ISR pathway or any combination thereof in a patient in need thereof, the method comprising administering to the patient an effective amount of a compound of Formula (I) or Formula (II), or a pharmaceutically acceptable salt, co-crystal, solvate, hydrate, tautomer, ester, N-oxide or stereoisomer thereof, wherein the patient has been diagnosed with a disease, disorder, or condition described herein and wherein the disease, disorder or condition is characterized by increased levels of protein activity. In some embodiments, administering to the patient in need thereof an effective amount of a compound of Formula (I) or Formula (II), or a pharmaceutically acceptable salt, co-crystal, solvate, hydrate, tautomer, ester, N-oxide or stereoisomer thereof decreases the activity of eIF2B, eIF2a, a component of the eIF2 pathway, a component of the ISR pathway or any combination thereof in the patient by about 1%, about 2%, about 3%, about 4%, about 5%, about 6%, about 7%, about 8%, about 9%, about 10%, about 15%, about 20%, about 25%, about 30%, about 40%, about 45%, about 50%, about 60%, about 65%, about 70%, about 75%, about 80%, about 85%, about 90%, about 95%, or about 100%, thereby treating the disease, disorder or condition.

In some embodiments, the compound of Formula (I) or Formula (II) is chemically modified, prior to (ex vivo) or after (in vivo) contacting with a cell, forming a biologically active compound that decreases the expression and/or activity of eIF2B, eIF2a, a component of the eIF2 pathway, component of the ISR pathway or any combination thereof in the cell. In some embodiments, the compound of Formula (I) or Formula (II) is metabolized by the patient forming a biologically active compound that decreases the expression and/or activity of eIF2B, eIF2a, a component of the eIF2 pathway, component of the ISR pathway or any combination thereof in the patients cells, thereby treating a condition, disease or disorder disclosed herein. In some embodiments, the biologically active compound is the compound of Formula (I) or Formula (II).

In some embodiments, the compounds set forth herein are provided as pharmaceutical compositions including a compound of Formula (I) or Formula (II), or a pharmaceutically acceptable salt, solvate, hydrate, tautomer, or stereoisomer thereof and a pharmaceutically acceptable excipient. In embodiments of the method, a compound of Formula (I) or Formula (II), or a pharmaceutically acceptable salt, solvate, hydrate, tautomer, or stereoisomer thereof, is coadministered with a second agent (e.g. therapeutic agent). In other embodiments of the method, a compound of Formula (I) or Formula (II), or a pharmaceutically acceptable salt, solvate, hydrate, tautomer, or stereoisomer thereof, is co-administered with a second agent (e.g. therapeutic agent), which is administered in a therapeutically effective amount. In embodiments, the second agent is an agent for improving memory.

Combination Therapy

In one aspect, the present invention features a pharmaceutical composition comprising a compound of Formula (I) or Formula (II), or a pharmaceutically acceptable salt, solvate, hydrate, tautomer, or stereoisomer thereof as well as a second agent (e.g. a second therapeutic agent). In some embodiments, the pharmaceutical composition includes a second agent (e.g. a second therapeutic agent) in a therapeutically effective amount. In some embodiments, the second agent is an agent for treating cancer, a neurodegenerative disease, a leukodystrophy, an inflammatory disease, a musculoskeletal disease, a metabolic disease, or a disease or disorder associated with impaired function of eIF2B, eIF2a, or a component of the eIF2 pathway or ISR pathway.

The compounds described herein can be used in combination with one another, with other active agents known to be useful in treating cancer, a neurodegenerative disease, an inflammatory disease, a musculoskeletal disease, a metabolic disease, or a disease or disorder associated with impaired function of eIF2B, eIF2a, or a component of the eIF2 pathway or ISR pathway or with adjunctive agents that may not be effective alone, but may contribute to the efficacy of the active agent.

In some embodiments, co-administration includes administering one active agent within 0.5, 1 , 2, 4, 6, 8, 10, 12, 16, 20, or 24 hours of a second active agent. Co-administration includes administering two active agents simultaneously, approximately simultaneously (e.g., within about 1 , 5, 10, 15, 20, or 30 minutes of each other), or sequentially in any order. In some embodiments, co- administration can be accomplished by co-formulation, i.e., preparing a single pharmaceutical composition including both active agents. In other embodiments, the active agents can be formulated separately. In another embodiment, the active and/or adjunctive agents may be linked or conjugated to one another. In some embodiments, the compounds described herein may be combined with treatments for a cancer, a neurodegenerative disease, a leukodystrophy, an inflammatory disease, a musculoskeletal disease, a metabolic disease, or a disease or disorder associated with impaired function of eIF2B, eIF2a, or a component of the eIF2 pathway or ISR pathway. In embodiments, the second agent is an anti-cancer agent. In embodiments, the second agent is a chemotherapeutic. In embodiments, the second agent is an agent for improving memory. In embodiments, the second agent is an agent for treating a neurodegenerative disease. In embodiments, the second agent is an agent for treating a leukodystrophy. In embodiments, the second agent is an agent for treating vanishing white matter disease. In embodiments, the second agent is an agent for treating childhood ataxia with CNS hypo-myelination. In embodiments, the second agent is an agent for treating an intellectual disability syndrome. In embodiments, the second agent is an agent for treating pancreatic cancer. In embodiments, the second agent is an agent for treating breast cancer. In embodiments, the second agent is an agent for treating multiple myeloma. In embodiments, the second agent is an agent for treating myeloma. In embodiments, the second agent is an agent for treating a cancer of a secretory cell. In embodiments, the second agent is an agent for reducing eIF2a phosphorylation. In embodiments, the second agent is an agent for inhibiting a pathway activated by eIF2a phosphorylation. In embodiments, the second agent is an agent for inhibiting a pathway activated by eIF2a. In embodiments, the second agent is an agent for inhibiting the integrated stress response. In embodiments, the second agent is an anti-inflammatory agent. In embodiments, the second agent is an agent for treating postsurgical cognitive dysfunction. In embodiments, the second agent is an agent for treating traumatic brain injury. In embodiments, the second agent is an agent for treating a musculoskeletal disease. In embodiments, the second agent is an agent for treating a metabolic disease. In embodiments, the second agent is an antidiabetic agent.

Anti-cancer agents

"Anti-cancer agent" is used in accordance with its plain ordinary meaning and refers to a composition (e.g. compound, drug, antagonist, inhibitor, modulator) having antineoplastic properties or the ability to inhibit the growth or proliferation of cells. In some embodiments, an anti-cancer agent is a chemotherapeutic. In some embodiments, an anti-cancer agent is an agent identified herein having utility in methods of treating cancer. In some embodiments, an anticancer agent is an agent approved by the FDA or similar regulatory agency of a country other than the USA, for treating cancer. Examples of anti-cancer agents include, but are not limited to, MEK (e.g. MEK1 , MEK2, or MEK1 and MEK2) inhibitors (e.g. XL518, CI- 1040, PD035901 , selumetinib/ AZD6244, GSK1120212/ trametinib, GDC-0973, ARRY-162, ARRY-300, AZD8330, PD0325901 , U0126, PD98059, TAK-733, PD318088, AS703026, BAY 869766), alkylating agents (e.g., cyclophosphamide, ifosfamide, chlorambucil, busulfan, melphalan, mechlorethamine, uramustine, thiotepa, nitrosoureas, nitrogen mustards (e.g., mechloroethamine, cyclophosphamide, chlorambucil, meiphalan), ethylenimine and methylmelamines (e.g., hexamethlymelamine, thiotepa), alkyl sulfonates (e.g., busulfan), nitrosoureas (e.g., carmustine, lomusitne, semustine, streptozocin), triazenes (decarbazine), anti-metabolites (e.g., 5- azathioprine, leucovorin, capecitabine, fludarabine, gemcitabine, pemetrexed, raltitrexed, folic acid analog (e.g., methotrexate), or pyrimidine analogs (e.g., fluorouracil, floxouridine,

Cytarabine), purine analogs (e.g., mercaptopurine, thioguanine, pentostatin), etc.), plant alkaloids (e.g., vincristine, vinblastine, vinorelbine, vindesine, podophyllotoxin, paclitaxel, docetaxel, etc.), topoisomerase inhibitors (e.g., irinotecan, topotecan, amsacrine, etoposide (VP 16), etoposide phosphate, teniposide, etc.), antitumor antibiotics (e.g., doxorubicin, adriamycin, daunorubicin, epirubicin, actinomycin, bleomycin, mitomycin, mitoxantrone, plicamycin, etc.), platinum-based compounds (e.g. cisplatin, oxaloplatin, carboplatin), anthracenedione (e.g., mitoxantrone), substituted urea (e.g., hydroxyurea), methyl hydrazine derivative (e.g., procarbazine), adrenocortical suppressant (e.g., mitotane, aminoglutethimide),

epipodophyllotoxins (e.g., etoposide), antibiotics (e.g., daunorubicin, doxorubicin, bleomycin), enzymes (e.g., L-asparaginase), inhibitors of mitogen-activated protein kinase signaling (e.g. U0126, PD98059, PD184352, PD0325901 , ARRY-142886, SB239063, SP600125, BAY 43- 9006, wortmannin, or LY294002, Syk inhibitors, mTOR inhibitors, antibodies (e.g., rituxan), gossyphol, genasense, polyphenol E, Chlorofusin, all trans-retinoic acid (ATRA), bryostatin, tumor necrosis factor-related apoptosis-inducing ligand (TRAIL), 5-aza-2'-deoxycytidine, all trans retinoic acid, doxorubicin, vincristine, etoposide, gemcitabine, imatinib (Gleevec.RTM.), geldanamycin, 17-N-Allylamino-17-Demethoxygeldanamycin (17-AAG), flavopiridol,

LY294002, bortezomib, trastuzumab, BAY 1 1-7082, PKC412, PD184352, 20-epi-l, 25 dihydroxyvitamin D3; 5-ethynyluracil; abiraterone; aclarubicin; acylfulvene; adecypenol;

adozelesin; aldesleukin; ALL-TK antagonists; altretamine; ambamustine; amidox; amifostine; aminolevulinic acid; amrubicin; amsacrine; anagrelide; anastrozole; andrographolide;

angiogenesis inhibitors; antagonist D; antagonist G; antarelix; anti-dorsalizing morphogenetic protein- 1 ; antiandrogen, prostatic carcinoma; antiestrogen; antineoplaston; antisense oligonucleotides; aphidicolin glycinate; apoptosis gene modulators; apoptosis regulators;

apurinic acid; ara-CDP-DL-PTBA; arginine deaminase; asulacrine; atamestane; atrimustine; axinastatin 1 ; axinastatin 2; axinastatin 3; azasetron; azatoxin; azatyrosine; baccatin III derivatives; balanol; batimastat; BCR/ABL antagonists; benzochlorins; benzoylstaurosporine; beta lactam derivatives; beta-ale thine; betaclamycin B ; betulinic acid; bFGF inhibitor;

bicalutamide; bisantrene; bisaziridinylspermine; bisnafide; bistratene A; bizelesin; breflate; bropirimine; budotitane; buthionine sulfoximine; calcipotriol; calphostin C; camptothecin derivatives; canarypox IL-2; capecitabine; carboxamide-amino-triazole; carboxyamidotriazole; CaRest M3; CARN 700; cartilage derived inhibitor; carzelesin; casein kinase inhibitors (ICOS); castanospermine; cecropin B ; cetrorelix; chlorins; chloroquinoxaline sulfonamide; cicaprost; cis- porphyrin; cladribine; clomifene analogues; clotrimazole; collismycin A; collismycin B;

combretastatin A4; combretastatin analogue; conagenin; crambescidin 816; crisnatol;

cryptophycin 8; cryptophycin A derivatives; curacin A; cyclopentanthraquinones; cycloplatam; cypemycin; cytarabine ocfosfate; cytolytic factor; cytostatin; dacliximab; decitabine;

dehydrodidemnin B ; deslorelin; dexamethasone; dexifosf amide; dexrazoxane; dexverapamil; diaziquone; didemnin B ; didox; diethylnorspermine; dihydro-5-azacytidine; 9-dioxamycin; diphenyl spiromustine; docosanol; dolasetron; doxifluridine; droloxifene; dronabinol;

duocarmycin SA; ebselen; ecomustine; edelfosine; edrecolomab; eflornithine; elemene; emitefur; epirubicin; epristeride; estramustine analogue; estrogen agonists; estrogen antagonists;

etanidazole; etoposide phosphate; exemestane; fadrozole; fazarabine; fenretinide; filgrastim; finasteride; flavopiridol; flezelastine; fluasterone; fludarabine; fluorodaunorunicin

hydrochloride; forfenimex; formestane; fostriecin; fotemustine; gadolinium texaphyrin; gallium nitrate; galocitabine; ganirelix; gelatinase inhibitors; gemcitabine; glutathione inhibitors;

hepsulfam; heregulin; hexamethylene bisacetamide; hypericin; ibandronic acid; idarubicin; idoxifene; idramantone; ilmofosine; ilomastat; imidazoacridones; imiquimod; immunostimulant peptides; insulin-like growth factor- 1 receptor inhibitor; interferon agonists; interferons;

interleukins; iobenguane; iododoxorubicin; ipomeanol, 4-; iroplact; irsogladine; isobengazole; isohomohalicondrin B ; itasetron; jasplakinolide; kahalalide F; lamellarin-N triacetate; lanreotide; leinamycin; lenograstim; lentinan sulfate; leptolstatin; letrozole; leukemia inhibiting factor; leukocyte alpha interferon; leuprolide+estrogen+progesterone; leuprorelin; levamisole; liarozole; linear polyamine analogue; lipophilic disaccharide peptide; lipophilic platinum compounds; lissoclinamide 7; lobaplatin; lombricine; lometrexol; lonidamine; losoxantrone; lovastatin;

loxoribine; lurtotecan; lutetium texaphyrin; lysofylline; lytic peptides; maitansine; mannostatin A; marimastat; masoprocol; maspin; matrilysin inhibitors; matrix metalloproteinase inhibitors; menogaril; merbarone; meterelin; methioninase; metoclopramide; MIF inhibitor; mifepristone; miltefosine; mirimostim; mismatched double stranded RNA; mitoguazone; mitolactol;

mitomycin analogues; mitonafide; mitotoxin fibroblast growth factor-saporin; mitoxantrone; mofarotene; molgramostim; monoclonal antibody, human chorionic gonadotrophin;

monophosphoryl lipid A+myobacterium cell wall sk; mopidamol; multiple drug resistance gene inhibitor; multiple tumor suppressor 1 -based therapy; mustard anticancer agent; mycaperoxide B ; mycobacterial cell wall extract; myriaporone; N-acetyldinaline; N-substituted benzamides; nafarelin; nagrestip; naloxone+pentazocine; napavin; naphterpin; nartograstim; nedaplatin; nemorubicin; neridronic acid; neutral endopeptidase; nilutamide; nisamycin; nitric oxide modulators; nitroxide antioxidant; nitrullyn; 06-benzylguanine; octreotide; okicenone;

oligonucleotides; onapristone; ondansetron; ondansetron; oracin; oral cytokine inducer;

ormaplatin; osaterone; oxaliplatin; oxaunomycin; palauamine; palmitoylrhizoxin; pamidronic acid; panaxytriol; panomifene; parabactin; pazelliptine; pegaspargase; peldesine; pentosan polysulfate sodium; pentostatin; pentrozole; perflubron; perfosfamide; perillyl alcohol;

phenazinomycin; phenylacetate; phosphatase inhibitors; picibanil; pilocarpine hydrochloride; pirarubicin; piritrexim; placetin A; placetin B; plasminogen activator inhibitor; platinum complex; platinum compounds; platinum- triamine complex; porfimer sodium; porfiromycin; prednisone; propyl bis-acridone; prostaglandin J2; proteasome inhibitors; protein A-based immune modulator; protein kinase C inhibitor; protein kinase C inhibitors, microalgal; protein tyrosine phosphatase inhibitors; purine nucleoside phosphorylase inhibitors; purpurins;

pyrazoloacridine; pyridoxylated hemoglobin polyoxyethylerie conjugate; raf antagonists;

raltitrexed; ramosetron; ras farnesyl protein transferase inhibitors; ras inhibitors; ras-GAP inhibitor; retelliptine demethylated; rhenium Re 186 etidronate; rhizoxin; ribozymes; RII retinamide; rogletimide; rohitukine; romurtide; roquinimex; rubiginone Bl; ruboxyl; safingol; saintopin; SarCNU; sarcophytol A; sargramostim; Sdi 1 mimetics; semustine; senescence derived inhibitor 1 ; sense oligonucleotides; signal transduction inhibitors; signal transduction modulators; single chain antigen-binding protein; sizofuran; sobuzoxane; sodium borocaptate; sodium phenylacetate; solverol; somatomedin binding protein; sonermin; sparfosic acid;

spicamycin D; spiromustine; splenopentin; spongistatin 1 ; squalamine; stem cell inhibitor; stem- cell division inhibitors; stipiamide; stromelysin inhibitors; sulfinosine; superactive vasoactive intestinal peptide antagonist; suradista; suramin; swainsonine; synthetic glycosaminoglycans; tallimustine; tamoxifen methiodide; tauromustine; tazarotene; tecogalan sodium; tegafur;

tellurapyrylium; telomerase inhibitors; temoporfin; temozolomide; teniposide;

tetrachlorodecaoxide; tetrazomine; thaliblastine; thiocoraline; thrombopoietin; thrombopoietin mimetic; thymalfasin; thymopoietin receptor agonist; thymotrinan; thyroid stimulating hormone; tin ethyl etiopurpurin; tirapazamine; titanocene bichloride; topsentin; toremifene; totipotent stem cell factor; translation inhibitors; tretinoin; triacetyluridine; triciribine; trimetrexate; triptorelin; tropisetron; turosteride; tyrosine kinase inhibitors; tyrphostins; UBC inhibitors; ubenimex;

urogenital sinus-derived growth inhibitory factor; urokinase receptor antagonists; vapreotide; variolin B ; vector system, erythrocyte gene therapy; velaresol; veramine; verdins; verteporfin; vinorelbine; vinxaltine; vitaxin; vorozole; zanoterone; zeniplatin; zilascorb; zinostatin stimalamer, Adriamycin, Dactinomycin, Bleomycin, Vinblastine, Cisplatin, acivicin; aclarubicin; acodazole hydrochloride; acronine; adozelesin; aldesleukin; altretamine; ambomycin;

ametantrone acetate; aminoglutethimide; amsacrine; anastrozole; anthramycin; asparaginase; asperlin; azacitidine; azetepa; azotomycin; batimastat; benzodepa; bicalutamide; bisantrene hydrochloride; bisnafide dimesylate; bizelesin; bleomycin sulfate; brequinar sodium;

bropirimine; busulfan; cactinomycin; calusterone; caracemide; carbetimer; carboplatin;

carmustine; carubicin hydrochloride; carzelesin; cedefingol; chlorambucil; cirolemycin;

cladribine; crisnatol mesylate; cyclophosphamide; cytarabine; dacarbazine; daunorubicin hydrochloride; decitabine; dexormaplatin; dezaguanine; dezaguanine mesylate; diaziquone; doxorubicin; doxorubicin hydrochloride; droloxifene; droloxifene citrate; dromostanolone propionate; duazomycin; edatrexate; eflornithine hydrochloride; elsamitrucin; enloplatin;

enpromate; epipropidine; epirubicin hydrochloride; erbulozole; esorubicin hydrochloride;

estramustine; estramustine phosphate sodium; etanidazole; etoposide; etoposide phosphate; etoprine; fadrozole hydrochloride; fazarabine; fenretinide; floxuridine; fludarabine phosphate; fluorouracil; fluorocitabine; fosquidone; fostriecin sodium; gemcitabine; gemcitabine hydrochloride; hydroxyurea; idarubicin hydrochloride; ifosfamide; iimofosine; interleukin II

(including recombinant interleukin II, or rlL.sub.2), interferon alfa-2a; interferon alfa-2b;

interferon alfa-nl; interferon alfa-n3; interferon beta- la; interferon gamma-lb; iprop latin;

irinotecan hydrochloride; lanreotide acetate; letrozole; leuprolide acetate; liarozole

hydrochloride; lometrexol sodium; lomustine; losoxantrone hydrochloride; masoprocol;

maytansine; mechlorethamine hydrochloride; megestrol acetate; melengestrol acetate;

melphalan; menogaril; mercaptopurine; methotrexate; methotrexate sodium; metoprine;

meturedepa; mitindomide; mitocarcin; mitocromin; mitogillin; mitomalcin; mitomycin;

mitosper; mitotane; mitoxantrone hydrochloride; mycophenolic acid; nocodazoie; nogalamycin; ormaplatin; oxisuran; pegaspargase; peliomycin; pentamustine; peplomycin sulfate;

perfosfamide; pipobroman; piposulfan; piroxantrone hydrochloride; plicamycin; plomestane; porfimer sodium; porfiromycin; prednimustine; procarbazine hydrochloride; puromycin;

puromycin hydrochloride; pyrazofurin; riboprine; rogletimide; safingol; safingol hydrochloride; semustine; simtrazene; sparfosate sodium; sparsomycin; spirogermanium hydrochloride;

spiromustine; spiroplatin; streptonigrin; streptozocin; sulofenur; talisomycin; tecogalan sodium; tegafur; teloxantrone hydrochloride; temoporfin; teniposide; teroxirone; testolactone;

thiamiprine; thioguanine; thiotepa; tiazofurin; tirapazamine; toremifene citrate; trestolone acetate; triciribine phosphate; trimetrexate; trimetrexate glucuronate; triptorelin; tubulozole hydrochloride; uracil mustard; uredepa; vapreotide; verteporfin; vinblastine sulfate; vincristine sulfate; vindesine; vindesine sulfate; vinepidine sulfate; vinglycinate sulfate; vinleurosine sulfate; vinorelbine tartrate; vinrosidine sulfate; vinzolidine sulfate; vorozole; zeniplatin;

zinostatin; zorubicin hydrochloride, agents that arrest cells in the G2-M phases and/or modulate the formation or stability of microtubules, (e.g. Taxol (i.e. paclitaxel), Taxotere compounds comprising the taxane skeleton, Erbulozole (i.e. R-55104), Dolastatin 10 (i.e. DLS-10 and NSC- 376128), Mivobulin isethionate (i.e. as CI-980), Vincristine, NSC-639829, Discodermolide (i.e. as NVP-XX-A-296), ABT-751 (Abbott, i.e. E-7010), Altorhyrtins (e.g. Altorhyrtin A and Altorhyrtin C), Spongistatins (e.g. Spongistatin 1, Spongistatin 2, Spongistatin 3, Spongistatin 4, Spongistatin 5, Spongistatin 6, Spongistatin 7, Spongistatin 8, and Spongistatin 9), Cemadotin hydrochloride (i.e. LU-103793 and SC-D-669356), Epothilones (e.g. Epothilone A, Epothilone B, Epothilone C (i.e. desoxyepothilone A or dEpoA), Epothilone D (i.e. KOS-862, dEpoB, and desoxyepothilone B), Epothilone E, Epothilone F, Epothilone B N-oxide, Epothilone A N-oxide, 16-aza-epothilone B, 21 -aminoepothilone B (i.e. BMS-310705), 21-hydroxyepothilone D (i.e. Desoxyepothilone F and dEpoF), 26-fluoroepothilone, Auristatin PE (i.e. NSC-654663),

Soblidotin (i.e. TZT-1027), LS-4559-P (Pharmacia, i.e. LS-4577), LS-4578 (Pharmacia, i.e. LS- 477-P), LS-4477 (Pharmacia), LS-4559 (Pharmacia), RPR-1 12378 (Aventis), Vincristine sulfate, DZ-3358 (Daiichi), FR-182877 (Fujisawa, i.e. WS-9885B), GS-164 (Takeda), GS-198 (Takeda), KAR-2 (Hungarian Academy of Sciences), BSF-223651 (BASF, i.e. ILX-651 and LU- 223651), SAH-49960 (Lilly/No vartis), SDZ-268970 (Lilly/Novartis), AM-97 (Armad/Kyowa Hakko), AM- 132 (Armad), AM- 138 (Armad/Kyowa Hakko), IDN-5005 (Indena),

Cryptophycin 52 (i.e. LY-355703), AC-7739 (Ajinomoto, i.e. AVE-8063A and CS-39.HC1), AC-7700 (Ajinomoto, i.e. AVE-8062, AVE-8062A, CS-39-L-Ser.HCl, and RPR-258062A), Vitilevuamide, Tubulysin A, Canadensol, Centaureidin (i.e. NSC-106969), T-138067 (Tularik, i.e. T-67, TL-138067 and TI- 138067), COBRA-1 (Parker Hughes Institute, i.e. DDE-261 and WHI-261), H10 (Kansas State University), H16 (Kansas State University), Oncocidin A 1 (i.e. BTO-956 and DIME), DDE- 313 (Parker Hughes Institute), Fijianolide B, Laulimalide, SPA-2 (Parker Hughes Institute), SPA-1 (Parker Hughes Institute, i.e. SPIKET-P), 3-IAABU (Cytoskeleton/Mt. Sinai School of Medicine, i.e. MF-569), Narcosine (also known as NSC- 5366), Nascapine, D-24851 (Asta Medica), A-105972 (Abbott), Hemiasterlin, 3-BAABU (Cytoskeleton/Mt. Sinai School of Medicine, i.e. MF-191), TMPN (Arizona State University), Vanadocene acetylacetonate, T- 138026 (Tularik), Monsatrol, Inanocine (i.e. NSC-698666), 3- I A ABE (Cytoskeleton/Mt. Sinai School of Medicine), A-204197 (Abbott), T-607 (Tularik, i.e. T-900607), RPR-115781 (A vends), Eleutherobins (such as Desmethyleleutherobin,

Desaetyleleutherobin, lsoeleutherobin A, and Z-Eleutherobin), Caribaeoside, Caribaeolin, Halichondrin B, D-64131 (Asta Medica), D-68144 (Asta Medica), Diazonamide A, A-293620 (Abbott), NPI-2350 (Nereus), Taccalonolide A, TUB-245 (A vends), A-259754 (Abbott), Diozostatin, (-)-Phenylahistin (i.e. NSCL-96F037), D-68838 (Asta Medica), D-68836 (Asta Medica), Myoseverin B, D-43411 (Zentaris, i.e. D-81862), A-289099 (Abbott), A-318315 (Abbott), HTI-286 (i.e. SPA-110, trifluoroacetate salt) (Wyeth), D-82317 (Zentaris), D-82318 (Zentaris), SC- 12983 (NCI), Resverastatin phosphate sodium, BPR-OY-007 (National Health Research Institutes), and SSR-25041 1 (Sanofi), steroids (e.g., dexamethasone), finasteride, aromatase inhibitors, gonadotropin-releasing hormone agonists (GnRH) such as goserelin or leuprolide, adrenocorticosteroids (e.g., prednisone), progestins (e.g., hydroxyprogesterone caproate, megestrol acetate, medroxyprogesterone acetate), estrogens (e.g., diethlystilbestrol, ethinyl estradiol), antiestrogen (e.g., tamoxifen), androgens (e.g., testosterone propionate, fluoxymesterone), antiandrogen (e.g., flutamide), immunostimulants (e.g., Bacillus Calmette- Guerin (BCG), levamisole, interleukin-2, alpha-interferon, etc.), monoclonal antibodies (e.g., anti-CD20, anti-HER2, anti-CD52, anti-HLA-DR, and anti-VEGF monoclonal antibodies), immunotoxins (e.g., anti-CD33 monoclonal antibody-calicheamicin conjugate, anti-CD22 monoclonal antibody-pseudomonas exotoxin conjugate, etc.), radioimmunotherapy (e.g., anti- CD20 monoclonal antibody conjugated to ^{u J} ln, ⁹⁰ Y, or ¹³¹ I, etc. ), triptolide, homoharringtonine, dactinomycin, doxorubicin, epirubicin, topotecan, itraconazole, vindesine, cerivastatin, vincristine, deoxy adenosine, sertraline, pitavastatin, irinotecan, clofazimine, 5- nonyloxytryptamine, vemurafenib, dabrafenib, erlotinib, gefitinib, EGFR inhibitors, epidermal growth factor receptor (EGFR)-targeted therapy or therapeutic (e.g. gefitinib (Iressa™), erlotinib (Tarceva™), cetuximab (Erbitux™), lapatinib (Tykerb™), panitumumab (Vectibix™), vandetanib (Caprelsa™), afatinib/BIBW2992, CI-1033/canertinib, neratinib/HKI-272, CP-

724714, TAK-285, AST- 1306, ARRY334543, ARRY-380, AG-1478, dacomitinib/PF299804, OSI-420/desmethyl erlotinib, AZD8931 , AEE788, pelitinib/EKB-569, CUDC- 101 , WZ8040, WZ4002, WZ3146, AG-490, XL647, PD153035, BMS-599626), sorafenib, imatinib, sunitinib, dasatinib, or the like.

"Chemotherapeutic" or "chemotherapeutic agent" is used in accordance with its plain ordinary meaning and refers to a chemical composition or compound having antineoplastic properties or the ability to inhibit the growth or proliferation of cells.

Additionally, the compounds described herein can be co-administered with conventional immunotherapeutic agents including, but not limited to, immunostimulants (e.g., Bacillus Calmette-Guerin (BCG), levamisole, interleukin-2, alpha- interferon, etc.), monoclonal antibodies (e.g., anti-CD20, anti-HER2, anti-CD52, anti-HLA-DR, and anti-VEGF monoclonal antibodies), immunotoxins (e.g., anti-CD33 monoclonal antibody-calicheamicin conjugate, anti- CD22 monoclonal antibody -pseudomonas exotoxin conjugate, etc.), and radioimmunotherapy (e.g., anti-CD20 monoclonal antibody conjugated to ^m In, ⁹⁰ Y, or ¹³¹ I, etc.).

In a further embodiment, the compounds described herein can be co-administered with conventional radiotherapeutic agents including, but not limited to, radionuclides such as ⁴⁷ Sc, ⁶⁴ Cu, ⁶⁷ Cu, ⁸⁹ Sr, ⁸⁶ Y, ⁸⁷ Y, ⁹⁰ Y, ¹⁰⁵ Rh, ^m Ag, ^m In, ^117m Sn, ¹⁴⁹ Pm, ¹⁵³ Sm, ¹⁶⁶ Ho, ¹⁷⁷ Lu, ¹⁸⁶ Re, ¹⁸⁸ Re,

211 212

At, and Bi, optionally conjugated to antibodies directed against tumor antigens.

Additional Agents

In some embodiments, the second agent for use in combination with a compound (e.g., a compound of Formula (I) or Formula (II)) or composition thereof described herein is an agent for use in treating a neurodegenerative disease, a leukodystrophy, an inflammatory disease, a musculoskeletal disease, or a metabolic disease. In some embodiments, a second agent for use in combination with a compound (e.g., a compound of Formula (I) or Formula (II)) or composition thereof described herein is an agent approved by the FDA or similar regulatory agency of a country other than the USA, for treating a disease, disorder, or condition described herein.

In some embodiments, a second agent for use in treating a neurodegenerative disease, a leukodystrophy, an inflammatory disease, a musculoskeletal disease, or a metabolic disease includes, but is not limited to, an anti-psychotic drug, anti-depressive drug, anti-anxiety drug, analgesic, a stimulant, a sedative, a pain reliever, an anti-inflammatory agent, a benzodiazepine, a cholinesterase inhibitor, a non-steroidal anti-inflammatory drug (NSAID), a corticosteroid, a MAO inhibitor, a beta-blocker, a calcium channel blocker, an antacid, or other agent.

Exemplary second agents may include donepezil, galantamine, rivastigmine, memantine, levodopa, dopamine, pramipexole, ropinirole, rotigotine, doxapram, oxazepam, quetiapine, selegiline, rasagiline, entacapone, benztropine, trihexyphenidyl, riluzole, diazepam,

chlorodiazepoxide, lorazepam, alprazolam, buspirone, gepirone, ispapirone, hydroxyzine, propranolol, hydroxyzine, midazolam, trifluoperazine, methylphenidate, atomoxetine, methylphenidate, pemoline, perphenazine, divalproex, valproic acid, sertraline, fluoxetine, citalopram, escitalopram, paroxetine, fluvoxamine, trazodone, desvenlafaxine, duloxetine, venlafaxine, amitriptyline, amoxapine, clomipramine, desipramine, imipramine, nortriptyline, protriptyline, trimipramine, maprotiline, bupropion, nefazodone, vortioxetine, lithium, clozapine, fluphenazine, haloperidol, paliperidone, loxapine, thiothixene, pimozide, thioridazine, risperidone, aspirin, ibuprofen, naproxen, acetaminophen, azathioprine, methotrexate, mycophenolic acid, leflunomide, dibenzoylmethane, cilostazol, pentoxifylline, duloxetine, a cannabinoid (e.g, nabilone), simethicone, magaldrate, aluminum salts, calcium salts, sodium salts, magnesium salts, alginic acid, acarbose, albiglutide, alogliptin, metformin, insulin, lisinopril, atenolol, atorvastatin, fluvastatin, lovastatin, pitavastatin, simvastatin, rosuvastatin, and the like.

Naturally derived agents or supplements may also be used in conjunction with a compound of Formula (I) or Formula (II), or a composition thereof to treat a neurodegenerative disease, an inflammatory disease, a musculoskeletal disease, or a metabolic disease. Exemplary naturally derived agents or supplements include omega-3 fatty acids, carnitine, citicoline, curcumin, gingko, vitamin E, vitamin B (e.g., vitamin B5, vitamin B6, or vitamin B 12), huperzine A, phosphatidylserine, rosemary, caffeine, melatonin, chamomile, St. John's wort, tryptophan, and the like.

EXAMPLES

In order that the invention described herein may be more fully understood, the following examples are set forth. The synthetic and biological examples described in this application are offered to illustrate the compounds, pharmaceutical compositions, and methods provided herein and are not to be construed in any way as limiting their scope.

Synthetic Protocols

The compounds provided herein can be prepared from readily available starting materials using modifications to the specific synthesis protocols set forth below that would be well known to those of skill in the art. It will be appreciated that where typical or preferred process conditions (i.e., reaction temperatures, times, mole ratios of reactants, solvents, pressures, etc.) are given, other process conditions can also be used unless otherwise stated. Optimum reaction conditions may vary with the particular reactants or solvents used, but such conditions can be determined by those skilled in the art by routine optimization procedures. General scheme relating to methods of making exemplary compounds of the invention are additionally described in the section entitled Methods of Making Compounds.

Additionally, as will be apparent to those skilled in the art, conventional protecting groups may be necessary to prevent certain functional groups from undergoing undesired reactions. The choice of a suitable protecting group for a particular functional group as well as suitable conditions for protection and deprotection are well known in the art. For example, numerous protecting groups, and their introduction and removal, are described in Greene et al, Protecting Groups in Organic Synthesis, Second Edition, Wiley, New York, 1991, and references cited therein.

Abbreviations

APCI for atmospheric pressure chemical ionization; DMSO for dimethyl sulfoxide; HPLC for high performance liquid chromatography; MS for mass spectrum; and NMR for nuclear magnetic resonance.

Example 1: 3-[2-(4-chlorophenoxy)acetamido]-N-[2-(4-chlorophenoxy)ethyl ]bicyclo[l.l.l]- pentane-l-carboxamide (Compound 100)

Example 1A: methyl 3-(2-(4-chlorophenoxy)acetamido)bicyclo[l.l.l]pentane-l-carb oxylate

To a solution of 2-(4-chlorophenoxy)acetic acid (10.88 g, 58.5 mmol) in N,N- dimethylformamide (150 mL) were added methyl 3-aminobicyclo[l.l. l]pentane-l-carboxylate (Pharmablock, 10.5 g, 53.2 mmol), N,N-diisopropylethylamine (27.5 g, 213 mmol) and 2-(3H- [l,2,3]triazolo[4,5-¾]pyridin-3-yl)-l,l,3,3-tetramethylisou ronium hexafluorophosphate(V) (30.3 g, 80 mmol). The reaction mixture was stirred at ambient temperature for 3 hours, and then partitioned between ethyl acetate (250 mL) and water (250 mL). The aqueous layer was extracted with ethyl acetate (3 x 200 mL). The combined organic layers were washed with brine (5 x 300 mL), dried (Na ₂ SO/ _t ), filtered and concentrated under reduced pressure. The crude product was purified by flash chromatography (silica gel, 10-20% ethyl acetate/heptane) to provide 15.4 g (94%) of the title compound as light yellow solid. MS (APCI) m/z 310 (M+H) ⁺ . Example IB: 3-(2-(4-chlorophenoxy)acetamido)bicyclo[l .1.1 ]pentane-l -carboxylic acid A solution of Example 1A (0.52 g, 0.169 mmol) in tetrahydrofuran (3 mL) was treated with 1 N LiOH solution (3.34 mL) and stirred at ambient temperature for 0.5 hour. The reaction mixture was concentrated and neutralized with 6 N HC1. The resultant precipitate was collected by filtration, washed with water, and dried in a vacuum oven to provide the title compound. MS (APCI) m/z 296 (M+H) ⁺ .

Example 1 C: 3-[ 2-( 4-chlorophenoxy )acetamido ]-N-[ 2-( 4-chlorophenoxy)ethyl ]bicyclo[ 1.1.1]- pentane-l-carboxamide (Compound 100)

To a solution of Example IB (0.025 g, 0.085 mmol) in N,N-dimethylformamide (0.5 mL) was added 2-(4-chlorophenoxy)ethan-l -amine (0.015 g, 0.085 mmol), N,N- diisopropylethylamine (0.04 mL, 0.212 mmol) and 2-(7-aza-lH-benzotriazole- l-yl)-l, 1 ,3,3- tetramethyluronium hexafluorophosphate (0.035 g, 0.093 mmol) at ambient temperature. The reaction mixture was stirred for 3 hours, and then it was partitioned between ethyl acetate (20 mL) and water (20 mL). The aqueous layer was extracted with ethyl acetate (3 x 20 mL). The combined organic layers were washed with brine (5 x 30 mL), dried (Na ₂ S04), filtered and concentrated under reduced pressure. The residue was purified by HPLC (Phenomenex® Luna® C18(2) 5 μπι 100 A AXIA™ column 250 mm x 21.2 mm, flow rate 25 mL/minute, 10-80% gradient of acetonitrile in buffer (0.1 % trifluoroacetic acid in water)) to provide 0.028 g (74%) of the title compound as light yellow solid. ^J H NMR (400 MHz, DMSO- ₆ ) δ ppm 8.65 (s, 1H), 7.96 (t, / = 5.7 Hz, 1H), 7.40 - 7.25 (m, 4H), 7.05 - 6.90 (m, 4H), 4.38 (s, 2H), 3.95 (t, / = 5.9 Hz, 2H), 3.35 (q, / = 5.9 Hz, 2H), 2.13 (s, 6H). MS (APCI) m/z 450 (M+H) ⁺ .

Example 2: 3-[2-(4-chlorophenoxy)acetamido]-N-[2-(3-methylphenoxy)ethyl ]bicyclo[l.l.l]- pentane-l-carboxamide (Compound 101)

A solution of Example IB (25 mg, 0.08 mmol) in N,N-dimethylformamide (1.0 mL) was treated with a solution of 2-(3H-[l ,2,3]triazolo[4,5-¾]pyridin-3-yl)- l, 1 ,3,3- tetramethylisouronium hexafluorophosphate(V) (35 mg, 0.09 mmol) in N,N-dimethylformamide (0.5 mL). Then a solution of 2-(m-tolyloxy)ethanamine (12 mg, 0.08 mmol) in N,N- dimethylacetamide (0.15 mL) was added followed by N,N-diisopropylethylamine (0.037 mL, 0.21 mmol). The reaction was shaken at ambient temperature overnight and purified by HPLC (2-coupled C8 5 μπι 100 A columns 30 mm x 75 mm each, flow rate of 50 mL/minute, 5-90% gradient of acetonitrile in buffer (0.1 % trifluoroacetic acid in water)) to provide the title compound. ^J H NMR (400 MHz, DMSO-<¾/D ₂ 0, temperature = 27 °C ) δ ppm 8.06 (t, / = 5.7 Hz, 1H), 7.36 - 7.29 (m, 2H), 7.15 (t, / = 8.0 Hz, 1H), 7.01 - 6.93 (m, 2H), 6.77 - 6.68 (m, 3H), 4.40 (s, 2H), 3.95 (t, / = 5.9 Hz, 2H), 3.43 - 3.31 (m, 2H), 2.25 (s, 3H), 2.17 (s, 6H). MS (APCI+) m/z 429.2 (M+H) ⁺ .

Example 3: 3-[2-(4-chlorophenoxy)acetamido]-N-[2-(4-fluorophenoxy)ethyl ]bicyclo[l.l.l]- pentane-l-carboxamide (Compound 102)

The title compound was prepared using the method described in Example 2 by replacing 2-(m-tolyloxy)ethanamine with 2-(4-fluorophenoxy)ethanamine (12.4 mg, 0.08 mmol). ^J H NMR (400 MHz, DMSO-<¾/D ₂ 0, temperature = 27 °C ) δ ppm 8.07 (t, / = 5.7 Hz, 1H), 7.38 - 7.32 (m, 2H), 7.15 - 7.06 (m, 2H), 7.02 - 6.90 (m, 4H), 4.40 (s, 2H), 3.95 (t, / = 5.8 Hz, 2H), 3.46 - 3.36 (m, 2H), 2.17 (s, 6H). MS (APCI+) m/z 433.2 (M+H) ⁺ .

Example 4 : iV- [2-(4-chloro-3-methy lphenoxy)ethyl] -3 - [2-(4-chlorophenoxy)acetamido] - bicyclo[l.l.l]pentane-l-carboxamide (Compound 103)

The title compound was prepared using the method described in Example 2 by replacing 2-(m-tolyloxy)ethanamine with 2-(4-chloro-3-methylphenoxy)ethanamine (14.8 mg, 0.08 mmol). ^J H NMR (400 MHz, DMSO-<¾/D ₂ 0, temperature = 27 °C ) δ ppm 8.07 (t, / = 5.7 Hz, 1H), 7.37 - 7.31 (m, 2H), 7.27 (d, / = 8.7 Hz, 1H), 7.03 - 6.96 (m, 2H), 6.95 - 6.91 (m, 1H), 6.83 - 6.77 (m, 1H), 4.40 (s, 2H), 3.97 (t, / = 5.9 Hz, 2H), 3.45 - 3.35 (m, 2H), 2.27 (s, 3H), 2.17 (s, 6H). MS (APCI+) m/z 463.2 (M+H) ⁺ .

Example 5: 3-[2-(4-chlorophenoxy)acetamido]-N-[2-(3-fluorophenoxy)ethyl ]bicyclo- [l.l.l]pentane-l-carboxamide (Compound 104)

The title compound was prepared using the method described in Example 2 by replacing 2-(m-tolyloxy)ethanamine with 2-(3-fluorophenoxy)ethanamine (12.4 mg, 0.08 mmol). ^J H NMR (400 MHz, DMSO-<¾/D ₂ 0, temperature = 27 °C ) δ ppm 8.75 (s, 1H), 8.08 (t, / = 5.7 Hz, 1H), 7.36 - 7.28 (m, 3H), 7.03 - 6.93 (m, 2H), 6.82 - 6.74 (m, 3H), 4.40 (s, 2H), 4.00 (t, / = 5.8 Hz, 2H), 3.43 - 3.34 (m, 2H), 2.17 (s, 6H). MS (APCI+) m/z 433.2 (M+H) ⁺ .

Example 6: 3-[2-(4-chlorophenoxy)acetamido]-N-[2-(4-methylphenoxy)ethyl ]bicyclo- [l.l.l]pentane-l-carboxamide (Compound 105)

The title compound was prepared using the method described in Example 2 by replacing 2-(m-tolyloxy)ethanamine with 2-(p-tolyloxy)ethanamine (12.4 mg, 0.08 mmol). ^J H NMR (400 MHz, DMSO-<¾/D ₂ 0, temperature = 27 °C ) δ ppm 8.75 (s, 1H), 8.06 (t, / = 5.7 Hz, 1H), 7.39 - 7.31 (m, 2H), 7.12 - 7.05 (m, 2H), 7.01 - 6.94 (m, 2H), 6.86 - 6.78 (m, 2H), 4.40 (s, 2H), 3.93 (t, / = 6.0 Hz, 2H), 3.43 - 3.34 (m, 2H), 2.21 (s, 3H), 2.17 (s, 6H). MS (APCI+) m/z 429.2 (M+H) ⁺ . Example 7: 4-[2-(4-chloro-3-fluorophenoxy)acetamido]-2-hydroxy-iV-{[5- (trifluoromethyl)pyridin-2-yl]methyl}bicyclo[2.2.2]octane-l- carboxamide (Compound 106)

Example 7 : ethyl l,4-dioxaspiro[4.5]decane-8-carboxylate

A mixture of ethyl 4-oxocyclohexanecarboxylate (11.70 mL, 73.4 mmol), ethane- 1 ,2-diol (12.29 mL, 220 mmol), and p-toluenesulfonic acid monohydrate (1.397 g, 7.34 mmol) in toluene (200 mL) was stirred at 120 °C with a Dean-Stark trap apparatus for 180 minutes. The reaction mixture was neutralized with N-ethyl-N-isopropylpropan-2-amine and then concentrated. The residue was purified on silica gel (0-30% ethyl acetate in heptane) to give 12.77 g of the title compound as a clear oil. ^J H NMR (400 MHz, DMSO-<¾) δ ppm 4.01 (q, / = 7.1 Hz, 2H), 3.81 (s, 4H), 2.32 (tt, / = 10.4, 3.8 Hz, 1H), 1.83 - 1.71 (m, 2H), 1.66 - 1.57 (m, 1H), 1.62 - 1.38 (m, 5H), 1.13 (t, J = 7.1 Hz, 3H).

Example 7B: ethyl 8-acetyl-l,4-dioxaspiro[4.5]decane-8-carboxylate

To a solution of diisopropylamine (5.19 mL, 36.4 mmol) in tetrahydrofuran (25 mL) at 0 °C was added «-butyllithium slowly below 5 °C. After stirring for 30 minutes, the solution was cooled to -78 °C under nitrogen, and a solution of Example 7A (6.0 g, 28.0 mmol) in tetrahydrofuran (3 mL) was added slowly, and the resultant mixture was stirred for 30 minutes at the same temperature. Then acetyl chloride (2.59 mL, 36.4 mmol) was added slowly to maintain the temperature below -60 °C, and the mixture was stirred at -70 °C for 2 hours. The reaction was quenched with saturated NH4CI solution, and the aqueous phase was extracted with ethyl acetate. The organic layer was washed with brine, dried over magnesium sulfate and filtered. The filtrate was concentrated, and the residue was purified on silica gel (0-70% ethyl acetate in heptane) to give 6.78 g of the title compound as a clear oil. ^J H NMR (500 MHz, DMSO- ) δ ppm 4.19 - 4.11 (m, 2H), 3.85 (s, 4H), 2.13 (s, 3H), 2.10 - 2.01 (m, 2H), 1.90 (ddd, / = 13.9, 9.6, 4.6 Hz, 2H), 1.54 (th, / = 13.6, 4.7 Hz, 4H), 1.18 (dd, / = 7.6, 6.5 Hz, 3H).

Example 7 C: ethyl l-acetyl-4-oxocyclohexane-l-carboxylate

A mixture of Example 7B (6.5 g, 25.4 mmol) and HC1 (21.13 mL, 127 mmol) in acetone (60 mL) was stirred at ambient temperature overnight. Volatiles were removed under reduced pressure, and the residue was partitioned between water and dichlorome thane. The organic layer was washed with brine, dried over magnesium sulfate and filtered. The filtrate was concentrated to give 5.46 g of the title compound as a clear oil, used without further purification. ^J H NMR

(400 MHz, DMSO- ) δ ppm 4.16 (q, / = 7.1 Hz, 2H), 2.17 (s, 3H), 2.35 2.07 (m, 8H), 1.17 (t, / = 7.1 Hz, 3H).

Example 7D: ethyl 4-(benzylamino )-2-oxobicyclo[ 2.2.2 ] octane- 1-carboxylate A mixture of Example 7C (9.7 g, 45.7 mmol), benzylamine (14.98 mL, 137 mmol), and /?-toluenesulfonic acid monohydrate (0.087 g, 0.457 mmol) in toluene (100 mL) was stirred at 130 °C with a Dean-Stark trap apparatus overnight. The mixture was concentrated, and the residue was stirred with a mixture of ethyl acetate (50 mL) and 3 N HC1 (100 mL) for 30 minutes. The precipitate was collected by filtration, washed with mixture of ethyl

acetate/heptane, air-dried to give 11.3 g of title compound as a HC1 salt. The filtrate was neutralized with 6 N NaOH and extracted with ethyl acetate (100 mL x 2). The organic layer was washed with brine, dried over magnesium sulfate and filtered. The residue was purified on silica gel (0-70% ethyl acetate in heptane) to give another 0.77 g of the title compound as yellow solid. ^J H NMR (400 MHz, DMSO-<¾) δ ppm 9.73 (t, / = 6.2 Hz, 2H), 7.87 - 7.12 (m, 5H), 4.09 (m, 4H), 2.88 (s, 2H), 2.08 (dt, / = 20.7, 13.4 Hz, 6H), 1.16 (t, / = 7.1 Hz, 3H); MS (ESI ⁺ ) m/z 302.1 (M+H) ⁺ .

Example 7E: ethyl 4-amino-2-oxobicyclo[2.2.2] octane- 1-carboxylate, hydrochloric acid

To a mixture of Example 7D (11.2 g, 33.2 mmol) in tetrahydrofuran (1 10 mL) in a 50 mL pressure bottle was added 20% Pd(OH)2/C, wet (2.2 g, 1.598 mmol), and the reaction was shaken at 50 °C under 50 psi of hydrogen for 22 hours. The reaction mixture was cooled to ambient temperature, and solids were removed by filtration and washed with methanol (1 L).

The filtrate and wash were concentrated to give 7.9 g of the title compound as a light yellow solid. ^J H NMR (400 MHz, DMSO-<¾) δ ppm 8.46 (s, 3H), 4.07 (q, / = 7.1 Hz, 2H), 2.62 (s, 2H), 2.17 - 2.05 (m, 2H), 2.04 - 1.78 (m, 6H), 1.14 (t, / = 7.1 Hz, 3H).

Example 7F: ethyl 4-[2-(4-chloro-3-fluorophenoxy)acetamido]-2-oxobicyclo[2.2.2 ]octane-l- carboxylate

To a suspension of Example 7E (7.8 g, 31.5 mmol), N-ethyl-N-isopropylpropan-2-amine (22.00 mL, 126 mmol) and 2-(4-chloro-3-fluorophenoxy)acetic acid (7.41 g, 36.2 mmol) in N,N- dimethylformamide (200 mL), 2-(3H-[l ,2,3]triazolo[4,5- ?]pyridin-3-yl)-l, 1,3,3- tetramethylisouronium hexafluorophosphate(V) (14.97 g, 39.4 mmol) was added, and the resulting brown solution was stirred at ambient temperature for 16 hours. Water was added, and the mixture was stirred for 15 minutes. The precipitate was collected by filtration, washed with water, and air-dried to give 12.1 g of the title compound as an off-white solid. ^J H NMR (400 MHz, DMSO- ) δ ppm 7.87 (s, 1H), 7.45 (t, / = 8.9 Hz, 1H), 7.00 (dd, / = 11.4, 2.9 Hz, 1H), 6.79 (ddd, / = 8.9, 2.9, 1.2 Hz, 1H), 4.45 (s, 2H), 4.06 (q, / = 7.1 Hz, 2H), 2.73 (s, 2H), 2.07 (m, 1H), 2.01 - 1.84 (m, 6H), 1.14 (t, / = 7.1 Hz, 3H); MS (ESI ⁺ ) m/z 398.0 (M+H) ⁺ . Example 7G: 4-[2-(4-chloro-3-fluorophenoxy)acetamido]-2-oxobicyclo[2.2.2 ]octane-l- carboxylic acid

A suspension of Example 7F (11.37 g, 28.6 mmol) and sodium hydroxide (7.15 mL, 57.2 mmol, 8 M solution) in methanol (100 mL) was stirred at ambient temperature for 16 hours. Volatiles were removed, and the residue was acidified with 1 N HC1. The precipitate was collected by filtration and dried in vacuum oven to give 9.9 g of the title compound as a white solid. ^J H NMR (400 MHz, DMSO-<¾) δ ppm 12.49 (s, 1H), 7.86 (s, 1H), 7.45 (t, / = 8.9 Hz, 1H), 7.00 (dd, / = 11.4, 2.9 Hz, 1H), 6.83 - 6.74 (m, 1H), 4.45 (s, 2H), 2.71 (s, 2H), 2.01 - 1.81 (m, 7H); MS (ESI ) m/z 368.1 (M-H)\

Example 7H: 4-(2-(4-chloro-3-fluorophenoxy)acetamido)-2-hydroxybicyclo[2 .2.2]octane-l- carboxylic acid

A suspension of Example 7G (2.6 g, 7.03 mmol) and sodium borohydride (1.330 g, 35.2 mmol) (8 M solution) in methanol (50.0 mL) was stirred at ambient temperature for 30 minutes. The mixture was concentrated, and the residue was acidified with 1 N HC1. The resultant precipitate was collected by filtration and dried in vacuum oven to give 2.63 g of product as a white solid. ^J H NMR (400 MHz, DMSO-<¾) δ ppm 11.93 (s, 1H), 7.50 - 7.39 (m, 2H), 6.98 (dd, J = 11.4, 2.8 Hz, 1H), 6.77 (ddd, J = 9.0, 2.8, 1.2 Hz, 1H), 4.79 (d, J = 4.9 Hz, 1H), 4.40 (s, 2H), 4.02 (dd, J = 8.9, 4.1 Hz, 1H), 2.20 (ddd, J = 12.7, 9.4, 2.9 Hz, 1H), 2.02 (tdd, J = 11.4, 4.4, 2.0 Hz, 1H), 1.85 - 1.44 (m, 8H); MS (ESI ⁺ ) m/z 372.0 (M+H) ⁺ .

Example 71: 4-[2-( 4-chloro-3-fluorophenoxy )acetamido ]-2-hydroxy-N-{ [ 5- (trifluoromethyl)pyridin-2-yl]methyl}bicyclo[2.2.2] octane- 1-carboxamide

A mixture of Example 7G (50 mg, 0.135 mmol), (5-(trifluoromethyl)pyridin-2- yl)methanamine (29.8 mg, 0.169 mmol) and N-ethyl-N-isopropylpropan-2- amine (0.059 mL, 0.338 mmol) in N,N-dimethylformamide (1.5 mL) was treated with 2-(3H-[l ,2,3]triazolo[4,5- Z?]pyridin-3-yl)- l ,l ,3,3-tetramethylisouronium hexafluorophosphate(V) (77 mg, 0.203 mmol), and the reaction was stirred at ambient temperature for 16 hours. The mixture was concentrated, and the residue was dissolved in dichloromethane/methanol (1 : 1 mixture, 2 mL) and treated with sodium borohydride (25.6 mg, 0.676 mmol). The mixture was stirred at ambient temperature for 1 hour. The mixture was concentrated under vacuum, and the crude residue was purified by HPLC (performed on a Phenomenex® Luna® CI 8(2) 5 μπι 100A AXIA™ column (250 mm x 21.2 mm). A gradient of acetonitrile (A) and 0.1 % trifluoroacetic acid in water (B) is used, at a flow rate of 25 mL/minute. A linear gradient is used from about 5% of A to about 95% of A over about 10 minutes. Detection method is UV at wave length of 218 nM and 254 nM) to give 46 mg of product as a white solid. H NMR (400 MHz, DMSO- ) δ ppm 8.82 (d, J = 2.2 Hz, 1H), 8.17 (t, J = 5.9 Hz, 1H), 8.09 (dd, J = 8.4, 2.4 Hz, 1H), 7.53 - 7.40 (m, 3H), 6.99 (dd, J = 11.4, 2.8 Hz, 1H), 6.78 (dd, J = 8.9, 2.8 Hz, 1H), 4.40 (d, J = 6.0 Hz, 4H), 4.07 (dd, J = 9.4, 2.7 Hz, 1H), 2.23 (ddd, J = 12.6, 9.2, 2.8 Hz, 1H), 2.11 (td, J = 11.9, 3.7 Hz, 1H), 1.86 (tt, J = 15.4, 7.8 Hz, 1H), 1.78 - 1.54 (m, 7H); MS (ESI ⁺ ) nt/z 530.2 (M+H) ⁺ .

Example 8: 4-[2-(4-chloro-3-fluorophenoxy)acetamido]-N-[2-(4-chlorophen oxy)ethyl]-2- hydroxybicyclo[2.2.2]octane-l-carboxamide (Compound 107)

The title compound was prepared using the methodologies described in Example 7 substituting 2-(4-chlorophenoxy)ethanamine for (5-(trifluoromethyl)pyridin-2-yl)methanamine. ^J H NMR (400 MHz, DMSO-<¾) δ ppm 7.64 (t, J = 5.6 Hz, 1H), 7.50 - 7.39 (m, 2H), 7.28 (d, J = 8.9 Hz, 2H), 7.03 - 6.87 (m, 3H), 6.77 (dd, J = 9.0, 2.9 Hz, 1H), 4.89 (s, 1H), 4.40 (s, 2H), 4.03 - 3.88 (m, 3H), 3.37 (t, J = 5.9 Hz, 2H), 2.18 (ddd, J = 12.6, 9.2, 2.9 Hz, 1H), 1.99 (tt, J = 12.0, 3.3 Hz, 1H), 1.90 - 1.77 (m, 1H), 1.74 - 1.57 (m, 5H), 1.52 (tt, J = 12.2, 5.2 Hz, 2H); MS (ESI ⁺ )

Example 9: 4-[2-(4-chloro-3-fluorophenoxy)acetamido]-N-[(5-chloropyridi n-2-yl)methyl]- 2-hydroxybicyclo[2.2.2]octane-l-carboxamide (Compound 108)

The title compound was prepared using the methodologies described in Example 7 substituting (5-chloropyridin-2-yl)methanamine for (5-(trifluoromethyl)pyridin-2- yl)methanamine. ^J H NMR (400 MHz, DMSO- ) δ ppm 8.47 (d, J = 2.5 Hz, 1H), 8.10 (t, J = 6.0 Hz, 1H), 7.88 - 7.75 (m, 1H), 7.56 - 7.32 (m, 2H), 7.27 (d, J = 8.5 Hz, 1H), 6.99 (dd, J = 11.4, 2.8 Hz, 1H), 6.78 (dd, J = 8.8, 2.7 Hz, 1H), 4.41 (s, 2H), 4.30 (d, J = 5.9 Hz, 2H), 4.06 (dd, J = 9.4, 2.7 Hz, 1H), 2.22 (ddd, J = 12.6, 9.2, 2.9 Hz, 1H), 2.08 (tt, J = 11.7, 3.2 Hz, 1H), 1.85 (ddd, J = 23.0, 14.3, 8.5 Hz, 2H), 1.69 (qt, J = 12.7, 2.7 Hz, 6H), 1.65 - 1.53 (m, 1H); MS (ESI ⁺ ) m/z 496.2 (M+H) ⁺ .

Example 10: 4-[2-(4-chloro-3-fluorophenoxy)acetamido]-2-hydroxy-N-{[3-(p ropan-2-yl)- l,2-oxazol-5-yl]methyl}bicyclo[2.2.2]octane-l-carboxamide (Compound 109)

The title compound was prepared using the methodologies described in Example 7 substituting 3-isopropyl-isoxazol-5-ylmethylamine hydrochloride for (5-

(trifluoromethyl)pyridin-2-yl)methanamine. ^J H NMR (400 MHz, DMSO- ¾) δ ppm 8.03 (t, J = 5.9 Hz, 1H), 7.46 (dd, J = 18.3, 9.4 Hz, 2H), 6.99 (dd, J = 11.4, 2.9 Hz, 1H), 6.77 (ddd, J = 9.0, 2.9, 1.2 Hz, 1H), 6.13 (s, 1H), 4.96 (s, 1H), 4.40 (s, 2H), 4.28 (d, J = 5.8 Hz, 2H), 4.04 (d, J = 9.1 Hz, 1H), 2.90 (hept, J = 6.9 Hz, 1H), 2.21 (ddd, J = 12.7, 9.2, 2.8 Hz, 1H), 2.10 - 1.99 (m, 1H), 1.85 (td, J = 11.9, 7.9 Hz, 1H), 1.75 - 1.50 (m, 7H), 1.15 (d, J = 6.9 Hz, 6H); MS (ESI ⁺ ) m/z 494.1 (M+H) ⁺ .

Example 11: 4-[2-(4-chloro-3-fluorophenoxy)acetamido]-2-hydroxy-N-{[4- (trifluoromethyl)phenyl]methyl}bicyclo[2.2.2]octane-l-carbox amide (Compound 110) The title compound was prepared using the methodologies described in Example 7 substituting (4-(trifluoromethyl)phenyl)methanamine for (5-(trifluoromethyl)pyridin-2- yl)methanamine. ^J H NMR (400 MHz, DMSO- ) δ ppm 8.05 (t, J = 6.0 Hz, 1H), 7.61 (d, J = 8.1 Hz, 2H), 7.49 (s, 1H), 7.49 - 7.37 (m, 3H), 6.99 (dd, J = 11.4, 2.9 Hz, 1H), 6.78 (dt, J = 8.8, 1.8 Hz, 1H), 4.93 (s, 1H), 4.41 (s, 2H), 4.31 (d, J = 5.9 Hz, 2H), 4.06 (dt, J = 9.2, 2.2 Hz, 1H), 2.21 (ddd, J = 12.6, 9.2, 2.8 Hz, 1H), 2.14 - 2.02 (m, 1H), 1.86 (tdd, J = 11.4, 5.4, 1.7 Hz, 1H), 1.78 - 1.53 (m, 7H); MS (ESI ⁺ ) m/z 529.2 (M+H) ⁺ .

Example 12: 4-[2-(4-chloro-3-fluorophenoxy)acetamido]-N-[(4,6-dimethylpy ridin-3- yl)methyl]-2-hydroxybicyclo[2.2.2]octane-l-carboxamide (Compound 111)

A mixture of Example 7H (48 mg, 0.129 mmol), (4,6-dimethylpyridin-3-yl)methanamine (21.98 mg, 0.161 mmol) and N-ethyl-N-isopropylpropan-2-amine (0.056 mL, 0.323 mmol) in N,N-dimethylformamide(1.5 mL) was treated with 2-(3H-[l ,2,3]triazolo[4,5-¾]pyridin-3-yl)- 1 , 1 ,3,3-tetramethylisouronium hexafluorophosphate(V) (73.6 mg, 0.194 mmol), and the reaction mixture was stirred at ambient temperature for 16 hours. The reaction mixture was concentrated, and the crude residue was purified by HPLC (10- 100% acetonitrile in 0.1 % trifluoroacetic acid/water at 25 mL/minute on a Phenomenex® C18 5μπι column (250 mm x 21.2 mm)) to give 69 mg of the title compound as a white solid. ^J H NMR (400 MHz, DMSO- ) δ ppm 8.22 (t, J = 5.8 Hz, 1H), 7.53 (s, 1H), 7.50 - 7.38 (m, 2H), 7.37 (s, 1H), 6.99 (dd, J = 1 1.4, 2.8 Hz, 1H), 6.78 (ddd, J = 9.0, 3.0, 1.2 Hz, 1H), 4.48 - 4.37 (m, 4H), 4.06 (dt, J = 8.9, 2.4 Hz, 1H), 2.57 (s, 3H), 2.42 (s, 3H), 2.24 (ddd, J = 12.5, 9.2, 2.9 Hz, 1H), 2.11 (td, J = 11.6, 4.0 Hz, 1H), 1.95 - 1.78 (m, 1H), 1.78 - 1.63 (m, 7H); MS (ESI ⁺ ) m/z 494.2 (M+H) ⁺ .

Example 13: 4-[2-(4-chloro-3-fluorophenoxy)acetamido]-N-[(5-fluoropyridi n-3-yl)methyl]- 2-hydroxybicyclo[2.2.2]octane-l-carboxamide (Compound 112)

The title compound was prepared using the methodologies described in Example 12 substituting (5-fluoropyridin-3-yl)methanamine for (4,6-dimethylpyridin-3-yl)methanamine. ^J H NMR (400 MHz, DMSO-<¾) δ ppm 8.39 (d, J = 2.9 Hz, 1H), 8.31 (s, 1H), 8.04 (t, J = 6.0 Hz,

1H), 7.56 - 7.37 (m, 3H), 6.99 (dd, J = 11.4, 2.8 Hz, 1H), 6.77 (dd, J = 9.0, 2.7 Hz, 1H), 4.40 (s, 2H), 4.39 - 4.22 (m, 2H), 4.05 (dd, J = 9.9, 2.8 Hz, 1H), 2.21 (ddd, J = 12.6, 9.2, 2.9 Hz, 1H), 2.07 (td, J = 11.8, 3.8 Hz, 1H), 1.91 - 1.75 (m, 1H), 1.76 - 1.51 (m, 7H); MS (ESI ⁺ ) m/z 480.2 (M+H) ⁺ .

Example 14: (2/?)-4-[2-(4-chloro-3-fluorophenoxy)acetamido]-2-hydroxy-N- {[5- (trifluoromethyl)pyridin-2-yl]methyl}bicyclo[2.2.2]octane-l- carboxamide (Compound 113) The title compound was isolated by chiral preparative SFC (Supercritical Fluid

Chromatography) of Example 7 as the second eluting peak. Preparative SFC was performed on a THAR/W aters SFC 80 system running under SuperChrom™ software control. The preparative SFC system was equipped with an 8-way preparative column switcher, C(¾ pump, modifier pump, automated back pressure regulator (ABPR), UV detector, and 6-position fraction collector. The mobile phase was comprised of supercritical C(¾ supplied by a Dewar of bone- dry non-certified C(¾ pressurized to 350 psi with a modifier of methanol at a flow rate of 70 g/minute. The column was at ambient temperature and the backpressure regulator was set to maintain 100 bar. The sample was dissolved in a mixture of methanol and dichloromethane (1 : 1) at a concentration of 14 mg/mL. The sample was loaded into the modifier stream in 1 mL (10 mg) injections. The mobile phase was held isocratically at 30% methanol :C(¾. Fraction collection was time triggered. The instrument was fitted with a Chiralpak® AD-H column with dimensions 21 mm i.d. x 250 mm length with 5 μπι particles. ^J H NMR (400 MHz, DMSO-<¾) δ ppm 8.82 (dt, J = 2.2, 0.9 Hz, 1H), 8.17 (t, J = 5.9 Hz, 1H), 8.09 (dd, J = 8.4, 2.4 Hz, 1H), 7.53 - 7.40 (m, 3H), 6.99 (dd, J = 11.4, 2.9 Hz, 1H), 6.78 (ddd, J = 9.0, 2.9, 1.2 Hz, 1H), 5.01 (d, J = 4.2 Hz, 1H), 4.40 (d, J = 6.3 Hz, 4H), 2.23 (ddd, J = 12.5, 9.2, 2.9 Hz, 1H), 2.16 - 2.06 (m, 1H), 1.87 (td, J = 11.7, 4.9 Hz, 1H), 1.78 - 1.55 (m, 7H); MS (ESI ⁺ ) m/z 530.1 (M+H) ⁺ .

Example 15: (2S)-4-[2-(4-chloro-3-fluorophenoxy)acetamido]-2-hydroxy-N-{ [5- (trifluoromethyl)pyridin-2-yl]methyl}bicyclo[2.2.2]octane-l- carboxamide (Compound 114) The title compound was isolated by chiral preparative SFC of Example 7 as the first peak eluted off the column using the methodologies described in Example 14. ^J H NMR (400 MHz, DMSO- ) δ ppm 8.82 (dt, J = 1.8, 0.9 Hz, 1H), 8.17 (t, J = 5.9 Hz, 1H), 8.09 (dd, J = 8.4, 2.4 Hz, 1H), 7.53 - 7.39 (m, 3H), 6.99 (dd, J = 11.4, 2.9 Hz, 1H), 6.78 (ddd, J = 8.9, 2.9, 1.2 Hz, 1H), 5.01 (d, J = 4.2 Hz, 1H), 4.40 (d, J = 6.5 Hz, 4H), 4.08 (dq, J = 8.6, 3.4, 2.8 Hz, 1H), 2.23 (ddd, J = 12.6, 9.1 , 2.9 Hz, 1H), 2.16 - 2.01 (m, 1H), 1.87 (td, J = 11.3, 4.7 Hz, 1H), 1.78 - 1.62 (m, 6H), 1.61 (td, J = 11.5, 4.2 Hz, 1H); MS (ESI ⁺ ) m/z 530.2 (M+H) ⁺ .

Example 16: 4-[2-(4-chloro-3-fluorophenoxy)acetamido]-2-hydroxy-N-[(l,3- oxazol-4- yl)methyl]bicyclo[2.2.2]octane-l-carboxamide (Compound 115) The title compound was prepared using the methodologies described in Example 12 substituting 4-oxazolemethanamine hydrochloride for (4,6-dimethylpyridin-3-yl)methanamine. ^J H NMR (400 MHz, DMSO-<¾) δ ppm 7.87 (t, J = 5.8 Hz, 1H), 7.75 (s, 1H), 7.52 - 7.39 (m, 2H), 6.98 (dd, J = 11.4, 2.9 Hz, 1H), 6.77 (dd, J = 9.1, 2.8 Hz, 1H), 4.39 (s, 2H), 4.11 (d, J = 5.6 Hz, 2H), 4.06 - 3.98 (m, 1H), 2.20 (ddd, J = 12.6, 9.2, 2.9 Hz, 1H), 2.02 (tt, J = 11.8, 3.3 Hz, 1H), 1.84 (td, J = 11.6, 5.1 Hz, 1H), 1.68 (ddd, J = 12.4, 8.2, 4.7 Hz, 5H), 1.64 - 1.48 (m, 2H); MS (ESI ⁺ ) m/z 452.2 (M+H) ⁺ .

Example 17: 4-[2-(4-chloro-3-fluorophenoxy)acetamido]-2-hydroxy-N-[(l-me thyl-lH- pyrazol-3-yl)methyl]bicyclo[2.2.2]octane-l-carboxamide (Compound 116)

The title compound was prepared using the methodologies described in Example 12 substituting (l-methyl-lH-pyrazol-3-yl)methanamine dihydrochloride for (4,6-dimethylpyridin- 3-yl)methanamine. ^J H NMR (400 MHz, DMSO-<¾) δ ppm 7.81 (t, J = 5.8 Hz, 1H), 7.54 - 7.46 (m, 2H), 7.43 (t, J = 8.9 Hz, 1H), 6.98 (dd, J = 11.4, 2.9 Hz, 1H), 6.77 (ddd, J = 9.0, 2.9, 1.2 Hz, 1H), 6.00 (d, J = 2.3 Hz, 1H), 4.47 (s, 1H), 4.39 (s, 2H), 4.14 (d, J = 5.7 Hz, 2H), 4.02 (dt, J = 8.9, 2.1 Hz, 1H), 3.71 (s, 3H), 2.19 (ddd, J = 12.5, 9.2, 2.9 Hz, 1H), 2.01 (tt, J = 11.8, 3.4 Hz, 1H), 1.83 (ddd, J = 12.9, 10.9, 4.7 Hz, 1H), 1.76 - 1.48 (m, 7H); MS (ESI ⁺ ) m/z 465.2 (M+H) ⁺ . Example 18: 3-[2-(4-chloro-3-fluorophenoxy)acetamido]-N-[(4- chlorophenyl)methyl]bicyclo[l.l.l]pentane-l-carboxamide (Compound 117)

Example 18A: 3-(2-(4-chloro-3-fluorophenoxy)acetamido)bicyclo[ l.l.l]pentane-l-carboxylic acid

The reaction and purification conditions described in Example 1A and Example IB, substituting 2-(4-chloro-3-fluorophenoxy)acetic acid (Aldlab) for 2-(4-chlorophenoxy)acetic acid gave the title compound. MS (APCI ⁺ ) m/z 314 (M+H) ⁺ .

Example 18B: 3-[2-(4-chloro-3-fluorophenoxy)acetamido]-N-[(4- chlorophenyl)methyl]bicyclo[l.l.l]pentane-l-carboxamide

The product of Example 18A (52 mg, 0.166 mmol) was suspended in dichloromethane (2 mL) and 1 drop of N,N-dimethylformamide was added followed by the addition of oxalyl chloride (2.0 M solution in dichloromethane, 0.124 mL) in one portion. After stirring at ambient temperature for 10 minutes, the reaction mixture was concentrated under reduced pressure. The residue was taken up in dichloromethane (1 mL), and the mixture was transferred to a pyridine (2 mL) solution of 4-chlorobenzylamine (Aldrich, 23.5 mg, 0.166 mmol). The resulting solution was stirred at ambient temperature for 20 minutes and concentrated under reduced pressure. The residue was taken up in N,N-dimethylformamide (3 mL), filtered through a glass microfiber frit, and purified by preparative HPLC [YMC TriArt™ CI 8 Hybrid 20 μηι column, 25 x 150 mm, flow rate 80 mL/minute, 5-100% gradient of acetonitrile in buffer (0.025 M aqueous ammonium bicarbonate, adjusted to pH 10 with ammonium hydroxide)] to give the title compound (41 mg, 0.094 mmol, 57% yield). ^J H NMR (501 MHz, DMSO-<¾) δ ppm 8.74 (s, 1H), 8.39 (t, J = 6.1 Hz, 1H), 7.48 (t, J = 8.9 Hz, 1H), 7.39 - 7.32 (m, 2H), 7.26 - 7.20 (m, 2H), 7.06 (dd, J = 11.4, 2.8 Hz, 1H), 6.85 (ddd, J = 9.0, 2.9, 1.2 Hz, 1H), 4.46 (s, 2H), 4.22 (d, J = 6.1 Hz, 2H), 2.20 (s, 6H); MS (ESI ⁺ ) m/z 437 (M+H) ⁺ .

Example 19: 3-[2-(4-chloro-3-fluorophenoxy)acetamido]-N-{[5-(trifluorome thyl)pyridin-2- yl]methyl}bicyclo[l.l.l]pentane-l-carboxamide (Compound 118)

A mixture of the product of Example 18A (70 mg, 0.223 mmol), (5-

(trifluoromethyl)pyridin-2-yl)methanamine (47.2 mg, 0.27 mmol), N-[(dimethylamino)-lH- l,2,3-triazolo-[4,5-¾]pyridin-l-ylmethylene]-N-methylmethan aminium hexafluorophosphate N- oxide (HATU, 102 mg, 0.27 mmol), and triethylamine (0.062 mL, 0.45 mmol) in tetrahydrofuran (3 mL) was stirred for 16 hours. The reaction mixture was treated with water and brine and extracted with ethyl acetate. The combined organic layers were concentrated under reduced pressure, and the residue was purified by reverse -phase HPLC performed on a Phenomenex® Zorbax® Rx-C18 column (250 x 21.2 mm, 7 μπι particle size) using a gradient of 10% to 95% acetonitrile/0.1% aqueous trifluoroacetic acid over 30 minutes at a flow rate of 18 mL/minute to provide the title compound (38.0 mg, 0.081 mmol, 36% yield). ^J H NMR (501 MHz, DMSO-<¾) <5 ppm 8.89 (dt, J = 1.9, 1.0 Hz, 1H), 8.73 (s, 1H), 8.52 (t, J = 6.0 Hz, 1H), 8.23 - 8.11 (m, 1H), 7.57 - 7.39 (m, 2H), 7.08 (dd, J = 11.4, 2.9 Hz, 1H), 6.86 (ddd, J = 9.0, 2.9, 1.2 Hz, 1H), 4.48 (s, 2H), 4.43 (d, J = 6.0 Hz, 2H), 2.24 (s, 6H); MS (ESI ⁺ ) m/z 472.1 (M+H) ⁺ .

Example 20: 4-[2-(4-chloro-3-fluorophenoxy)acetamido]-2-hydroxy-N-[(5-me thylpyrazin- 2-yl)methyl]bicyclo[2.2.2]octane-l-carboxamide (Compound 119)

The title compound was prepared using the methodologies described in Example 12 substituting (5-methylpyrazin-2-yl)methanamine for (4,6-dimethylpyridin-3-yl)methanamine. ^J H NMR (400 MHz, DMSO-<¾) δ ppm 8.43 - 8.36 (m, 2H), 8.12 (t, J = 5.9 Hz, 1H), 7.47 (dd, J = 17.3, 8.5 Hz, 2H), 7.01 (dd, J = 11.4, 2.9 Hz, 1H), 6.79 (ddd, J = 8.9, 2.8, 1.2 Hz, 1H), 4.42 (s, 2H), 4.34 (d, J = 5.8 Hz, 2H), 4.07 (dt, J = 9.0, 2.2 Hz, 1H), 2.43 (s, 3H), 2.23 (ddd, J = 12.7, 9.3, 2.9 Hz, 1H), 2.10 (tt, J = 11.6, 3.3 Hz, 1H), 1.88 (td, J = 11.0, 10.6, 4.6 Hz, 1H), 1.78 - 1.54 (m, 7H); MS (ESI ⁺ ) m/z All .2 (M+H) ⁺ .

Example 21: 4-[2-(4-chloro-3-fluorophenoxy)acetamido]-2-hydroxy-N-{[4- (trifluoromethyl)pyridin-2-yl]methyl}bicyclo[2.2.2]octane-l- carboxamide (Compound 120) The title compound was prepared using the methodologies described in Example 12 substituting (4-(trifluoromethyl)pyridin-2-yl)methanamine hydrochloride for (4,6- dimethylpyridin-3-yl)methanamine. ^J H NMR (400 MHz, DMSO- ) δ ppm 8.74 (d, J = 5.2 Hz, 1H), 8.18 (t, J = 5.9 Hz, 1H), 7.59 (d, J = 4.5 Hz, 2H), 7.52 (s, 1H), 7.46 (t, J = 8.9 Hz, 1H), 7.01 (dd, J = 11.4, 2.8 Hz, 1H), 6.80 (dd, J = 8.9, 2.6 Hz, 1H), 4.50 - 4.37 (m, 2H), 4.43 (s, 2H), 4.12 - 4.06 (m, 1H), 2.25 (ddd, J = 12.7, 9.3, 3.0 Hz, 1H), 2.12 (td, J = 12.0, 4.1 Hz, 1H), 1.89 (td, J = 11.7, 5.0 Hz, 1H), 1.79 - 1.57 (m, 7H); MS (ESI ⁺ ) m/z 530.2 (M+H) ⁺ .

Example 22: 4-[2-(4-chloro-3-fluorophenoxy)acetamido]-2-hydroxy-N-{[5- (methanesulfonyl)pyridin-2-yl]methyl}bicyclo[2.2.2]octane-l- carboxamide (Compound 121)

The title compound was prepared using the methodologies described in Example 12 substituting (5-(methylsulfonyl)pyridin-2-yl)methanamine for (4,6-dimethylpyridin-3- yl)methanamine. ^J H NMR (400 MHz, DMSO- ) δ ppm 8.92 (d, J = 2.3 Hz, 1H), 8.23 - 8.15 (m, 2H), 7.53 - 7.39 (m, 3H), 6.99 (dd, J = 11.4, 2.9 Hz, 1H), 6.82 - 6.73 (m, 1H), 4.98 (s, 1H), 4.41 (d, J = 6.3 Hz, 1H), 4.41 (s, 2H), 4.12 - 4.04 (m, 1H), 3.26 (s, 3H), 2.23 (ddd, J = 12.7, 9.3, 2.9 Hz, 1H), 2.12 (tt, J = 12.2, 6.2 Hz, 1H), 1.86 (tt, J = 14.6, 7.3 Hz, 1H), 1.73 - 1.50 (m, 7H); MS (ESI ⁺ ) m/z 540.2 (M+H) ⁺ .

Example 23: 4-[2-(4-fluorophenoxy)acetamido]-2-hydroxy-N-{[5-(trifluorom ethyl)pyridin- 2-yl]methyl}bicyclo[2.2.2]octane-l-carboxamide (Compound 122)

Example 23A: 4-(2-(4-fluorophenoxy)acetamido)-2-oxobicyclo[2.2.2]octane-l -carboxylic acid The title compound was prepared using the methodologies described in Examples 7F-7G substituting 2-(4-fluorophenoxy)acetic acid for 2-(4-chloro-3-fluorophenoxy)acetic acid. ^J H NMR (400 MHz, DMSO-de) δ ppm 7.81 (s, 1H), 7.16 - 7.04 (m, 2H), 6.97 - 6.87 (m, 2H), 4.39 (s, 2H), 2.73 (s, 2H), 2.10 - 1.83 (m, 7H); MS (ESI ⁺ ) m/z 336.0 (M+H) ⁺ .

Example 23B: 4-[2-(4-fluorophenoxy)acetamido]-2-hydroxy-N-{[5-(trifluorom ethyl)pyridin-2- yl ]methyl}bicyclo[ 2.2.2 ] octane- 1 -carboxamide

The title compound was prepared using the methodologies described in Examples 7H-7I substituting Example 23A for Example 7G. ^J H NMR (400 MHz, DMSO-<¾) δ ppm 8.82 (d, J = 2.2 Hz, 1H), 8.18 (t, J = 5.9 Hz, 1H), 8.09 (dd, J = 8.3, 2.4 Hz, 1H), 7.49 - 7.39 (m, 2H), 7.14 - 7.03 (m, 2H), 6.95 - 6.84 (m, 2H), 4.43 - 4.29 (m, 4H), 4.07 (dd, J = 9.2, 2.7 Hz, 1H), 2.23 (ddd, J = 12.6, 9.2, 2.9 Hz, 1H), 2.10 (td, J = 12.2, 3.4 Hz, 1H), 1.87 (td, J = 11.7, 5.0 Hz, 1H), 1.78 - 1.54 (m, 7H); MS (ESI ⁺ ) m/z 496.2 (M+H) ⁺ . Example 24: 4-[2-(4-fluorophenoxy)acetamido]-2-hydroxy-N-{[4- (trifluoromethyl)phenyl]methyl}bicyclo[2.2.2]octane-l-carbox amide (Compound 123)

The title compound was prepared using the methodologies described in Example 23 substituting (4-(trifluoromethyl)phenyl)methanamine for (5-(trifluoromethyl)pyridin-2- yl)methanamine. ^J H NMR (400 MHz, DMSO- ) δ ppm 8.05 (t, J = 6.0 Hz, 1H), 7.61 (d, J = 8.1 Hz, 2H), 7.44 - 7.37 (m, 3H), 7.14 - 7.03 (m, 2H), 6.95 - 6.84 (m, 2H), 4.37 - 4.27 (m, 4H), 4.06 (dd, J = 9.4, 2.6 Hz, 1H), 2.22 (ddd, J = 12.7, 9.2, 2.9 Hz, 1H), 2.07 (tt, J = 11.7, 3.1 Hz, 1H), 1.86 (td, J = 12.1, 11.4, 5.0 Hz, 1H), 1.77 - 1.53 (m, 7H); MS (ESI ⁺ ) m/z 496.2 (M+H) ⁺ . Example 25: 4-[2-(4-chloro-3-fluorophenoxy)acetamido]-2-hydroxy-N-[(3- methylphenyl)methyl]bicyclo[2.2.2]octane-l-carboxamide (Compound 124)

The product of Example 7H (37 mg, 0.10 mmol) and l-[bis(dimethylamino)methylene]- lH-l,2,3-triazolo[4,5-¾]pyridinium 3-oxid hexafluorophosphate (HATU, 57 mg, 0.15 mmol) were mixed in N,N-dimethylacetamide (1.0 mL). m-Tolylmethanamine (15 mg, 0.12 mmol) and N,N-diisopropylethylamine (43 μΕ, 0.25 mmol) were added. The reaction mixture was stirred at room temperature for 16 hours before being purified by reverse phase chromatography: A

Phenomenex® Luna® C8(2) 5 μηι 100A AXIA™ column (50 mm x 30 mm) with a gradient of acetonitrile (A) and 0.1% trifluoroacetic acid in ¾0 (B) was used at a flow rate of 40 mL/minute (0-0.5 minute 5% A, 0.5-6.5 minutes linear gradient 5-100% A, 6.5-8.5 minutes 100% A, 8.5-9.0 minutes linear gradient 100-5% A, 9.0-10.0 minutes 5% A) to yield the title compound (33 mg, 69%). ^J H NMR (400 MHz, DMSO-<¾) δ ppm 7.48 (t, J = 8.9 Hz, 1H), 7.18 (t, J = 7.9 Hz, 1H), 7.08 - 6.95 (m, 4H), 6.82 (ddd, J = 9.0, 2.9, 1.2 Hz, 1H), 4.43 (s, 2H), 4.23 (s, 2H), 4.10 (dt, J = 8.9, 2.0 Hz, 1H), 2.27 (m, 4H), 2.08 (dd, J = 12.9, 9.6 Hz, 1H), 1.90 (td, J = 11.3, 10.6, 4.8 Hz, 1H), 1.80 - 1.54 (m, 7H); MS (ESI ⁺ ) m/z 475 (M+H) ⁺ .

Example 26: 4-[2-(4-chloro-3-fluorophenoxy)acetamido]-2-hydroxy-N-[(4- methylphenyl)methyl]bicyclo[2.2.2]octane-l-carboxamide (Compound 125)

The title compound was prepared using the methodologies described in Example 25 substituting /?-tolylmethanamine for m-tolylmethanamine. ^J H NMR (400 MHz, DMSO- e) δ ppm 7.48 (t, J = 8.9 Hz, 1H), 7.11 (s, 4H), 7.01 (dd, J = 11.3, 2.9 Hz, 1H), 6.82 (ddd, J = 9.0, 2.9, 1.2 Hz, 1H), 4.43 (s, 2H), 4.22 (s, 2H), 4.08 (dt, J = 8.8, 2.1 Hz, 1H), 2.26 (s, 4H), 2.07 (dd, J = 13.4, 10.1 Hz, 1H), 1.89 (td, J = 11.5, 5.2 Hz, 1H), 1.80 - 1.52 (m, 6H); MS (ESI ⁺ ) m/z 475 (M+H) ⁺ . Example 27: 4-[2-(4-chloro-3-fluorophenoxy)acetamido]-N-{[3-fluoro-5- (trifluoromethyl)phenyl]methyl}-2-hydroxybicyclo[2.2.2]octan e-l-carboxamide

(Compound 126)

The title compound was prepared using the methodologies described in Example 25 substituting (3-fluoro-5-(trifluoromethyl)phenyl)methanamine for m-tolylmethanamine. ^J H NMR (400 MHz, DMSO-<¾) δ ppm 7.52 - 7.44 (m, 3H), 7.38 (d, J = 9.5 Hz, 1H), 7.01 (dt, J = 11.4, 3.1 Hz, 1H), 6.82 (ddt, J = 9.1, 3.4, 1.7 Hz, 1H), 4.43 (s, 2H), 4.36 (t, J = 5.1 Hz, 2H), 4.16 - 4.02 (m, 1H), 2.28 (td, J = 9.6, 4.8 Hz, 1H), 2.11 (t, J = 12.2 Hz, 1H), 1.90 (td, J = 11.8, 4.9 Hz, 1H), 1.85 - 1.52 (m, 7H); MS (ESI ⁺ ) m/z 547 (M+H) ⁺ .

Example 28: 4-[2-(4-chloro-3-fluorophenoxy)acetamido]-2-hydroxy-N-[(3- methoxyphenyl)methyl]bicyclo[2.2.2]octane-l-carboxamide (Compound 127)

The title compound was prepared using the methodologies described in Example 25 substituting (3-methoxyphenyl)methanamine for m-tolylmethanamine. ^J H NMR (400 MHz, DMSO- ) δ ppm 7.48 (t, J = 8.9 Hz, 1H), 7.25 - 7.15 (m, 1H), 7.01 (dd, J = 11.4, 2.8 Hz, 1H), 6.86 - 6.73 (m, 4H), 4.44 (s, 2H), 4.25 (s, 2H), 4.10 (dt, J = 8.9, 2.2 Hz, 1H), 3.72 (s, 3H), 2.27 (ddd, J = 12.5, 9.2, 2.9 Hz, 1H), 2.15 - 2.03 (m, 1H), 1.90 (td, J = 11.5, 11.0, 5.1 Hz, 1H), 1.82 - 1.56 (m, 7H); MS (ESI ⁺ ) m/z 491 (M+H) ⁺ .

Example 29: 4-[2-(4-chloro-3-fluorophenoxy)acetamido]-2-hydroxy-N-[(4- methoxyphenyl)methyl]bicyclo[2.2.2]octane-l-carboxamide (Compound 128)

The title compound was prepared using the methodologies described in Example 25 substituting (4-methoxyphenyl)methanamine for m-tolylmethanamine. ^J H NMR (400 MHz, DMSO- ) δ ppm 7.47 (t, J = 8.9 Hz, 1H), 7.20 - 7.10 (m, 2H), 7.01 (dd, J = 11.4, 2.9 Hz, 1H), 6.89 - 6.76 (m, 3H), 4.43 (s, 2H), 4.20 (s, 2H), 4.08 (dt, J = 9.0, 2.1 Hz, 1H), 3.72 (s, 3H), 2.26 (ddd, J = 12.6, 9.2, 2.9 Hz, 1H), 2.12 - 1.99 (m, 1H), 1.89 (td, J = 11.5, 11.1, 5.2 Hz, 1H), 1.80 - 1.53 (m, 7H); MS (ESI ⁺ ) m/z 491 (M+H) ⁺ .

Example 30: 4-[2-(4-chloro-3-fluorophenoxy)acetamido]-N-[(3-fluorophenyl )methyl]-2- hydroxybicyclo[2.2.2]octane-l-carboxamide (Compound 129)

The title compound was prepared using the methodologies described in Example 25 substituting (3-fluorophenyl)methanamine for m-tolylmethanamine. ^J H NMR (400 MHz, DMSO- ) δ ppm 7.48 (t, J = 8.9 Hz, 1H), 7.38 - 7.24 (m, 1H), 7.13 - 6.91 (m, 4H), 6.83 (ddd, J = 9.2, 2.8, 1.2 Hz, 1H), 4.44 (s, 2H), 4.29 (d, J = 4.7 Hz, 2H), 4.10 (dt, J = 9.1, 2.3 Hz, 1H), 2.28 (ddd, J = 12.6, 9.2, 2.9 Hz, 1H), 2.10 (t, J = 11.6 Hz, 1H), 1.90 (td, J = 11.5, 5.1 Hz, 1H), 1.81 - 1.52 (m, 7H); MS (ESI ⁺ ) m/z 479 (M+H) ⁺ . Example 31: 4-[2-(4-chloro-3-fluorophenoxy)acetamido]-N-[(4-fluorophenyl )methyl]-2- hydroxybicyclo[2.2.2]octane-l-carboxamide (Compound 130)

The title compound was prepared using the methodologies described in Example 25 substituting (4-fluorophenyl)methanamine for m-tolylmethanamine. ^J H NMR (400 MHz, DMSO- ) δ ppm 7.48 (t, J = 8.9 Hz, 1H), 7.31 - 7.20 (m, 2H), 7.15 - 7.07 (m, 2H), 7.01 (dd, J = 11.4, 2.9 Hz, 1H), 6.82 (ddd, J = 9.1, 2.9, 1.2 Hz, 1H), 4.43 (s, 2H), 4.25 (s, 2H), 4.09 (dt, J = 9.0, 2.1 Hz, 1H), 2.27 (ddd, J = 12.6, 9.2, 2.9 Hz, 1H), 2.15 - 2.02 (m, 1H), 1.90 (td, J = 11.6, 5.2 Hz, 1H), 1.68 (dddd, J = 33.6, 17.3, 12.2, 6.7 Hz, 7H); MS (ESI ⁺ ) m/z 479 (M+H) ⁺ .

Example 32: 4-[2-(4-chloro-3-fluorophenoxy)acetamido]-N-[(3-chlorophenyl )methyl]-2- hydroxybicyclo[2.2.2]octane-l-carboxamide (Compound 131)

The title compound was prepared using the methodologies described in Example 25 substituting (3-chlorophenyl)methanamine for m-tolylmethanamine. ^J H NMR (400 MHz, DMSO- ) δ ppm 7.48 (t, J = 8.9 Hz, 1H), 7.33 (dd, J = 8.7, 7.4 Hz, 1H), 7.29 - 7.25 (m, 2H), 7.19 (dt, J = 7.5, 1.4 Hz, 1H), 7.01 (dd, J = 11.4, 2.8 Hz, 1H), 6.82 (ddd, J = 8.8, 2.9, 1.1 Hz, 1H), 4.44 (s, 2H), 4.27 (d, J = 4.9 Hz, 2H), 4.10 (dt, J = 9.0, 2.4 Hz, 1H), 2.28 (ddd, J = 12.6, 9.3, 2.8 Hz, 1H), 2.10 (t, J = 11.6 Hz, 1H), 1.90 (td, J = 11.6, 5.1 Hz, 1H), 1.71 (qt, J = 15.5, 6.8 Hz, 7H); MS (ESI ⁺ ) m/z 495 (M+H) ⁺ .

Example 33: 4-[2-(4-chloro-3-fluorophenoxy)acetamido]-N-[(4-chlorophenyl )methyl]-2- hydroxybicyclo[2.2.2]octane-l-carboxamide (Compound 132)

The title compound was prepared using the methodologies described in Example 25 substituting (4-chlorophenyl)methanamine for m-tolylmethanamine. ^J H NMR (400 MHz, DMSO- ) δ ppm 7.48 (t, J = 8.9 Hz, 1H), 7.38 - 7.31 (m, 2H), 7.28 - 7.18 (m, 2H), 7.01 (dd, J = 11.4, 2.8 Hz, 1H), 6.82 (ddd, J = 9.0, 2.9, 1.2 Hz, 1H), 4.43 (s, 2H), 4.30 - 4.20 (m, 2H), 4.09 (dt, J = 9.0, 2.1 Hz, 1H), 2.27 (ddd, J = 12.7, 9.3, 2.9 Hz, 1H), 2.09 (t, J = 11.8 Hz, 1H), 1.90 (td, J = 11.5, 5.1 Hz, 1H), 1.68 (dddd, J = 29.0, 18.0, 8.8, 4.6 Hz, 7H); MS (ESI ⁺ ) m/z 495 (M+H) ⁺ . Example 34: 4-[2-(4-chloro-3-fluorophenoxy)acetamido]-2-hydroxy-N-{[4- (trifluoromethoxy)phenyl]methyl}bicyclo[2.2.2]octane-l-carbo xamide (Compound 133)

The title compound was prepared using the methodologies described in Example 25 substituting (4-(trifluoromethoxy)phenyl)methanamine for m-tolylmethanamine. ^J H NMR (400 MHz, DMSO- ) δ ppm 7.48 (t, J = 8.9 Hz, 1H), 7.38 - 7.31 (m, 2H), 7.27 (dd, J = 8.6, 1.1 Hz, 2H), 7.01 (dd, J = 11.4, 2.9 Hz, 1H), 6.82 (ddd, J = 9.0, 2.9, 1.2 Hz, 1H), 4.43 (s, 2H), 4.34 - 4.23 (m, 2H), 4.16 - 4.01 (m, 1H), 2.27 (ddd, J = 12.5, 9.2, 2.8 Hz, 1H), 2.10 (t, J = 11.7 Hz, 1H), 1.90 (td, J = 11.5, 5.1 Hz, 1H), 1.79 - 1.56 (m, 7H); MS (ESI ⁺ ) m/z 545 (M+H) ⁺ . Example 35: 4-[2-(4-chloro-3-fluorophenoxy)acetamido]-N-{[4-

(dimethylamino)phenyl]methyl}-2-hydroxybicyclo[2.2.2]octa ne-l-carboxamide (Compound 134)

The title compound was prepared using the methodologies described in Example 25 substituting (4-(dimethylamino)phenyl)methanamine for m-tolylmethanamine. ^J H NMR (400 MHz, DMSO- ) δ ppm 7.48 (t, J = 8.9 Hz, 1H), 7.36 - 7.23 (m, 4H), 7.01 (dd, J = 11.4, 2.9 Hz, 1H), 6.82 (ddd, J = 9.0, 2.9, 1.2 Hz, 1H), 4.44 (s, 2H), 4.26 (s, 2H), 4.09 (dt, J = 9.0, 2.2 Hz, 1H), 3.07 (s, 6H), 2.27 (ddd, J = 12.7, 9.1, 2.8 Hz, 1H), 2.08 (t, J = 11.6 Hz, 1H), 1.90 (td, J = 11.5, 5.1 Hz, 1H), 1.84 - 1.50 (m, 7H); MS (ESI ⁺ ) m/z 504 (M+H) ⁺ .

Example 36: 4-[2-(4-chloro-3-fluorophenoxy)acetamido]-2-hydroxy-N-{[3-

(trifluoromethyl)phenyl]methyl}bicyclo[2.2.2]octane-l-car boxamide (Compound 135) The title compound was prepared using the methodologies described in Example 25 substituting (3-(trifluoromethyl)phenyl)methanamine for m-tolylmethanamine. ^J H NMR (400 MHz, DMSO- ) δ ppm 7.58 - 7.52 (m, 4H), 7.48 (t, J = 8.9 Hz, 1H), 7.01 (dd, J = 11.4, 2.9 Hz, 1H), 6.82 (ddd, J = 9.0, 2.9, 1.2 Hz, 1H), 4.44 (s, 2H), 4.38 - 4.27 (m, 2H), 4.14 - 4.03 (m, 1H), 2.28 (ddd, J = 12.5, 9.2, 2.8 Hz, 1H), 2.11 (t, J = 11.6 Hz, 1H), 1.90 (td, J = 11.5, 5.0 Hz, 1H), 1.82 - 1.56 (m, 7H); MS (ESI ⁺ ) m/z 529 (M+H) ⁺ .

Example 37: 4-[2-(4-chloro-3-fluorophenoxy)acetamido]-2-hydroxy-N-{[3- (trifluoromethoxy)phenyl]methyl}bicyclo[2.2.2]octane-l-carbo xamide (Compound 136) The title compound was prepared using the methodologies described in Example 25 substituting (3-(trifluoromethoxy)phenyl)methanamine for m-tolylmethanamine. ^J H NMR (400 MHz, DMSO- ) δ ppm 7.51 - 7.38 (m, 2H), 7.26 (dt, J = 7.7, 1.2 Hz, 1H), 7.20 (d, J = 6.7 Hz, 2H), 7.01 (dd, J = 11.4, 2.9 Hz, 1H), 6.83 (ddd, J = 9.0, 2.9, 1.2 Hz, 1H), 4.44 (s, 2H), 4.34 - 4.24 (m, 2H), 4.10 (d, J = 8.7 Hz, 1H), 2.28 (ddd, J = 12.5, 9.2, 2.8 Hz, 1H), 2.10 (t, J = 11.5 Hz, 1H), 1.90 (td, J = 11.5, 5.1 Hz, 1H), 1.82 - 1.50 (m, 7H); MS (ESI ⁺ ) m/z 545 (M+H) ⁺ .

Example 38: N-[(4-tert-butylphenyl)methyl]-4-[2-(4-chloro-3-fluorophenox y)acetamido]-2- hydroxybicyclo[2.2.2]octane-l-carboxamide (Compound 137)

The title compound was prepared using the methodologies described in Example 25 substituting (4-teri-butylphenyl)methanamine for m-tolylmethanamine. ^J H NMR (400 MHz, DMSO- ) δ ppm 7.48 (t, J = 8.9 Hz, 1H), 7.37 - 7.26 (m, 2H), 7.19 - 7.08 (m, 2H), 7.01 (dd, J = 11.4, 2.8 Hz, 1H), 6.82 (ddd, J = 9.0, 2.9, 1.2 Hz, 1H), 4.43 (s, 2H), 4.23 (s, 2H), 4.12 - 4.00 (m, 1H), 2.27 (ddd, J = 12.4, 9.1, 2.8 Hz, 1H), 2.08 (t, J = 11.7 Hz, 1H), 1.90 (td, J = 11.4, 5.0 Hz, 1H), 1.81 - 1.52 (m, 7H), 1.26 (s, 9H); MS (ESI ⁺ ) m/z 517 (M+H) ⁺ . Example 39: 4-[2-(4-chloro-3-fluorophenoxy)acetamido]-2-hydroxy-N-{2-[4- (trifluoromethyl)phenyl]ethyl}bicyclo[2.2.2]octane-l-carboxa mide (Compound 138)

The title compound was prepared using the methodologies described in Example 25 substituting (4-(trifluoromethyl)phenyl)methanamine for m-tolylmethanamine. ^J H NMR (400 MHz, DMSO- ) δ ppm 7.64 (d, J = 8.0 Hz, 2H), 7.51 - 7.34 (m, 3H), 7.01 (dd, J = 11.4, 2.9 Hz, 1H), 6.82 (ddd, J = 8.9, 2.9, 1.2 Hz, 1H), 4.43 (s, 2H), 4.08 - 3.92 (m, 1H), 3.30 (t, J = 7.1 Hz, 2H), 2.80 (t, J = 7.1 Hz, 2H), 2.23 (ddd, J = 12.7, 9.2, 2.9 Hz, 1H), 1.99 (dd, J = 13.5, 10.0 Hz, 1H), 1.87 (td, J = 11.8, 11.4, 5.2 Hz, 1H), 1.80 - 1.38 (m, 7H); MS (ESI ⁺ ) m/z 543 (M+H) ⁺ . Example 40: 4-[2-(4-chloro-3-fluorophenoxy)acetamido]-2-hydroxy-N-[(pyri din-2- yl)methyl]bicyclo[2.2.2]octane-l-carboxamide (Compound 139)

The title compound was prepared using the methodologies described in Example 25 substituting pyridine-2-ylmethanamine for m-tolylmethanamine. ^J H NMR (400 MHz, DMSO- d ₆ ) δ ppm 8.74 - 8.64 (m, 1H), 8.32 (td, J = 7.9, 1.6 Hz, 1H), 7.79 - 7.67 (m, 2H), 7.48 (t, J = 8.9 Hz, 1H), 7.01 (dd, J = 11.3, 2.8 Hz, 1H), 6.82 (ddt, J = 9.1 , 3.2, 1.6 Hz, 1H), 4.53 (s, 2H), 4.44 (s, 2H), 4.10 (dt, J = 9.1, 2.4 Hz, 1H), 2.29 (ddd, J = 12.6, 9.1, 2.8 Hz, 1H), 2.18 - 2.06 (m, 1H), 1.93 (qd, J = 11.3, 10.5, 5.0 Hz, 1H), 1.81 - 1.59 (m, 7H); MS (ESI ⁺ ) m/z 462 (M+H) ⁺ .

Example 41: 4-[2-(4-chloro-3-fluorophenoxy)acetamido]-2-hydroxy-N-[l-(py ridin-3- yl)ethyl]bicyclo[2.2.2]octane-l-carboxamide (Compound 140)

The title compound was prepared using the methodologies described in Example 25 substituting l-(pyridin-3-yl)ethanamine for m-tolylmethanamine. ^J H NMR (400 MHz, DMSO- d ₆ ) δ ppm 8.84 - 8.64 (m, 2H), 8.45 (ddt, J = 8.1, 4.1, 1.7 Hz, 1H), 8.01 - 7.90 (m, 1H), 7.48 (t, J = 8.9 Hz, 1H), 7.01 (dd, J = 11.4, 2.8 Hz, 1H), 6.82 (ddd, J = 9.0, 2.9, 1.2 Hz, 1H), 5.05 (p, J = 7.1 Hz, 1H), 4.44 (s, 2H), 4.20 - 4.03 (m, 1H), 2.33 - 2.20 (m, 1H), 2.18 - 1.98 (m, 1H), 1.98 - 1.81 (m, 1H), 1.80 - 1.56 (m, 7H), 1.45 (d, J = 7.2 Hz, 3H); MS (ESI ⁺ ) m/z 476 (M+H) ⁺ .

Example 42: 4-[2-(4-chloro-3-fluorophenoxy)acetamido]-N-[(5-cyanopyridin -2-yl)methyl]- 2-hydroxybicyclo[2.2.2]octane-l-carboxamide (Compound 141)

The title compound was prepared using the methodologies described in Example 25 substituting (5-cyanopyridin-2-yl)methanamine for m-tolylmethanamine. ^J H NMR (400 MHz, DMSO- ) δ ppm 8.90 (dd, J = 2.1, 0.8 Hz, 1H), 8.21 (dd, J = 8.2, 2.2 Hz, 1H), 7.52 - 7.39 (m, 2H), 7.02 (dd, J = 11.4, 2.8 Hz, 1H), 6.83 (ddd, J = 9.1, 2.9, 1.2 Hz, 1H), 4.44 (d, J = 4.1 Hz, 4H), 4.11 (dt, J = 8.9, 2.2 Hz, 1H), 2.29 (ddd, J = 12.6, 9.3, 2.9 Hz, 1H), 2.18 - 2.07 (m, 1H), 1.92 (td, J = 11.5, 4.9 Hz, 1H), 1.82 - 1.54 (m, 7H); MS (ESI ⁺ ) m/z 487 (M+H) ⁺ . Example 43: 4-[2-(4-chloro-3-fluorophenoxy)acetamido]-2-hydroxy-N-[(5-me thylpyridin- 2-yl)methyl]bicyclo[2.2.2]octane-l-carboxamide (Compound 142)

The title compound was prepared using the methodologies described in Example 25 substituting (5-methylpyridin-2-yl)methanamine for m-tolylmethanamine. ^J H NMR (400 MHz, DMSO- ) δ ppm 8.56 (t, J = 5.9 Hz, 1H), 7.71 - 7.61 (m, 2H), 7.54 - 7.35 (m, 1H), 7.01 (dd, J = 11.4, 2.8 Hz, 1H), 6.83 (ddd, J = 9.0, 2.9, 1.2 Hz, 1H), 4.51 (d, J = 5.9 Hz, 2H), 4.45 (d, J = 5.5 Hz, 3H), 4.17 - 4.03 (m, 1H), 2.40 - 2.24 (m, 1H), 2.20 - 2.06 (m, 1H), 2.00 - 1.84 (m, 2H), 1.81 - 1.57 (m, 8H); MS (ESI ⁺ ) m/z 476 (M+H) ⁺ .

Example 44: 4-[2-(4-chloro-3-fluorophenoxy)acetamido]-2-hydroxy-N-[(4-me thylpyridin- 2-yl)methyl]bicyclo[2.2.2]octane-l-carboxamide (Compound 143)

The title compound was prepared using the methodologies described in Example 25 substituting (4-methylpyridin-2-yl)methanamine for m-tolylmethanamine. ^J H NMR (400 MHz, DMSO- ) δ ppm 8.65 - 8.51 (m, 1H), 8.24 (dd, J = 8.4, 2.0 Hz, 1H), 7.68 (d, J = 8.2 Hz, 1H), 7.48 (t, J = 8.9 Hz, 1H), 7.01 (dd, J = 11.4, 2.9 Hz, 1H), 6.83 (ddd, J = 9.0, 2.9, 1.2 Hz, 1H), 4.50 (s, 2H), 4.44 (s, 2H), 4.14 - 4.03 (m, 1H), 2.43 (s, 3H), 2.29 (ddd, J = 12.7, 9.3, 2.9 Hz, 1H), 2.12 (dt, J = 11.9, 6.1 Hz, 1H), 1.92 (td, J = 11.6, 4.7 Hz, 1H), 1.84 - 1.55 (m, 6H); MS (ESI ⁺ ) m/z 476 (M+H) ⁺ .

Example 45: 4-[2-(4-chloro-3-fluorophenoxy)acetamido]-2-hydroxy-N-[(pyra zin-2- yl)methyl]bicyclo[2.2.2]octane-l-carboxamide (Compound 144)

The title compound was prepared using the methodologies described in Example 25 substituting (pyrazin-2-yl)methanamine for m-tolylmethanamine. ^J H NMR (400 MHz, DMSO- d ₆ ) δ ppm 8.57 - 8.40 (m, 3H), 7.48 (t, J = 8.9 Hz, 1H), 7.02 (dd, J = 11.4, 2.9 Hz, 1H), 6.83 (ddd, J = 9.0, 2.9, 1.2 Hz, 1H), 4.52 - 4.36 (m, 4H), 4.11 (dt, J = 9.0, 2.4 Hz, 1H), 2.28 (ddd, J = 12.5, 9.3, 2.8 Hz, 1H), 2.17 - 2.06 (m, 1H), 1.91 (td, J = 11.5, 4.9 Hz, 1H), 1.85 - 1.55 (m, 7H); MS (ESI ⁺ ) m/z 463 (M+H) ⁺ .

Example 46: 4-[2-(4-chloro-3-fluorophenoxy)acetamido]-2-hydroxy-N-methyl -N-{[4- (trifluoromethyl)phenyl]methyl}bicyclo[2.2.2]octane-l-carbox amide (Compound 145) The title compound was prepared using the methodologies described in Example 12 substituting N-methyl-l-(4-(trifluoromethyl)phenyl)methanamine for (4,6-dimethylpyridin-3- yl)methanamine. ^J H NMR (400 MHz, DMSO- ) δ ppm 7.66 (d, J = 8.1 Hz, 2H), 7.52 (s, 1H), 7.46 (t, J = 8.9 Hz, 1H), 7.39 (d, J = 8.0 Hz, 2H), 7.00 (dd, J = 11.4, 2.8 Hz, 1H), 6.83 - 6.76 (m, 1H), 4.64 (q, J = 16.0 Hz, 2H), 4.42 (s, 2H), 4.36 (ddd, J = 9.4, 3.9, 1.6 Hz, 1H), 2.99 (s, 3H), 2.26 (ddd, J = 12.5, 9.3, 2.9 Hz, 1H), 2.15 (tdt, J = 11.2, 6.2, 2.4 Hz, 1H), 1.94 - 1.69 (m, 7H),

I.65 (ddd, J = 12.8, 3.9, 2.1 Hz, 1H); MS (ESI ⁺ ) m/z 543.2 (M+H) ⁺ .

Example 47: 4-[2-(4-chloro-3-fluorophenoxy)acetamido]-N-{[5-(difluoromet hoxy)pyridin- 2-yl]methyl}-2-hydroxybicyclo[2.2.2]octane-l-carboxamide (Compound 146)

The title compound was prepared using the methodologies described in Example 12 substituting (5-(difluoromethoxy)pyridin-2-yl)methanamine for (4,6-dimethylpyridin-3- yl)methanamine. ^J H NMR (400 MHz, DMSO- ) δ ppm 8.34 (d, J = 2.8 Hz, 1H), 8.10 (t, J = 5.9 Hz, 1H), 7.58 (dd, J = 8.6, 2.9 Hz, 1H), 7.53 - 7.40 (m, 2H), 7.31 (d, J = 8.6 Hz, 1H), 7.08 - 6.95 (m, 1H), 6.78 (dd, J = 9.0, 2.8 Hz, 1H), 4.41 (s, 2H), 4.32 (d, J = 5.8 Hz, 2H), 4.06 (dd, J = 9.5, 2.8 Hz, 1H), 2.22 (ddd, J = 12.7, 9.2, 2.9 Hz, 1H), 2.09 (tt, J = 11.5, 3.2 Hz, 1H), 1.86 (td, J =

I I.6, 5.1 Hz, 1H), 1.71 (q, J = 3.9 Hz, 2H), 1.72 - 1.53 (m, 5H); MS (ESI ⁺ ) m/z 528.2 (M+H) ⁺ . Example 48: 3-[2-(4-chloro-3-fluorophenoxy)acetamido]-N-{[5-(difluoromet hoxy)pyridin- 2-yl]methyl}bicyclo[l.l.l]pentane-l-carboxamide (Compound 147)

N,N-Dimethylformamide (2 mL), triethylamine (0.079 mL, 0.57 mmol) and 1- [bis(dimethylamino)methylene]-lH-l,2,3-triazolo[4,5-¾]pyrid inium 3-oxid hexafluorophosphate (79 mg, 0.208 mmol, HATU) were added to a mixture of the product of Example 18A (59.4 mg, 0.189 mmol) and (5-(difluoromethoxy)pyridin-2-yl)methanamine (Enamine, 33 mg, 0.189 mmol) in sequential order. The reaction mixture was then stirred at ambient temperature for 30 minutes. The resulting solution was filtered through a glass microfiber frit and purified by preparative HPLC [YMC TriArt™ CI 8 Hybrid 5 μπι column, 50 x 100 mm, flow rate 90 mL/minute, 5-100% gradient of acetonitrile in buffer (0.025 M aqueous ammonium bicarbonate, adjusted to pH 10 with ammonium hydroxide)] to give the title compound (56 mg, 0.119 mmol, 63% yield). ^J H NMR (501 MHz, DMSO-de) δ ppm 8.73 (s, 1H), 8.44 (t, J = 6.1 Hz, 1H), 8.40 (d, J = 2.8 Hz, 1H), 7.64 (dd, J = 8.6, 2.9 Hz, 1H), 7.50 (t, J = 8.9 Hz, 1H), 7.29 (dd, J = 8.6, 0.7 Hz, 1H), 7.27 (t, J = 73.5 Hz, 1H), 7.08 (dd, J = 11.4, 2.9 Hz, 1H), 6.86 (ddd, J = 8.9, 2.9, 1.2 Hz, 1H), 4.47 (s, 2H), 4.33 (d, J = 6.1 Hz, 2H), 2.22 (s, 6H); MS (ESI ⁺ ) m/z 470 (M+H) ⁺ .

Example 49: 3-[2-(3,4-dichlorophenoxy)acetamido]-N-{[5-(difluoromethoxy) pyridin-2- yl]methyl}bicyclo[l.l.l]pentane-l-carboxamide (Compound 148)

Example 49A: 3-(2-(3,4-dichlorophenoxy)acetamido)bicyclo[ l.l.l]pentane-l-carboxylic acid The reaction and purification conditions described in Example 1A and Example IB, substituting 2-(3,4-dichlorophenoxy)acetic acid (Aldrich) for 2-(4-chlorophenoxy)acetic acid gave the title compound. MS (APCI ⁺ ) m/z 330 (M+H) ⁺ . Example 49B: 3-[ 2-( 3,4-dichlorophenoxy)acetamido ]-N-{[5-( difluoromethoxy)pyridin-2- yl]methyl}bicyclo[l.l.l]pentane-l-carboxamide

The reaction and purification conditions described in Example 48 substituting the product of Example 49 A for the product of Example 18A gave the title compound. ^J H NMR (501 MHz, DMSO- ) δ ppm 8.73 (s, 1H), 8.45 (t, J = 6.1 Hz, 1H), 8.40 (d, J = 2.7 Hz, 1H), 7.64 (dd, J = 8.6, 2.9 Hz, 1H), 7.55 (d, J = 8.9 Hz, 1H), 7.30 (d, J = 8.6 Hz, 1H), 7.27 (t, J = 73.5 Hz, 1H), 7.27 (d, J = 2.9 Hz, 1H), 6.99 (dd, J = 8.9, 2.9 Hz, 1H), 4.49 (s, 2H), 4.33 (d, J = 6.1 Hz, 2H), 2.22 (s, 6H); MS (ESI ⁺ ) m/z 486 (M+H) ⁺ .

Example 50: 3-[2-(4-chloro-3-fluorophenoxy)acetamido]-N-{[6-(trifluorome thyl)pyridin-3- yl]methyl}bicyclo[l.l.l]pentane-l-carboxamide (Compound 149)

The reaction and purification conditions described in Example 48 substituting 3- (aminomethyl)-6-(trifluoromethyl)pyridine (Matrix) for (5-(difluoromethoxy)pyridin-2- yl)methanamine gave the title compound. ^J H NMR (400 MHz, DMSO- ) δ ppm 8.73 (s, 1H), 8.64 (d, J = 1.9 Hz, 1H), 8.49 (t, J = 6.0 Hz, 1H), 7.93 - 7.84 (m, 2H), 7.49 (t, J = 8.8 Hz, 1H), 7.07 (dd, J = 11.4, 2.8 Hz, 1H), 6.85 (ddd, J = 9.0, 2.9, 1.2 Hz, 1H), 4.47 (s, 2H), 4.37 (d, J = 6.0 Hz, 2H), 2.22 (s, 6H); MS (ESI ⁺ ) m/z All [M+H] ⁺ .

Example 51: 3-[2-(3,4-dichlorophenoxy)acetamido]-N-{[6-(trifluoromethyl) pyridin-3- yl]methyl}bicyclo[l.l.l]pentane-l-carboxamide (Compound 150)

The reaction and purification conditions described in Example 48 substituting the product of Example 49A for the product of Example 18 A, and 3-(aminomethyl)-6-

(trifluoromethyl)pyridine (Matrix) for (5-(difluoromethoxy)pyridin-2-yl)methanamine gave the title compound. ^J H NMR (501 MHz, DMSO- ) δ ppm 8.73 (s, 1H), 8.65 - 8.63 (m, 1H), 8.49 (t, J = 6.0 Hz, 1H), 7.92 - 7.86 (m, 2H), 7.55 (d, J = 8.9 Hz, 1H), 7.26 (d, J = 2.9 Hz, 1H), 6.99 (dd, J = 9.0, 2.9 Hz, 1H), 4.48 (s, 2H), 4.37 (d, J = 6.0 Hz, 2H), 2.22 (s, 6H); MS (ESI ⁺ ) m/z 488 (M+H) ⁺ .

Example 52: 3-[2-(4-chloro-3-fluorophenoxy)acetamido]-N-[(l,3-dimethyl-l H-pyrazol-5- yl)methyl]bicyclo[l.l.l]pentane-l-carboxamide (Compound 151)

The reaction and purification conditions described in Example 19 substituting (1,3- dimethyl-lH-pyrazol-5-yl)methanamine for (5-(trifluoromethyl)pyridin-2-yl)methanamine gave the titled compound (56 mg, 0.105 mmol, 82% yield). ^J H NMR (501 MHz, DMSO-<¾) δ ppm

8.71 (s, 1H), 8.25 (t, J = 5 Hz, 1H), 7.49 (t, J = 8 Hz, 1H), 7.05 (dd, J = 9, 3 Hz, 1H), 6.83 (br d, J = 8 Hz, 1H), 5.86 (s, 1H), 4.46 (s, 2H), 4.21 (d, J = 5 Hz, 2H), 3.65 (s, 3H), 2.20 (s, 6H), 2.06 (s, 3H); MS (ESI ⁺ ) m/z 421 (M+H) ⁺ . Example 53: 3-[2-(4-chloro-3-fluorophenoxy)acetamido]-N-[(l,3-dimethyl-l H-pyrazol-4- yl)methyl]bicyclo[l.l.l]pentane-l-carboxamide (Compound 152)

The reaction and purification conditions described in Example 19 substituting (1 ,3- dimethyl-lH-pyrazol-4-yl)methanamine for (5-(trifluoromethyl)pyridin-2-yl)methanamine gave the titled compound (47 mg, 0.088 mmol, 69% yield). ^J H NMR (501 MHz, DMSO-<¾) δ ppm 8.68 (s, 1H), 7.98 (t, J = 5 Hz, 1H), 7.48 (t, J = 8 Hz, 1H), 7.40 (s, 1H), 7.05 (dd, J = 9, 3 Hz, 1H), 6.83 (br d, J = 8 Hz, 1H), 4.44 (s, 2H), 4.00 (d, J = 5 Hz, 2H), 3.69 (s, 3H), 2.15 (s, 6H), 2.05 (s, 3H); MS (ESI ⁺ ) m/z 421 (M+H) ⁺ .

Example 54: 3-[2-(4-chloro-3-fluorophenoxy)acetamido]-N-[2-(pyridin-2- yl)ethyl]bicyclo[l.l.l]pentane-l-carboxamide (Compound 153)

The reaction and purification conditions described in Example 19 substituting 2-(pyridin- 2-yl)ethanamine for (5-(trifluoromethyl)pyridin-2-yl)methanamine gave the titled compound (40 mg, 0.075 mmol, 59% yield). ^J H NMR (501 MHz, DMSO-<¾) δ ppm 8.70 (s, 1H), 8.68 (s, 1H), 8.18 (br t, J = 8 Hz, 1H), 7.90 (br t, J = 8 Hz, 1H), 7.63 (m, 2H), 7.50 (t, J = 8 Hz, 1H), 7.06 (dd, J = 9, 3 Hz, 1H), 6.84 (br d, J = 8 Hz, 1H), 4.46 (s, 2H), 3.44 (m, 2H), 3.03 (t, J = 7 Hz, 2H), 2.13 (s, 6H); MS (ESI ⁺ ) m/z 418 (M+H) ⁺ .

Example 55: 3-[2-(3,4-dichlorophenoxy)acetamido]-N-[(l,3-dimethyl-lH-pyr azol-5- yl)methyl]bicyclo[l.l.l]pentane-l-carboxamide (Compound 154)

The reaction and purification conditions described in Example 49B substituting (1,3- dimethyl- lH-pyrazol-5-yl)methanamine for (5-(difluoromethoxy)pyridin-2-yl)methanamine gave the titled compound (48 mg, 0.087 mmol, 68%). ^J H NMR (501 MHz, DMSO-de) δ ppm 8.73 (s, 1H), 8.28 (t, J = 5 Hz, 1H), 7.54 (d, J = 9 Hz, 1H), 7.26 (d, J = 3 Hz, 1H), 6.98 (dd, J = 9, 3 Hz, 1H), 5.87 (s, 1H), 4.48 (s, 2H), 4.22 (d, J = 5 Hz, 2H), 3.65 (s, 3H), 2.20 (s, 6H), 2.08 (s, 3H); MS (ESI ⁺ ) m/z 437 (M+H) ⁺ .

The compounds in the following table were prepared using the methodologies described above.

Name

Example NMR MS

(Compound Number)

3-[2-(4-chloro-3- MS fluorophenoxy)acetamido] - (APCI ⁺ )

Example 56

N-[(6-methylpyridin-3- m/z 418 yl)methyl] bicyclo [ 1.1.1 ]pen tane- 1 -carboxamide (M+H) ⁺

(Compound 155)

3-[2-(4-chloro-3- ^J H NMR (400 MHz, DMSO- MS fluorophenoxy)acetamido] - de O) δ ppm 7.67 (d, J = 8.1 (APCI ⁺ )

N-{ [4- Hz, 2H), 7.48 (t, J = 8.9 Hz, m/z 471

(trifluoromethyl)phenyl] met 1H), 7.45 - 7.40 (m, 2H), 7.05 (M+H) ⁺

Example 57

hyl } bicyclo [1.1.1] pentane- (dd, J = 11.3, 2.8 Hz, 1H), 6.85

1 -carboxamide (Compound (ddd, J = 9.0, 2.9, 1.2 Hz, 1H),

156) 4.46 (s, 2H), 4.32 (s, 2H), 2.23

(s, 6H)

3-[2-(4-chloro-3- MS fluorophenoxy)acetamido] - (APCI ⁺ )

N-[(6-methoxypyridin-3- m/z 434

Example 58

yl)methyl] bicyclo [ 1.1.1 ]pen (M+H) ⁺ tane- 1 -carboxamide

(Compound 157)

3-[2-(4-chloro-3- Ή NMR (400 MHz, DMSO- MS fluorophenoxy)acetamido] - de O) δ ppm 7.47 (t, J = 8.9 (APCI ⁺ )

N-[2-(3,4- Hz, 1H), 7.04 (dd, J = 11.3, 2.8 m/z 461 dimethylphenoxy)ethyl] bicy Hz, 1H), 7.01 (d, J = 8.3 Hz, (M+H) ⁺ clo[ 1.1.1 ]pentane- 1 - 1H), 6.85 (ddd, J = 9.0, 2.9,

Example 59 carboxamide (Compound 1.2 Hz, 1H), 6.71 (d, J = 2.7

158) Hz, 1H), 6.63 (dd, J = 8.2, 2.7

Hz, 1H), 4.45 (s, 2H), 3.92 (t, J

= 6.0 Hz, 2H), 3.37 (t, J = 6.0

Hz, 2H), 2.18 (s, 6H), 2.16 (s,

3H), 2.12 (s, 3H)

3-[2-(4-chloro-3- MS

Example 60 fluorophenoxy)acetamido] - (APCI ⁺ )

N-[(3-methyl-l,2,4- m/z 409 oxadiazol-5- (M+H) ⁺ yl)methyl] bicyclo [ 1.1.1 ]pen

tane- 1 -carboxamide

(Compound 159)

3-[2-(4-chloro-3- MS fluorophenoxy)acetamido] - (APCI ⁺ )

N-[(2,5-dimethylfuran-3- m/z 421

Example 61

yl)methyl] bicyclo [ 1.1.1 ]pen (M+H) ⁺ tane- 1 -carboxamide

(Compound 160)

3-[2-(4-chloro-3- MS fluorophenoxy)acetamido] - (APCI ⁺ )

N-{ [3- m/z 487

Example 62 (trifluoromethoxy)phenyl] m (M+H) ⁺ ethyl } bicyclo [1.1.1] pentane

-1 -carboxamide (Compound

161)

N-benzyl-3-[2-(4-chloro-3- MS fluorophenoxy)acetamido]bi (APCI ⁺ )

Example 63 cyclo[ 1.1.1 ]pentane- 1 - m/z 403 carboxamide (Compound (M+H) ⁺

162)

3-[2-(4-chloro-3- MS fluorophenoxy)acetamido] - (APCI ⁺ )

N-[(2,6- m/z

Example 64 dichlorophenyl)methyl] bicy 4101413 clo[ 1.1.1 ]pentane- 1 - (M+H) ⁺ carboxamide (Compound

163) 3-[2-(4-chloro-3- Ή NMR (501 MHz, DMSO- fluorophenoxy)acetamido] - d ₆ _O ₂ 0) δ ppm 8.58 (dd, J =

N-[(pyrazin-2- 2.6, 1.5 Hz, 1H), 8.54 - 8.51

yl)methyl] bicyclo [ 1.1.1 ]pen (m, 2H), 7.49 (t, J = 8.9 Hz,

Example 65

tane- 1 -carboxamide 1H), 7.06 (dd, J = 11.3, 2.9 Hz,

(Compound 164) 1H), 6.90 - 6.83 (m, 1H), 4.47

(s, 2H), 4.40 (s, 2H), 2.25 (s,

6H)

3-[2-(4-chloro-3- MS fluorophenoxy)acetamido] - (APCI ⁺ ) N- [(4-methylpyridin-3- m/z 418

Example 66

yl)methyl] bicyclo [ 1.1.1 ]pen (M+H) ⁺ tane- 1 -carboxamide

(Compound 165)

3-[2-(4-chloro-3- MS fluorophenoxy)acetamido] - (APCI ⁺ ) N-[(3- m/z 417

Example 67 methylphenyl)methyl] bicycl (M+H) ⁺ o[l. l.l]pentane-l- carboxamide (Compound

166)

N-[(4-tert- Ή NMR (400 MHz, DMSO- butylphenyl)methyl] -3- [2- _D ₂ 0) δ ppm 7.49 (t, J = 8.9 (4-chloro-3- Hz, 1H), 7.36 - 7.31 (m, 2H), fluorophenoxy)acetamido]bi 7.18 - 7.13 (m, 2H), 7.06 (dd,

Example 68

cyclo[ 1.1.1 Jpentane- 1 - J = 11.3, 2.9 Hz, 1H), 6.86 carboxamide (Compound (ddd, J = 9.1, 2.9, 1.2 Hz, 1H),

167) 4.46 (s, 2H), 4.21 (s, 2H), 2.22

(s, 6H), 1.26 (s, 9H)

Example 69 3-[2-(4-chloro-3- Ή NMR (400 MHz, DMSO- MS fluorophenoxy)acetamido] - ¾_Ι¾0) δ ppm 8.55 (n, J = (APCI ⁺ )

N- [(5-methylpyridin-2- 2.0, 0.8 Hz, IH), 8.18 (dd, J = m/z 418 yl)methyl] bicyclo [ 1.1.1 ]pen 8.3, 2.0 Hz, IH), 7.60 (d, J = (M+H) ⁺ tane- 1 -carboxamide 8.3 Hz, IH), 7.48 (t, J = 8.9

(Compound 168) Hz, IH), 7.05 (dd, J = 11.3, 2.8

Hz, IH), 6.85 (ddd, J = 9.0,

2.9, 1.2 Hz, IH), 4.47 (s, 2H),

4.46 (s, 2H), 2.41 (s, 3H), 2.24

(s, 6H)

3-[2-(4-chloro-3- Ή NMR (400 MHz, DMSO- MS fluorophenoxy)acetamido] - i¾_D ₂ 0) δ ppm 7.47 (t, J = 8.9 (APCI ⁺ )

N-{ [4- Hz, IH), 7.32 - 7.23 (m, 2H), m/z 469

(difluoromethoxy)phenyl]m 7.16 - 7.08 (m, 2H), 7.12 (t, J (M+H) ⁺

Example 70

ethyl } bicyclo [1.1.1] pentane = 74.2 Hz, IH), 7.05 (dd, J = -1 -carboxamide (Compound 11.3, 2.9 Hz, IH), 6.85 (ddd, J

169) = 8.9, 2.9, 1.1 Hz, IH), 4.45 (s,

2H), 4.22 (s, 2H), 2.21 (s, 6H)

3-[2-(4-chloro-3- MS fluorophenoxy)acetamido] - (APCI ⁺ )

N-[(l,2-oxazol-4- m/z 394

Example 71

yl)methyl] bicyclo [ 1.1.1 ]pen (M+H) ⁺ tane- 1 -carboxamide

(Compound 170)

3-[2-(4-chloro-3- Ή NMR (400 MHz, DMSO- MS fluorophenoxy)acetamido] - i¾_D ₂ 0) δ ppm 7.48 (t, J = 8.9 (APCI ⁺ )

N-[l-(4- Hz, IH), 7.22 - 7.14 (m, 2H), m/z 449

Example 72 fluorophenyl)propan-2- 7.09 - 7.01 (m, 3H), 6.85 (ddd, (M+H) ⁺ yl] bicyclo [ 1.1.1 ] pentane- 1 - J = 9.0, 2.9, 1.2 Hz, IH), 4.44 carboxamide (Compound (s, 2H), 3.92 (h, J = 6.7 Hz, 171) IH), 2.71 - 2.60 (m, 2H), 2.11

(s, 6H), 1.03 (d, J = 6.7 Hz, 3H)

3-[2-(4-chloro-3- MS fluorophenoxy)acetamido] - (APCI ⁺ ) N-(l- m/z 417

Example 73

phenylethyl)bicyclo[ 1.1.1 ]p (M+H) ⁺ entane- 1 -carboxamide

(Compound 172)

3-[2-(4-chloro-3- MS fluorophenoxy)acetamido] - (APCI ⁺ ) N-[(3-fluoro-4- m/z 451

Example 74 methoxyphenyl)methyl]bicy (M+H) ⁺ clo[ 1.1.1 Jpentane- 1 - carboxamide (Compound

173)

3-[2-(4-chloro-3- MS fluorophenoxy)acetamido] - (APCI ⁺ ) N-[(2-fluoro-5- m/z ^5

Example 75 methylphenyl)methyl] bicycl (M+H) ⁺ o[l. l.l]pentane-l- carboxamide (Compound

174)

N-benzyl-3-[2-(4-chloro-3- MS fluorophenoxy)acetamido] - (APCI ⁺ ) N- m/z 417

Example 76

methylbicyclo[ 1.1.1 Jpentan (M+H) ⁺ e-1 -carboxamide

(Compound 175)

3-[2-(4-chloro-3- MS

Example 77 fluorophenoxy)acetamido] - (APCI ⁺ )

N- [(4-methyl- 1 ,3-thiazol-2- m/z 424 yl)methyl] bicyclo [ 1.1.1 ]pen (M+H) ⁺ tane- 1 -carboxamide

(Compound 176)

3-[2-(4-chloro-3- MS fluorophenoxy)acetamido] - (APCI ⁺ )

N-[(5-methyl-l,3-oxazol-2- m/z 40S

Example 78

yl)methyl] bicyclo [ 1.1.1 ]pen (M+H) ⁺ tane- 1 -carboxamide

(Compound 177)

3-[2-(4-chloro-3- MS fluorophenoxy)acetamido] - (APCI ⁺ )

N-[(5-methyl-l,3-thiazol-2- m/z 424

Example 79

yl)methyl] bicyclo [ 1.1.1 ]pen (M+H) ⁺ tane- 1 -carboxamide

(Compound 178)

3-[2-(4-chloro-3- MS fluorophenoxy)acetamido] - (APCI ⁺ )

N- [( 1 -methyl- 1 H-pyrazol-3 - m/z 407

Example 80

yl)methyl] bicyclo [ 1.1.1 ]pen (M+H) ⁺ tane- 1 -carboxamide

(Compound 179)

3-[2-(4-chloro-3- MS fluorophenoxy)acetamido] - (APCI ⁺ )

N-{ [4-fluoro-3- m/z 9

Example 81 (trifluoromethyl)phenyl] met (M+H) ⁺ hyl } bicyclo [1.1.1] pentane- 1 -carboxamide (Compound

180)

Example 82 N-[(4-chloro-2,6- MS difluorophenyl)methyl] -3- (APCI ⁺ ) [2-(4-chloro-3- m/z 473 fluorophenoxy)acetamido]bi (M+H) ⁺ cyclo[ 1.1.1 Jpentane- 1 - carboxamide (Compound

181)

3-[2-(4-chloro-3- MS fluorophenoxy)acetamido] - (APCI ⁺ )

N-[(2- m/z 447

Example 83 ethoxyphenyl)methyl] bicycl (M+H) ⁺ o[l. l.l]pentane-l- carboxamide (Compound

182)

3-[2-(4-chloro-3- MS fluorophenoxy)acetamido] - (APCI ⁺ )

N-[(15)-l-(4- m/z 451

Example 84 chlorophenyl)ethyl] bicyclo [ (M+H) ⁺ l.l.l]pentane-l- carboxamide (Compound

183)

3-[2-(4-chloro-3- MS fluorophenoxy)acetamido] - (APCI ⁺ )

N- [( 1 -methyl- 1 H-pyrazol-5 - m/z 407

Example 85

yl)methyl] bicyclo [ 1.1.1 ]pen (M+H) ⁺ tane- 1 -carboxamide

(Compound 184)

3-[2-(4-chloro-3- MS fluorophenoxy)acetamido] - (APCI ⁺ )

Example 86 N-[(3,4- m/z 439 difluorophenyl)methyl] bicy (M+H) ⁺ clo[ 1.1.1 Jpentane- 1 - carboxamide (Compound

185)

3-[2-(4-chloro-3- MS fluorophenoxy)acetamido] - (APCI ⁺ )

N- [( 1 -methyl- 1 H-imidazol- m/z 407

Example 87 2- (M+H) ⁺ yl)methyl] bicyclo [ 1.1.1 ]pen

tane- 1 -carboxamide

(Compound 186)

3-[2-(4-chloro-3- MS fluorophenoxy)acetamido] - (APCI ⁺ )

N-[(15)-l-(3-

Example 88 methylphenyl)ethyl] bicyclo[ (M+H) ⁺ l.l.l]pentane-l- carboxamide (Compound

187)

3-[2-(4-chloro-3- MS fluorophenoxy)acetamido] - (APCI ⁺ )

N-[2-(lH-imidazol-4- m/z 407

Example 89

yl)ethyl] bicyclo [ 1.1. l]penta (M+H) ⁺ ne- 1 -carboxamide

(Compound 188)

3-[2-(4-chloro-3- MS fluorophenoxy)acetamido] - (APCI ⁺ )

N-[(l#)-l-(3- m/z ^l

Example 90 methylphenyl)ethyl] bicyclo[ (M+H) ⁺ l.l.l]pentane-l- carboxamide (Compound

189) 3-[2-(4-chloro-3- MS fluorophenoxy)acetamido] - (APCI ⁺ )

N-[(2,5- m/z 431

Example 91 dimethylphenyl)methyl] bicy (M+H) ⁺ clo[ 1.1.1 Jpentane- 1 - carboxamide (Compound

190)

3-[2-(4-chloro-3- Ή NMR (400 MHz, DMSO- MS fluorophenoxy)acetamido] - de O) δ ppm 8.81 - 8.73 (m, (APCI ⁺ )

N- [(imidazo[ 1 ,2-a]pyridin- 1H), 8.08 (s, 1H), 7.88 - 7.83 m/z 443

2- (m, 2H), 7.48 (t, J = 8.9 Hz, (M+H) ⁺

Example 92 yl)methyl] bicyclo [ 1.1.1 ]pen 1H), 7.44 - 7.38 (m, 1H), 7.05

tane- 1 -carboxamide (dd, J = 11.3, 2.9 Hz, 1H), 6.85

(Compound 191) (ddd, J = 9.0, 2.9, 1.2 Hz, 1H),

4.48 (br s, 2H), 4.46 (s, 2H),

2.25 (s, 6H)

3-[2-(4-chloro-3- MS fluorophenoxy)acetamido] - (APCI ⁺ )

N- [(3-methylthiophen-2- m/z 423

Example 93

yl)methyl] bicyclo [ 1.1.1 ]pen (M+H) ⁺ tane- 1 -carboxamide

(Compound 192)

3-[2-(4-chloro-3- Ή NMR (400 MHz, DMSO- MS fluorophenoxy)acetamido] - d ₆ _O ₂ ) δ ppm 7.51 (t, J = 8.0 (APCI ⁺ )

N-[(4-chloro-3- Hz, 1H), 7.47 (t, J = 8.9 Hz, m/z 455

Example 94 fluorophenyl)methyl] bicycl 1H), 7.21 (dd, J = 10.4, 2.0 Hz, (M+H) ⁺ o[l. l.l]pentane-l- 1H), 7.12 - 7.07 (m, 1H), 7.05 carboxamide (Compound (dd, J = 11.3, 2.8 Hz, 1H), 6.85

193) (ddd, J = 9.0, 2.9, 1.2 Hz, 1H),

4.45 (s, 2H), 4.23 (s, 2H), 2.22 (s, 6Η)

3-[2-(4-chloro-3- Ή NMR (400 MHz, DMSO- MS fluorophenoxy)acetamido] - d ₆ _O ₂ 0) δ ppm 7.98 (t, J = 5.8 (APCI ⁺ )

N-[2-(lH-indol-3- Hz, 1H), 7.54 (dt, J = 7.9, 1.0 m/z 456 yl)ethyl] bicyclo [ 1.1. l]penta Hz, 1H), 7.49 (t, J = 8.9 Hz, (M+H) ⁺ ne- 1 -carboxamide 1H), 7.35 (dt, J = 8.2, 0.9 Hz,

(Compound 194) 1H), 7.15 - 7.12 (m, 1H), 7.11

Example 95

- 7.04 (m, 2H), 6.99 (ddd, J =

8.0, 7.0, 1.1 Hz, 1H), 6.87

(ddd, J = 9.0, 2.9, 1.2 Hz, 1H),

4.47 (s, 2H), 3.36 - 3.26 (m,

2H), 2.83 (t, J = 7.4 Hz, 2H),

2.18 (s, 6H)

3-[2-(4-chloro-3- MS fluorophenoxy)acetamido] - (APCI ⁺ )

N-[(4- m/z 433

Example 96 methoxyphenyl)methyl]bicy (M+H) ⁺ clo[ 1.1.1 Jpentane- 1 - carboxamide (Compound

195)

3-[2-(4-chloro-3- MS fluorophenoxy)acetamido] - (APCI ⁺ )

N- [( 1 -methyl- 1 H-imidazol- m/z 407

Example 97 4- (M+H) ⁺ yl)methyl] bicyclo [ 1.1.1 ]pen

tane- 1 -carboxamide

(Compound 196)

3-[2-(4-chloro-3- MS

Example 98 fluorophenoxy)acetamido] - (APCI ⁺ )

N-[(2- m/z 417 methylphenyl)methyl] bicycl (M+H) ⁺ o[l. l.l]pentane-l- carboxamide (Compound

197)

3-[2-(4-chloro-3- MS fluorophenoxy)acetamido] - (APCI ⁺ ) N-[(lR)-l-(4- m/z 451

Example 99 chlorophenyl)ethyl] bicyclo [ (M+H) ⁺ l.l.l]pentane-l- carboxamide (Compound

198)

3-[2-(4-chloro-3- MS fluorophenoxy)acetamido] - (APCI ⁺ ) N-[2-(4- m/z 496

Example 100 sulf amoylphenyl)ethyl] bicy (M+H) ⁺ clo[ 1.1.1 Jpentane- 1 - carboxamide (Compound

199)

3-[2-(4-chloro-3- MS fluorophenoxy)acetamido] - (APCI ⁺ ) N- [(2-methoxypyrimidin-5- m/z ^5

Example 101

yl)methyl] bicyclo [ 1.1.1 ]pen (M+H) ⁺ tane- 1 -carboxamide

(Compound 200)

3-[2-(4-chloro-3- Ή NMR (400 MHz, DMSO- MS fluorophenoxy)acetamido] - d ₆ _O ₂ ) S ppm 8.12 - 8.06 (m, (APCI ⁺ )

Example 102 N- [(5-phenyl- 1,2,4- 2H), 7.74 - 7.68 (m, 1H), 7.67 m/z 471 oxadiazol-3- - 7.61 (m, 2H), 7.48 (t, J = 8.9 (M+H) ⁺ yl)methyl] bicyclo [ 1.1.1 ]pen Hz, 1H), 7.05 (dd, J = 11.3, 2.9 tane- 1 -carboxamide Hz, 1H), 6.85 (ddd, J = 9.0, (Compound 201) 2.8, 1.2 Hz, 1H), 4.50 - 4.41

(m, 4H), 2.23 (s, 6H)

3-[2-(4-chloro-3- MS fluorophenoxy)acetamido] - (APCI ⁺ )

N-[(3,4- m/z 463

Example 103 dimethoxyphenyl)methyl]bi (M+H) ⁺ cyclo[ 1.1.1 Jpentane- 1 - carboxamide (Compound

202)

3-[2-(4-chloro-3- MS fluorophenoxy)acetamido] - (APCI ⁺ )

N-{ [2-(2,2- m/z 483

Example 104 difluoroethoxy)phenyl] meth (M+H) ⁺ yl } bicyclo [1.1.1] pentane- 1 - carboxamide (Compound

203)

3-[2-(4-chloro-3- Ή NMR (400 MHz, DMSO- MS fluorophenoxy)acetamido] - de O) δ ppm 7.47 (t, J = 8.8 (APCI ⁺ )

N-[3-(4- Hz, 1H), 7.25 - 7.17 (m, 2H), m/z 449 fluorophenyl)propyl] bicyclo 7.11 - 7.02 (m, 3H), 6.85 (ddd, (M+H) ⁺

Example 105

[ 1.1.1 ]pentane-l- J = 9.0, 2.9, 1.2 Hz, 1H), 4.45 carboxamide (Compound (s, 2H), 3.03 (t, J = 7.1 Hz, 204) 2H), 2.56 - 2.50 (m, 2H), 2.17

(s, 6H), 1.75 - 1.60 (m, 2H)

3-[2-(4-chloro-3- MS fluorophenoxy)acetamido] - (APCI ⁺ )

N-[(pyridazin-3- m/z 405

Example 106

yl)methyl] bicyclo [ 1.1.1 ]pen (M+H) ⁺ tane- 1 -carboxamide

(Compound 205) 3-[2-(4-chloro-3- MS fluorophenoxy)acetamido] - (APCI ⁺ )

N-[(3,5-difluoro-4- m/z 469

Example 107 methoxyphenyl)methyl]bicy (M+H) ⁺ clo[ 1.1.1 Jpentane- 1 - carboxamide (Compound

206)

3-[2-(4-chloro-3- MS fluorophenoxy)acetamido] - (APCI ⁺ )

N-({4-[(propan-2- m/z 461

Example 108 yl)oxy]phenyl } methyl)bicyc (M+H) ⁺ lo[ 1.1.1 ]pentane-l- carboxamide (Compound

207)

3-[2-(4-chloro-3- MS fluorophenoxy)acetamido] - (APCI ⁺ )

N-[(l,3-thiazol-2- m/z 410

Example 109

yl)methyl] bicyclo [ 1.1.1 ]pen (M+H) ⁺ tane- 1 -carboxamide

(Compound 208)

3-[2-(4-chloro-3- MS fluorophenoxy)acetamido] - (APCI ⁺ )

N-[(3-fluoro-5- m/z 451

Example 110 methoxyphenyl)methyl]bicy (M+H) ⁺ clo[ 1.1.1 Jpentane- 1 - carboxamide (Compound

209)

3-[2-(4-chloro-3- MS

Example 111 fluorophenoxy)acetamido] - (APCI ⁺ )

N-[(2- m/z M fluorophenyl)methyl] bicycl (M+H) ⁺ o[l.l .l]pentane-l- carboxamide (Compound

210)

3-[2-(4-chloro-3- ¾ NMR (400 MHz, DMSO- MS fluorophenoxy)acetamido] - d ₆ _O ₂ 0) S ppm 7.52 (s, 2H), (APCI ⁺ ) N- [2-(2,6-dimethylpyridin- 7.48 (t, J = 8.9 Hz, 1H), 7.04 m/z 446 4- (dd, J = 11.3, 2.8 Hz, 1H), 6.85 (M+H) ⁺

Example 112

yl)ethyl] bicyclo [ 1.1. l]penta (ddd, J = 9.0, 2.9, 1.2 Hz, 1H), ne- 1 -carboxamide 4.45 (s, 2H), 3.37 (t, J = 6.8 (Compound 211) Hz, 2H), 2.89 (t, J = 6.8 Hz,

2H), 2.62 (s, 6H), 2.15 (s, 6H)

3-[2-(4-chloro-3- MS fluorophenoxy)acetamido] - (APCI ⁺ ) N- { [3-(2-methylpropyl)- 1 ,2- m/z 450

Example 113 oxazol-5- (M+H) ⁺ yl] methyl } bicyclo [1.1.1] pen

tane- 1 -carboxamide

(Compound 212)

3-[2-(4-chloro-3- MS fluorophenoxy)acetamido] - (APCI ⁺ ) N-{2-[5- m/z 486

Example 114 (trifluoromethyl)pyridin-2- (M+H) ⁺ yl] ethyl } bicyclo [ 1.1.1 ]penta

ne- 1 -carboxamide

(Compound 213)

3-[2-(4-chloro-3- MS fluorophenoxy)acetamido] - (APCI ⁺ )

Example 115

N- { [2-(3-methylphenyl)- m/z 500 l,3-thiazol-4- (M+H) ⁺ yl] methyl } bicyclo [1.1.1] pen

tane- 1 -carboxamide

(Compound 214)

3-[2-(4-chloro-3- MS fluorophenoxy)acetamido] - (APCI ⁺ )

N-{ [5- m/z 461

Example 116 (trifluoromethyl)furan-2- (M+H) ⁺ yl] methyl } bicyclo [1.1.1] pen

tane- 1 -carboxamide

(Compound 215)

3-[2-(4-chloro-3- MS fluorophenoxy)acetamido] - (APCI ⁺ )

N-[(3- m/z 433

Example 117 methoxyphenyl)methyl]bicy (M+H) ⁺ clo[ 1.1.1 ]pentane- 1 - carboxamide (Compound

216)

3-[2-(4-chloro-3- MS fluorophenoxy)acetamido] - (APCI ⁺ )

N- [(2-ethylpyrimidin-4- m/z 433

Example 118

yl)methyl] bicyclo [ 1.1.1 ]pen (M+H) ⁺ tane- 1 -carboxamide

(Compound 217)

3-[2-(4-chloro-3- MS fluorophenoxy)acetamido] - (APCI ⁺ )

N- [2-(3-methylpyridin-2- m/z 432

Example 119

yl)ethyl] bicyclo [ 1.1. l]penta (M+H) ⁺ ne- 1 -carboxamide

(Compound 218) 3-[2-(4-chloro-3- MS fluorophenoxy)acetamido] - (APCI ⁺ )

N-[(3- m/z 431

Example 120 chlorophenyl)methyl] bicycl (M+H) ⁺ o[l. l.l]pentane-l- carboxamide (Compound

219)

3-[2-(4-chloro-3- MS fluorophenoxy)acetamido] - (APCI ⁺ )

N-[3-(3,5-dimethyl-l,2- m/z 450

Example 121 oxazol-4- (M+H) ⁺ yl)propyl] bicyclo [1.1.1 ]pent

ane- 1 -carboxamide

(Compound 220)

3-[2-(4-chloro-3- MS fluorophenoxy)acetamido] - (APCI ⁺ )

N- [(4-methylpyridin-2- m/z 418

Example 122

yl)methyl] bicyclo [ 1.1.1 ]pen (M+H) ⁺ tane- 1 -carboxamide

(Compound 221)

3-[2-(4-chloro-3- MS fluorophenoxy)acetamido] - (APCI ⁺ )

N-[(l,2-oxazol-5- m/z 394

Example 123

yl)methyl] bicyclo [ 1.1.1 ]pen (M+H) ⁺ tane- 1 -carboxamide

(Compound 222)

3-[2-(4-chloro-3- MS fluorophenoxy)acetamido] - (APCI ⁺ )

Example 124

#-[(5,6,7,8- m/z 448 tetrahydro[l,2,4]triazolo[4,3 (M+H) ⁺ -fl]pyridin-3- yl)methyl] bicyclo [ 1.1.1 ]pen

tane- 1 -carboxamide

(Compound 223)

3-[2-(4-chloro-3- MS fluorophenoxy)acetamido] - (APCI ⁺ )

N-[(pyridin-2- m/z 404

Example 125

yl)methyl] bicyclo [ 1.1.1 ]pen (M+H) ⁺ tane- 1 -carboxamide

(Compound 224)

3-[2-(4-chloro-3- MS fluorophenoxy)acetamido] - (APCI ⁺ )

N-{ [4- m/z 487

Example 126 (trifluoromethoxy)phenyl] m (M+H) ⁺ ethyl } bicyclo [1.1.1] pentane

-1 -carboxamide (Compound

225)

3-[2-(4-chloro-3- MS fluorophenoxy)acetamido] - (APCI ⁺ )

N- [(6-cyanopyridin-3- m/z 29

Example 127

yl)methyl] bicyclo [ 1.1.1 ]pen (M+H) ⁺ tane- 1 -carboxamide

(Compound 226)

3-[2-(4-chloro-3- MS fluorophenoxy)acetamido] - (APCI ⁺ )

N-{ [4-(propan-2- m/z 445

Example 128

yl)phenyl] methyl } bicyclo [ 1. (M+H) ⁺ 1.1 ]pentane- 1 -carboxamide

(Compound 227) 3-[2-(4-chloro-3- MS fluorophenoxy)acetamido] - (APCI ⁺ )

N- [(5-methylpyrazin-2- m/z 419

Example 129

yl)methyl] bicyclo [ 1.1.1 ]pen (M+H) ⁺ tane- 1 -carboxamide

(Compound 228)

3-[2-(4-chloro-3- MS fluorophenoxy)acetamido] - (APCI ⁺ )

N-{ [4- m/z 447

Example 130 (methoxymethyl)phenyl] me (M+H) ⁺ thyl } bicyclo [ 1.1.1 Jpentane- 1 -carboxamide (Compound

229)

3-[2-(4-chloro-3- MS fluorophenoxy)acetamido] - (APCI ⁺ )

N- [2-(4-ethyl- 1 ,3-thiazol-2- m/z 452

Example 131

yl)ethyl] bicyclo [ 1.1. l]penta (M+H) ⁺ ne- 1 -carboxamide

(Compound 230)

3-[2-(4-chloro-3- MS fluorophenoxy)acetamido] - (APCI ⁺ )

N-{ [3-fluoro-5- m/z 9

Example 132 (trifluoromethyl)phenyl] met (M+H) ⁺ hyl } bicyclo [1.1.1] pentane- 1 -carboxamide (Compound

231)

3-[2-(4-chloro-3- MS fluorophenoxy)acetamido] - (APCI ⁺ )

Example 133

N- [(6-methoxypyridin-2- m/z 434 yl)methyl] bicyclo [ 1.1.1 ]pen (M+H) ⁺ tane- 1 -carboxamide

(Compound 232)

3-[2-(4-chloro-3- MS fluorophenoxy)acetamido] - (APCI ⁺ ) N-[(pyridin-4- m/z 404

Example 134

yl)methyl] bicyclo [ 1.1.1 ]pen (M+H) ⁺ tane- 1 -carboxamide

(Compound 233)

3-[2-(4-chloro-3- MS fluorophenoxy)acetamido] - (APCI ⁺ ) N-[2-(pyridin-4- m/z 418

Example 135

yl)ethyl] bicyclo [ 1.1. l]penta (M+H) ⁺ ne- 1 -carboxamide

(Compound 234)

3-[2-(4-chloro-3- MS fluorophenoxy)acetamido] - (APCI ⁺ ) N-[(l,2-oxazol-3- m/z 460

Example 136

yl)methyl] bicyclo [ 1.1.1 ]pen (M+H) ⁺ tane- 1 -carboxamide

(Compound 235)

3-[2-(4-chloro-3- MS fluorophenoxy)acetamido] - (APCI ⁺ ) N-[(2,5- m/z 463

Example 137 dimethoxyphenyl)methyl]bi (M+H) ⁺ cyclo[ 1.1.1 Jpentane- 1 - carboxamide (Compound

236)

3-[2-(4-chloro-3- MS

Example 138 fluorophenoxy)acetamido] - (APCI ⁺ )

N-[(3- m/z M fluorophenyl)methyl] bicycl (M+H) ⁺ o[l. l.l]pentane-l- carboxamide (Compound

237)

N- [(4-butylphenyl)methyl] - MS

3-[2-(4-chloro-3- (APCI ⁺ ) fluorophenoxy)acetamido]bi m/z 459

Example 139

cyclo[ 1.1.1 Jpentane- 1 - (M+H) ⁺ carboxamide (Compound

238)

3-[2-(4-chloro-3- MS fluorophenoxy)acetamido] - (APCI ⁺ )

N-[2-(4- m/z 435

Example 140 fluorophenyl)ethyl] bicyclo [ (M+H) ⁺ l.l.l]pentane-l- carboxamide (Compound

239)

3-[2-(4-chloro-3- MS fluorophenoxy)acetamido] - (APCI ⁺ )

N-[(4- m/z 447

Example 141 ethoxyphenyl)methyl] bicycl (M+H) ⁺ o[l. l.l]pentane-l- carboxamide (Compound

240)

3-[2-(4-chloro-3- MS fluorophenoxy)acetamido] - (APCI ⁺ )

Example 142 N-[(3,4- m/z

dichlorophenyl)methyl] bicy 471/473 clo[ 1.1.1 Jpentane- 1 - (M+H) ⁺ carboxamide (Compound 241)

3-[2-(4-chloro-3- MS fluorophenoxy)acetamido] - (APCI ⁺ ) N-[2-(pyridin-3- m/z 418

Example 143

yl)ethyl] bicyclo [ 1.1. l]penta (M+H) ⁺ ne- 1 -carboxamide

(Compound 242)

3-[2-(4-chloro-3- MS fluorophenoxy)acetamido] - (APCI ⁺ ) N-{ [2- m/z 469

Example 144 (difluoromethoxy)phenyl]m (M+H) ⁺ ethyl } bicyclo [1.1.1] pentane

-1-carboxamide (Compound

243)

3-[2-(4-chloro-3- MS fluorophenoxy)acetamido] - (APCI ⁺ ) N- [(2-methylfuran-3- m/z 407

Example 145

yl)methyl] bicyclo [ 1.1.1 ]pen (M+H) ⁺ tane- 1 -carboxamide

(Compound 244)

3-[2-(4-chloro-3- MS fluorophenoxy)acetamido] - (APCI ⁺ ) N-[(4- m/z M

Example 146 fluorophenyl)methyl] bicycl (M+H) ⁺ o[l. l.l]pentane-l- carboxamide (Compound

245)

Example 147 3-[2-(4-chloro-3- MS fluorophenoxy)acetamido] - (APCI ⁺ ) N-({4- m/z 503

[(trifluoromethyl)sulfanyl]p (M+H) ⁺ henyl } methyl)bicyclo [1.1.1]

pentane- 1 -carboxamide

(Compound 246)

3-[2-(4-chloro-3- MS fluorophenoxy)acetamido] - (APCI ⁺ ) N- [(3 -propyl- 1 ,2-oxazol- 5 - m/z 436

Example 148

yl)methyl] bicyclo [ 1.1.1 ]pen (M+H) ⁺ tane- 1 -carboxamide

(Compound 247)

3-[2-(4-chloro-3- MS fluorophenoxy)acetamido] - (APCI ⁺ ) N-[2-(3-chloro-4- m/z

Example 149 methoxyphenyl)ethyl] bicycl (M+H) ⁺ o[l. l.l]pentane-l- carboxamide (Compound

248)

3-[2-(4-chloro-3- MS fluorophenoxy)acetamido] - (APCI ⁺ ) N-[(3-chloro-4- m/z 467

Example 150 methoxyphenyl)methyl]bicy (M+H) ⁺ clo[ 1.1.1 ]pentane- 1 - carboxamide (Compound

249)

3-[2-(4-chloro-3- MS fluorophenoxy)acetamido] - (APCI ⁺ )

Example 151

N-{ [3- m/z 469

(difluoromethoxy)phenyl]m (M+H) ⁺ ethyl } bicyclo [1.1.1] pentane

-1-carboxamide (Compound

250)

3-[2-(4-chloro-3- MS fluorophenoxy)acetamido] - (APCI ⁺ )

N- [(2,6-dimethylpyridin-3- m/z 432

Example 152

yl)methyl] bicyclo [ 1.1.1 ]pen (M+H) ⁺ tane- 1 -carboxamide

(Compound 251)

3-[2-(4-chloro-3- Ή NMR (400 MHz, DMSO- MS fluorophenoxy)acetamido] - d ₆ _O ₂ 0) S ppm 7.62 (dd, J = (APCI ⁺ )

N-[2-(lH-pyrazol-l- 2.3, 0.7 Hz, 1H), 7.49 (t, J = m/z 407 yl)ethyl] bicyclo [ 1.1. l]penta 8.9 Hz, 1H), 7.45 (dd, J = 1.8, (M+H) ⁺ ne- 1 -carboxamide 0.7 Hz, 1H), 7.06 (dd, J = 11.3,

Example 153

(Compound 252) 2.8 Hz, 1H), 6.86 (ddd, J = 9.0,

2.9, 1.2 Hz, 1H), 6.24 (t, J =

2.1 Hz, 1H), 4.46 (s, 2H), 4.17

(t, J = 6.4 Hz, 2H), 3.41 (t, J =

6.4 Hz, 2H), 2.16 (s, 6H)

Example 154: 3-[2-(4-chloro-3-fluorophenoxy)acetamido]-N-[3-(pyridin-3- yl)propyl]bicyclo[l.l.l]pentane-l-carboxamide (Compound 253)

The reaction and purification conditions described in Example 48 substituting 3-(pyridin- 3-yl)propan-l-amine, hydrochloric acid (AniChem) for (5-(difluoromethoxy)pyridin-2- yl)methanamine gave the title compound. ^J H NMR (400 MHz, DMSO- ) δ ppm 8.70 (s, 1H), 8.43 (dd, J = 2.3, 0.8 Hz, 1H), 8.39 (dd, J = 4.8, 1.7 Hz, 1H), 7.77 (t, J = 5.7 Hz, 1H), 7.65 - 7.60 (m, 1H), 7.49 (t, J = 8.9 Hz, 1H), 7.30 (ddd, J = 7.8, 4.8, 0.9 Hz, 1H), 7.07 (dd, J = 11.4, 2.9 Hz, 1H), 6.85 (ddd, J = 8.9, 2.8, 1.2 Hz, 1H), 4.47 (s, 2H), 3.05 (td, J = 7.1, 5.9 Hz, 2H), 2.57 (t, J = 7.6 Hz, 2H), 2.16 (s, 6H), 1.72 (p, J = 7.4 Hz, 2H); MS (ESI ⁺ ) m/z 432 (M+H) ⁺ .

Example 155: 3-[2-(4-chloro-3-fluorophenoxy)acetamido]-N-[3-(pyridin-2- yl)propyl]bicyclo[l.l.l]pentane-l-carboxamide (Compound 254) The reaction and purification conditions described in Example 48 substituting 3-(pyridin- 2-yl)propan-l-amine (ChemBridge) for (5-(difluoromethoxy)pyridin-2-yl)methanamine gave the title compound. ^J H NMR (400 MHz, DMSO- ) δ ppm 8.69 (s, 1H), 8.46 (ddd, J = 4.8, 1.9, 0.9 Hz, 1H), 7.79 (t, J = 5.7 Hz, 1H), 7.68 (td, J = 7.6, 1.9 Hz, 1H), 7.49 (t, J = 8.9 Hz, 1H), 7.24 (dt, J = 7.8, 1.1 Hz, 1H), 7.19 (ddd, J = 7.5, 4.9, 1.2 Hz, 1H), 7.07 (dd, J = 11.3, 2.9 Hz, 1H), 6.85 (ddd, J = 9.0, 2.9, 1.2 Hz, 1H), 4.46 (s, 2H), 3.07 (td, J = 7.3, 5.9 Hz, 2H), 2.74 - 2.66 (m, 2H), 2.16 (s, 6H), 1.87 - 1.74 (m, 2H); MS (ESI ⁺ ) m/z 432 (M+H) ⁺ .

Example 156: 4-[2-(3,4-dichlorophenoxy)acetamido]-2-hydroxy-N-{[4- (trifluoromethyl)phenyl]methyl}bicyclo[2.2.2]octane-l-carbox amide (Compound 255) Example 156A: 4-(benzylamino)-2-oxobicyclo[2.2.2]octane-l-carboxylic acid

A mixture of Example 7D (20.7 g, 61.3 mmol) and sodium hydroxide (49.0 mL, 306 mmol) in methanol/water (1 : 1 , 200 mL) was stirred for 24 hours at ambient temperature. The reaction mixture was concentrated, and the residue was acidified with 1 N HC1. The precipitate was collected by filtration, washed with water, and air-dried to give the title compound. ^J H NMR (400 MHz, DMSO-<¾) δ ppm 12.70 (s, 1H), 9.67 (s, 2H), 7.62 (dd, J = 7.5, 2.0 Hz, 2H), 7.43 (d, J = 6.6 Hz, 3H), 4.13 (s, 2H), 2.87 (s, 2H), 2.08 (tdq, J = 14.4, 10.8, 5.8, 5.0 Hz, 8H). Example 156B: 4-(benzylamino )-2-oxo-N-(4-( trifluoromethyl)benzyl)bicyclo[ 2.2.2]octane-l- carboxamide

To a mixture of Example 156A (1 100 mg, 4.02 mmol), (4- (trifluoromethyl)phenyl)methanamine, hydrochloric acid (1065 mg, 5.03 mmol), and N-ethyl-N- isopropylpropan-2-amine (2.460 mL, 14.09 mmol) in N,N-dimethylformamide (25 mL), was added 2-(3H-[l ,2,3]triazolo[4,5-¾]pyridin-3-yl)-l , l,3,3-tetramethylisouronium

hexafluorophosphate(V) (2295 mg, 6.04 mmol), and the reaction mixture was stirred at ambient temperature overnight. Water was added, and the mixture was extracted with dichloromethane. The organic layer was concentrated, and the residue was purified on silica gel (30-100% ethyl acetate in heptane) to give the title compound. MS (ESI ⁺ ) m/z 431.3 (M+H) ⁺ .

Example 156C: 4-amino-2-oxo-N-(4-( trifluoromethyl)benzyl)bicyclo[ 2.2.2] octane- 1- carboxamide

A mixture of Example 156B (1.29 g, 2.55 mmol) and 20% Pd(OH) ₂ /C, wet (0.24 g, 0.872 mmol) in tetrahydrofuran (14 mL) in a 20 mL stainless steel pressure vessel was stirred under 50 psi hydrogen at ambient temperature overnight. The suspension was filtered, and the filtrate was concentrated. The residue was purified by by reverse phase preparative HPLC (30- 100% acetonitrile in 0.1 % trifluoroacetic acid/water at 50 mL/minute on Phenomenex® C18 ΙΟμπι 250 mm x 50 mm column) to give 380 mg of the title compound. H NMR (400 MHz, DMSO- ¾) δ ppm 8.25 (m, 4H), 7.67 (d, J = 8.1 Hz, 2H), 7.53 (d, J = 8.0 Hz, 2H), 4.40 (d, J = 5.8 Hz, 2H), 2.59 (s, 2H), 2.20 (td, J = 11.2, 9.6, 2.4 Hz, 2H), 2.05 1.87 (m, 4H), 1.82 (td, J = 10.9, 10.2, 3.5 Hz, 2H).

Example 156D: 4-[2-( 3,4-dichlorophenoxy )acetamido ]-2-hydroxy-N-{ [4- (trifluoromethyl)phenyl]methyl}bicyclo[2.2.2]octane-l-carbox amide

To a mixture of Example 156C (185 mg, 0.407 mmol), 2-(3,4-dichlorophenoxy)acetic acid (112 mg, 0.509 mmol), and N-ethyl-N-isopropylpropan-2-amine (0.249 mL, 1.425 mmol) in N,N-dimethylformamide (5.0 mL), 2-(3H-[l,2,3]triazolo[4,5- ?]pyridin-3-yl)-l, 1,3,3- tetramethylisouronium hexafluorophosphate(V) (232 mg, 0.611 mmol) was added. The solution was stirred at ambient temperature for 2 hours. The reaction mixture was concentrated, and the residue was purified by reverse phase HPLC (30-100% acetonitrile in 0.1% trifluoroacetic acid/water at 50 mL/minute on Phenomenex® C18 10 μπι 250 mm x 50 mm column) to give 220 mg of 4-[2-(3,4-dichlorophenoxy)acetamido]-2-oxo-N-{ [4- (trifluoromemyl)phenyl]memyl}bicyclo[2.2.2]octane-l-carboxam ide with about 85% purity. This 4-[2-(3,4-dichlorophenoxy)acetamido]-2-oxo-N-{ [4-

(trifluoromemyl)phenyl]methyl}bicyclo[2.2.2]octane-l-carb oxarnide was dissolved in a mixture of dichloromethane/methanol (5 mL, 1: 1) and treated sodium tetrahydroborate (30.8 mg, 0.814 mmol). The mixture was stirred at ambient temperature for 2 hours. The reaction mixture was concentrated, and the residue was purified by preparative reverse phase HPLC (30-100% acetonitrile in 0.1% trifluoroacetic acid/water at 50 mL/minute on Phenomenex® C18 10 μπι 250 mm x 50 mm column) to give 114 mg of the title compound. ^J H NMR (400 MHz, DMSO- d ₆ ) δ ppm 8.04 (t, J = 6.1 Hz, 1H), 7.61 (d, J = 8.1 Hz, 2H), 7.53 7.46 (m, 2H), 7.41 (d, J = 8.0 Hz, 2H), 7.17 (d, J = 2.9 Hz, 1H), 6.91 (dd, J = 9.0, 2.9 Hz, 1H), 4.94 (d, J = 4.2 Hz, 1H), 4.42 (s, 2H), 4.31 (d, J = 5.9 Hz, 2H), 4.10 4.02 (m, 1H), 2.21 (ddd, J = 12.5, 9.1, 2.8 Hz, 1H), 2.08 (t, J = 11.4 Hz, 1H), 1.86 (td, J = 11.4, 5.0 Hz, 1H), 1.77 1.64 (m, 5H), 1.61 (dtd, J = 17.2, 11.8, 10.7, 6.0 Hz, 2H); MS (ESI ⁺ ) m/z 545.1 (M+H) ⁺ .

Example 157

4-[2-(4-chloro-3-fluorophenoxy)acetamido]-/V-{[5-(difluorome thoxy)pyridin-2- yl]methyl}bicyclo[2.1.1]hexane-l-carboxamide (Compound 256)

Example 157 : methyl 4-(2-(4-chloro-3-fluorophenoxy)acetamido)bicyclo[2.1.1]hexan e-l- carboxylate The reaction and purification conditions described in Example 48 substituting 2-(4- chloro-3-fluorophenoxy)acetic acid (Aldlab) for the product of Example 18 A, and methyl 4- aminobicyclo[2.1.1]hexane-l-carboxylate, hydrochloric acid (Pharmablock) for (5- (difluoromethoxy)pyridin-2-yl)methanamine gave the title compound. MS (ESI ⁺ ) m/z 342 (M+H) ⁺ .

Example 157B: sodium 4-(2-(4-chloro-3-fluorophenoxy)acetamido)bicyclo[2.1.1]hexan e-l- carboxylate, 2 sodium hydroxide

The product of Example 157A (0.4 g, 1.17 mmol) was dissolved in methanol (10 mL) and stirred at ambient temperature. An aqueous NaOH solution (2.5 M, 1.4 mL) was added. After stirring at 40 °C for 1 hour, the reaction mixture was concentrated under reduced pressure to give the title compound (0.5 g, 1.12 mmol, 95% yield). MS (ESI ⁺ ) m/z 328 (M+H) ⁺ .

Example 157C: 4-[ 2-(4-chloro-3-fluorophenoxy)acetamido ]-N-{ [5-( difluoromethoxy )pyridin-2- yl]methyl}bicyclo[2.1.1]hexane-l-carboxamide

The product of Example 157B (60 mg, 0.134 mmol) was combined with trifluoroacetic acid (0.062 mL, 0.80 mmol) and methanol (1 mL), and concentrated under reduced pressure. To the resulting residue was added [5-(difluoromethoxy)pyridin-2-yl]methanamine (27 mg, 0.15 mmol, Enamine), triethylamine (0.075 mL, 0.54 mmol), N,N-dimethylformamide (2 mL), and (l -[bis(dimethylamino)methylene]-lH-l,2,3-triazolo[4,5-¾]pyri dinium 3-oxid

hexafluorophosphate) (HATU, 56.1 mg, 0.15 mmol) sequentially. After stirring at ambient temperature for 30 minutes, the reaction mixture was filtered through a glass microfiber frit and purified by preparative HPLC [YMC TriArt™ CI 8 Hybrid 5 μπι column, 50 x 100 mm, flow rate 70 mL/minute, 5-100% gradient of acetonitrile in buffer (0.1 % TFA)] to give the title compound (41 mg, 0.085 mmol, 63% yield). ^J H NMR (400 MHz, DMSO- ) δ ppm 8.53 (s, 1H), 8.39 (d, J = 2.8 Hz, 1H), 8.29 (t, J = 6.0 Hz, 1H), 7.64 (dd, J = 8.6, 2.8 Hz, 1H), 7.49 (t, J = 8.9 Hz, 1H), 7.28 (d, J = 8.7 Hz, 1H), 7.27 (t, J = 73.5 Hz, 1H), 7.08 - 7.03 (m, 1H), 6.85 (ddd, J = 9.0, 2.8, 1.2 Hz, 1H), 4.49 (s, 2H), 4.35 (d, J = 6.1 Hz, 2H), 2.09 - 2.00 (m, 2H), 1.89 - 1.76 (m, 4H), 1.74 - 1.67 (m, 2H); MS (ESI ⁺ ) m/z 484 (M+H) ⁺ .

Example 158: 4-[2-(4-chloro-3-fluorophenoxy)acetamido]-N-[(5-chloropyridi n-2- yl)methyl]bicyclo[2.2.2]octane-l-carboxamide (Compound 257)

Example 158A: methyl 4-(2-(4-chloro-3-fluorophenoxy)acetamido)bicyclo[2.2.2]octan e-l- carboxylate

The reaction and purification conditions described in Example 48 substituting 2-(4- chloro-3-fluorophenoxy)acetic acid (Advanced Chemblocks) for the product of Example 18 A, methyl 4-aminobicyclo[2.2.2]octane-l-carboxylate hydrochloride (ArkPharm) for (5- (difluoromethoxy)pyridin-2-yl)methanamine, and (l-cyano-2-ethoxy-2- oxoethylidenaminooxy)dimethylamino-mo holino-carbenium hexafluorophosphate (COMU) for (l-[bis(dimethylamino)methylene]-lH-l ,2,3-triazolo[4,5-¾]pyridinium 3-oxid

hexafluorophosphate) (HATU) gave the title compound. MS (APCI ⁺ ) m/z 370 (M+H) ⁺ .

Example 158B: 4-(2-(4-chloro-3-fluorophenoxy)acetamido)bicyclo[2.2.2]octan e-l-carboxylic acid, 4 sodium chloride

The product of Example 158 A (0.78 g, 2.11 mmol) was dissolved in methanol (6 mL) and stirred at ambient temperature. An aqueous NaOH solution (2.5 M, 3.37 mL) was added. After stirring at 40 °C for 1 hour, the reaction mixture was left stirring at ambient temperature for 72 hours. Aqueous HC1 (6.0 M, 2.11 mL) was added, and the resulting solution was concentrated under reduced pressure to give the title compound (1.22 g, 2.07 mmol, 98% yield). MS (ESI ⁺ ) m/z 356 (M+H) ⁺ .

Example 158C: 4-[ 2-(4-chloro-3-fluorophenoxy)acetamido ]-N-[ ( 5-chloropyridin-2- yl )methyl ]bicyclo[ 2.2.2 ] octane- 1-carboxamide

The reaction and purification conditions described in Example 48 substituting the product of Example 158B for the product of Example 18A, and (5-chloropyridin-2-yl)methanamine hydrochloride (Frontier) for (5-(difluoromethoxy)pyridin-2-yl)methanamine gave the title compound. ^J H NMR (501 MHz, DMSO-<¾) δ ppm 8.52 (dd, J = 2.6, 0.7 Hz, 1H), 8.09 (t, J = 6.0 Hz, 1H), 7.86 (dd, J = 8.4, 2.5 Hz, 1H), 7.50 - 7.45 (m, 2H), 7.19 (dd, J = 8.4, 0.7 Hz, 1H), 7.03 (dd, J = 11.4, 2.9 Hz, 1H), 6.81 (ddd, J = 9.0, 2.9, 1.2 Hz, 1H), 4.44 (s, 2H), 4.30 (d, J = 5.9 Hz, 2H), 1.89 - 1.76 (m, 12H); MS (ESI ⁺ ) m/z 480 (M+H) ⁺ .

Example 159: 4-[2-(4-chloro-3-fluorophenoxy)acetamido]-N-[(5-methylpyrazi n-2- yl)methyl]bicyclo[2.2.2]octane-l-carboxamide (Compound 258)

The reaction and purification conditions described in Example 48 substituting the product of Example 158B for the product of Example 18A, and (5-methylpyrazin-2-yl)methanamine (Aldrich) for (5-(difluoromethoxy)pyridin-2-yl)methanamine gave the title compound. ^J H NMR (501 MHz, DMSO- ) δ ppm 8.44 - 8.42 (m, 1H), 8.31 (d, J = 1.5 Hz, 1H), 8.09 (t, J = 5.9 Hz, 1H), 7.51 - 7.45 (m, 2H), 7.03 (dd, J = 11.4, 2.9 Hz, 1H), 6.81 (ddd, J = 9.0, 2.9, 1.2 Hz, 1H), 4.44 (s, 2H), 4.32 (d, J = 5.8 Hz, 2H), 2.46 (s, 3H), 1.88 - 1.74 (m, 12H); MS (ESI ⁺ ) m/z 461 (M+H) ⁺ .

Example 160: 4-[2-(4-chloro-3-fluorophenoxy)acetamido]-N-[(pyridin-2- yl)methyl]bicyclo[2.2.2]octane-l-carboxamide (Compound 259) The reaction and purification conditions described in Example 48 substituting the product of Example 158B for the product of Example 18 A, and pyridin-2-ylmethanamine (Aldrich) for (5-(difluoromethoxy)pyridin-2-yl)methanamine gave the title compound. ^J H NMR (501 MHz, DMSO- ) δ ppm 8.47 (ddd, J = 4.9, 1.8, 0.9 Hz, 1H), 8.03 (t, J = 6.0 Hz, 1H), 7.73 (td, J = 7.7, 1.8 Hz, 1H), 7.51 - 7.46 (m, 2H), 7.23 (ddd, J = 7.6, 4.8, 1.1 Hz, 1H), 7.17 - 7.13 (m, 1H), 7.03 (dd, J = 11.4, 2.8 Hz, 1H), 6.81 (ddd, J = 9.0, 2.9, 1.2 Hz, 1H), 4.44 (s, 2H), 4.32 (d, J = 6.0 Hz, 2H), 1.90 - 1.77 (m, 12H); MS (ESI ⁺ ) m/z 446 (M+H) ⁺ .

Example 161: 4-[2-(4-chloro-3-fluorophenoxy)acetamido]-N-[(4- chlorophenyl)methyl]bicyclo[2.2.2]octane-l-carboxamide (Compound 260)

The reaction and purification conditions described in Example 48 substituting the product of Example 158B for the product of Example 18 A, and (4-chlorophenyl)methanamine for (5- (difluoromethoxy)pyridin-2-yl)methanamine gave the title compound. ^J H NMR (501 MHz, DMSO- ) δ ppm 8.00 (t, J = 6.1 Hz, 1H), 7.53 - 7.44 (m, 2H), 7.37 - 7.33 (m, 2H), 7.22 - 7.18 (m, 2H), 7.03 (dd, J = 11.4, 2.8 Hz, 1H), 6.81 (ddd, J = 8.9, 2.9, 1.2 Hz, 1H), 4.44 (s, 2H), 4.21 (d, J = 6.0 Hz, 2H), 1.89 - 1.72 (m, 12H); MS (ESI ⁺ ) m/z 479 (M+H) ⁺ .

Example 162: 4-[2-(4-chloro-3-fluorophenoxy)acetamido]-N-{[5-(trifluorome thyl)pyridin-

2- yl]methyl}bicyclo[2.2.2]octane-l-carboxamide (Compound 261)

The reaction and purification conditions described in Example 48 substituting the product of Example 158B for the product of Example 18A, and (5-(trifluoromethyl)pyridin-2- yl)methanamine hydrochloride (PharmaBlock) for (5-(difluoromethoxy)pyridin-2- yl)methanamine gave the title compound. ^J H NMR (501 MHz, DMSO- ) δ ppm 8.89 - 8.85 (m, 1H), 8.21 - 8.13 (m, 2H), 7.51 - 7.46 (m, 2H), 7.39 - 7.36 (m, 1H), 7.03 (dd, J = 11.4, 2.9 Hz, 1H), 6.82 (ddd, J = 8.9, 2.9, 1.2 Hz, 1H), 4.45 (s, 2H), 4.41 (d, J = 5.9 Hz, 2H), 1.92 - 1.74 (m, 12H); MS (APCI ⁺ ) m/z 514 (M+H) ⁺ .

Example 163: 4-[2-(4-chloro-3-fluorophenoxy)acetamido]-N-{[6-(difluoromet hoxy)pyridin-

3- yl]methyl}bicyclo[2.2.2]octane-l-carboxamide (Compound 262)

The reaction and purification conditions described in Example 48 substituting the product of Example 158B for the product of Example 18A, and (6-(difluoromethoxy)pyridin-3- yl)methanamine (ArkPharm) for (5-(difluoromethoxy)pyridin-2-yl)methanamine gave the title compound. ^J H NMR (400 MHz, DMSO-<¾) δ ppm 8.09 - 8.06 (m, 1H), 8.04 (t, J = 6.0 Hz, 1H), 7.72 (dd, J = 8.4, 2.5 Hz, 1H), 7.67 (t, J = 73.0 Hz, 1H), 7.53 - 7.43 (m, 2H), 7.06 - 6.98 (m, 2H), 6.81 (ddd, J = 9.0, 2.9, 1.2 Hz, 1H), 4.43 (s, 2H), 4.22 (d, J = 5.9 Hz, 2H), 1.87 - 1.69 (m, 12H); MS (ESI ⁺ ) m/z 512 (M+H) ⁺ . Example 164: (2/?)-4-[2-(3,4-dichlorophenoxy)acetamido]-2-hydroxy-N-{[4- (trifluoromethyl)phenyl]methyl}bicyclo[2.2.2]octane-l-carbox amide (Compound 263)

The title compound was isolated by chiral preparative SFC of Example 156D as the second peak eluted off the column using the methodologies described in Example 14. ^J H NMR (400 MHz, DMSO- ) δ ppm 8.09 (t, J = 6.0 Hz, 1H), 7.64 (d, J = 8.1 Hz, 2H), 7.57 - 7.50 (m, 2H), 7.45 (d, J = 8.0 Hz, 2H), 7.21 (d, J = 2.9 Hz, 1H), 6.95 (dd, J = 9.0, 2.9 Hz, 1H), 5.00 (s, 1H), 4.46 (s, 2H), 4.35 (d, J = 5.9 Hz, 2H), 4.10 (dt, J = 9.0, 2.2 Hz, 1H), 2.25 (ddd, J = 12.7, 9.2, 3.0 Hz, 1H), 2.12 (tt, J = 11.8, 3.3 Hz, 1H), 1.90 (tdd, J = 11.5, 5.6, 2.0 Hz, 1H), 1.80 - 1.58 (m, 7H); MS (ESI ⁺ ) m/z 545.1 (M+H) ⁺ . Stereochemistry of this compound was arbitrarily assigned. Example 165: (25)-4-[2-(3,4-dichlorophenoxy)acetamido]-2-hydroxy-N-{[4-

(trifluoromethyl)phenyl]methyl}bicyclo[2.2.2]octane-l-car boxamide (Compound 264)

The title compound was isolated by chiral preparative SFC of Example 156D as the first peak eluted off the column using the methodologies described in Example 14. ^J H NMR (400 MHz, DMSO- ) δ ppm 8.09 (t, J = 6.0 Hz, 1H), 7.64 (d, J = 8.1 Hz, 2H), 7.53 (d, J = 9.2 Hz, 2H), 7.47 - 7.42 (m, 2H), 7.21 (d, J = 2.9 Hz, 1H), 6.95 (dd, J = 9.0, 2.9 Hz, 1H), 4.99 (s, 1H), 4.46 (s, 2H), 4.34 (d, J = 6.0 Hz, 2H), 4.10 (d, J = 9.0 Hz, 1H), 2.30 - 2.20 (m, 1H), 2.11 (td, J = 11.9, 5.9 Hz, 1H), 1.95 - 1.85 (m, 1H), 1.80 - 1.58 (m, 7H); MS (ESI ⁺ ) m/z 545.2 (M+H) ⁺ .

Stereochemistry of this compound was arbitrarily assigned.

Example 166: 4-[2-(4-chloro-3-fluorophenoxy)acetamido]-N-{[5-(difluoromet hoxy)pyridin- 2-yl]methyl}bicyclo[2.2.2]octane-l-carboxamide (Compound 265)

The reaction and purification conditions described in Example 48 substituting the product of Example 158B for the product of Example 18A, and (5-(difluoromethoxy)pyridin-2- yl)methanamine (Enamine) for (5-(difluoromethoxy)pyridin-2-yl)methanamine gave the title compound. ^J H NMR (501 MHz, DMSO-<¾) δ ppm 8.38 (d, J = 2.8 Hz, 1H), 8.08 (t, J = 6.0 Hz, 1H), 7.62 (dd, J = 8.6, 2.8 Hz, 1H), 7.49 (br s, 1H), 7.48 (t, J = 8.9 Hz, 1H), 7.34 (d, J = 73.5 Hz, 1H), 7.22 (dd, J = 8.6, 0.8 Hz, 1H), 7.03 (dd, J = 11.4, 2.8 Hz, 1H), 6.81 (ddd, J = 9.0, 2.9, 1.2 Hz, 1H), 4.44 (s, 2H), 4.31 (d, J = 5.9 Hz, 2H), 1.91 - 1.73 (m, 12H); MS (APCI ⁺ ) m/z 512 (M+H) ⁺ .

Example 167: (25)-4-[2-(4-chloro-3-fluorophenoxy)acetamido]-2-hydroxy-N-{ [4- (trifluoromethyl)phenyl]methyl}bicyclo[2.2.2]octane-l-carbox amide (Compound 266)

The title compound was isolated by chiral preparative SFC of Example 11 as the first peak eluted off the column using the methodologies described in Example 14. ^J H NMR (400 MHz, DMSO- ) δ ppm 8.08 (t, J = 6.1 Hz, 1H), 7.64 (d, J = 8.1 Hz, 2H), 7.54 - 7.41 (m, 4H), 7.03 (dd, J = 11.4, 2.8 Hz, 1H), 6.81 (ddd, J = 9.0, 2.9, 1.2 Hz, 1H), 4.98 (s, 1H), 4.44 (s, 2H), 4.34 (d, J = 5.9 Hz, 2H), 4.10 (d, J = 9.0 Hz, 1H), 2.25 (ddd, J = 12.6, 9.2, 2.9 Hz, 1H), 2.11 (ddd, J = 13.9, 8.8, 3.0 Hz, 1H), 1.89 (ddd, J = 12.6, 8.8, 3.4 Hz, 1H), 1.80 - 1.57 (m, 7H); MS (ESI ⁺ ) m/z 529.1 (M+H) ⁺ . Stereochemistry of this compound was arbitrarily assigned.

Example 168: (2/?)-4-[2-(4-chloro-3-fluorophenoxy)acetamido]-2-hydroxy-iV -{[4-

(trifluoromethyl)phenyl]methyl}bicyclo[2.2.2]octane-l-car boxamide (Compound 267)

The title compound was isolated by chiral preparative SFC of Example 11 as the second peak eluted off the column using the methodologies described in Example 14. ^J H NMR (400 MHz, DMSO- ) δ ppm 8.08 (t, J = 6.0 Hz, 1H), 7.64 (d, J = 8.0 Hz, 2H), 7.55 - 7.41 (m, 4H), 7.03 (dd, J = 11.5, 2.9 Hz, 1H), 6.81 (ddd, J = 8.9, 2.9, 1.2 Hz, 1H), 4.98 (s, 1H), 4.44 (s, 2H), 4.34 (d, J = 5.9 Hz, 2H), 4.10 (d, J = 9.3 Hz, 1H), 2.25 (ddd, J = 12.6, 9.2, 2.8 Hz, 1H), 2.12 (td, J = 11.5, 11.0, 5.8 Hz, 1H), 1.90 (td, J = 11.4, 4.9 Hz, 1H), 1.80 - 1.57 (m, 7H); MS (ESI ⁺ ) m/z 529.2 (M+H) ⁺ . Stereochemistry of this compound was arbitrarily assigned.

Example 169: 4-[2-(4-chloro-3-fluorophenoxy)acetamido]-N-[6-(difluorometh oxy)pyridin- 3-yl]bicyclo[2.1.1]hexane-l-carboxamide (Compound 268)

The reaction and purification conditions described in Example 157C substituting 6- (difluoromethoxy)pyridin-3-amine (Enamine) for [5-(difluoromethoxy)pyridin-2- yl]methanamine, and (l-cyano-2-ethoxy-2-oxoethylidenaminooxy)dimethylamino-mo holino- carbenium hexafluorophosphate (COMU) for (l-[bis(dimethylamino)methylene]-lH-l,2,3- triazolo[4,5- ?]pyridinium 3-oxid hexafluorophosphate) (HATU) gave the title compound. ^J H NMR (400 MHz, DMSO-de) δ ppm 9.66 (s, 1H), 8.58 (s, 1H), 8.52 (dd, J = 2.7, 0.6 Hz, 1H),

8.14 (dd, J = 8.9, 2.7 Hz, 1H), 7.63 (t, J = 73.2 Hz, 1H), 7.50 (t, J = 8.9 Hz, 1H), 7.11 - 7.03 (m, 2H), 6.86 (ddd, J = 9.0, 2.9, 1.2 Hz, 1H), 4.50 (s, 2H), 2.18 - 2.10 (m, 2H), 1.97 - 1.86 (m, 4H), 1.85 - 1.78 (m, 2H); MS (APCI ⁺ ) m/z 471 (M+H) ⁺ .

Example 170: (3 ?)-4-[2-(4-chloro-3-fluorophenoxy)acetamido]-3-hydroxy-N-{[4 -

(trifluoromethyl)phenyl]methyl}bicyclo[2.2.2]octane-l-car boxamide (Compound 269)

The title compound was isolated by chiral preparative SFC of Example 175 as the second peak eluted off the column using the methodologies described in Example 14. ^J H NMR (400 MHz, DMSO-<¾) δ ppm 8.11 (t, J = 6.0 Hz, 1H), 7.66 (d, J = 8.1 Hz, 2H), 7.49 (t, J = 8.9 Hz, 1H), 7.40 (d, J = 8.0 Hz, 2H), 7.31 (s, 1H), 7.06 (dd, J = 11.4, 2.9 Hz, 1H), 6.84 (ddd, J = 9.0, 2.9, 1.2 Hz, 1H), 5.12 (s, 1H), 4.48 (s, 2H), 4.30 (d, J = 5.9 Hz, 2H), 4.03 (d, J = 9.1 Hz, 1H),

2.15 (ddd, J = 13.5, 9.3, 2.2 Hz, 1H), 2.03 (ddd, J = 12.7, 10.9, 4.6 Hz, 1H), 1.88 (tt, J = 9.2, 4.3 Hz, 1H), 1.86 1.77 (m, 1H), 1.82 1.70 (m, 4H), 1.74 1.61 (m, 1H), 1.58 (dt, J = 13.5, 3.0 Hz, 1H); MS (ESI ⁺ ) m/z 529.2 (M+H) ⁺ . Stereochemistry of this compound was arbitrarily assigned. Example 171: (35)-4-[2-(4-chloro-3-fluorophenoxy)acetamido]-3-hydroxy-N-{ [4- (trifluoromethyl)phenyl]methyl}bicyclo[2.2.2]octane-l-carbox amide (Compound 270) The title compound was isolated by chiral preparative SFC of Example 175 as the first peak eluted off the column using the methodologies described in Example 14. ^J H NMR (400 MHz, DMSO- ) δ ppm 8.11 (t, J = 6.0 Hz, 1H), 7.66 (d, J = 8.1 Hz, 2H), 7.49 (t, J = 8.9 Hz, 1H), 7.40 (d, J = 8.0 Hz, 2H), 7.31 (s, 1H), 7.06 (dd, J = 11.4, 2.9 Hz, 1H), 6.84 (ddd, J = 9.0, 2.9, 1.2 Hz, 1H), 5.12 (s, 1H), 4.48 (s, 2H), 4.30 (d, J = 5.9 Hz, 2H), 4.03 (d, J = 9.1 Hz, 1H), 2.15 (ddd, J = 13.5, 9.3, 2.2 Hz, 1H), 2.03 (ddd, J = 12.7, 10.9, 4.6 Hz, 1H), 1.88 (tt, J = 9.2, 4.3 Hz, 1H), 1.86 - 1.77 (m, 1H), 1.82 - 1.70 (m, 4H), 1.74 - 1.61 (m, 1H), 1.58 (dt, J = 13.5, 3.0 Hz, 1H); MS (ESI ⁺ ) m/z 529.1 (M+H) ⁺ . Stereochemistry of this compound was arbitrarily assigned. Example 172: (3 ?)-4-[2-(4-chloro-3-fluorophenoxy)acetamido]-3-hydroxy-N-{[5 - (trifluoromethyl)pyridin-2-yl]methyl}bicyclo[2.2.2]octane-l- carboxamide (Compound 271) The title compound was isolated by chiral preparative SFC of Example 176 as the second peak eluted off the column using the methodologies described in Example 14. H NMR (400 MHz, DMSO- ) δ ppm 8.87 (dt, J = 1.9, 0.9 Hz, 1H), 8.23 8.12 (m, 2H), 7.49 (t, J = 8.9 Hz, 1H), 7.37 (d, J = 8.3 Hz, 1H), 7.31 (s, 1H), 7.06 (dd, J = 11.4, 2.9 Hz, 1H), 6.84 (ddd, J = 9.0, 2.9, 1.2 Hz, 1H), 5.12 (d, J = 4.3 Hz, 1H), 4.48 (s, 2H), 4.40 (d, J = 5.8 Hz, 2H), 4.05 (dt, J = 8.6, 3.5 Hz, 1H), 2.18 (ddd, J = 13.6, 9.4, 2.1 Hz, 1H), 2.04 (ddd, J = 12.5, 10.8, 4.6 Hz, 1H), 1.96 1.64 (m, 7H), 1.60 (dt, J = 13.5, 3.0 Hz, 1H); MS (ESI ⁺ ) m/z 530.1 (M+H) ⁺ . Stereochemistry of this compound was arbitrarily assigned.

Example 173: (35)-4-[2-(4-chloro-3-fluorophenoxy)acetamido]-3-hydroxy-N-{ [5- (trifluoromethyl)pyridin-2-yl]methyl}bicyclo[2.2.2]octane-l- carboxamide (Compound 272) The title compound was isolated by chiral preparative SFC of Example 176 as the first peak eluted off the column using the methodologies described in Example 14 ^J H NMR (400 MHz, DMSO- ) δ ppm 8.87 (dt, J = 2.0, 1.0 Hz, 1H), 8.23 8.12 (m, 2H), 7.49 (t, J = 8.9 Hz, 1H), 7.37 (d, J = 8.3 Hz, 1H), 7.31 (s, 1H), 7.06 (dd, J = 11.4, 2.9 Hz, 1H), 6.84 (ddd, J = 9.0, 2.9, 1.2 Hz, 1H), 5.11 (d, J = 4.3 Hz, 1H), 4.48 (s, 2H), 4.40 (d, J = 5.8 Hz, 2H), 4.05 (dt, J = 8.4, 3.6 Hz, 1H), 2.18 (ddd, J = 13.6, 9.3, 2.0 Hz, 1H), 2.04 (ddd, J = 12.5, 10.8, 4.5 Hz, 1H), 1.95 1.82 (m, 1H), 1.87 1.72 (m, 5H), 1.77 1.65 (m, 1H), 1.60 (dt, J = 13.4, 3.0 Hz, 1H); MS (ESI ⁺ ) m/z 530.2 (M+H) ⁺ . Stereochemistry of this compound was arbitrarily assigned. Example 174: (25)-4-[2-(4-chloro-3-fluorophenoxy)acetamido]-N-[2-(4-chlor ophenyl)-2- oxoethyl]-2-hydroxybicyclo[2.2.2]octane-l-carboxamide (Compound 273)

Example 174A: ethyl l,4-dioxaspiro[4.5]decane-8-carboxylate

A mixture of ethyl 4-oxocyclohexanecarboxylate (11.70 mL, 73.4 mmol), ethane- 1 ,2-diol (12.29 mL, 220 mmol), and p-toluenesulfonic acid monohydrate (1.397 g, 7.34 mmol) in toluene (200 mL) was stirred at 120 °C with a Dean-Stark trap apparatus for 180 minutes. The reaction mixture was neutralized with N-ethyl-N-isopropylpropan-2-amine and then concentrated. The residue was purified by silica gel column chromatography (0-30% ethyl acetate in heptane) to give 12.77 g of the title compound. ^J H NMR (400 MHz, DMSO-<¾) δ ppm 4.01 (q, / = 7.1 Hz, 2H), 3.81 (s, 4H), 2.32 (tt, / = 10.4, 3.8 Hz, 1H), 1.83 - 1.71 (m, 2H), 1.66 - 1.57 (m, 1H), 1.62 - 1.38 (m, 5H), 1.13 (t, / = 7.1 Hz, 3H).

Example 174B: ethyl 8-acetyl-l,4-dioxaspiro[4.5]decane-8-carboxylate

To a solution of diisopropylamine (5.19 mL, 36.4 mmol) in tetrahydrofuran (25 mL) at 0 °C was added «-butyllithium slowly below 5 °C. After stirring for 30 minutes, the solution was cooled to -78 °C under nitrogen, and a solution of Example 174A (6.0 g, 28.0 mmol) in tetrahydrofuran (3 mL) was added slowly, and the resultant mixture was stirred for 30 minutes at the same temperature. Then acetyl chloride (2.59 mL, 36.4 mmol) was added slowly to maintain the temperature below -60 °C, and the mixture was stirred at -70 °C for 2 hours. The reaction was quenched with saturated NH4CI solution, and the aqueous phase was extracted with ethyl acetate. The organic layer was washed with brine, dried over magnesium sulfate and filtered. The filtrate was concentrated, and the residue was purified chromatographically on silica gel (0- 70% ethyl acetate in heptane) to give 6.78 g of the title compound. ^J H NMR (500 MHz, DMSO- d ₆ ) S ppm 4.19 - 4.11 (m, 2H), 3.85 (s, 4H), 2.13 (s, 3H), 2.10 - 2.01 (m, 2H), 1.90 (ddd, / = 13.9, 9.6, 4.6 Hz, 2H), 1.54 (th, / = 13.6, 4.7 Hz, 4H), 1.18 (dd, / = 7.6, 6.5 Hz, 3H).

Example 174C: ethyl 1 -acetyl-4-oxocyclohexane-l -carboxylate

A mixture of Example 174B (6.5 g, 25.4 mmol) and HQ (21.13 mL, 127 mmol) in acetone (60 mL) was stirred at ambient temperature overnight. Volatiles were removed under reduced pressure, and the residue was partitioned between water and dichlorome thane. The organic layer was washed with brine, dried over magnesium sulfate and filtered. The filtrate was concentrated to give 5.46 g of the title compound which was used without further purification. ^J H NMR (400 MHz, DMSO-<¾) δ ppm 4.16 (q, / = 7.1 Hz, 2H), 2.17 (s, 3H), 2.35 2.07 (m, 8H), 1.17 (t, J = 7.1 Hz, 3H). Example 174D: ethyl 4-(benzylamino)-2-oxobicyclo[2.2.2] Octane- 1-carboxylate, hydrochloric acid

A mixture of Example 174C (9.7 g, 45.7 mmol), benzylamine (14.98 mL, 137 mmol), and /?-toluenesulfonic acid monohydrate (0.087 g, 0.457 mmol) in toluene (100 mL) was stirred at 130 °C with a Dean-Stark trap apparatus overnight. The mixture was concentrated, and the residue was stirred with a mixture of ethyl acetate (50 mL) and 3 N HC1 (100 mL) for 30 minutes. The precipitate was collected by filtration, washed with mixture of ethyl

acetate/heptane, and air-dried to give 11.3 g of title compound as an HC1 salt. The filtrate was neutralized with 6 N NaOH and extracted with ethyl acetate (100 mL x 2). The organic layer was washed with brine, dried over magnesium sulfate and filtered. The residue was purified on silica gel (0-70% ethyl acetate in heptane) to give another 0.77 g of the title compound. ^J H NMR (400 MHz, DMSO-<¾) δ ppm 9.73 (t, / = 6.2 Hz, 2H), 7.87 - 7.12 (m, 5H), 4.09 (m, 4H), 2.88 (s, 2H), 2.08 (dt, / = 20.7, 13.4 Hz, 6H), 1.16 (t, / = 7.1 Hz, 3H); MS (ESI ⁺ ) m/z 302.1 (M+H) ⁺ .

Example 174E: ethyl 4-amino-2-oxobicyclo[2.2.2]octane-l-carboxylate, hydrochloric acid

To a mixture of Example 174D (11.2 g of HC1 salt, 33.2 mmol) in tetrahydrofuran (110 mL) in a 50 mL pressure bottle was added 20% Pd(OH)2/C, wet (2.2 g, 1.598 mmol), and the reaction mixture was shaken at 50 °C under 50 psi of hydrogen for 22 hours. The reaction mixture was cooled to ambient temperature, solids were removed by filtration and washed with methanol (1 L). The filtrate and wash were concentrated to give 7.9 g of the title compound. ^J H NMR (400 MHz, DMSO-de) δ ppm 8.46 (s, 3H), 4.07 (q, / = 7.1 Hz, 2H), 2.62 (s, 2H), 2.17 - 2.05 (m, 2H), 2.04 - 1.78 (m, 6H), 1.14 (t, / = 7.1 Hz, 3H).

Example 174F: ethyl 4-[2-(4-chloro-3-fluorophenoxy)acetamido]-2-oxobicyclo[2.2.2 ] octane- 1- carboxylate

To a suspension of Example 174E (7.8 g, 31.5 mmol), N-ethyl-N-isopropylpropan-2- amine (22.00 mL, 126 mmol) and 2-(4-chloro-3-fluorophenoxy)acetic acid (7.41 g, 36.2 mmol) in N,N-dimethylformamide (200 mL), 2-(3H-[l,2,3]triazolo[4,5- ?]pyridin-3-yl)-l, 1,3,3- tetramethylisouronium hexafluorophosphate(V) (14.97 g, 39.4 mmol) was added, and the resulting solution was stirred at ambient temperature for 16 hours. Water was added, and the mixture was stirred for 15 minutes. The precipitate was collected by filtration, washed with water, and air-dried to give 12.1 g of the title compound. ^J H NMR (400 MHz, DMSO-<¾) δ ppm 7.87 (s, 1H), 7.45 (t, / = 8.9 Hz, 1H), 7.00 (dd, / = 11.4, 2.9 Hz, 1H), 6.79 (ddd, / = 8.9, 2.9, 1.2 Hz, 1H), 4.45 (s, 2H), 4.06 (q, / = 7.1 Hz, 2H), 2.73 (s, 2H), 2.07 (m, 1H), 2.01 - 1.84 (m, 6H), 1.14 (t, / = 7.1 Hz, 3H); MS (ESI ⁺ ) m/z 398.0 (M+H) ⁺ .

Example 174G: 4-[2-(4-chloro-3-fluorophenoxy)acetamido]-2-oxobicyclo[2.2.2 ] octane- 1- carboxylic acid

A suspension of Example 174F (11.37 g, 28.6 mmol) and sodium hydroxide (7.15 mL,

57.2 mmol, 8 M solution) in methanol (100 mL) was stirred at ambient temperature for 16 hours. Volatiles were removed, and the residue was acidified with 1 N HC1. The precipitate was collected by filtration and dried in vacuum oven to give 9.9 g of the title compound. ^J H NMR (400 MHz, DMSO- ) δ ppm 12.49 (s, 1H), 7.86 (s, 1H), 7.45 (t, / = 8.9 Hz, 1H), 7.00 (dd, / = 11.4, 2.9 Hz, 1H), 6.83 - 6.74 (m, 1H), 4.45 (s, 2H), 2.71 (s, 2H), 2.01 - 1.81 (m, 7H); MS (ESI ^" ) m/z 368.1 (M-H) ^~ .

Example 174H: ( S )-4-(2-(4-chloro-3-fluorophenoxy )acetamido )-2-hydroxybicyclo[ 2.2.2]octane- 1-carboxylic acid

To a solution of Example 174G (10 g, 25.7 mmol) in methanol (200 mL) was added NaB¾ (1.069 g, 28.3 mmol) at -20°C, and the reaction mixture was stirred for 2 hours at the same temperature. Solvent was removed under reduced pressure, and the residue was quenched with aqueous HC1 (1.5 M) to pH =1. Water (50 mL) was added, and the resulting mixture was filtered. The collected solid was washed with water (100 mL) and ethyl acetate (100 mL), and dried under high vacuum to give 8.7 g of the racemic title compound. This intermediate was then subjected to preparative chiral SFC purification to give Example 174H as the first peak eluted off the column. The method of separation by chiral SFC (Instrument: Thar SFC80 preparative SFC; Column: Chiralpak AD-H 250x30mm i.d. 5μπι; Mobile phase: A for C(¾ and B for CH ₃ OH (0.1 % ΝΗ ₃ Ή ₂ Ο) Eluent B 35% isocratic for 4 minute runtime; Flow rate:70 g/minute; Wavelength = 220 nm; Column temperature: 40 °C; System back pressure: 100 bar; Cycle time:4 minutes; Injection amount: 25 mg per injection. Work up: the resulting solution was concentrated under reduced pressure at 40 °C, and the residue was diluted with water (150 mL), adjusted to pH =1 with aqueous HC1 (1.5 M) to pH=l . The resulting mixture was filtered, and the cake was washed with water (100 mL) and ethyl acetate (100 mL), and dried under high vacuum to give the title compound. MS (ESI+) m/z 372.0 (M+H) ⁺ .

Example 1741: (2S)-4-[2-(4-chloro-3-fluorophenoxy)acetamido]-N-[2-(4-chlor ophenyl)-2- oxoethyl]-2-hydroxybicyclo[ 2.2.2 ] octane- 1-carboxamide

A mixture of 2-amino-l-(4-chlorophenyl)ethanone hydrochloride (133 mg, 0.646 mmol), (5)-4-(2-(4-chloro-3-fluorophenoxy)acetamido)-2-hydroxybicyc lo[2.2.2]octane-l-carboxylic acid (200 mg, 0.538 mmol, Example 174H), N-ethyl-N-isopropylpropan-2-amine (0.282 mL, 1.614 mmol) in N,N-dimethylformamide (DMF) (2 mL) was treated with 2-(3H- [l,2,3]triazolo[4,5-¾]pyridin-3-yl)-l,l,3,3-tetramethylisou ronium hexafluorophosphate(V) (307 mg, 0.807 mmol), and the reaction mixture was stirred at ambient temperature for 12 hours. The reaction mixture was diluted with methanol (2 mL) and then purified by preparative reverse phase HPLC (Phenomenex® Luna® CI 8(2) 10 μπι 100A AXIA™ column (250 mm x 50 mm). A 30-100% gradient of acetonitrile (A) and 0.1 % trifluoroacetic acid in water (B) is used over 30 minutes, at a flow rate of 50 mL/minute) to give the title compound (250 mg, 89% yield). ^J H NMR (400 MHz, CDC1 ₃ ) δ ppm 7.98 - 7.83 (m, 2H), 7.57 - 7.40 (m, 2H), 7.32 (t, J = 8.6 Hz, 1H), 7.00 (t, J = 4.5 Hz, 1H), 6.74 (dd, J = 10.3, 2.9 Hz, 1H), 6.66 (ddd, J = 8.9, 2.9, 1.3 Hz, 1H), 6.16 (s, 1H), 4.70 (qd, J = 19.7, 4.5 Hz, 2H), 4.35 (s, 2H), 4.27 (dt, J = 9.1, 2.2 Hz, 1H), 2.50 (ddd, J = 13.4, 9.3, 3.0 Hz, 1H), 2.43 - 2.31 (m, 1H), 2.30 - 1.86 (m, 5H), 1.86 - 1.45 (m, 3H); MS(APCI) m/z 523.2 (M+H) ⁺ .

Example 175: 4-[2-(4-chloro-3-fluorophenoxy)acetamido]-3-hydroxy-iV-{[4- (trifluoromethyl)phenyl]methyl}bicyclo[2.2.2]octane-l-carbox amide (Compound 274)

Example 175 A: dimethyl 2-oxobicyclo[2.2.2] octane- 1,4-dicarboxylate:

To a mixture of dimethyl bicyclo[2.2.2]octane- 1,4-dicarboxylate (3.89 g, 17.19 mmol) in acetic acid (40 mL) was added chromium trioxide (3.44 g, 34.4 mmol) at 20 °C, then the mixture was stirred at 90 °C for 18 hours. The reaction mixture was diluted with ethyl acetate (200 mL), poured into water (100 mL) and adjusted to pH = 9 with solid NaHCC>3. The aqueous layer was extracted with ethyl acetate (3 x 200 mL). The organic phase was washed with brine (300 mL), dried over Na2SC>4 and concentrated under reduced pressure. The residue was purified by column chromatography on silica gel (petroleum ether: ethyl acetate = 20:1-10: 1) to give crude title compound which was treated with petroleum ether (50 mL). The solid was collected by filtration and dried under high vacuum to give 0.8 g of the title compound. ^J H NMR (400 MHz, DMSO- ), δ ppm 1.68-2.16 (m, 8H), 2.25-2.35 (m, 2H), 2.58 (s, 2H), 3.64 (s, 1H), 3.70 (s, 3H), 3.74 (s, 3H).

Example 175B: 4-(methoxycarbonyl)-2-oxobicyclo[2.2.2] octane- 1-carboxylic acid

To a solution of Example 175A (8.4 g, 33.2 mmol) in tetrahydrofuran (80 mL) and methanol (20 mL) was added a solution of lithium hydroxide monohydrate (1.116 g, 26.6 mmol) in water (20 mL) at 0 °C, and the resulting mixture was stirred for 48 hours at 25 °C. The mixture was concentrated under reduced pressure at 25°C, and the residue was diluted with water (40 mL) and extracted with 2-methoxy-2-methylpropane (2 x 80 mL). The aqueous layer was adjusted to pH =2 with aqueous 0.5 N HCl, and the precipitate was collected by filtration and dried under high vacuum to give the title compound (4 g, yield 50.6%). ^J H NMR (400 MHz, CDC1 ₃ ) δ ppm 1.88-2.12 (m, 7H), 2.27-2.39 (m, 2H), 2.60 (s, 2H), 3.72 (s, 1H), 3.75 (s, 3H). Example 175C: 4-tert-butyl 1 -methyl 2-oxobicyclo[2.2.2]octane-l,4-dicarboxylate

To a solution of Example 175B (4 g, 16.80 mmol) in i-butanol (60 mL) was added pyridine (9.57 g, 121 mmol) and N,N-dimethylpyridin-4-amine (2.052 g, 16.80 mmol). Then di- teri-butyl dicarbonate (18.33 g, 84 mmol) was added slowly at 20 °C, and the mixture was stirred at 35 °C for 24 hours. The resulting solution was concentrated under reduced pressure, and the residue was partitioned between ethyl acetate (100 mL) and water (100 mL). The organic phase was washed with water (2 x 100 mL), dried with Na2SC>4 and concentrated under reduced pressure to give the title compound (5.5 g) which was used in the subsequent step without further purification. ^J H NMR (400 MHz, CDC1 ₃ ) δ ppm 1.37 (s, 9H), 1.79 (br d, /=12.35 Hz, 2H), 1.83-2.00 (m, 4H), 2.21 (br d, /=13.33 Hz, 2H), 2.46 (s, 2H), 3.68 (s, 3H). Example 175D: 4-(tert-butoxycarbonyl)-2-oxobicyclo[2.2.2]octane-l-carboxyl ic acid

To a solution of Example 175C (5.5 g, 19.48 mmol) in tetrahydrofuran (80 mL) and methanol (20 mL) was added a solution of NaOH (0.779 g, 19.48 mmol) in water (20 mL) at 0 °C, and the mixture was stirred at 0 °C to 25 °C for 12 hours. The mixture was concentrated under reduced pressure at 25 °C. The residue was diluted with water (30 mL) and washed with 2-methoxy-2-methylpropane (2 x 50 mL). The aqueous layer was acidified to pH =1 with aqueous 1 N HCl, and the precipitate was collected by filtration and dried under high vacuum to give the title compound (2.4 g, yield 41 %). ^J H NMR (400 MHz, CDCI ₃ ), δ ppm 1.22 (s, 1H), 1.41- 1.53 (m, 9H), 1.78-1.98 (m, 2H), 2.03-2.27 (m, 6H), 2.57-2.69 (m, 2H).

Example 175E: tert-butyl 4-(((benzyloxy)carbonyl)amino)-3-oxobicyclo[2.2.2]octane-l- carboxylate

To a solution of Example 175D (1 g, 3.73 mmol) in toluene (100 mL) was added triethylamine (1.558 mL, 11.18 mmol) and diphenyl phosphorazidate (2.051 g, 7.45 mmol) sequentially at 20 °C, and the mixture was stirred for 2 hours at 120 °C under N ₂ . Then benzyl alcohol (1.163 mL, 11.18 mmol) was added at 120 °C, and the mixture was stirred at 120 °C for 12 hours. The reaction mixture was cooled to 25 °C and concentrated under reduced pressure. The residue was diluted with water (50 mL) and extracted with ethyl acetate (2 x 100 mL). The organic phase was dried with Na2SC>4 and concentrated under reduced pressure, and the residue was purified by column chromatography on silica gel eluted with petroleum ether and ethyl acetate (100: 1 to 30: 1 to 10: 1) to give the title compound (0.95 g, yield 62.5%). ^J H NMR (400 MHz, CDCI ₃ ) δ ppm 1.37 (s, 9H), 1.50-1.56 (m, 2H), 1.70-1.88 (m, 3H), 1.97-2.12 (m, 3H), 2.55 (s, 2H), 2.72-2.90 (m, 2H), 4.99 (s, 2H), 5.92 (br s, 1H), 7.25-7.31 (m, 5H).

Example 175F: tert-butyl 4-amino-3-oxobicyclo[2.2.2] octane- 1-carboxylate

To a mixture of Pd(OH)2 (600 mg, 4.27 mmol) in tetrahydrofuran (60 mL) was added a solution of Example 175E (2 g, 4.82 mmol) in tetrahydrofuran (60 mL) at 20 °C under argon, and the resulting mixture was stirred for 2 hours under ¾ at 15 psi. The resulting mixture was filtered through a pad of diatomaceous earth, and the cake was washed with ethyl acetate (30 mL). Water (20 mL) was added, and the resulting mixture was adjusted to pH = 1 with aqueous 1.2 M HC1. The two phases were cut, and the aqueous layer was washed with ethyl acetate (2 x 20 mL). The aqueous layer was lyophilized to give the title compound (1.2 g, yield 88%). ^J H NMR (400 MHz, CD ₃ OD) δ ppm 1.46-1.49 (m, 9H), 1.94-2.07 (m, 4H), 2.13-2.25 (m, 4H), 2.74 (s, 2H).

Example 175G: tert-butyl 4-(2-(4-chloro-3-fluorophenoxy)acetamido)-3- oxobicyclo[ 2.2.2 ] octane- 1-carboxylate

A mixture of Example 175F (0.51 g, 1.849 mmol), 2-(4-chloro-3-fluorophenoxy)acetic acid (0.435 g, 2.127 mmol) and N-ethyl-N-isopropylpropan-2-amine (0.969 mL, 5.55 mmol) in N,N-dimethylformamide (10.0 mL) was treated with 2-(3H-[l,2,3]triazolo[4,5-¾]pyridin-3-yl)- 1 , 1 ,3,3-tetramethylisouronium hexafluorophosphate(V) (0.703 g, 1.849 mmol), and the reaction mixture was stirred at ambient temperature overnight. Water (100 mL) was added drop wise, and stirring was continued for 15 minutes. The precipitate was collected by filtration, washed with water and heptane, and dried under vacuum to give 0.74 g of the title compound. ^J H NMR (400 MHz, DMSO- ) δ ppm 7.67 (s, 1H), 7.45 (t, J = 8.9 Hz, 1H), 7.04 (dd, J = 11.3, 2.9 Hz, 1H), 6.81 (ddd, J = 9.0, 2.9, 1.2 Hz, 1H), 4.52 (s, 2H), 2.53 (d, J = 1.3 Hz, 2H), 2.46 2.29 (m, 2H), 1.94 (t, J = 9.9 Hz, 2H), 1.87 1.79 (m, 1H), 1.78 (d, J = 10.5 Hz, 3H), 1.36 (s, 9H); MS (ESI ⁺ ) m/z 426 A (M+H) ⁺ .

Example 175H: 4-(2-(4-chloro-3-fluorophenoxy)acetamido)-3-oxobicyclo[2.2.2 ] octane- 1- carboxylic acid

To a solution of teri-butyl 4-(2-(4-chloro-3-fluorophenoxy)acetamido)-3- oxobicyclo[2.2.2]octane-l-carboxylate (0.73 g, 1.714 mmol, Example 175G) in dichloromethane (10.0 mL) was added 2,2,2-trifluoroacetic acid (1.321 mL, 17.14 mmol), and the reaction mixture was stirred at ambient temperature for 2 hours and 50 °C for 1 hour. Volatiles were removed under high vacuum. The residue was triturated with dichloromethane/heptane to give 0.63 g of the title compound. ^J H NMR (400 MHz, DMSO-<¾) δ ppm 12.53 (s, 1H), 7.71 (s, 1H), 7.49 (t, J = 8.8 Hz, 1H), 7.08 (dd, J = 11.4, 2.9 Hz, 1H), 6.85 (ddd, J = 8.9, 2.9, 1.2 Hz, 1H), 4.57 (s, 2H), 2.59 (d, J = 1.3 Hz, 2H), 2.42 (dd, J = 11.5, 8.5 Hz, 2H), 2.09 1.93 (m, 2H), 1.84 (d, J = 8.3 Hz, 4H); MS (ESI ⁺ ) m/z 370.2 (M+H) ⁺ .

Example 1751: 4-(2-( 4-chloro-3-fluorophenoxy )acetamido )-3-hydroxybicyclo[ 2.2.2 ] octane- 1- carboxylic acid

To a mixture of 4-(2-(4-chloro-3-fluorophenoxy)acetamido)-3-oxobicyclo[2.2.2 ]octane- 1-carboxylic acid (0.25 g, 0.676 mmol, Example 175H) in dichloromethane (2.5 mL) and methanol (2.5 mL), sodium tetrahydroborate (0.064 g, 1.690 mmol) was added, and the mixture was stirred at ambient temperature for 2 days. The reaction mixture was concentrated, and the residue was purified by reverse phase preparative HPLC (30-100% acetonitrile in 0.1 % trifluoroacetic acid/water over 25 minutes at 50 mL/minute on a Phenomenex® CI 8 10 μπι 250 mm x 50 mm column) to give 154 mg of the title compound. ^J H NMR (400 MHz, DMSO-<¾) δ ppm 12.08 (s, 1H), 7.48 (t, J = 8.9 Hz, 1H), 7.29 (s, 1H), 7.05 (dd, J = 11.4, 2.9 Hz, 1H), 6.83 (ddd, J = 9.0, 2.9, 1.2 Hz, 1H), 5.07 (d, J = 4.2 Hz, 1H), 4.47 (s, 2H), 4.06 - 3.97 (m, 1H), 2.12 (ddd, J = 13.6, 9.3, 2.4 Hz, 1H), 2.01 (ddd, J = 12.8, 10.9, 4.7 Hz, 1H), 1.94 - 1.59 (m, 7H), 1.55 (dt, J = 13.6, 3.0 Hz, 1H); MS (ESI ⁺ ) m/z 372.3 (M+H) ⁺ .

Example 175 J: 4-[2-( 4-chloro-3-fluorophenoxy )acetamido ]-3-hydroxy-N-{ [4- (trifluoromethyl)phenyl]methyl}bicyclo[2.2.2]octane-l-carbox amide

To a mixture of 4-(2-(4-chloro-3-fluorophenoxy)acetamido)-3- hydroxybicyclo[2.2.2]octane-l-carboxylic acid (75 mg, 0.202 mmol, Example 1751), 4-

(trifluoromethyl)benzylamine (44.2 mg, 0.252 mmol), and N-ethyl-N-isopropylpropan-2-amine (0.141 mL, 0.807 mmol) in N,N-dimethylformamide (1.5 mL) was added 2-(3H- [l ,2,3]triazolo[4,5-¾]pyridin-3-yl)-l , l ,3,3-tetramethylisouronium hexafluorophosphate(V) (115 mg, 0.303 mmol) followed by stirring at ambient temperature for 60 minutes. The reaction mixture was concentrated, and the residue was purified by preparative reverse phase HPLC

(Phenomenex® Luna® C18(2) 10 μπι 100A AXIA™ column (250 mm x 50 mm). A 30-100% gradient of acetonitrile (A) and 0.1% trifluoroacetic acid in water (B) is used over 25 minutes, at a flow rate of 50 mL/minute) to give 90 mg of the title compound. ^J H NMR (400 MHz, DMSO- d ₆ ) δ ppm 8.11 (t, J = 6.0 Hz, 1H), 7.66 (d, J = 8.1 Hz, 2H), 7.49 (t, J = 8.9 Hz, 1H), 7.40 (d, J = 8.0 Hz, 2H), 7.30 (s, 1H), 7.06 (dd, J = 11.4, 2.8 Hz, 1H), 6.84 (ddd, J = 8.9, 2.9, 1.2 Hz, 1H), 5.11 (s, 1H), 4.48 (s, 2H), 4.30 (d, J = 5.9 Hz, 2H), 4.04 (dd, J = 9.5, 3.0 Hz, 1H), 2.16 (ddd, J =

13.4, 9.3, 2.2 Hz, 1H), 2.03 (ddd, J = 12.6, 10.8, 4.6 Hz, 1H), 1.96 1.62 (m, 7H), 1.58 (dt, J =

13.5, 3.0 Hz, 1H); MS (ESI ⁺ ) m/z 529.2 (M+H) ⁺ . Example 176: 4-[2-(4-chloro-3-fluorophenoxy)acetamido]-3-hydroxy-iV-{[5- (trifluoromethyl)pyridin-2-yl]methyl}bicyclo[2.2.2]octane-l- carboxamide (Compound 275)

The title compound was prepared by using the methodologies described in Example 175 J substituting (5-(trifluoromethyl)pyridin-2-yl)methanamine, hydrochloric acid for 4- (trifluoromethyl)benzylamine. ^J H NMR (400 MHz, DMSO-<¾) δ ppm 8.87 (d, J = 2.3 Hz, IH), 8.23 - 8.12 (m, 2H), 7.49 (t, J = 8.8 Hz, IH), 7.38 (d, J = 8.3 Hz, IH), 7.31 (s, IH), 7.06 (dd, J = 11.4, 2.9 Hz, IH), 6.84 (dd, J = 9.1, 2.5 Hz, IH), 4.48 (s, 2H), 4.40 (d, J = 5.8 Hz, 2H), 4.05 (dd, J = 9.4, 3.0 Hz, IH), 2.18 (ddd, J = 13.6, 9.3, 2.1 Hz, IH), 2.04 (ddd, J = 12.6, 10.9, 4.6 Hz, IH), 1.96 - 1.56 (m, 8H); MS (ESI ⁺ ) m/z 530.3 (M+H) ⁺ .

Example 177: (2/?)-4-[2-(4-chloro-3-fluorophenoxy)acetamido]-N-[2-(4-chlo rophenyl)-2- oxoethyl]-2-hydroxybicyclo[2.2.2]octane-l-carboxamide (Compound 276)

Example 177 A: (R)-4-(2-(4-chloro-3-fluorophenoxy)acetamido)-2-hydroxybicyc lo[2.2.2]octane- 1-carboxylic acid

The title compound was prepared using the procedures described in Examples 174A- 174H and was isolated from the chiral SFC purification method described in Example 174H as the second peak eluted off column. ^J H NMR (400 MHz, DMSO-<¾) δ ppm 1.54-1.77 (m, 7H), 1.84 (td, J=11.55, 4.89 Hz, IH), 1.96-2.13 (m, IH), 2.18-2.30 (m, IH), 2.31-2.45 (m, IH), 2.53- 2.58 (m, IH), 4.06 (br d, J=7.83 Hz, IH), 4.44 (s, 2H), 4.49 (s, IH), 4.84 (br s, IH), 6.81 (dt, J=8.93, 1.41 Hz, IH), 7.03 (dd, J=11.49, 2.81 Hz, IH), 7.43-7.56 (m, 2H), 11.84-12.12 (m, IH); MS (+ESI) m/z = 372.0 (M+H)

Example 177B: (2R)-4-[2-(4-chloro-3-fluorophenoxy)acetamido]-N-[2-(4-chlor ophenyl)-2- oxoethyl]-2-hydroxybicyclo[ 2.2.2 ] octane- 1-carboxamide

The title compound was prepared using the procedure described in Example 1741 substituting Example 177A for Example 174H. ^J H NMR (400 MHz, CDC1 ₃ ) δ ppm 8.06 - 7.79 (m, 2H), 7.58 - 7.42 (m, 2H), 7.32 (t, J = 8.6 Hz, IH), 6.99 (t, J = 4.4 Hz, IH), 6.74 (dd, J = 10.3, 2.8 Hz, IH), 6.66 (ddd, J = 8.9, 2.9, 1.3 Hz, IH), 6.15 (s, IH), 4.70 (qd, J = 19.7, 4.5 Hz, 2H), 4.35 (s, 2H), 4.26 (dq, J = 9.2, 2.2 Hz, IH), 3.71 (d, J = 2.2 Hz, IH), 2.50 (ddd, J = 13.3, 9.3, 3.0 Hz, IH), 2.38 (ddt, J = 13.2, 10.8, 3.8 Hz, IH), 2.17 - 1.89 (m, 5H), 1.90 - 1.67 (m, 3H); MS (APCI) m/z 523.2 (M+H) ⁺ .

Example 178: (25)-4-[2-(4-chloro-3-fluorophenoxy)acetamido]-2-hydroxy-/V- (2-oxo-3- phenylpropyl)bicyclo[2.2.2]octane-l-carboxamide (Compound 277)

The title compound was prepared using the procedure described in Example 174 and substituting l-amino-3-phenylpropan-2-one hydrochloride for 2-amino-l-(4- chlorophenyl)ethanone hydrochloride . H NMR (500 MHz, CDC1 ₃ ) δ ppm 7.39 - 7.27 (m, 4H), 7.24 - 7.15 (m, 2H), 6.73 (dd, J = 10.3, 2.9 Hz, 2H), 6.65 (ddd, J = 8.9, 2.9, 1.3 Hz, 1H), 6.16 (s, 1H), 4.34 (s, 2H), 4.26 - 4.16 (m, 2H), 4.15 - 4.05 (m, 1H), 3.75 (s, 2H), 2.45 (ddd, J = 13.4, 9.3, 3.1 Hz, 1H), 2.29 (ddt, J = 12.8, 11.1 , 3.6 Hz, 1H), 2.07 - 1.85 (m, 6H), 1.82 - 1.73 (m, 1H), 1.73 - 1.62 (m, 1H); MS(APCI) m/z 503.2 (M+H) ⁺ .

Example 179: 4-[2-(4-chloro-3-fluorophenoxy)acetamido]-N-[6-(difluorometh oxy)pyridin- 3-yl]bicyclo[2.2.2]octane-l-carboxamide (Compound 278)

The reaction and purification conditions described in Example 48 substituting the product of Example 158B for the product of Example 18A, 6-(difluoromethoxy)pyridin-3-amine (Enamine) for (5-(difluoromethoxy)pyridin-2-yl)methanamine, and (l-cyano-2-ethoxy-2- oxoethylidenaminooxy)dimethylamino-mo holino-carbenium hexafluorophosphate (COMU) for (l-[bis(dimethylamino)methylene]-lH-l ,2,3-triazolo[4,5-¾]pyridinium 3-oxid

hexafluorophosphate) (HATU) gave the title compound. ^J H NMR (400 MHz, DMSO- ¾) δ ppm 9.41 (s, 1H), 8.47 (dd, J = 2.7, 0.6 Hz, 1H), 8.11 (dd, J = 8.9, 2.7 Hz, 1H), 7.62 (t, J = 73.2 Hz, 1H), 7.53 (s, 1H), 7.49 (t, J = 8.9 Hz, 1H), 7.08 - 7.00 (m, 2H), 6.82 (ddd, J = 9.0, 2.9, 1.2 Hz, 1H), 4.45 (s, 2H), 1.89 (s, 12H); MS (APCI ⁺ ) m/z 498 (M+H) ⁺ .

Example 180: 4-[2-(4-chloro-3-fluorophenoxy)acetamido]-N-[5-(trifluoromet hoxy)pyridin- 2-yl]bicyclo[2.2.2]octane-l-carboxamide (Compound 279)

The product of Example 158B (62 mg, 0.11 mmol) and

bis(tetramethylene)fluoroformamidinium hexafluorophosphate (50 mg, 0.16 mmol, Alfa) were charged to a sealed tube, and a solvent mixture of dichloromethane (0.26 mL) and N,N- diisopropylethylamine (0.083 mL, 0.47 mmol) was added in one portion. The resulting mixture was stirred at ambient temperature for 30 minutes and 5-(trifluoromethoxy)pyridin-2-amine (22.5 mg, 0.13 mmol, Astatech) was added. The tube was sealed and stirred at 75 °C for 18 hours. The reaction mixture was cooled to ambient temperature and concentrated under reduced pressure. The resulting residue was dissolved in N,N-dimethylformamide (3 mL), filtered through a glass microfiber frit and purified by preparative HPLC [YMC TriArt™ CI 8 Hybrid 5 μπι column, 50 x 100 mm, flow rate 70 mL/minute, 5-100% gradient of acetonitrile in buffer (0.025 M aqueous ammonium bicarbonate, adjusted to pH 10 with ammonium hydroxide)] to give the title compound (12 mg, 0.023 mmol, 22% yield). ^J H NMR (400 MHz, DMSO-<¾) $ ppm 9.95 (s, 1H), 8.39 - 8.36 (m, 1H), 8.11 (dd, J = 9.2, 0.6 Hz, 1H), 7.83 (ddd, J = 9.2, 3.0, 1.0 Hz, 1H), 7.48 - 7.41 (m, 2H), 7.00 (dd, J = 11.4, 2.8 Hz, 1H), 6.78 (ddd, J = 9.0, 2.8, 1.2 Hz, 1H), 4.42 (s, 2H), 1.92 - 1.78 (m, 12H). MS (APCI ⁺ ) m/z 516 (M+H) ⁺ . Example 181 : 4-[2-(4-chloro-3-fluorophenoxy)acetamido]-N-[6-(trifluoromet hoxy)pyridin- 3-yl]bicyclo[2.2.2]octane-l-carboxamide (Compound 280)

The reaction and purification conditions described in Example 48 substituting the product of Example 158B for the product of Example 18A, 6-(trifluoromethoxy)pyridin-3-amine (BePharm) for (5-(difluoromethoxy)pyridin-2-yl)methanamine, and (7-azabenzotriazol-l- yloxy)tripyrrolidinophosphonium hexafluorophosphate (PyAOP) for (1- [bis(dimethylamino)methylene]-lH-l,2,3-triazolo[4,5-¾]pyrid inium 3-oxid

hexafluorophosphate) (HATU) gave the title compound. ^J H NMR (400 MHz, DMSO- ¾) δ ppm 9.57 (s, 1H), 8.57 (d, J = 2.7 Hz, 1H), 8.23 (dd, J = 8.9, 2.7 Hz, 1H), 7.55 (s, 1H), 7.49 (t, J = 8.9 Hz, 1H), 7.26 (d, J = 8.8 Hz, 1H), 7.04 (dd, J = 11.4, 2.9 Hz, 1H), 6.83 (ddd, J = 9.0, 3.0, 1.2 Hz, 1H), 4.45 (s, 2H), 1.89 (s, 12H); MS (APCI ⁺ ) m/z 516 (M+H) ⁺ .

Example 182: 4-[2-(4-chloro-3-fluorophenoxy)acetamido]-N-[6-(2,2,2- trifluoroethoxy)pyridin-3-yl]bicyclo[2.2.2]octane-l-carboxam ide (Compound 281)

The reaction and purification conditions described in Example 48 substituting the product of Example 158B for the product of Example 18A, and 6-(2,2,2-trifluoroethoxy)pyridin-3-amine (Enamine) for (5-(difluoromethoxy)pyridin-2-yl)methanamine gave the title compound. ^J H NMR (400 MHz, DMSO-<¾) δ ppm 9.30 (s, 1H), 8.40 (dd, J = 2.7, 0.7 Hz, 1H), 7.98 (dd, J = 8.9, 2.7 Hz, 1H), 7.53 (s, 1H), 7.49 (t, J = 8.9 Hz, 1H), 7.04 (dd, J = 11.4, 2.9 Hz, 1H), 6.93 (dd, J = 8.9, 0.6 Hz, 1H), 6.82 (ddd, J = 9.0, 2.9, 1.2 Hz, 1H), 4.93 (q, J = 9.1 Hz, 2H), 4.45 (s, 2H), 1.88 (br s, 12H); MS (ESI ⁺ ) m/z 530 (M+H) ⁺ .

Example 183: 3-[2-(4-chloro-3-fluorophenoxy)acetamido]-N-[6-(difluorometh oxy)pyridin- 3-yl]bicyclo[l.l.l]pentane-l-carboxamide (Compound 282)

The reaction and purification conditions described in Example 48 substituting (1-cyano- 2-ethoxy-2-oxoethylidenaminooxy)dimethylamino-mo holino-carbenium hexafluorophosphate (COMU) for (l-[bis(dimethylamino)methylene]-lH-l,2,3-triazolo[4,5-¾]py ridinium 3-oxid hexafluorophosphate) (HATU), and 6-(difluoromethoxy)pyridin-3-amine (Enamine) for (5- (difluoromethoxy)pyridin-2-yl)methanamine gave the title compound. ^J H NMR (500 MHz, DMSO- ) δ ppm 9.87 (s, 1H), 8.81 (s, 1H), 8.50 (dd, J = 2.7, 0.7 Hz, 1H), 8.12 (dd, J = 8.9, 2.7 Hz, 1H), 7.83 - 7.47 (m, 2H), 7.11 - 7.05 (m, 2H), 6.87 (ddd, J = 8.9, 2.8, 1.2 Hz, 1H), 4.50 (s, 2H), 2.34 (s, 6H); MS (ESI ⁺ ) m/z 456 (M+H) ⁺ .

Example 184: 3-[2-(4-chloro-3-fluorophenoxy)acetamido]-N-(4- chlorophenyl)bicyclo[l.l.l]pentane-l-carboxamide (Compound 283) To a dichloromethane (2.0 mL) solution of the product of Example 18A (52 mg, 0.17 mmol) was added one drop of N,N-dimethylformamide followed by oxalyl chloride (2.0 M solution in dichloromethane, 0.124 mL). After stirring at ambient temperature for 10 minutes, the reaction mixture was concentrated under reduced pressure and taken up in dichloromethane (1.0 mL). The resulting solution was transferred to a pyridine (2 mL) solution of 4-chloroaniline (21.2 mg, 0.17 mmol). After stirring at ambient temperature for 30 minutes, the reaction mixture was concentrated under reduced pressure. The resulting residue was taken up in N,N- dimethylformamide (3 mL), filtered through a glass microfiber frit and purified by preparative HPLC [YMC TriArt™ C18 Hybrid 20 μπι column, 25 x 150 mm, flow rate 80 mL/minute, 5- 100% gradient of acetonitrile in buffer (0.025 M aqueous ammonium bicarbonate, adjusted to pH 10 with ammonium hydroxide)] to give the title compound (25 mg, 0.06 mmol, 36% yield). ^J H NMR (400 MHz, DMSO-<¾) δ ppm 9.70 (s, 1H), 8.78 (s, 1H), 7.72 - 7.63 (m, 2H), 7.50 (t, J = 8.9 Hz, 1H), 7.39 - 7.32 (m, 2H), 7.08 (dd, J = 11.4, 2.8 Hz, 1H), 6.87 (ddd, J = 9.0, 2.9, 1.2 Hz, 1H), 4.49 (s, 2H), 2.32 (s, 6H); MS (ESI ) m/z 421 (M-H) ^~ .

Example 185: 3-[2-(4-chloro-3-fluorophenoxy)acetamido]-N-[5-(difluorometh yl)pyrazin-2- yl]bicyclo[l.l.l]pentane-l-carboxamide (Compound 284)

The reaction and purification conditions described in Example 184 substituting 5- (difluoromethyl)pyrazin-2-amine (Aldrich) for 4-chloroaniline gave the title compound. ^J H NMR (501 MHz, DMSO-<¾) δ ppm 11.01 (s, 1H), 9.37 (d, J = 1.5 Hz, 1H), 8.78 (s, 1H), 8.73 - 8.71 (m, 1H), 7.50 (t, J = 8.9 Hz, 1H), 7.08 (dd, J = 11.4, 2.9 Hz, 1H), 7.07 (t, J = 54.4 Hz, 1H), 6.87 (ddd, J = 9.0, 2.9, 1.2 Hz, 1H), 4.49 (s, 2H), 2.39 (s, 6H); MS (ESI ⁺ ) m/z 441 (M+H) ⁺ . Example 186: 3-[2-(4-chloro-3-fluorophenoxy)acetamido]-N-phenylbicyclo[l. l.l]pentane- 1-carboxamide (Compound 285)

The reaction and purification conditions described in Example 48 substituting aniline for (5-(difluoromethoxy)pyridin-2-yl)methanamine gave the title compound. ^J H NMR (500 MHz, DMSO- ) δ ppm 9.56 (s, 1H), 8.78 (s, 1H), 7.65 - 7.61 (m, 2H), 7.50 (t, J = 8.9 Hz, 1H), 7.32 - 7.27 (m, 2H), 7.09 (dd, J = 11.4, 2.9 Hz, 1H), 7.05 (tt, J = 7.4, 1.2 Hz, 1H), 6.87 (ddd, J = 9.0, 2.9, 1.2 Hz, 1H), 4.49 (s, 2H), 2.32 (s, 6H); MS (ESI ⁺ ) m/z 389 (M+H) ⁺ .

Example 187: 4-[2-(4-chloro-3-fluorophenoxy)acetamido]-N-(4- chlorophenyl)bicyclo[2.1.1]hexane-l-carboxamide (Compound 286)

Example 187 : tert-butyl (4-((4-chlorophenyl)carbamoyl)bicyclo[2.1.1]hexan-l-yl)carba mate

The reaction and purification conditions described in Example 48 substituting 4- chloroaniline for (5-(difluoromethoxy)pyridin-2-yl)methanamine, and 4-((tert- butoxycarbonyl)amino)bicyclo[2.1.1]hexane-l-carboxylic acid (Enamine) for the product of

Example 18A gave the title compound. MS (ESI ) m/z 349 (M-H)\

Example 187B: 4-amino-N-(4-chlorophenyl)bicyclo[2.1.1]hexane-l-carboxamide

The product of Example 187 A (0.1 g, 0.29 mmol) was stirred in dichloromethane (1 mL) at 0 °C. Trifluoroacetic acid (1 mL, 12.98 mmol) was added in one portion. The reaction mixture was allowed to warm up to ambient temperature over 30 minutes and continued to stir for 1 hour. The resulting mixture was concentrated under reduced pressure, and the resulting residue was purified by preparative HPLC [YMC TriArt™ CI 8 Hybrid 20 μπι column, 25 x 150 mm, flow rate 80 mL/minute, 5-100% gradient of acetonitrile in buffer (0.025 M aqueous ammonium bicarbonate, adjusted to pH 10 with ammonium hydroxide)] to give the title compound (0.06 g, 0.24 mmol, 84% yield). MS (ESI ⁺ ) m/z 251 (M+H) ⁺ .

Example 187C: 4-[2-(4-chloro-3-fluorophenoxy)acetamido]-N-(4- chlorophenyl )bicyclo[ 2.1.1 ]hexane-l -carboxamide

The reaction and purification conditions described in Example 48 substituting the product of Example 187B for (5-(difluoromethoxy)pyridin-2-yl)methanamine, and 2-(4-chloro-3- fluorophenoxy)acetic acid for the product of Example 18A gave the title compound. ¹ H NMR (400 MHz, DMSO- ) δ ppm 9.48 (s, 1H), 8.54 (s, 1H), 7.69 - 7.62 (m, 2H), 7.46 (t, J = 8.9 Hz, 1H), 7.33 - 7.27 (m, 2H), 7.04 (dd, J = 11.4, 2.9 Hz, 1H), 6.82 (ddd, J = 9.0, 2.9, 1.2 Hz, 1H), 4.46 (s, 2H), 2.10 - 2.03 (m, 2H), 1.91 - 1.82 (m, 4H), 1.80 - 1.75 (m, 2H); MS (ESI ⁺ ) m/z 437 (M+H) ⁺ .

Example 188: 3-[2-(4-chloro-3-fluorophenoxy)acetamido]-N-[5-(trifluoromet hoxy)pyridin- 2-yl]bicyclo[l.l.l]pentane-l-carboxamide (Compound 287)

The reaction and purification conditions described in Example 180 substituting the product of Example 18A for the product of Example 158B gave the title compound. ^J H NMR (501 MHz, DMSO-de) δ ppm 10.57 (s, 1H), 8.76 (s, 1H), 8.42 (d, J = 3.0 Hz, 1H), 8.16 (dd, J = 9.2, 0.6 Hz, 1H), 7.90 (ddd, J = 9.2, 3.0, 1.1 Hz, 1H), 7.50 (t, J = 8.9 Hz, 1H), 7.08 (dd, J = 11.4, 2.8 Hz, 1H), 6.86 (ddd, J = 9.0, 2.9, 1.2 Hz, 1H), 4.48 (s, 2H), 2.36 (s, 6H); MS (ESI ⁺ ) m/z 474 (M+H) ⁺ .

Example 189: 4-[2-(4-chloro-3-fluorophenoxy)acetamido]-N-[5-(trifluoromet hoxy)pyridin- 2-yl]bicyclo[2.1.1]hexane-l-carboxamide (Compound 288)

Example 189 : tert-butyl (4-((5-(trifluoromethoxy)pyridin-2-yl)carbamoyl)bicyclo[2.1. 1]hexan- 1 -yl)carbamate The reaction and purification conditions described in Example 180 substituting A-{{tert- butoxycarbonyl)amino)bicyclo[2.1.1]hexane-l-carboxylic acid (Enamine) for the product of Example 158B gave the title compound. MS (ESI ⁺ ) m/z 402 (M+H) ⁺ .

Example 189B: 4-[2-( 4-chloro-3-fluorophenoxy )acetamido ]-N-[ 5-( trifluoromethoxy )pyridin-2- yl ]bicyclo[ 2.1.1 ]hexane-l-carboxamide

Trifluoroacetic acid (0.25 mL, 3.24 mmol) was added to the product of Example 189A (30 mg, 0.075 mmol), and the mixture was stirred at ambient temperature. After 30 minutes, dichloromethane (2 mL) was added followed by dropwise addition of aqueous sodium carbonate (1.0 M, 10 mL) over a period of 2 minutes. In a separate vial, 2-(4-chloro-3- fluorophenoxy)acetic acid (18.4 mg, 0.09 mmol, Aldlab) was suspended in dichloromethane (2. mL) and 1 drop of N,N-dimethylformamide was added followed by oxalyl chloride (2 M solution in dichloromethane, 0.075 mL). After stirring for 10 minutes at ambient temperature, the resulting clear solution was added in one portion to the fast stirring suspension from the previous step and was kept stirring for 20 minutes. The layers were separated, and the organic phase was dried over sodium sulfate and concentrated under reduced pressure. The resulting residue was taken up in N,N-dimethylformamide (2mL), filtered through a glass microfiber frit, and purified by preparative HPLC [YMC TriArt™ CI 8 Hybrid 20 μπι column, 25 x 250 mm, flow rate 70 mL/minute, 5-100% gradient of acetonitrile in buffer (0.025 M aqueous ammonium bicarbonate, adjusted to pH 10 with ammonium hydroxide)] to give the crude product which was further purified by preparative HPLC [Waters XBridge™ CI 8 5 μπι OBD column, 30 x 100 mm, flow rate 40 mL/minute, 5-100% gradient of MeOH in buffer (0.025 M aqueous ammonium bicarbonate, adjusted to pH 10 with ammonium hydroxide)] to give the title compound (15 mg, 0.03 mmol, 41% yield). ^J H NMR (400 MHz, DMSO-de) δ ppm 10.28 (s, 1H), 8.42 (d, J = 2.9 Hz, 1H), 8.19 (d, J = 9.2 Hz, 1H), 7.89 (dd, J = 8.9, 2.4 Hz, 1H), 7.34 (s, 1H), 2.11 - 1.98 (m, 2H), 1.95 - 1.86 (m, 2H), 1.82 - 1.67 (m, 4H), 1.39 (s, 9H); MS (ESI ⁺ ) m/z 402 (M+H) ⁺ .

Example 190: 3-[2-(3,4-dichlorophenoxy)acetamido]-/V-(pyridin-2- yl)bicyclo[l.l.l]pentane-l-carboxamide (Compound 289)

The reaction and purification conditions described in Example 180 substituting the product of Example 49A for the product of Example 158B, and 2-aminopyridine for (5- (trifluoromethoxy )pyridin-2-amine gave the title compound. ^J H NMR (400 MHz, DMSO-<¾) δ ppm 10.24 (s, 1H), 8.75 (s, 1H), 8.33 (ddd, J = 4.9, 2.0, 0.9 Hz, 1H), 8.04 (dt, J = 8.4, 1.0 Hz, 1H), 7.78 (ddd, J = 8.9, 7.3, 1.9 Hz, 1H), 7.55 (d, J = 8.9 Hz, 1H), 7.27 (d, J = 2.9 Hz, 1H), 7.11 (ddd, J = 7.3, 4.9, 1.0 Hz, 1H), 7.00 (dd, J = 8.9, 2.9 Hz, 1H), 4.49 (s, 2H), 2.35 (br s, 5H); MS (ESI ⁺ ) m/z 406 (M+H) ⁺ .

Example 191: 3-[2-(4-chloro-3-fluorophenoxy)acetamido]-N-(pyridin-2- yl)bicyclo[l.l.l]pentane-l-carboxamide (Compound 290)

The reaction and purification conditions described in Example 180 substituting the product of Example 18A for the product of Example 158B, and 2-aminopyridine for (5- (trifluoromethoxy)pyridin-2-amine gave the title compound. ^J H NMR (400 MHz, DMSO-<¾) δ ppm 10.24 (s, 1H), 8.75 (s, 1H), 8.33 (ddd, J = 4.9, 2.0, 0.9 Hz, 1H), 8.04 (dt, J = 8.5, 1.0 Hz, 1H), 7.78 (ddd, J = 8.8, 7.4, 1.9 Hz, 1H), 7.50 (t, J = 8.8 Hz, 1H), 7.15 - 7.06 (m, 2H), 6.86 (ddd, J = 9.0, 2.8, 1.2 Hz, 1H), 4.48 (s, 2H), 2.35 (s, 6H); MS (ESI ⁺ ) m/z 390 (M+H) ⁺ .

Example 192: 3-[2-(3,4-dichlorophenoxy)acetamido]-N-[5-(trifluoromethoxy) pyridin-2- yl]bicyclo[l.l.l]pentane-l-carboxamide (Compound 291)

The reaction and purification conditions described in Example 180 substituting the product of Example 49A for the product of Example 158B gave the title compound. ^J H NMR (400 MHz, DMSO- ) δ ppm 10.59 (s, 1H), 8.76 (s, 1H), 8.44 - 8.42 (m, 1H), 8.17 (dd, J = 9.2, 0.6 Hz, 1H), 7.90 (ddd, J = 9.2, 3.2, 1.1 Hz, 1H), 7.55 (d, J = 8.9 Hz, 1H), 7.27 (d, J = 2.9 Hz, 1H), 7.00 (dd, J = 9.0, 2.9 Hz, 1H), 4.50 (s, 2H), 2.36 (s, 6H); MS (ESI ⁺ ) m/z 490 (M+H) ⁺ . Example 193: 4-[2-(3,4-dichlorophenoxy)acetamido]-N-[5-(trifluoromethoxy) pyridin-2- yl]bicyclo[2.1.1]hexane-l-carboxamide (Compound 292)

Example 193A: 4-amino-N-(5-(trifluoromethoxy)pyridin-2-yl)bicyclo[2.1.1]he xane-l- carboxamide, trifluoro acetic acid

The product of Example 189 A (60 mg, 0.15 mmol) was dissolved in dichloromethane (0.5 mL) and trifluoroacetic acid (0.5 mL, 6.49 mmol) was added. After stirring at ambient temperature for 15 minutes, the resulting solution was concentrated under reduced pressure to give the title compound. MS (ESI ⁺ ) m/z 302 (M+H) ⁺ .

Example 193B: 4-[2-(3,4-dichlorophenoxy)acetamido]-N-[5-(trifluoromethoxy) pyridin-2- yl ]bicyclo[ 2.1.1 ]hexane-l-carboxamide

The reaction and purification conditions described in Example 48 substituting 2-(3,4- dichlorophenoxy)acetic acid (Aldrich) for the product of Example 18 A, and the product of Example 193A for (5-(difluoromethoxy)pyridin-2-yl)methanamine gave the title compound. ^J H NMR (400 MHz, DMSO-<¾) δ ppm 10.59 (s, 1H), 8.76 (s, 1H), 8.44 - 8.42 (m, 1H), 8.17 (dd, J = 9.2, 0.6 Hz, 1H), 7.90 (ddd, J = 9.2, 3.2, 1.1 Hz, 1H), 7.55 (d, J = 8.9 Hz, 1H), 7.27 (d, J = 2.9 Hz, 1H), 7.00 (dd, J = 9.0, 2.9 Hz, 1H), 4.50 (s, 2H), 2.36 (s, 6H); MS (ESI ⁺ ) m/z 490 (M+H) ⁺ . Example 194: 4-{2-[(2,2-difluoro-2H-l,3-benzodioxol-5-yl)oxy]acetamido}-N -[5- (trifluoromethoxy)pyridin-2-yl]bicyclo[2.1.1]hexane-l-carbox amide (Compound 293)

Example 194A: 2,2-difluorobenzo[d] [ 1 ,3]dioxol-5-ol

To a cold solution of 5-bromo-2,2-difluorobenzo[(f] [l ,3]dioxole (5.75 mL, 42.2 mmol) in tetrahydrofuran (80 mL) was added a 2.0 M solution of isopropylmagnesium chloride in tetrahydrofuran (28.1 mL, 56.1 mmol) within 5- 10 minutes while maintaining the temperature in the range of 10-20 °C. The reaction mixture was stirred at the same temperature for another 15 minutes and then allowed to attain room temperature with continued overnight stirring. The reaction mixture was cooled with an ice bath, triisopropyl borate (12.74 mL, 54.9 mmol) was added dropwise over 2 minutes, and stirring at room temperature was continued for 30 minutes. The reaction mixture was cooled to 10 °C and 10% H2SO4 solution (50 mL) was added slowly which resulted in a slight exotherm to 20 °C. After stirring for 15 minutes, the mixture was partitioned between water and ethyl acetate, and the combined organic extracts were washed with saturated NaHCC>3 solution. The organic layer was separated, dried over magnesium sulfate, filtered, and concentrated. The residue was dissolved in 100 mL of teri-butyl methyl ether and cooled to 0 °C. 30% Hydrogen peroxide solution in water (5.39 mL, 52.7 mmol) was added slowly followed by water (60 mL), and the mixture was stirred overnight while warming up to ambient temperature. The reaction mixture was diluted with ethyl acetate and washed twice with sodium thiosulfate solution and brine. The organic layer was dried with magnesium sulfate and filtered. The filtrate was concentrated, and the residue was purified on silica gel

(0-50% ethyl acetate in heptane) to give 6.43 g of the title compound as an amber oil. ^J H NMR (400 MHz, DMSO- ) δ ppm 9.75 (s, 1H), 7.12 (d, / = 8.7 Hz, 1H), 6.75 (d, / = 2.4 Hz, 1H), 6.52 (dd, / = 8.7, 2.5 Hz, 1H); MS (ESI-) mJz 173.1 (M-H)\

Example 194B: 2-((2,2-difluorobenzo[d] [ 1 ,3]dioxol-5-yl)oxy)acetic acid

To a solution of Example 194A (3.0 g, 17.23 mmol) in N,N-dimethylformamide (30 mL) at ambient temperature was added potassium carbonate (4.76 g, 34.5 mmol) and teri-butyl bromoacetate (2.91 mL, 19.82 mmol). This mixture was warmed to 65 °C and was allowed to stir for 1.5 hours. The mixture was allowed to cool to ambient temperature and was then partitioned between ethyl acetate (50 mL) and ¾0 (50 mL). The layers were separated, and the aqueous layer was extracted with ethyl acetate (3 x 15 mL). The combined organic fractions were dried over anhydrous Na2SO/t, filtered, and concentrated under reduced pressure to give 5.5 g of teri-butyl 2-((2,2-difluorobenzo[(f] [l ,3]dioxol-5-yl)oxy)acetate, which was used without further purification. To a mixture of teri-butyl 2-((2,2-difluorobenzo[i ] [l ,3]dioxol-5- yl)oxy)acetate (5.0 g, 17.35 mmol) in methanol (60 mL) and water (20.00 mL) was added NaOH (17.35 mL, 87 mmol, 5 M aqueous solution). This mixture was allowed to stir at ambient temperature for 2 hours, and then it was concentrated under reduced pressure. The residue was dissolved in water, and the pH was adjusted to ~1 with 1 N HC1. The resulting solid was collected by filtration to give the title compound (3.28 g, 14.13 mmol, 81% yield) as a white solid. ^J H NMR (400 MHz, DMSO-<¾) δ ppm 13.10 (s, 1H), 7.30 (d, / = 8.9 Hz, 1H), 7.13 (d, / = 2.6 Hz, 1H), 6.73 (dd, / = 8.9, 2.6 Hz, 1H), 4.69 (s, 2H).

Example 194C: 4-{2-[(2,2-difluoro-2H-l,3-benzodioxol-5-yl)oxy]acetamido}-N -[5- ( trifluoromethoxy )pyridin-2-yl ]bicyclo[ 2.1.1 ]hexane-l -carboxamide

The reaction and purification conditions described in Example 48 substituting the product of Example 194B for the product of Example 18A, and the product of Example 193A for (5- (difluoromethoxy)pyridin-2-yl)methanamine gave the title compound. ^J H NMR (400 MHz, DMSO- ) δ ppm 10.35 (s, 1H), 8.52 (s, 1H), 8.42 (dt, J = 2.9, 0.8 Hz, 1H), 8.20 (dd, J = 9.2, 0.6 Hz, 1H), 7.90 (ddd, J = 9.2, 3.0, 1.0 Hz, 1H), 7.33 (d, J = 8.9 Hz, 1H), 7.14 (d, J = 2.5 Hz, 1H), 6.78 (dd, J = 8.9, 2.6 Hz, 1H), 4.45 (s, 2H), 2.12 - 2.04 (m, 2H), 2.01 - 1.84 (m, 6H); MS (ESI ⁺ ) m/z 516 (M+H) ⁺ .

Example 195: 3-{2-[(2,2-difluoro-2H-l,3-benzodioxol-5-yl)oxy]acetamido}-N -[5- (trifluoromethoxy)pyridin-2-yl]bicyclo[l.l.l]pentane-l-carbo xamide (Compound 294)

Example 195A: tert-butyl (3-((5-(trifluoromethoxy)pyridin-2- yl)carbamoyl)bicyclo[l .1.1 ]pentan-l -yl)carbamate

The reaction and purification conditions described in Example 180 substituting 3-((tert- butoxycarbonyl)amino)bicyclo[l. l. l]pentane-l-carboxylic acid (Enamine) for the product of

Example 158B gave the title compound. MS (ESI ⁺ ) m/z 388 (M+H) ⁺ .

Example 195B: 3-amino-N-(5-(trifluoromethoxy)pyridin-2-yl)bicyclo[ 1.1.1 ]pentane-l- carboxamide bistrifluoroacetate

The reaction and purification conditions described in Example 193 A substituting the product of Example 195 A for the product of Example 189 A gave the title compound. MS (ESI ⁺ ) m/z 288 (M+H) ⁺ .

Example 195C: 3-{2-[(2,2-difluoro-2H-l,3-benzodioxol-5-yl)oxy]acetamido}-N -[5- ( trifluoromethoxy )pyridin-2-yl ]bicyclo[ 1.1.1 ]pentane-l -carboxamide

The reaction and purification conditions described in Example 48 substituting the product of Example 194B for the product of Example 18 A, and the product of Example 195B for (5- (difluoromethoxy)pyridin-2-yl)methanamine gave the title compound. ^J H NMR (400 MHz, DMSO- ) δ ppm 10.58 (s, 1H), 8.74 (s, 1H), 8.43 (dt, J = 3.0, 0.8 Hz, 1H), 8.17 (dd, J = 9.2, 0.6 Hz, 1H), 7.90 (ddd, J = 9.1, 3.0, 1.1 Hz, 1H), 7.33 (d, J = 8.9 Hz, 1H), 7.15 (d, J = 2.6 Hz, 1H), 6.78 (dd, J = 8.9, 2.6 Hz, 1H), 4.45 (s, 2H), 2.36 (s, 6H); MS (ESI ⁺ ) m/z 502 (M+H) ⁺ .

Example 196: 3-[2-(3,4-dichlorophenoxy)acetamido]-N-(pyridin-3- yl)bicyclo[l.l.l]pentane-l-carboxamide (Compound 295)

The reaction and purification conditions described in Example 180 substituting the product of Example 49A for the product of Example 158B, and 3-aminopyridine for (5- (trifluoromethoxy)pyridin-2-amine gave the title compound. ^J H NMR (500 MHz, DMSO-<¾) δ ppm 9.82 (s, 1H), 8.82 - 8.79 (m, 2H), 8.26 (dd, J = 4.7, 1.5 Hz, 1H), 8.05 (ddd, J = 8.4, 2.6, 1.5 Hz, 1H), 7.56 (d, J = 8.9 Hz, 1H), 7.34 (ddd, J = 8.3, 4.7, 0.8 Hz, 1H), 7.28 (d, J = 2.9 Hz, 1H), 7.00 (dd, J = 8.9, 2.9 Hz, 1H), 4.51 (s, 2H), 2.34 (s, 6H); MS (ESI ⁺ ) m/z 406 (M+H) ⁺ .

Example 197: 3-[2-(3,4-dichlorophenoxy)acetamido]-N-(pyridin-4- yl)bicyclo[l.l.l]pentane-l-carboxamide (Compound 296)

The reaction and purification conditions described in Example 180 substituting the product of Example 49A for the product of Example 158B, and 4-aminopyridine for (5-

(trifluoromethoxy)pyridin-2-amine gave the title compound. H NMR (400 MHz, DMSO-<¾) δ ppm 9.94 (s, 1H), 8.80 (s, 1H), 8.45 - 8.39 (m, 2H), 7.66 - 7.61 (m, 2H), 7.56 (d, J = 8.9 Hz, 1H), 7.28 (d, J = 2.9 Hz, 1H), 7.00 (dd, J = 8.9, 2.9 Hz, 1H), 4.51 (s, 2H), 2.35 (s, 6H); MS (ESI ⁺ ) m/z 406 (M+H) ⁺ .

Example 198: N-[5-(trifluoromethoxy)pyridin-2-yl]-3-(2-{[6-(trifluorometh yl)pyridin-3- yl]oxy}acetamido)bicyclo[l.l.l]pentane-l-carboxamide (Compound 297)

Example 198A: 2-((6-(trtfluoromethyl)pyridin-3-yl)oxy)acetic acid

The reaction and purification conditions described in Example 194B substituting 6-

(trifluoromethyl)pyridin-3-ol (Combi-B locks) for the product of Example 194A gave the title compound. MS (DCI ⁺ ) m/z 296 (M+NH ₄ ) ⁺ .

Example 198B: N-[5-(trifluoromethoxy)pyridin-2-yl]-3-(2-{[6-(trifluorometh yl)pyridin-3- yl]oxy}acetamido)bicyclo[l.l.l]pentane-l-carboxamide

The reaction and purification conditions described in Example 48 substituting the product of Example 195B for (5-(difluoromethoxy)pyridin-2-yl)methanamine, and the product of Example 198A for the product of Example 18A gave the title compound. ^J H NMR (400 MHz,

DMSO- ) δ ppm 10.58 (s, 1H), 8.85 (s, 1H), 8.47 (d, J = 2.9 Hz, 1H), 8.43 (dt, J = 2.9, 0.8 Hz,

1H), 8.16 (dd, J = 9.1, 0.6 Hz, 1H), 7.92 - 7.88 (m, 1H), 7.87 (d, J = 8.8 Hz, 1H), 7.60 - 7.56 (m,

1H), 4.67 (s, 2H), 2.36 (s, 6H); MS (ESI ⁺ ) m/z 490 (M+H) ⁺ . Example 199: 3-[2-(4-chloro-3-fluorophenoxy)acetamido]-N-[5-(difluorometh yl)pyridin-2- yl]bicyclo[l.l.l]pentane-l-carboxamide (Compound 298)

Example 199 : 5-( difluoromethyl )pyridin-2- amine

To a solution of 6-aminonicotinaldehyde (0.2 g, 1.64 mmol) in CH2CI2 (7.5 mL) at 0 °C was added bis(2-methoxyethyl)aminosulfur trifluoride (0.91 mL, 4.9 mmol) in CH2CI2 (5 mL) dropwise via syringe pump over 10 minutes. The mixture was allowed to stir at 0 °C for 20 minutes, then the ice-bath was removed, and the mixture was allowed to warm to ambient temperature. The mixture was then allowed to stir for an additional 90 minutes and was quenched by slow addition of saturated, aqueous NaHCC>3 (25 mL) added via addition funnel over 1 hour. The mixture was diluted with CH2CI2 (15 mL), and the layers were separated. The aqueous layer was extracted with CH2CI2 (3 x 7 mL). The combined organic fractions were dried over anhydrous Na2SO/t, filtered, and concentrated under reduced pressure. The residue was purified via column chromatography (Si(¾, 50% ethyl acetate/heptanes) to give the title compound (0.06 g, 0.42 mmol, 25% yield). MS (ESI ⁺ ) mJz 145.1 (M+H) ⁺ .

Example 199B: 3-[2-(4-chloro-3-fluorophenoxy)acetamido]-N-[5-(difluorometh yl)pyridin-2- yl]bicyclo[ 1.1.1 ]pentane-l -carboxamide

To the product of Example 18A (0.06 g, 0.19 mmol) and l-(fluoro(pyrrolidin- l- yl)methylene)pyrrolidin-l-ium hexafluorophosphate(V) (HATU, 0.091 g, 0.29 mmol) was added a mixture of CH2CI2 (0.3 mL) and N-ethyl-N-isopropylpropan-2-amine (0.15 mL, 0.86 mmol). This mixture was allowed to stir at ambient temperature for 30 minutes, and then the product of Example 199A (0.050 g, 0.344 mmol) inCH ₂ Cl ₂ (0.5 mL) was added. The vial was sealed and the mixture was warmed to 78 °C and was allowed to stir for 16 hours. The mixture was allowed to cool to ambient temperature, then was dissolved in ethyl acetate, and filtered through silica gel with ethyl acetate. The filtrate was concentrated under reduced pressure and was purified by preparative HPLC [Waters XBridge™ CI 8 5 μηι OBD™ column, 50 x 100 mm, flow rate 90 mL/minute, 5- 100% gradient of acetonitrile in buffer (0.025 M aqueous ammonium bicarbonate, adjusted to pH 10 with ammonium hydroxide)] to give the title compound (0.04 g, 0.091 mmol, 48% yield). ^J H NMR (400 MHz, DMSO-<¾) δ ppm 10.55 (s, 1H), 8.74 (s, 1H), 8.50 (d, J = 2.2 Hz, 1H), 8.15 (d, J = 8.7 Hz, 1H), 8.02 7.91 (m, 1H), 7.46 (t, J = 8.9 Hz, 1H), 7.25 6.89 (m, 2H), 6.83 (ddd, J = 9.0, 2.8, 1.2 Hz, 1H), 4.45 (s, 2H), 2.34 (s, 6H); MS (ESI ⁺ ) m/z 440.1 (M+H) ⁺ .

Example 200: 3-[2-(4-chloro-3-fluorophenoxy)acetamido]-N-(5-methylpyridin -2- yl)bicyclo[l.l.l]pentane-l-carboxamide (Compound 299) To the product of Example 18A (0.06 g, 0.19 mmol) and l-(fluoro(pyrrolidin- l- yl)methylene)pyrrolidin-l-ium hexafluorophosphate(V) (HATU, 0.091 g, 0.29 mmol) was added a mixture of CH2CI2 (0.5 mL) and N-ethyl-N-isopropylpropan-2-amine (0.15 mL, 0.86 mmol). This mixture was allowed to stir at ambient temperature for 30 minutes, and then 2-amino-5- methylpyridine (0.041 g, 0.38 mmol) was added. The vial was sealed, and the mixture was warmed to 78 °C and was allowed to stir for 16 hours. The mixture was allowed to cool to ambient temperature, then was dissolved in ethyl acetate, and filtered through silica gel with ethyl acetate. The filtrate was concentrated under reduced pressure and was purified by preparative HPLC [Waters XBridge™ C18 5 μπι OBD™ column, 50 x 100 mm, flow rate 90 mL/minute, 5- 100% gradient of acetonitrile in buffer (0.025 M aqueous ammonium bicarbonate, adjusted to pH 10 with ammonium hydroxide)] to give the title compound (0.035 g, 0.087 mmol, 45% yield). ^J H NMR (400 MHz, DMSO-<¾) δ ppm 10.10 (s, 1H), 8.71 (s, 1H), 8.12 (d, J = 2.2 Hz, 1H), 7.89 (d, J = 8.5 Hz, 1H), 7.56 (dd, J = 8.6, 2.4 Hz, 1H), 7.47 (t, J = 8.9 Hz, 1H), 7.05 (dd, J = 11.4, 2.8 Hz, 1H), 6.83 (ddd, J = 8.9, 2.9, 1.2 Hz, 1H), 4.44 (s, 2H), 2.30 (s, 6H), 2.21 (s, 3H); MS (ESI ⁺ ) m/z 404.0 (M+H) ⁺ .

Example 201: 3-[2-(4-chloro-3-fluorophenoxy)acetamido]-N-(pyridin-3- yl)bicyclo[l.l.l]pentane-l-carboxamide (Compound 300)

The reaction and purification conditions described in Example 48 substituting 3- aminopyridine for (5-(difluoromethoxy)pyridin-2-yl)methanamine gave the title compound. ^J H NMR (400 MHz, DMSO-<¾) δ ppm 9.80 (s, 1H), 8.81 - 8.78 (m, 2H), 8.26 (dd, J = 4.7, 1.5 Hz, 1H), 8.05 (ddd, J = 8.3, 2.6, 1.5 Hz, 1H), 7.51 (t, J = 8.9 Hz, 1H), 7.34 (ddd, J = 8.4, 4.7, 0.8 Hz, 1H), 7.09 (dd, J = 11.4, 2.9 Hz, 1H), 6.87 (ddd, J = 9.0, 2.9, 1.2 Hz, 1H), 4.50 (s, 2H), 2.34 (s, 6H); MS (ESI ⁺ ) m/z 390 (M+H) ⁺ .

Example 202: 3-[2-(4-chloro-3-fluorophenoxy)acetamido]-N-(pyridin-4- yl)bicyclo[l.l.l]pentane-l-carboxamide (Compound 301)

The reaction and purification conditions described in Example 180 substituting the product of Example 18A for the product of Example 158B, and 4-aminopyridine for 5- (trifluoromethoxy)pyridin-2-amine gave the title compound. ^J H NMR (400 MHz, DMSO-<¾) δ ppm 9.94 (s, 1H), 8.80 (s, 1H), 8.44 - 8.40 (m, 2H), 7.66 - 7.62 (m, 2H), 7.51 (t, J = 8.9 Hz, 1H), 7.09 (dd, J = 11.4, 2.8 Hz, 1H), 6.87 (ddd, J = 8.8, 2.8, 1.2 Hz, 1H), 4.50 (s, 2H), 2.35 (s, 6H); MS (ESI ⁺ ) m/z 390 (M+H) ⁺ . Example 203: 3-[2-(4-chloro-3-fluorophenoxy)acetamido]-N-(5-methoxypyrimi din-2- yl)bicyclo[l.l.l]pentane-l-carboxamide (Compound 302)

The reaction and purification conditions described in Example 180 substituting the product of Example 18A for the product of Example 158B, and 2-amino-5-methoxypyrirnidine (Combi-Blocks) for 5-(trifluoromethoxy)pyridin-2-amine gave the title compound. ^J H NMR (400 MHz, DMSO- ) δ ppm 10.29 (s, 1H), 8.74 (s, 1H), 8.44 (s, 2H), 7.50 (t, J = 8.9 Hz, 1H), 7.08 (dd, J = 11.4, 2.8 Hz, 1H), 6.86 (ddd, J = 9.0, 2.9, 1.2 Hz, 1H), 4.48 (s, 2H), 3.88 (s, 3H), 2.32 (s, 6H); MS (ESI ⁺ ) m/z 421 (M+H) ⁺ .

Example 204: 3-[2-(4-chloro-3-fluorophenoxy)acetamido]-N-(5-methoxypyridi n-2- yl)bicyclo[l.l.l]pentane-l-carboxamide (Compound 303)

The reaction and purification conditions described in Example 180 substituting the product of Example 18A for the product of Example 158B, and 2-amino-5-methoxypyridine (ArkPharm) for 5-(trifluoromethoxy)pyridin-2-amine gave the title compound. ^J H NMR (400 MHz, DMSO- ) δ ppm 10.11 (s, 1H), 8.74 (s, 1H), 8.03 (dd, J = 3.2, 0.7 Hz, 1H), 7.95 (d, J = 8.8 Hz, 1H), 7.50 (t, J = 8.9 Hz, 1H), 7.42 (dd, J = 9.1 , 3.1 Hz, 1H), 7.08 (dd, J = 11.4, 2.8 Hz, 1H), 6.86 (ddd, J = 8.9, 2.8, 1.2 Hz, 1H), 4.48 (s, 2H), 3.80 (s, 3H), 2.33 (s, 6H); MS (ESI ⁺ ) m/z 420 (M+H) ⁺ .

Example 205: 3-[2-(4-chloro-3-fluorophenoxy)acetamido]-N-(5-methylpyrazin -2- yl)bicyclo[l.l.l]pentane-l-carboxamide (Compound 304)

The reaction and purification conditions described in Example 180 substituting the product of Example 18A for the product of Example 158B, and 5-methylpyrazin-2-amine (AK Scientific) for 5-(trifluoromethoxy)pyridin-2-amine gave the title compound. ^J H NMR (400 MHz, DMSO-de) δ ppm 10.51 (s, 1H), 9.14 (d, J = 1.5 Hz, 1H), 8.76 (s, 1H), 8.32 - 8.28 (m, 1H), 7.50 (t, J = 8.9 Hz, 1H), 7.08 (dd, J = 11.4, 2.9 Hz, 1H), 6.86 (ddd, J = 9.0, 2.9, 1.2 Hz, 1H), 4.49 (s, 2H), 2.45 (s, 3H), 2.36 (s, 6H); MS (ESI ⁺ ) m/z 405 (M+H) ⁺ .

Example 206: 3-[2-(4-chloro-3-fluorophenoxy)acetamido]-N-(5-cyanopyridin- 2- yl)bicyclo[l.l.l]pentane-l-carboxamide (Compound 305)

The reaction and purification conditions described in Example 180 substituting the product of Example 18A for the product of Example 158B, and 2-amino-5-cyanopyridine (Aldrich) for 5-(trifluoromethoxy)pyridin-2-amine gave the title compound. ^J H NMR (501

MHz, DMSO-<¾) δ ppm 10.86 (s, 1H), 8.81 (dd, J = 2.3, 0.9 Hz, 1H), 8.77 (s, 1H), 8.28 - 8.19 (m, 2H), 7.50 (t, J = 8.9 Hz, 1H), 7.08 (dd, J = 11.4, 2.8 Hz, 1H), 6.86 (ddd, J = 9.0, 2.9, 1.2 Hz, 1H), 4.48 (s, 2H), 2.38 (s, 6H); MS (ESI ⁺ ) m/z 415 (M+H) ⁺ . Example 207: 3-[2-(4-chloro-3-fluorophenoxy)acetamido]-N-(5-cyclopropylpy ridin-2- yl)bicyclo[l.l.l]pentane-l-carboxamide (Compound 306)

The reaction and purification conditions described in Example 180 substituting the product of Example 18A for the product of Example 158B, and 5-cyclopropylpyridin-2-amine (CombiPhos) for 5-(trifluoromethoxy)pyridin-2-amine gave the title compound. ^J H NMR (501 MHz, DMSO- ) δ ppm 10.15 (s, 1H), 8.75 (s, 1H), 8.16 (d, J = 2.4 Hz, 1H), 7.91 (d, J = 8.4 Hz, 1H), 7.50 (t, J = 8.9 Hz, 1H), 7.41 (dd, J = 8.7, 2.5 Hz, 1H), 7.08 (dd, J = 11.4, 2.8 Hz, 1H), 6.86 (ddd, J = 9.0, 2.8, 1.2 Hz, 1H), 4.48 (s, 2H), 2.33 (s, 6H), 1.92 (tt, J = 8.3, 5.1 Hz, 1H), 1.00 - 0.90 (m, 2H), 0.74 - 0.63 (m, 2H); MS (ESI ⁺ ) m/z 430 (M+H) ⁺ .

Example 208: 3-[2-(4-chloro-3-fluorophenoxy)acetamido]-N-(5-ethoxypyrazin -2- yl)bicyclo[l.l.l]pentane-l-carboxamide (Compound 307)

The reaction and purification conditions described in Example 180 substituting the product of Example 18A for the product of Example 158B, and 5-ethoxypyrazin-2-amine (ArkPharm) for 5-(trifluoromethoxy)pyridin-2-amine gave the title compound. ^J H NMR (400 MHz, DMSO- ) δ ppm 10.36 (s, 1H), 8.77 (d, J = 1.5 Hz, 1H), 8.75 (s, 1H), 8.08 (d, J = 1.5 Hz, 1H), 7.50 (t, J = 8.9 Hz, 1H), 7.08 (dd, J = 11.4, 2.8 Hz, 1H), 6.86 (ddd, J = 9.0, 2.8, 1.2 Hz, 1H), 4.48 (s, 2H), 4.32 (q, J = 7.0 Hz, 2H), 2.34 (s, 6H), 1.33 (t, J = 7.0 Hz, 3H); MS (ESI ⁺ ) m/z 435 (M+H) ⁺ .

Example 209: 3-[2-(3,4-difluorophenoxy)acetamido]-N-[5-(trifluoromethoxy) pyridin-2- yl]bicyclo[l.l.l]pentane-l-carboxamide (Compound 308)

The reaction and purification conditions described in Example 48 substituting 2-(3,4- difluorophenoxy)acetic acid (Combi-B locks) for the product of Example 18 A, and the product of Example 195B for (5-(difluoromethoxy)pyridin-2-yl)methanamine. ^J H NMR (400 MHz, DMSO- ) δ ppm 10.58 (s, 1H), 8.74 (s, 1H), 8.43 (d, J = 2.9 Hz, 1H), 8.17 (dd, J = 9.1, 0.6 Hz, 1H), 7.90 (dd, J = 8.9, 2.9 Hz, 1H), 7.37 (dt, J = 10.7, 9.3 Hz, 1H), 7.10 (ddd, J = 12.6, 6.7, 3.0 Hz, 1H), 6.83 - 6.78 (m, 1H), 4.45 (s, 2H), 2.36 (s, 6H); MS (APCI ⁺ ) m/z 458 (M+H) ⁺ .

Example 210: 3-[2-(4-chloro-3-fluorophenoxy)acetamido]-N-[5-(difluorometh oxy)pyridin- 2-yl]bicyclo[l.l.l]pentane-l-carboxamide (Compound 309)

The reaction and purification conditions described in Example 180 substituting the product of Example 18A for the product of Example 158B, and 5-(difluoromethoxy)pyridin-2- amine dihydrochloride (Oakwood) for 5-(trifluoromethoxy)pyridin-2-amine gave the title compound. ^J H NMR (400 MHz, DMSO-<¾) δ ppm 8.79 (s, 1H), 8.19 (d, J = 2.9 Hz, 1H), 8.11 (d, J = 9.0 Hz, 1H), 7.62 (dd, J = 9.1, 2.9 Hz, 1H), 7.38 (t, J = 8.7 Hz, 1H), 6.97 - 6.91 (m, 1H), 6.84 (t, J = 73.0 Hz, 1H), 6.84 - 6.80 (m, 1H), 4.49 (s, 2H), 2.46 (s, 6H); MS (ESI ⁺ ) m/z 456 (M+H) ⁺ .

Example 211: 3-[2-(4-chloro-3-fluorophenoxy)acetamido]-N-[6-(2,2,2- trifluoroethoxy)pyridin-3-yl]bicyclo[l.l.l]pentane-l-carboxa mide (Compound 310)

The reaction and purification conditions described in Example 180 substituting the product of Example 18A for the product of Example 158B, and 6-(2,2,2-trifluoroethoxy)pyridin- 3-amine (Enamine) for 5-(trifluoromethoxy)pyridin-2-amine gave the title compound. ^J H NMR (400 MHz, DMSO- ) δ ppm 9.74 (s, 1H), 8.79 (s, 1H), 8.43 (d, J = 2.6 Hz, 1H), 8.01 (dd, J = 8.9, 2.7 Hz, 1H), 7.50 (t, J = 8.9 Hz, 1H), 7.09 (dd, J = 11.4, 2.8 Hz, 1H), 6.96 (d, J = 8.9 Hz, 1H), 6.87 (ddd, J = 9.0, 2.9, 1.2 Hz, 1H), 4.94 (q, J = 9.1 Hz, 2H), 4.49 (s, 2H), 2.33 (s, 6H); MS (ESI ⁺ ) m/z 488 (M+H) ⁺ .

Example 212: ethyl 6-({3-[2-(4-chloro-3-fluorophenoxy)acetamido]bicyclo[l.l.l]p entane-l- carbonyl}amino)pyridine-3-carboxylate (Compound 311)

The reaction and purification conditions described in Example 180 substituting the product of Example 18A for the product of Example 158B, and ethyl 6-aminonicotinate

(ArkPharm) for 5-(trifluoromethoxy)pyridin-2-amine gave the title compound. ^J H NMR (400 MHz, DMSO- ) δ ppm 10.74 (s, 1H), 8.85 (dd, J = 2.4, 0.8 Hz, 1H), 8.77 (s, 1H), 8.28 (dd, J = 8.8, 2.4 Hz, 1H), 8.19 (dd, J = 8.9, 0.8 Hz, 1H), 7.50 (t, J = 8.9 Hz, 1H), 7.08 (dd, J = 11.4, 2.8 Hz, 1H), 6.86 (ddd, J = 9.0, 2.8, 1.2 Hz, 1H), 4.48 (s, 2H), 4.33 (q, J = 7.1 Hz, 2H), 2.38 (s, 6H), 1.33 (t, J = 7.1 Hz, 3H); MS (ESI ⁺ ) m/z 462 (M+H) ⁺ .

Example 213: ethyl 2-({3-[2-(4-chloro-3-fluorophenoxy)acetamido]bicyclo[l.l.l]p entane-l- carbonyl}amino)-l,3-thiazole-4-carboxylate (Compound 312)

The reaction and purification conditions described in Example 180 substituting the product of Example 18A for the product of Example 158B, and ethyl 2-aminothiazole-4- carboxylate (Alfa Aesar) for 5-(trifluoromethoxy)pyridin-2-amine gave the title compound. ^J H NMR (501 MHz, DMSO-<¾) δ ppm 12.58 (s, 1H), 8.79 (s, 1H), 8.06 (s, 1H), 7.50 (t, J = 8.9 Hz, 1H), 7.08 (dd, J = 11.3, 2.9 Hz, 1H), 6.86 (ddd, J = 9.0, 2.8, 1.2 Hz, 1H), 4.49 (s, 2H), 4.28 (q, J = 7.1 Hz, 2H), 2.37 (s, 6H), 1.29 (t, J = 7.1 Hz, 3H); MS (ESI ⁺ ) m/z 468 (M+H) ⁺ .

Example 214: 3-[2-(4-chloro-3-fluorophenoxy)acetamido]-N-[4-(hydroxymethy l)pyridin-2- yl]bicyclo[l.l.l]pentane-l-carboxamide (Compound 313)

The reaction and purification conditions described in Example 48 substituting \-(tert- butyl-dimethyl-silanyloxymethyl)-pyridin-2-ylamine (Matrix) for (5-(difluoromethoxy)pyridin- 2-yl)methanamine gave the title compound. ^J H NMR (400 MHz, DMSO- ¾) δ ppm 10.16 (s, 1H), 8.75 (s, 1H), 8.23 (dd, J = 5.0, 0.8 Hz, 1H), 8.03 8.01 (m, 1H), 7.50 (t, J = 8.9 Hz, 1H), 7.08 (dd, J = 11.4, 2.9 Hz, 1H), 7.06 7.03 (m, 1H), 6.86 (ddd, J = 9.0, 2.9, 1.2 Hz, 1H), 5.40 (t, J = 5.7 Hz, 1H), 4.51 (d, J = 5.5 Hz, 2H), 4.48 (s, 2H), 2.34 (s, 6H); MS (ESI ⁺ ) m/z 420 (M+H) ⁺ .

Example 215: 3-[2-(4-chloro-3-fluorophenoxy)acetamido]-N-(2- fluorophenyl)bicyclo[l.l.l]pentane-l-carboxamide (Compound 314)

To a mixture of 3-(2-(4-chloro-3-fluorophenoxy)acetamido)bicyclo[l.l. l]pentane-l- carboxylic acid (40 mg, 0.128 mmol, Example 18A), and l-[bis(dimethylamino)methylene]-lH- l,2,3-triazolo[4,5-¾]pyridinium 3-oxid hexafluorophosphate (HATU, 48.5 mg, 0.128 mmol) was added 2-fluoroaniline (22.67 mg, 0.204 mmol) and N-ethyl-N-isopropylpropan-2-amine (49.4 mg, 0.383 mmol) in N,N-dimethylformamide (1 mL). The mixture was stirred at room temperature for 60 minutes. Then water (0.02 mL) was added to quench the reaction. The product was purified by flash column chromatography on silica gel (40g) eluted with 20 to 60% ethyl acetate in heptane to give titled compound (23 mg, 0.057 mmol, 44%). ^J H NMR (400 MHz, DMSO- ) δ ppm 9.42 (s, 1H), 8.74 (s, 1H), 7. 50 (m, 1H), 7.48 (t, J = 8 Hz, 1H), 7.17 (m, 3H), 7.05 (dd, J = 9, 3 Hz, 1H), 6.83 (br d, J = 8 Hz, 1H), 4.46 (s, 2H), 2.30 (s, 6H); MS (ESI+) m/z 407 (M+H) ⁺ .

Example 216: 5-(trifluoromethoxy)-N-(3-{[5-(trifluoromethoxy)pyridin-2- yl]carbamoyl}bicyclo[l.l.l]pentan-l-yl)pyridine-2-carboxamid e (Compound 315)

The reaction and purification conditions described in Example 48 substituting 5- (trifluoromethoxy)picolinic acid (ArkPharm) for the product of Example 18 A, and the product of Example 195B for (5-(difluoromethoxy)pyridin-2-yl)methanamine. ^J H NMR (400 MHz, DMSO- ) δ ppm 10.61 (s, 1H), 9.41 (s, 1H), 8.71 (dt, J = 2.7, 0.8 Hz, 1H), 8.44 (dt, J = 2.9, 0.8 Hz, 1H), 8.20 - 8.17 (m, 1H), 8.16 - 8.13 (m, 1H), 8.11 - 8.06 (m, 1H), 7.94 - 7.88 (m, 1H), 2.45 (s, 6H); MS (ESI ⁺ ) m/z Ml (M+H) ⁺ .

Example 217: 4-[2-(4-chloro-3-fluorophenoxy)acetamido]-2-hydroxy-N-[5-

(trifluoromethyl)pyridin-2-yl]bicyclo[2.2.2]octane-l-carb oxamide (Compound 316)

The title compound was prepared using the methodologies described in Example 7 substituting 5-(trifluoromethyl)pyridin-2-amine for (5-(trifluoromethyl)pyridin-2- yl)methanamine. ^J H NMR (400 MHz, DMSO- ) δ ppm 9.73 (s, 1H), 8.91 (d, J = 2.4 Hz, 1H), 8.32 (dd, J = 8.7, 2.5 Hz, 1H), 7.80 (d, J = 8.7 Hz, 1H), 7.54 (s, 1H), 7.45 (t, J = 8.9 Hz, 1H), 7.00 (dd, J = 11.4, 2.8 Hz, 1H), 6.79 (ddd, J = 9.0, 2.8, 1.2 Hz, 1H), 5.16 (d, J = 4.7 Hz, 1H), 4.42 (s, 2H), 4.23 (m, 1H), 2.34 2.23 (m, 1H), 2.18 (t, J = 11.4 Hz, 1H), 1.94 1.63 (m, 8H); MS (ESI ⁺ ) m/z 516.2 (M+H) ⁺ . Example 218: 3-[2-(4-chloro-3-fluorophenoxy)acetamido]-N-[2-(4-chlorophen yl)-2- hydroxypropyl]bicyclo[l.l.l]pentane-l-carboxamide (Compound 317)

3-(2-(4-Chloro-3-fluorophenoxy)acetamido)bicyclo[l .1.1 Jpentane- 1 -carboxylic acid (Example 18A, 200 mg, 0.638 mmol) triethylamine (0.267 mL, 1.913 mmol), and l-amino-2-(4- chlorophenyl)propan-2-ol (142 mg, 0.765 mmol) were combined with N,N-dimethylformamide (3 mL) and l-[bis(dimethylamino)methylene]-lH-l,2,3-triazolo[4,5-¾]pyr idinium 3-oxid hexafluorophosphate (HATU, 339 mg, 0.893 mmol) was added in one portion. The resulting mixture was stirred at room temperature for 14 hours and purified by preparative HPLC

(Phenomenex® Luna® C18(2) 10 μπι 100A AXIA™ column (250 mm x 50 mm). A 30-100% gradient of acetonitrile (A) and 0.1% trifluoroacetic acid in water (B) is used over 30 minutes, at a flow rate of 50 mL/minute) to give the title compound (273 mg, 0.567 mmol, 89 % yield). ^J H NMR (400 MHz, DMSO-<¾) δ ppm 8.69 (s, 1H), 7.54 - 7.38 (m, 4H), 7.38 - 7.31 (m, 2H), 7.07 (dd, J = 11.3, 2.9 Hz, 1H), 6.85 (ddd, J = 9.0, 2.9, 1.2 Hz, 1H), 4.46 (s, 2H), 3.36 - 3.23 (m, 2H), 2.11 (s, 6H), 1.36 (s, 3H); MS(APCI) m/z 481.2 (M+H) ⁺ . Example 219: 3-[2-(4-chloro-3-fluorophenoxy)acetamido]-N-[l-(4-chlorophen yl)-2- hydroxyethyl]bicyclo[l.l.l]pentane-l-carboxamide (Compound 318)The title compound was prepared using the protocol described for Example 218 substituting 2-amino-2-(4- chlorophenyl)ethanol hydrochloride for l-amino-2-(4-chlorophenyl)propan-2-ol. ^J H NMR (400 MHz, CDC1 ₃ ) δ ppm 7.34 (t, J = 8.6 Hz, 3H), 7.25 (t, J = 9.0 Hz, 2H), 6.88 (s, 1H), 6.77 (dd, J = 10.2, 2.8 Hz, 1H), 6.68 (ddd, J = 8.9, 2.9, 1.3 Hz, 1H), 6.27 (d, J = 7.2 Hz, 1H), 5.03 (dt, J = 7.2, 4.6 Hz, 1H), 4.40 (s, 2H), 3.90 (d, J = 4.7 Hz, 2H), 2.44 (s, 6H) ; MS(APCI) m/z 467.2 (M+H) ⁺ .

Example 220: 4-[2-(4-chloro-3-fluorophenoxy)acetamido]-N-[(5,6-difluoro-l H- benzimidazol-2-yl)methyl]-3-hydroxybicyclo[2.2.2]octane-l-ca rboxamide (Compound 319) To a mixture of Example 175Η (100 mg, 0.270 mmol), (5,6-difluoro-lH- benzo[(f]imidazol-2-yl)methanamine (52.0 mg, 0.284 mmol), and N-ethyl-N-isopropylpropan-2- amine (0.142 mL, 0.811 mmol) in N,N-dimethylformamide (2.5 mL), 2-(3H-[l,2,3]triazolo[4,5- Z?]pyridin-3-yl)-l,l,3,3-tetramethylisouronium hexafluorophosphate(V) (129 mg, 0.338 mmol) was added and stirred at ambient temperature for 60 minutes. Volatiles were removed, and the residue was dissolved in a mixture of methanol/dichloromethane (1 : 1, 5 mL). To this solution, sodium tetrahydroborate (102 mg, 2.70 mmol) was added, and the mixture was stirred at ambient temperature for 30 minutes. Volatiles were removed, and the residue was purified by HPLC (Phenomenex® Luna® CI 8(2) 10 μηι 100A AXIA™ column (250 mm x 50 mm). A 20-95% gradient of acetonitrile (A) and 0.1% trifluoroacetic acid in water (B) was used over 25 minutes, at a flow rate of 50 mL/minute) to give 63 mg of the title compound. ^J H NMR (400 MHz, DMSO- ) δ ppm 8.15 (t, J = 5.5 Hz, 1H), 7.67 (t, J = 8.8 Hz, 2H), 7.45 (t, J = 8.9 Hz, 1H), 7.27 (s, 1H), 7.02 (dd, J = 11.4, 2.9 Hz, 1H), 6.79 (dd, J = 9.1, 2.8 Hz, 1H), 4.46 (d, J = 8.0 Hz, 2H), 4.44 (s, 2H), 4.00 (dd, J = 9.4, 3.1 Hz, 1H), 2.17 - 2.07 (m, 1H), 1.98 (td, J = 11.8, 4.6 Hz, 1H), 1.89 - 1.81 (m, 1H), 1.80 (t, J = 7.6 Hz, 1H), 1.79 - 1.71 (m, 1H), 1.74 - 1.65 (m, 3H), 1.64 (dd, J = 12.8, 4.6 Hz, 1H), 1.56 (dt, J = 13.5, 3.1 Hz, 1H); MS (ESI+) m/z 537.0 (M+H) ⁺ .

Example 221 : N-(2-amino-2-oxoethyl)-4-[2-(4-chloro-3-fluorophenoxy)acetam ido]-iV-[(4- chloro-3-fluorophenyl)methyl]bicyclo[2.2.2]octane-l-carboxam ide (Compound 320)

Example 221 A: 2-((4-chloro-3-fluorobenzyl)amino)acetamide

A 20 mL vial was charged with dimethyl sulfoxide (5 mL), 4-chloro-3-fluorobenzyl bromide (500 mg, 2.24 mmol, Enamine), glycinamide hydrochloride (200 mg, 1.81 mmol, Enamine) and Hunig's base (2.0 mL). The vial was sealed and stirred at 85 °C for 18 hours. The reaction mixture was cooled to ambient temperature and methanol (3 mL) was added. The resulting solution was filtered through a glass microfiber frit and purified by preparative HPLC [Waters XBridge™ C18 5 μπι OBD column, 50 x 100 mm, flow rate 90 mL/minute, 5-100% gradient of acetonitrile in buffer (0.025 M aqueous ammonium bicarbonate, adjusted to pH 10 with ammonium hydroxide)] to give the title compound (80 mg, 0.37 mmol, 20 % yield). ^J H NMR (400 MHz, DMSO-<¾) δ ppm 7.47 (t, J = 8.0 Hz, 1H), 7.37 (dd, J = 10.6, 1.9 Hz, 1H), 7.26 (br s, 1H), 7.16 (ddd, J = 8.2, 1.9, 0.8 Hz, 1H), 6.99 (br s, 1H), 3.64 (s, 2H), 2.98 (s, 2H), 2.62 (br s, 1H); MS (APCI ⁺ ) m/z 217 (M+H) ⁺ .

Example 22 IB: N-(2-amino-2-oxoethyl)-4-[2-(4-chloro-3-fluorophenoxy)acetam ido]-N-[(4- chloro-3 -fluorophenyl )methyl ]bicyclo[ 2.2.2 ] octane- 1-carboxamide To a 4ml vial was added N,N-dimethylformamide (1.5 mL), triethylamine (0.032 mL), the product of Example 211 A (9.8 mg, 0.045 mmol), the product of Example 158B (16 mg, 0.045 mmol) and HATU (25.8 mg, 0.068 mmol) in sequential order. The resulting reaction mixture was stirred at ambient temperature for 1 hour and more product of Example 158B (16 mg, 0.045 mmol) was added followed by (7-azabenzotriazol-l-yloxy)tripyrrolidinophosphonium hexafluorophosphate (PyAOP, 24 mg, 0.045 mmol). After stirring at ambient temperature for 18 hours, water (0.3 mL) was added, and the resulting solution was filtered through a glass microfiber frit and purified by preparative HPLC [Waters XBridge™ CI 8 5 μηι OBD column, 30 x 100 mm, flow rate 40 mL/minute, 5-100% gradient of acetonitrile in buffer (0.025 M aqueous ammonium bicarbonate, adjusted to pH 10 with ammonium hydroxide)] to give the title compound (8 mg, 0.014 mmol, 32 % yield). ^J H NMR (400 MHz, DMSO-<¾, 120 °C) δ ppm 7.45 (t, J = 8.0 Hz, 1H), 7.42 - 7.36 (m, 1H), 7.13 (dd, J = 10.5, 2.0 Hz, 1H), 7.04 - 7.01 (m, 1H), 6.97 - 6.93 (m, 1H), 6.92 (br s, 1H), 6.83 - 6.78 (m, 1H), 6.69 (br s, 2H), 4.58 (s, 2H), 4.39 (d, J = 2.3 Hz, 2H), 3.92 (s, 2H), 1.94 - 1.83 (m, 12H); MS (APCI ⁺ ) m/z 554 (M+H) ⁺ .

Example 222: 4-[2-(4-chloro-3-fluorophenoxy)acetamido]-3-hydroxy-iV-[(6- methoxypyridazin-3-yl)methyl]bicyclo[2.2.2]octane-l-carboxam ide (Compound 321)

To a mixture of Example 175H (0.028 g, 0.076 mmol), (6-methoxypyridazin-3- yl)methanamine hydrochloride (0.014 g, 0.080 mmol), and N-ethyl-N-isopropylpropan-2-amine (0.040 mL, 0.23 mmol) in N,N-dimethylformamide (0.7 mL) was added 2-(3H- [l ,2,3]triazolo[4,5-¾]pyridin-3-yl)-l , l ,3,3-tetramethylisouronium hexafluorophosphate(V) (0.036 g, 0.095 mmol) followed by stirring at ambient temperature for 16 hours. The reaction mixture was concentrated, and the residue was taken up in dichloromethane (0.7 mL) and methanol (0.7 mL). To this solution was added sodium tetrahydroborate (0.029 g, 0.76 mmol), and the reaction mixture was stirred at ambient temperature for 30 minutes. The reaction mixture was concentrated, and the residue was purified by preparative HPLC (Waters

XBridge™ C18 5 urn OBD column, 30 x 100 mm, flow rate 40 mL/minute, 5-100% gradient of acetonitrile in 0.1 % trifluoroacetic acid/water) to give the title compound (0.030 g, 0.061 mmol, 80% yield). ^J H NMR (400 MHz, DMSO-<¾) δ ppm 8.13 (t, J = 5.9 Hz, 1H), 7.48 (t, J = 8.9 Hz, 1H), 7.41 (d, J = 9.1 Hz, 1H), 7.30 (s, 1H), 7.20 (d, J = 9.1 Hz, 1H), 7.06 (dd, J = 11.4, 2.8 Hz, 1H), 6.83 (ddd, J = 9.0, 2.9, 1.2 Hz, 1H), 4.48 (s, 2H), 4.42 (d, J = 5.9 Hz, 2H), 4.03 (dd, J = 9.6, 3.2 Hz, 1H), 4.00 (s, 3H), 2.14 (ddd, J = 13.4, 9.3, 2.3 Hz, 1H), 2.02 (ddd, J = 12.5, 10.8, 4.6 Hz, 1H), 1.89 (m, 1H), 1.93 1.61 (m, 5H), 1.57 (dt, J = 13.5, 3.0 Hz, 1H); MS (ESI ⁺ ) m/z 493 (M+H) ⁺ .

Example 223: 3-[2-(4-chloro-3-fluorophenoxy)acetamido]-/V-[(6-methoxypyri dazin-3- yl)methyl]bicyclo[l.l.l]pentane-l-carboxamide (Compound 322) The methodologies described in Example 48, substituting (6-methoxypyridazin-3- yl)methanamine hydrochloride for (5-(difluoromethoxy)pyridin-2-yl)methanamine and purifying by preparative HPLC (Waters XB ridge™ CI 8 5 μηι OBD column, 30 x 100 mm, flow rate 40 mL/minute, 5-100% gradient of acetonitrile in 0.1% trifluoroacetic acid/water) gave the title compound. ^J H NMR (400 MHz, DMSO-<¾) δ ppm 8.73 (s, 1H), 8.49 (t, J = 6.0 Hz, 1H), 7.54 - 7.45 (m, 2H), 7.22 (d, J = 9.1 Hz, 1H), 7.07 (dd, J = 11.3, 2.9 Hz, 1H), 6.86 (ddd, J = 9.0, 2.9, 1.2 Hz, 1H), 4.47 (s, 2H), 4.45 (d, J = 6.0 Hz, 2H), 4.01 (s, 3H), 2.22 (s, 6H); MS (ESI ⁺ ) m/z 435 (M+H) ⁺ .

Example 224: 4-[2-(4-chloro-3-fluorophenoxy)acetamido]-N-[(5-fluoro-l-met hyl-lH- benzimidazol-2-yl)methyl]bicyclo[2.2.2]octane-l-carboxamide (Compound 323)

The reaction and purification conditions described in Example 48 substituting the product of Example 158B for the product of Example 18A, and (5-fluoro-l -methyl- 1H- benzo[(f]imidazol-2-yl)methanamine dihydrochloride (Aldrich) for (5-(difluoromethoxy)pyridin- 2-yl)methanamine gave the title compound. ^J H NMR (500 MHz, DMSO- ¾) δ ppm 8.03 (t, J = 5.4 Hz, 1H), 7.56 - 7.45 (m, 3H), 7.38 (dd, J = 9.8, 2.5 Hz, 1H), 7.10 (ddd, J = 9.8, 8.8, 2.5 Hz, 1H), 7.03 (dd, J = 11.4, 2.9 Hz, 1H), 6.81 (ddd, J = 9.0, 2.9, 1.2 Hz, 1H), 4.51 (d, J = 5.4 Hz, 2H), 4.44 (s, 2H), 3.73 (s, 3H), 1.89 - 1.73 (m, 12H); MS (APCI ⁺ ) m/z 517 (M+H) ⁺ .

Example 225: 4-[2-(4-chloro-3-fluorophenoxy)acetamido]-N-[(5,6-difluoro-l H- benzimidazol-2-yl)methyl]bicyclo[2.2.2]octane-l-carboxamide (Compound 324)

The title compound was prepared using the methodologies described above. ^J H NMR (400 MHz, DMSO- ) δ ppm 12.12 (s, 1H), 8.02 (t, J = 5.7 Hz, 1H), 7.53 - 7.39 (m, 4H), 6.99 (dd, J = 11.4, 2.8 Hz, 1H), 6.78 (dd, J = 9.0, 2.8 Hz, 1H), 4.40 (s, 2H), 4.37 (d, J = 5.6 Hz, 2H), 1.85 - 1.70 (m, 12H); MS (APCI ⁺ ) m/z 521 (M+H) ⁺ .

Example 226: N-[(6-chloro-lH-benzimidazol-2-yl)methyl]-4-[2-(4-chloro-3- fluorophenoxy)acetamido]bicyclo[2.2.2]octane-l-carboxamide (Compound 325)

The title compound was prepared using the methodologies described above. ^J H NMR (400 MHz, DMSO-de) δ ppm 12.08 (br s, 1H), 8.02 (t, J = 5.7 Hz, 1H), 7.53 - 7.40 (m, 4H), 7.12 (dd, J = 8.5, 2.1 Hz, 1H), 6.99 (dd, J = 11.4, 2.9 Hz, 1H), 6.77 (ddd, J = 9.0, 3.0, 1.2 Hz, 1H), 4.44 _ 4.35 ( _m , 4H), 1.85 - 1.70 (m, 12H); MS (APCI ⁺ ) m/z 519 (M+H) ⁺ . Example 227: (25)-4-[2-(4-chloro-3-fluorophenoxy)acetamido]-N-[2-(4-chlor o-3- fluorophenyl)-2-oxoethyl]-2-hydroxybicyclo[2.2.2]octane-l-ca rboxamide (Compound 326)

The title compound was prepared using the methodologies described for Example 178. ^J H NMR (501 MHz, DMSO-<¾) δ ppm 8.03 - 7.93 (m, 2H), 7.85 - 7.74 (m, 2H), 7.55 - 7.44 (m, 2H), 7.03 (dd, J = 11.4, 2.9 Hz, 1H), 6.81 (ddd, J = 8.9, 2.9, 1.2 Hz, 1H), 5.00 (d, J = 3.8 Hz, 1H), 4.54 (dd, J = 5.4, 1.8 Hz, 2H), 4.45 (s, 2H), 4.06 (d, J = 9.2 Hz, 1H), 2.31 - 2.18 (m, 1H), 2.15 - 2.01 (m, 1H), 1.98 - 1.86 (m, 1H), 1.82 - 1.65 (m, 5H), 1.65 - 1.48 (m, 2H); MS (APCI) m/z 541.2 (M+H) ⁺ .

Example 228: N-[(lH-benzimidazol-2-yl)methyl]-4-[2-(4-chloro-3- fluorophenoxy)acetamido]bicyclo[2.2.2]octane-l-carboxamide (Compound 327)

The title compound was prepared using the methodologies described above. ^J H NMR (400 MHz, DMSO- ) δ ppm 11.98 (s, 1H), 8.03 (t, J = 5.7 Hz, 1H), 7.53 - 7.44 (m, 4H), 7.16 - 7.10 (m, 2H), 7.03 (dd, J = 11.4, 2.8 Hz, 1H), 6.81 (ddd, J = 8.9, 2.9, 1.2 Hz, 1H), 4.45 - 4.43 (m, 4H), 1.89 - 1.76 (m, 12H); MS (APCI ⁺ ) m/z 485 (M+H) ⁺ . Example 229: {2-[({3-[2-(4-chloro-3-fluorophenoxy)acetamido]bicyclo[l.l.l ]pentane-l- carbonyl}amino)methyl]-5,6-difluoro-lH-benzimidazol-l-yl}ace tic acid (Compound 328)

Example 229 : tert-butyl 2-(2-((3-(2-(4-chloro-3- fluorophenoxy )acetamido )bicyclo[ 1.1.1 ]pentane-l-carboxamido )methyl)-5, 6-difluoro-lH- benzo[ d ]imidazol-l-yl )acetate

To a solution of potassium hydroxide (0.053 g, 0.95 mmol, crushed pellets) in dimethyl sulfoxide (0.53 mL), which had stirred for 15 minutes, was added Example 232 (0.114 g, 0.238 mmol). The reaction mixture stirred for 1 hour, and then teri-butyl bromoacetate (0.14 mL, 0.95 mmol) was added. This reaction mixture was allowed to stir at ambient temperature for 1 hour, was diluted with ¾0 and diethyl ether, and the layers were separated. The aqueous layer was extracted with diethyl ether (2 x 5 mL), and the combined organic layers were dried (Na ₂ SO/ _t ), filtered, and concentrated. The residue was then diluted with N,N-dimethylformamide (1 mL) and purified by preparative HPLC (Waters XBridge™ C18 5 μπι OBD column, 30 x 100 mm, flow rate 40 mL/minute, 5-100% gradient of acetonitrile in 0.1% trifluoroacetic acid/water) to give the title compound (0.10 g, 0.17 mmol g, mmol, 71% yield). ^J H NMR (400 MHz, DMSO- d ₆ ) S ppm 8.71 (s, 1H), 8.51 (t, J = 5.8 Hz, 1H), 7.70 (ddd, J = 11.0, 9.2, 7.3 Hz, 2H), 7.49 (t, J = 8.9 Hz, 1H), 7.07 (dd, J = 11.4, 2.8 Hz, 1H), 6.85 (dt, J = 9.1 , 1.9 Hz, 1H), 5.15 (s, 2H), 4.46 (s, 2H), 4.44 (d, J = 5.9 Hz, 2H), 2.19 (s, 6H), 2.07 (s, 2H), 1.42 (s, 9H); MS (ESI ⁺ ) m/z 593 (M+H) ⁺ .

Example 229B: {2-[({ 3-[2-(4-chloro-3-fluorophenoxy)acetamido]bicyclo[ 1.1.1 ]pentane-l- carbonyl}amino)methyl] -5,6-difluoro-l H-benzimidazol-1 -yl] acetic acid

To a solution of Example 229A (0.10 g, 0.17 mmol) in tetrahydrofuran (0.19 mL) and water (0.063 mL) was added lithium hydroxide (0.012 g, 0.51 mmol), and the resulting mixture was stirred at ambient temperature for 1 hour. Then the mixture was concentrated. The residue was diluted with N,N-dimethylformamide/water (3: 1 , 1.2 mL) and purified by preparative HPLC [Waters XBridge™ C18 5 μπι OBD column, 30 x 100 mm, flow rate 40 mL/minute, 5-100% gradient of acetonitrile in buffer (0.025 M aqueous ammonium bicarbonate, adjusted to pH 10 with ammonium hydroxide)] to give the title compound (0.020 g, 0.037 mmol, 22% yield). ^J H NMR (500 MHz, DMSO-<¾) δ ppm 8.73 (d, J = 2.1 Hz, 2H), 7.62 (ddd, J = 10.7, 7.4, 3.4 Hz, 2H), 7.49 (t, J = 8.9 Hz, 1H), 7.07 (dd, J = 11.4, 2.8 Hz, 1H), 6.85 (dd, J = 9.1 , 2.8 Hz, 1H), 4.76 (s, 2H), 4.46 (s, 2H), 4.45 (d, J = 5.4 Hz, 2H), 2.18 (s, 6H); MS (ESI ⁺ ) m/z 537 (M+H) ⁺ .

Example 230: l-[2-(4-chloro-3-fluorophenoxy)acetamido]-2-(2-hydroxyethyl) -3-oxo-N-{[5- (trifluoromethyl)pyridin-2-yl]methyl}-2-azabicyclo[2.2.2]oct ane-4-carboxamide

(Compound 329)

To a solution of Example 234 (80 mg, 0.151 mmol) in N,N-dimethylformamide (2.0 mL) was added NaH (9.07 mg, 60% in mineral oil, 0.227 mmol), and the reaction was stirred at ambient temperature for 15 minutes. Then (2-bromoethoxy)(teri-butyl)dimethylsilane (0.049 mL, 0.073 mmol) was added to the mixture and stirring was continued for 16 hours. The reaction was quenched with methanol and volatiles were removed under vacuum. The residue was purified by HPLC (Phenomenex® Luna® CI 8(2) 10 μπι 100A AXIA™ column (250 mm x 50 mm). A 40-100% gradient of acetonitrile (A) and 0.1 % trifluoroacetic acid in water (B) was used over 25 minutes, at a flow rate of 50 mL/minute) to give 68 mg of intermediate (tert- butyl)dimethylsilyl ether. A solution of this intermediate (50 mg, 0.073 mmol) and hydrogen chloride (5.0 mL, 6.25 mmol) in methanol (5.0 mL) was stirred at ambient temperature for 16 hours. Solvent was removed, and the residue was purified by HPLC (Phenomenex® Luna® CI 8(2) 10 μπι 100A AXIA™ column (250 mm x 50 mm). A 30-100% gradient of acetonitrile (A) and 0.1 % trifluoroacetic acid in water (B) was used over 25 minutes, at a flow rate of 50 mL/minute) to give 8 mg of the title compound. H NMR (501 MHz, methanol-^) δ ppm 8.75 - 8.70 (m, 1H), 8.04 - 7.98 (m, 1H), 7.47 (d, J = 8.2 Hz, 1H), 7.30 (t, J = 8.7 Hz, 1H), 6.84 (dd, J = 10.9, 2.9 Hz, 1H), 6.74 (ddd, J = 8.9, 2.9, 1.3 Hz, 1H), 4.51 (s, 2H), 3.63 (t, J = 5.7 Hz, 2H), 3.38 (t, J = 5.7 Hz, 2H), 2.70 - 2.62 (m, 2H), 2.21 (ddd, J = 13.8, 11.3, 4.5 Hz, 2H), 1.97 (qd, J = 11.4, 5.6 Hz, 4H); MS (ESI+) nt/z 573.4 (M+H) ⁺ .

Example 231: N-[l-(5-chloro-l-benzofuran-2-yl)ethyl]-3-[2-(4-chloro-3- fluorophenoxy)acetamido]bicyclo[l.l.l]pentane-l-carboxamide (Compound 330)

The methodologies described in Example 48, substituting l-(5-chlorobenzofuran-2- yl)ethanamine hydrochloride for (5-(difluoromethoxy)pyridin-2-yl)methanamine and purifying by preparative HPLC (Waters XBridge™ CI 8 5 μπι OBD column, 30 x 100 mm, flow rate 40 mL/minute, 5-100% gradient of acetonitrile in 0.1% trifluoroacetic acid/water) gave the title compound. ^J H NMR (400 MHz, DMSO-<¾) δ ppm 8.74 (s, 1H), 8.34 (d, J = 8.2 Hz, 1H), 7.67 (d, J = 2.2 Hz, 1H), 7.57 (d, J = 8.7 Hz, 1H), 7.49 (t, J = 8.9 Hz, 1H), 7.28 (dd, J = 8.7, 2.3 Hz, 1H), 7.07 (dd, J = 11.4, 2.8 Hz, 1H), 6.86 (ddd, J = 9.0, 2.9, 1.2 Hz, 1H), 6.67 (d, J = 1.1 Hz, 1H), 5.14 (tt, J = 7.7, 6.4 Hz, 1H), 4.47 (s, 2H), 2.23 (s, 6H), 1.47 (d, J = 7.0 Hz, 3H); MS (ESI ⁺ )

Example 232: 3-[2-(4-chloro-3-fluorophenoxy)acetamido]-/V-[(5,6-difluoro- lH- benzimidazol-2-yl)methyl]bicyclo[l.l.l]pentane-l-carboxamide (Compound 331)

The methodologies described in Example 48, substituting (5,6-difluoro-lH- benzo[(f]imidazol-2-yl)methanamine for (5-(difluoromethoxy)pyridin-2-yl)methanamine and purifying by preparative HPLC (Waters XBridge™ C18 5 μπι OBD column, 30 x 100 mm, flow rate 40 mL/minute, 5-100% gradient of acetonitrile in 0.1 % trifluoroacetic acid/water) gave the title compound. ^J H NMR (400 MHz, DMSO- ) δ ppm 8.76 (s, 1H), 8.66 (t, J = 5.6 Hz, 1H), 7.80 (t, J = 8.7 Hz, 2H), 7.50 (t, J = 8.9 Hz, 1H), 7.11 6.99 (m, 1H), 6.86 (ddd, J = 9.0, 2.8, 1.2 Hz, 1H), 4.59 (d, J = 5.5 Hz, 2H), 4.48 (s, 2H), 2.25 (s, 6H); MS (ESI ⁺ ) nt/z 479 (M+H) ⁺ .

Example 233: 4-[2-(4-chloro-3-fluorophenoxy)acetamido]-iV-{[4-(trifluorom ethyl)pyridin- 2-yl]methyl}bicyclo[2.2.2]octane-l-carboxamide (Compound 332)

The title compound was prepared using the methodologies described above. ^J H NMR (400 MHz, DMSO- ) δ ppm 8.76 - 8.72 (m, 1H), 8.13 (t, J = 5.9 Hz, 1H), 7.61 - 7.58 (m, 1H), 7.48 - 7.38 (m, 3H), 6.99 (dd, J = 1 1.5, 2.8 Hz, 1H), 6.78 (ddd, J = 9.0, 2.9, 1.2 Hz, 1H), 4.41 (s, 2H), 4.38 (d, J = 5.9 Hz, 2H), 1.87 - 1.72 (m, 12H); MS (APCI ⁺ ) m/z 514 (M+H) ⁺ .

Example 234 : 1 - [2-(4-chloro-3-fluorophenoxy)acetamido] -3 -oxo-N-{ [5 - (trifluoromethyl)pyridin-2-yl]methyl}-2-azabicyclo[2.2.2]oct ane-4-carboxamide

(Compound 333)

Example 234A: l-(ethoxycarbonyl)-4-oxocyclohexanecarboxylic acid

To a suspension of diethyl 4-oxocyclohexane-l, l-dicarboxylate (4.24 g, 17.5 mmol) in ethanol (20 mL) and dichloromethane (30 mL), potassium hydroxide (1.155 g, 17.50 mmol) was added at ambient temperature and stirred at reflux for 3 hours. The mixture was concentrated, and the residue was partitioned between water and ethyl acetate. The aqueous layer was then acidified with 3 N aqueous HC1 solution to pH = 3, and then extracted with ethyl acetate (2x100 mL). The combined organic layers were dried over magnesium sulfate and filtered. The filtrate was concentrated to give 2.89 g of the title compound that was used without additional purification. ^J H NMR (400 MHz, DMSO-<¾) δ ppm 13.01 (s, 1H), 4.24 - 4.02 (m, 2H), 2.32 (d, J = 5.5 Hz, 2H), 2.32 - 2.20 (m, 5H), 2.24 - 2.10 (m, 1H), 1.20 (t, J = 7.1 Hz, 3H).

Example 234B: ethyl 4-oxo-l-(((5-(trifluoromethyl)pyridin-2- yl )methyl )carbamoyl )cyclohexanecarboxylate

To a mixture of Example 234A (0.37 g, 1.727 mmol), (5-(trifluoromethyl)pyridin-2- yl)methanamine, hydrochloric acid (0.459 g, 2.159 mmol), and N-ethyl-N-isopropylpropan-2- amine (1.056 mL, 6.05 mmol) in N,N-dimethylformamide (7.5 mL), 2-(3H-[l ,2,3]triazolo[4,5- Z?]pyridin-3-yl)- l ,l ,3,3-tetramethylisouronium hexafluorophosphate(V) (0.985 g, 2.59 mmol) was added, and the mixture was stirred at ambient temperature overnight. Water was added, and the aqueous phase was extracted with dichloromethane. The organic layer was dried over magnesium sulfate and filtered. The filtrate was concentrated, and the residue was purified on silica gel (5-100% ethyl acetate in heptane) to give 0.45 g of the title compound. ^J H NMR (400 MHz, DMSO- ) δ ppm 8.83 (d, J = 2.3 Hz, 1H), 8.64 (t, J = 5.9 Hz, 1H), 8.13 (ddd, J = 21.1 , 8.4, 2.4 Hz, 1H), 7.39 (dd, J = 19.7, 8.3 Hz, 1H), 4.45 (d, J = 5.8 Hz, 2H), 4.20 - 4.03 (m, 2H), 2.38 - 2.21 (m, 8H), 1.15 (td, J = 7.1, 1.8 Hz, 3H); MS (ESI+) m/z 373.4 (M+H) ⁺ .

Example 234C: l-amino-3-oxo-N-( ( 5-( trifluoromethyl)pyridin-2-yl)methyl)-2- azabicyclo[ 2.2.2 ]octane-4-carboxamide A mixture of Example 234B (0.45 g, 1.088 mmol) and ammonia (10.0 mL, 7 M solution in methanol, 70.0 mmol) in methanol (10.0 mL) was stirred at ambient temperature for 48 hours. Volatiles were removed, and the residue was purified on silica gel (0-12%

methanol/dichloromethane) to give 0.18 g of the title compound. ^J H NMR (400 MHz, DMSO- d ₆ ) δ ppm 9.19 (t, J = 5.9 Hz, 1H), 8.88 (d, J = 2.3 Hz, 1H), 8.15 (dd, J = 8.4, 2.4 Hz, 1H), 7.93 (s, 1H), 7.72 (d, J = 8.3 Hz, 1H), 4.52 (d, J = 5.9 Hz, 2H), 2.64 (s, 2H), 1.98 - 1.80 (m, 4H), 1.72 (td, J = 11.2, 10.6, 4.4 Hz, 2H), 1.57 (td, J = 10.8, 5.2 Hz, 2H); MS (ESI-) nt/z 340.9 (M-H)\

Example 234: l-(2-(4-chloro-3-fluorophenoxy)acetamido)-3-oxo-N-((5-(trifl uoromethyl)pyridin- 2-yl)methyl)-2-azabicyclo[ 2.2.2] octane-4-carboxamide To a mixture of Example 234C (80 mg, 0.234 mmol), 2-(4-chloro-3- fluorophenoxy)acetic acid (59.8 mg, 0.292 mmol), and N-ethyl-N-isopropylpropan-2-amine (0.143 mL, 0.818 mmol) in N,N-dimethylformamide (2.0 mL), 2-(3H-[l ,2,3]triazolo[4,5- ¾]pyridin-3-yl)- l ,l ,3,3-tetramethylisouronium hexafluorophosphate(V) (133 mg, 0.351 mmol) was added, and the mixture was stirred at ambient temperature for 2 hours. N,N- Dimethylformamide and volatiles were removed under high vacuum, and the residue was purified by HPLC (Phenomenex® Luna® CI 8(2) 10 μπι 100A AXIA™ column (250 mm x 50 mm). A 30- 100% gradient of acetonitrile (A) and 0.1 % trifluoroacetic acid in water (B) was used over 25 minutes, at a flow rate of 50 mL/minute) to give 110 mg of the title compound. ^J H NMR (400 MHz, DMSO-<¾) δ ppm 9.11 (t, J = 5.9 Hz, 1H), 8.88 (d, J = 2.3 Hz, 1H), 8.57 (s, 1H), 8.35 (s, 1H), 8.16 (dd, J = 8.3, 2.4 Hz, 1H), 7.73 (d, J = 8.3 Hz, 1H), 7.49 (t, J = 8.8 Hz, 1H), 7.09 (dd, J = 11.4, 2.9 Hz, 1H), 6.87 (dd, J = 9.3, 2.9 Hz, 1H), 4.53 (s, 2H), 4.52 (d, J = 6.1 Hz, 2H), 2.20 (dd, J = 10.8, 6.0 Hz, 2H), 2.02 - 1.82 (m, 6H); MS (ESI+) nt/z 529.3 (M+H) ⁺ .

Example 235: 4-[2-(4-chloro-3-fluorophenoxy)acetamido]-N-[(4-chloro-3- fluorophenyl)methyl]-2-oxabicyclo[2.2.2]octane-l-carboxamide (Compound 334) Example 235 : tert-butyl (l-vinyl-2-oxabicyclo [2.2.2] octan-4-yl)carbamate

To a solution of l-vinyl-2-oxabicyclo[2.2.2]octane-4-carboxylic acid (4.3 g, 23.60 mmol) in toluene (150 mL) was added 4A molecular sieve (6 g), diphenylphosphoryl azide (7.14 g, 26.0 mmol) and triethylamine (3.62 mL, 26.0 mmol) in order at 20 °C. The mixture was stirred for 2 hours at 20 °C and 2 hours at 120 °C under N ₂ . After insoluble materials were filtered off, the filtrate was concentrated in vacuo. To a solution of the residue in anhydrous tetrahydrofuran (120 mL) was added potassium teri-butoxide (5.83 g, 51.9 mmol) under cooling with ice. The mixture was stirred at 20 °C for 12 hours. The reaction mixture was quenched with 10% aqueous citric acid and concentrated in vacuo. The residue was treated with ethyl acetate, washed with saturated sodium hydrogen carbonate solution, water and brine, dried over anhydrous sodium sulfate, filtered, and concentrated in vacuo. The residue was purified by column chromatography on silica gel eluted with petroleum ether and ethyl acetate from 100: 1 to 10: 1 to provide the title compound (5.2 g, yield 85%). ^J H NMR (400 MHz, CDC1 ₃ ) δ ppm 1.42 (s, 9H), 1.74-1.91 (m, 4H), 1.91-2.02 (m, 2H), 2.05-2.16 (m, 2H), 3.99 (s, 2H), 4.29 (br s, 1H), 5.03 (d, J=10.96 Hz, 1H), 5.15 (d, J=17.54 Hz, 1H), 5.81 (dd, J=17.54, 10.96 Hz, 1H). Example 235B: tert-butyl (l-formyl-2-oxabicyclo[2.2.2]octan-4-yl)carbamate

To a solution of Example 235A (2.6 g, 9.75 mmol) in tetrahydrofuran (90 mL) and water (60 mL) was added sodium periodate (6.26 g, 29.2 mmol) and osmium tetroxide (1.239 g, 4.87 mmol) in order at 0 °C, and the mixture was stirred for 12 hours at 20 °C. The reaction mixture was diluted with water and extracted with ethyl acetate (2 x). The combined organic phases were dried with Na2SC>4 and concentrated under reduced pressure. The residue was purified by column chromatography on silica gel eluted with petroleum ether:ethyl acetate (100: 1 to 4: 1) to provide the title compound (1.85 g, yield 70.6%). ^J H NMR (400 MHz, CDC1 ₃ ) δ ppm 1.42 (s, 9H), 1.81-1.92 (m, 4H), 1.94-2.05 (m, 2H), 2.08-2.20 (m, 2H), 4.06 (s, 2H), 4.33 (br s, 1H), 7.26 (s, 1H), 9.57 (s, 1H). Example 235C: 4-((tert-butoxycarbonyl)amino)-2-oxabicyclo[2.2.2]octane-l-c arboxylic acid

To a solution of Example 235B (1.9 g, 7.07 mmol) in tetrahydrofuran (60 mL), 2- methylpropan-2-ol (60 mL, 656 mmol) and water (20 mL) was added sodium dihydrogen phosphate (3.39 g, 28.3 mmol), 2-methyl-2-butene (7.49 mL, 70.7 mmol), and sodium chlorite (1.279 g, 14.14 mmol) in order at 20 °C, and the mixture was stirred for 12 hours at 20 °C. The reaction mixture was concentrated under reduced pressure to remove most of the volatiles. The remaining mixture was diluted with water (50 mL), adjusted to pH = 12 by aqueous NaOH (1 M), and extracted with methyl teri-butyl ether (50 mL) and ethyl acetate (50 mL) in order. The aqueous layer was adjusted to pH=l with aqueous HC1 (1 M) and extracted with ethyl acetate (2 x 100 mL). The combined organic phases were dried with Na2SC>4 and concentrated under reduced pressure to provide the title compound (1.84 g, yield 91 %). ^J H NMR (400 MHz, DMSO-ifc) «5 ppm 1.35 (s, 9H), 1.73-1.84 (m, 2H), 1.85-1.99 (m, 1H), 1.85-1.99 (m, 5H), 3.80 (s, 2H), 6.68 (br s, 1H), 12.42 (br s, 1H).

Example 235D: methyl 4-((tert-butoxycarbonyl)amino)-2-oxabicyclo[2.2.2]octane-l- carboxylate A solution of Example 235C (1.00 g, 3.69 mmol) in methanol (MeOH) (10 mL) was treated with 2 N (diazomethyl)trimethylsilane (1.843 mL, 3.69 mmol) in ether drop-wise. After 10 minutes, the reaction mixture was concentrated and purified on an 80 g column using the Biotage® Isolera One flash system eluted with heptanes/ethyl acetate (7:3 to 6:4) to provide the title compound (0.358 g, 34%). MS (DCI ⁺ ) mJz 303.2 (M+NH ₄ ) ⁺ . Example 235E: methyl 4-amino-2-oxabicyclo[2.2.2] octane- 1-carboxylate hydrochloric acid

A suspension of Example 235D (0.350 g, 1.227 mmol) and trifluoroacetic acid (0.945 mL, 12.27 mmol) in CH2CI2 (4 mL) was stirred overnight. The reaction mixture was concentrated. The residue was dissolved in methanol and concentrated again. The residue was suspended in 2 mL of methanol and treated with 2 mL of 2 N HC1 in ether. The suspension was stirred for 15 minutes, diluted with ether, collected by filtration, washed with ether, and vacuum oven-dried to provide the title compound as an HC1 salt (0.245 g, 90%). MS (DCI ⁺ ) m/z 203.1 (M+NH ₄ ) ⁺ .

Example 235F: methyl 4-(2-(4-chloro-3-fluorophenoxy)acetamido)-2-oxabicyclo[2.2.2 ]octane- 1-carboxylate A mixture of Example 235E (0.230 g, 1.038 mmol), triethylamine (0.434 ml, 3.11 mmol), 2-(4-chloro-3-fluorophenoxy)acetic acid (0.255 g, 1.245 mmol) and HATU (1- [bis(dimethylamino)methylene]-lH-l,2,3-triazolo[4,5-¾]pyrid inium 3-oxid

hexafluorophosphate) (0.473 g, 1.245 mmol) in N,N-dimethylformamide (DMF) (6 ml) was stirred for 6 hours. The reaction mixture was quenched with brine and saturated NaHCC>3, and extracted with ethyl acetate (2x). The combined organic layers were dried over MgSO/ _t , filtered, and concentrated. The residue was purified on a 25 g column using the Biotage® Isolera One flash system eluted with heptanes/ethyl acetate (3:7 to 2:8) to provide the title compound (0.333g, 86%). MS (ESI ⁺ ) m/z 372.2 (M+H) ⁺ . Example G: 4-(2-(4-chloro-3-fluorophenoxy jacetamido )-2-oxabicyclo[ 2.2.2] octane- 1- carboxylic acid

A mixture of Example 235F (0.310 g, 0.834 mmol) in tetrahydrofuran (THF) (6 mL) and methanol (MeOH) (4 mL) was treated with a solution of lithium hydroxide (0.070 g, 2.92 mmol) in water (2 mL). The mixture was stirred for 4 hours. Most of the volatiles were evaporated. The residue was diluted with water (2 mL) and treated with 5% citric acid until pH=4. The resulting suspension was filtered, and the collected solid was rinsed with water and vacuum oven-dried to provide the title compound (0.255g, 85%). MS (ESI ⁺ ) m/z 358.2 (M+H) ⁺ .

Example 235H: 4-[2-(4-chloro-3-fluorophenoxy)acetamido]-N-[(4-chloro-3- fluorophenyl)methyl]-2-oxabicyclo[2.2.2]octane-l-carboxamide

A mixture of Example 235G (40.0 mg, 0.112 mmol), HATU (1- [bis(dimethylamino)methylene]-lH-l ,2,3-triazolo[4,5-¾]pyridinium 3-oxid

hexafluorophosphate) (51.0 mg, 0.134 mmol), (4-chloro-3-fluorophenyl)methanamine (0.015 mL, 0.123 mmol), and triethylamine (0.031 mL, 0.224 mmol) in N,N-dimethylformamide (DMF) (1.5 mL) was stirred for 3 hours. The reaction mixture was quenched with brine and extracted with ethyl acetate (2x). The combined organic layers were washed with brine, dried over MgSO/t, filtered, and concentrated. The residue was purified by HPLC performed on a Phenomenex® Luna® C18 column (250 x 30 mm, 10 μπι particle size) using a gradient of 20% to 100% acetonitrile:0.1 % aqueous trifluoroacetic acid over 26 minutes at a flow rate of 50 mL/minute to provide the title compound (49.6 mg, yield 89%). ^J H NMR (501 MHz, DMSO- ¾) δ ppm 8.29 (t, J = 6.3 Hz, 1H), 7.75 (s, 1H), 7.50 (dt, J = 15.1 , 8.5 Hz, 2H), 7.20 (dd, J = 10.4, 2.0 Hz, 1H), 7.11 - 6.99 (m, 2H), 6.82 (ddd, J = 9.0, 2.9, 1.1 Hz, 1H), 4.48 (s, 2H), 4.23 (d, J = 6.3 Hz, 2H), 4.03 (s, 2H), 2.13 - 1.95 (m, 4H), 1.95 - 1.77 (m, 4H); MS (ESI ⁺ ) m/z 449.3 (M+H) ⁺ . Example 236: 4-[2-(4-chloro-3-fluorophenoxy)acetamido]-N-{[5-(trifluorome thyl)pyridin- 2-yl]methyl}-2-oxabicyclo[2.2.2]octane-l-carboxamide (Compound 335)

A mixture of Example 235G (40.0 mg, 0.112 mmol), HATU (1- [bis(dimethylamino)methylene]-lH-l ,2,3-triazolo[4,5-¾]pyridinium 3-oxid

hexafluorophosphate) (51.0 mg, 0.134 mmol), (5-(trifluoromethyl)pyridin-2-yl)methanamine (21.66 mg, 0.123 mmol), and triethylamine (0.031 mL, 0.224 mmol) in N,N-dimethylformamide (DMF) (1.5 mL) was stirred for 3 hours. The reaction mixture was quenched with brine and extracted with ethyl acetate (2x). The combined organic layers were washed with brine, dried over MgSO/t, filtered, and concentrated. The residue was purified by HPLC (see protocol in Example 235H) to provide the title compound as a trifluoroacetic acid salt (29.2 mg, 42%). ^J H NMR (501 MHz, DMSO-<¾) δ ppm 8.88 (d, J = 2.3 Hz, 1H), 8.36 (t, J = 6.1 Hz, 1H), 8.16 (dd, J = 8.3, 2.4 Hz, 1H), 7.77 (s, 1H), 7.49 (t, J = 8.9 Hz, 1H), 7.42 (d, J = 8.2 Hz, 1H), 7.04 (dd, J = 11.4, 2.9 Hz, 1H), 6.82 (ddd, J = 9.0, 2.9, 1.1 Hz, 1H), 4.48 (s, 2H), 4.44 (d, J=5.0 Hz, 2H), 4.06 (s, 2H), 2.19 - 1.97 (m, 4H), 1.92 (q, J = 9.3, 7.6 Hz, 4H); MS (ESI ⁺ ) m/z 516.3 (M+H) ⁺ .

Example 237: 4-[2-(4-chloro-3-fluorophenoxy)acetamido]-N-[4-(trifluoromet hoxy)phenyl]- 2-oxabicyclo[2.2.2]octane-l-carboxamide (Compound 336)

A mixture of Example 235G (0.040 g, 0.112 mrnol), 4-(trifluoromethoxy)aniline (0.024 g, 0.134 mmol), PyBOP® ((lH-benzo[(i] [l ,2,3]triazol-l-yl)oxy)tri(pyrrolidin-l-yl)phosphonium hexafluorophosphate(V)) (0.070 g, 0.134 mmol), and triethylamine (0.023 mL, 0.168 mmol) in N,N-dimethylformamide (DMF) (1.5 mL) was stirred for 6 hours. The reaction mixture was quenched with brine and saturated NaHC(¾ and extracted with ethyl acetate (2x). The combined organic layers were washed with brine, dried over MgSC , filtered, and concentrated. The residue was purified by HPLC (see protocol in Example 235H) to provide the title compound (31.8 mg, 55%). ^J H NMR (400 MHz, DMSO-<¾) δ ppm 9.65 (s, 1H), 7.91 - 7.74 (m, 3H), 7.49 (t, J = 8.9 Hz, 1H), 7.34 - 7.23 (m, 2H), 7.04 (dd, J = 11.4, 2.9 Hz, 1H), 6.83 (ddd, J = 9.0, 2.9, 1.2 Hz, 1H), 4.49 (s, 2H), 4.10 (s, 2H), 2.21 - 1.82 (m, 8H); MS (ESI ⁺ ) m/z 517.1 (M+H) ⁺ .

Example 238: 4-[2-(4-chloro-3-fluorophenoxy)acetamido]-N-[4-(trifluoromet hyl)phenyl]-2- oxabicyclo[2.2.2]octane-l-carboxamide (Compound 337)

The reaction described in Example 237 substituting 4-aminobenzotrifluoride for 4- (trifluoromethoxy)aniline gave the title compound. ^J H NMR (400 MHz, DMSO- ¾) δ ppm 9.81 (s, 1H), 7.95 (d, J = 8.5 Hz, 2H), 7.80 (s, 1H), 7.65 (d, J = 8.6 Hz, 2H), 7.49 (t, J = 8.9 Hz, 1H), 7.05 (dd, J = 11.4, 2.9 Hz, 1H), 6.83 (ddd, J = 9.0, 2.9, 1.2 Hz, 1H), 4.50 (s, 2H), 4.11 (s, 2H), 2.19 - 1.82 (m, 8H); MS (ESI ⁺ ) m/z 501.4 (M+H) ⁺ . Example 239: 4-[2-(4-chloro-3-fluorophenoxy)acetamido]-N-(4-chloro-3-fluo rophenyl)-2- oxabicyclo[2.2.2]octane-l-carboxamide (Compound 338)

The reaction described in Example 237 substituting 4-chloro-3-fluoroaniline for 4- (trifluoromethoxy)aniline gave the title compound. ^J H NMR (500 MHz, DMSO-(f ₆ ) δ ppm 9.81 (s, 1H), 7.88 (dd, J = 12.1 , 2.4 Hz, 1H), 7.81 (s, 1H), 7.61 (ddd, J = 8.9, 2.4, 1.0 Hz, 1H), 7.49 (td, J = 8.8, 1.2 Hz, 2H), 7.04 (dd, J = 11.4, 2.9 Hz, 1H), 6.82 (ddd, J = 9.0, 2.9, 1.2 Hz, 1H), 4.49 (s, 2H), 4.10 (d, J = 1.6 Hz, 2H), 2.16 - 1.89 (m, 8H); MS (ESI ⁺ ) m/z 485.3 (M+H) ⁺ .

Example 240: 6-[({3-[2-(4-chloro-3-fluorophenoxy)acetamido]bicyclo[l.l.l] pentane-l- carbonyl}amino)methyl]pyridine-3-carboxamide (Compound 339) The title compound was prepared using the methodologies described above. ^J H NMR

(501 MHz, DMSO- ) δ ppm 8.94 (d, J = 2.2 Hz, 1H), 8.74 (s, 1H), 8.47 (t, J = 6.1 Hz, 1H), 8.17 (dd, J = 8.2, 2.3 Hz, 1H), 8.10 (s, 1H), 7.53 (s, 1H), 7.50 (t, J = 8.9 Hz, 1H), 7.29 (d, J = 8.2 Hz, 1H), 7.08 (dd, J = 11.4, 2.9 Hz, 1H), 6.91 - 6.81 (m, 1H), 4.48 (s, 2H), 4.38 (d, J = 6.0 Hz, 2H), 2.24 (s, 6H); MS (ESI ⁺ ) m/z 447 (M+H) ⁺ . Example 241: 3-[2-(4-chloro-3-fluorophenoxy)acetamido]-N-[2-(4-chloro-3- fluorophenoxy)ethyl]bicyclo[l.l.l]pentane-l-carboxamide (Compound 340)

The title compound was prepared using the methodologies described above. ^J H NMR (400 MHz, DMSO- ) δ ppm 8.71 (s, 1H), 8.01 (t, J = 5.7 Hz, 1H), 7.49 (t, J = 8.9 Hz, 1H), 7.46 (t, J = 8.9 Hz, 1H), 7.10 - 7.04 (m, 2H), 6.88 - 6.81 (m, 2H), 4.47 (s, 2H), 4.02 (t, J = 5.9 Hz, 2H), 3.39 (q, J = 5.9 Hz, 2H), 2.17 (s, 6H); MS (ESI ⁺ ) m/z 485 (M+H) ⁺ .

Example 242: 4-[2-(4-chloro-3-fluorophenoxy)acetamido]-N-[6-(trifluoromet hoxy)pyridin- 3-yl]-2-oxabicyclo[2.2.2]octane-l-carboxamide (Compound 341)

Example 242A: tert-butyl (l-((6-(trifluoromethoxy)pyridin-3-yl)carbamoyl)-2- oxabicyclo[ 2.2.2 ]octan-4-yl )carbamate A mixture of Example 235C (0.095 g, 0.350 mmol), PyBOP® ((1H- benzo[(i] [l ,2,3]triazol-l-yl)oxy)tri(pyrrolidin-l-yl)phosphonium hexafluorophosphate(V)) (0.219 g, 0.420 mmol), 6-(trifluoromethoxy)pyridin-3-amine (0.075 g, 0.420 mmol), and triethylamine (0.073 mL, 0.525 mmol) in N,N-dimethylformamide (DMF) (3 mL) was stirred for 3 hours. The reaction mixture was quenched with brine and saturated NaHC(¾, and extracted with ethyl acetate (2x). The combined organic layers were washed with brine, dried over

MgSO/t, filtered, and concentrated. The residue was purified on a 12 g column using the Biotage® Isolera One flash system eluted with heptanes/ethyl acetate (7:3 to 6:4) to provide the title compound (65.1 mg, 43%). MS (ESI ⁺ ) nt/z 432.3 (M+H) ⁺ . Example 242B: 4-amino-N-(6-(trifluoromethoxy)pyridin-3-yl)-2-oxabicyclo[2. 2.2]octane-l- carboxamide, hydrochloric acid

A mixture of Example 242A (62.0 mg, 0.144 mmol) and trifluoroacetic acid (0.111 mL, 1.437 mmol) in CH2CI2 (2 mL) was stirred for 4 hours. The reaction mixture was concentrated, and the residue was dissolved in 1 mL of methanol. The solution was treated with 1 mL of 2 M HC1 in ether and stirred for 15 minutes. The solution was concentrated to provide the title compound as an HC1 salt (60.8 mg, quantitative yield) that was used in the next step without further purifications. MS (ESI ⁺ ) nt/z 332.2 (M+H) ⁺ .

Example 242C 4-[2-(4-chloro-3-fluorophenoxy)acetamido]-N-[6-(trifluoromet hoxy)pyridin-3- yl]-2-oxabicyclo[2.2.2] octane- 1-carboxamide, trifluoroacetic acid salt A mixture of Example 242B (59.0 mg, 0.146 mmol), HATU (1-

[bis(dimethylamino)methylene]-lH-l,2,3-triazolo[4,5-¾]py ridinium 3-oxid

hexafluorophosphate) (66.6 mg, 0.175 mmol), 2-(4-chloro-3-fluorophenoxy)acetic acid (35.8 mg, 0.175 mmol), and triethylamine (0.081 mL, 0.584 mmol) in N,N-dimethylformamide (DMF) (2 mL) was stirred for 3 hours. The reaction mixture was quenched with brine and saturated NaHCC>3, and extracted with ethyl acetate (2x). The combined organic layers were washed with brine, dried over MgSO/t, filtered, and concentrated. The residue was purified by HPLC (see protocol in Example 235H) to provide the title compound as a trifluoroacetic acid salt (43.5 mg, 47%). ^J H NMR (400 MHz, DMSO-<¾) δ ppm 9.94 (s, 1H), 8.66 (d, J = 2.6 Hz, 1H), 8.32 (dd, J = 8.9, 2.7 Hz, 1H), 7.81 (s, 1H), 7.49 (t, J = 8.9 Hz, 1H), 7.27 (d, J = 8.8 Hz, 1H), 7.05 (dd, J = 11.4, 2.8 Hz, 1H), 6.83 (ddd, J = 9.0, 2.9, 1.2 Hz, 1H), 4.50 (s, 2H), 4.12 (s, 2H), 2.23 - 1.77 (m, 8H); MS (ESI ⁺ ) m/z 518.4 (M+H) ⁺ .

Example 243: 4-[2-(4-chloro-3-fluorophenoxy)acetamido]-N-[(5-chloropyridi n-2- yl)methyl]-2-oxabicyclo[2.2.2]octane-l-carboxamide (Compound 342)

Example 243 : tert-butyl (!-((( 5-chloropyridin-2-yl)methyl)carbamoyl)-2- oxabicyclo[ 2.2.2 ]octan-4-yl )carbamate A mixture of Example 235C (0.150 g, 0.553 mmol), HATU (1 - [bis(dimethylamino)methylene]-lH-l ,2,3-triazolo[4,5-¾]pyridinium 3-oxid

hexafluorophosphate) (0.231 g, 0.608 mmol), (5-chloropyridin-2-yl)methanamine hydrochloride (0.109 g, 0.608 mmol), and triethylamine (0.193 mL, 1.382 mmol) in N,N-dimethylformamide (DMF) (2.5 mL) was stirred overnight. The reaction mixture was quenched with brine and saturated NaHC(¾ and extracted with ethyl acetate (2x). The combined organic layers were washed with brine, dried over MgSO/t, filtered, and concentrated. The residue was purified on a 12 g column using the Biotage® Isolera One flash system eluting with heptanes/ethyl acetate (4:6 to 3:7) to provide the title compound (0.165 g, 75%). MS (ESI ⁺ ) mJz 396.2 (M+H) ⁺ . Example 243B: 4-amino-N-((5-chloropyridin-2-yl)methyl)-2-oxabicyclo[2.2.2] octane-l- carboxamide

A mixture of Example 243A (0.160 g, 0.404 mmol) and trifluoroacetic acid (0.311 mL, 4.04 mmol) in CH2CI2 (3 mL) was stirred for 4 hours. The reaction mixture was concentrated, and the residue was dissolved in 2 mL of methanol. The solution was treated with 1.5 mL of 2 M HC1 in ether and stirred for 15 minutes. The solution was concentrated to provide the title compound as an HC1 salt (0.140 g, 94%) that was used in the next step without further purification. MS (ESI ⁺ ) m/z 296.2 (M+H) ⁺ .

Example 243 C: 4-[2-(4-chloro-3-fluorophenoxy)acetamido]-N-[(5-chloropyridi n-2-yl)methyl]- 2-oxabicyclo[ 2.2.2 ] octane- 1-carboxamide A mixture of Example 243B (0.070 g, 0.190 mmol), HATU (1 -

[bis(dimethylamino)methylene]-lH-l ,2,3-triazolo[4,5-¾]pyridinium 3-oxid

hexafluorophosphate) (0.087 g, 0.228 mmol), 2-(4-chloro-3-fluorophenoxy)acetic acid (0.047 g, 0.228 mmol), and triethylamine (0.106 mL, 0.759 mmol) in N,N-dimethylformamide (DMF) (2.5 mL) was stirred for 3 hours. The reaction mixture was quenched with brine and saturated NaHCC>3 and extracted with ethyl acetate (2x). The combined organic layers were washed with brine, dried over MgSO/t, filtered, and concentrated. The residue was purified by HPLC (see protocol in Example 235H) to provide the title compound as a trifluoroacetic acid salt (46.3 mg, 41 %). ^J H NMR (400 MHz, DMSO-<¾) δ 8.53 (d, J = 2.4 Hz, 1H), 8.25 (t, J = 6.1 Hz, 1H), 7.88 (dd, J = 8.4, 2.5 Hz, 1H), 7.76 (s, 1H), 7.49 (t, J = 8.9 Hz, 1H), 7.24 (d, J = 8.4 Hz, 1H), 7.04 (dd, J = 11.4, 2.9 Hz, 1H), 6.82 (ddd, J = 9.0, 2.9, 1.2 Hz, 1H), 4.48 (s, 2H), 4.34 (d, J = 6.1 Hz, 2H), 4.04 (s, 2H), 2.17 - 1.81 (m, 8H); MS (ESI ⁺ ) m/z 482.3 (M+H) ⁺ . Example 244: 3-[2-(4-chloro-3-fluorophenoxy)acetamido]-N-[(4-chloro-3- fluorophenyl)methyl]-N-(2-hydroxyethyl)bicyclo[l.l.l]pentane -l-carboxamide (Compound 343)

Example 244A: 2-((4-chloro-3-fluorobenzyl)amino)ethanol To a solution of (4-chloro-3-fluorophenyl)methanamine (266 mg, 1.67 mmol, Alfa) in a methanol buffer (3.6 weight % sodium acetate trihydrate and 2.4 weight % acetic acid in methanol, 15mL) was added l,4-dioxane-2,5-diol (100 mg, 0.833 mmol, Aldrich) in one portion followed by sodium cyanoborohydride (105 mg, 1.67 mmol) and trifluoroacetic acid (0.1 mL). After stirring at ambient temperature for 10 minutes, the reaction mixture was concentrated under reduced pressure to less than 5 mL and was filtered through a glass microfiber frit. Then the filtrate was purified by preparative HPLC [YMC TriArt™ CI 8 Hybrid 5 μπι column, 50 x 100 mm, flow rate 140 mL/minute, 5-100% gradient of acetonitrile in buffer (0.025 M aqueous ammonium bicarbonate, adjusted to pH 10 with ammonium hydroxide)] to give the title compound (0.18 g, 0.88 mmol, 53.0 % yield). MS (ESI ⁺ ) mJz 204 (M+H) ⁺ . Example 244B: 3-[2-(4-chloro-3-fluorophenoxy)acetamido]-N-[(4-chloro-3- fluorophenyl )methyl]-N-( 2 -hydroxy ethyl )bicyclo[ 1.1.1 ]pentane-l -carboxamide

The reaction and purification conditions described in Example 48 substituting the product of Example 244A for (5-(difluoromethoxy)pyridin-2-yl)methanamine, and (7-azabenzotriazol- 1- yloxy)tripyrrolidinophosphonium hexafluorophosphate (PyAOP) for (1- [bis(dimethylamino)methylene]- 1H- 1 ,2,3-triazolo[4,5- ?]pyridinium 3-oxid

hexafluorophosphate) (HATU) gave the title compound. ^J H NMR (400 MHz, DMSO-<¾, 120 °C) δ ppm 8.19 (s, 1H), 7.47 (t, J = 8.0 Hz, 1H), 7.40 (t, J = 8.8 Hz, 1H), 7.14 (dd, J = 10.4, 1.9 Hz, 1H), 7.04 (ddd, J = 8.3, 2.0, 0.9 Hz, 1H), 6.97 (dd, J = 11.3, 2.8 Hz, 1H), 6.82 (ddd, J = 8.9, 2.8, 1.2 Hz, 1H), 4.60 (s, 2H), 4.42 (s, 2H), 4.30 (br s, 1H), 3.51 (q, J = 5.8 Hz, 2H), 3.42 - 3.37 (m, 2H), 2.30 (s, 6H); MS (ESI ⁺ ) m/z 499 (M+H) ⁺ .

Example 245: 4-[2-(4-chloro-3-fluorophenoxy)acetamido]-N-[(4-chloro-3- fluorophenyl)methyl]-N-(2-hydroxyethyl)bicyclo[2.2.2]octane- l-carboxamide (Compound 344)

The title compound was prepared using the methodologies described above. ^J H NMR (400 MHz, DMSO-<¾, 120 °C) δ ppm 7.44 (t, J = 8.0 Hz, 1H), 7.39 (t, J = 8.8 Hz, 1H), 7.09 (dd, J = 10.5, 1.9 Hz, 1H), 7.01 (dd, J = 8.3, 1.9 Hz, 1H), 6.97 - 6.90 (m, 2H), 6.80 (ddd, J = 8.9, 2.9, 1.2 Hz, 1H), 4.62 (s, 2H), 4.39 (s, 2H), 4.25 (br s, 1H), 3.55 - 3.50 (m, 2H), 3.46 - 3.40 (m, 2H),

1.96 - 1.83 (m, 12H); MS (APCI ⁺ ) m/z 541 (M+H) ⁺ .

Example 246: 3-[2-(4-chloro-3-fluorophenoxy)acetamido]-N-{[5-(difluoromet hyl)pyridin- 2-yl]methyl}bicyclo[l.l.l]pentane-l-carboxamide (Compound 345)

The title compound was prepared using the methodologies described above. ^J H NMR (500 MHz, DMSO-<¾) δ ppm 8.75 (s, 1H), 8.71 - 8.68 (m, 1H), 8.50 (t, J = 6.1 Hz, 1H), 8.00 -

7.97 (m, 1H), 7.50 (t, J = 8.9 Hz, 1H), 7.39 - 7.34 (m, 1H), 7.13 (t, J = 55.4 Hz, 1H), 7.08 (dd, J = 11.4, 2.9 Hz, 1H), 6.86 (ddd, J = 9.0, 2.9, 1.2 Hz, 1H), 4.48 (s, 2H), 4.39 (d, J = 6.0 Hz, 2H), 2.24 (s, 6H); MS (ESI ⁺ ) m/z 454 (M+H) ⁺ .

Example 247: 4-[2-(4-chloro-3-fluorophenoxy)acetamido]-N-{[5-(difluoromet hyl)pyridin- 2-yl]methyl}bicyclo[2.2.2]octane-l-carboxamide (Compound 346)

The title compound was prepared using the methodologies described above. ^J H NMR (400 MHz, DMSO-de) S ppm 8.69 - 8.66 (m, 1H), 8.12 (t, J = 6.0 Hz, 1H), 7.98 - 7.93 (m, 1H), 7.52 - 7.45 (m, 2H), 7.30 (d, J = 8.2 Hz, 1H), 7.12 (t, J = 55.4 Hz, 1H), 7.03 (dd, J = 11.5, 2.8 Hz, 1H), 6.81 (ddd, J = 9.0, 2.9, 1.2 Hz, 1H), 4.44 (s, 2H), 4.37 (d, J = 5.9 Hz, 2H), 1.90 - 1.75 (m, 12H); MS (ESI ⁺ ) m/z 496 (M+H) ⁺ .

Example 248: (2/?)-4-[2-(4-chloro-3-fluorophenoxy)acetamido]-N-[2-(4-chlo ro-3- fluorophenyl)-2-oxoethyl]-2-hydroxybicyclo[2.2.2]octane-l-ca rboxamide (Compound 347) The title compound was prepared using the methodologies described for Example 177.

^J H NMR (501 MHz, DMSO-de) δ ppm 8.00 (t, J = 5.4 Hz, 1H), 7.96 (dd, J = 9.9, 1.8 Hz, 1H), 7.82 (dd, J = 8.4, 1.9 Hz, 1H), 7.78 (dd, J = 8.4, 7.1 Hz, 1H), 7.53 (s, 1H), 7.48 (t, J = 8.9 Hz, 1H), 7.03 (dd, J = 11.4, 2.8 Hz, 1H), 6.81 (ddd, J = 9.0, 2.9, 1.1 Hz, 1H), 4.60 - 4.48 (m, 2H), 4.45 (s, 2H), 4.12 - 4.01 (m, 1H), 2.24 (ddd, J = 12.6, 9.1 , 3.0 Hz, 1H), 2.17 - 2.01 (m, 1H), 1.98 - 1.84 (m, 1H), 1.84 - 1.65 (m, 5H), 1.66 - 1.52 (m, 2H); MS (APCI) m/z 541.2 (M+H) ⁺ .

Example 249: Activity of exemplary compounds in an in vitro model of vanishing cell white matter disease (VWMD)

In order to test exemplary compounds of the invention in a cellular context, a stable VWMD cell line was first constructed. The ATF4 reporter was prepared by fusing the human full-length ATF4 5'-UTR (NCBI Accession No. BC022088.2) in front of the firefly luciferase (FLuc) coding sequence lacking the initiator methionine as described in Sidrauski et al (eLife 2013). The construct was used to produce recombinant retroviruses using standard methods and the resulting viral supernatant was used to transduce HEK293T cells, which were then subsequently selected with puromycin to generate a stable cell line.

HEK293T cells carrying the ATF4 luciferase reporter were plated on polylysine coated 384-well plates (Greiner Bio-one) at 30,000 cells per well. Cells were treated the next day with 1 μg/mL tunicamycin and 200 nM of a compound of Formula (I) for 7 hours. Luminescence was measured using One Glo (Promega) as specified by the manufacturer. Cells were maintained in DMEM with L-glutamine supplemented with 10% heat-inactivated FBS (Gibco) and Antibiotic-Antimycotic solution (Gibco).

Table 2 below summarizes the EC5 ₀ data obtained using the ATF4-Luc assay for exemplary compounds of the invention. In this table, "A" represents an EC5 ₀ of less than 250 nM; "B" an EC ₅₀ of between 250 nM and 500 nM; "C" an EC ₅₀ of between 500 nM and 1 μΜ; "D" an EC5 ₀ of between 1 μΜ and 2 μΜ; "E" an EC5 ₀ of greater than 2 μΜ; and "F" indicates that data is not available.

Table 2: EC5 ₀ values of exemplary compounds of the invention in the ATF4-Luc assay.

ATF4-Luc ATF4-Luc

Compound No. Com ound No.

100 A 106 A

101 D 107 A

102 B 108 A

103 B 109 C

104 B 110 A

105 C 111 E ATF4-Luc ATF4-Luc

Compound No. Com ound No.

112 E 132 A

113 A 133 A

114 A 134 A

115 E 135 A

116 E 136 C

117 A 137 C

118 A 138 A

119 D 139 D

120 A 140 E

121 E 141 A

122 A 142 C

123 A 143 A

124 C 144 E

125 A 145 A

126 E 146 A

127 D 147 B

128 A 148 A

129 B 149 B

130 A 150 A

131 B 151 E ATF4-Luc ATF4-Luc

Compound No. Com ound No.

152 E 172 E

153 E 173 E

154 E 174 E

155 E 175 E

156 A 176 E

157 E 177 E

158 A 178 E

159 E 179 E

160 E 180 E

161 E 181 E

162 E 182 E

163 E 183 E

164 E 184 E

165 E 185 E

166 E 186 E

167 E 187 E

168 D 188 E

169 C 189 E

170 E 190 E

171 D 191 D ATF4-Luc ATF4-Luc

Compound No. Com ound No.

192 E 212 E

193 B 213 E

194 A 214 E

195 E 215 E

196 E 216 E

197 C 217 E

198 E 218 F

199 E 219 E

200 E 220 E

201 D 221 E

202 E 222 E

203 E 223 E

204 A 224 E

205 E 225 E

206 E 226 E

207 E 227 E

208 E 228 E

209 E 229 E

210 E 230 E

211 D 231 E ATF4-Luc ATF4-Luc

Compound No. Com ound No.

232 E 252 E

233 E 253 D

234 E 254 D

235 E 255 A

236 E 256 D

237 E 257 A

238 E 258 C

239 E 259 C

240 E 260 A

241 E 261 A

242 E 262 A

243 E 263 A

244 E 264 A

245 E 265 A

246 E 266 A

247 E 267 A

248 E 268 B

249 E 269 A

250 E 270 A

251 E 271 A ATF4-Luc ATF4-Luc

Compound No. Com ound No.

272 A 292 A

273 A 293 B

274 A 294 A

275 A 295 A

276 A 296 A

277 A 297 A

278 A 298 A

279 A 299 A

280 A 300 A

281 E 301 A

282 A 302 B

283 A 303 B

284 A 304 A

285 A 305 A

286 E 306 A

287 A 307 B

288 A 308 A

289 A 309 A

290 A 310 A

291 A 311 B ATF4-Luc ATF4-Luc

Compound No. Com ound No.

312 B 330 D

313 D 331 A

314 C 332 A

315 C 333 A

316 C 334 B

317 D 335 A

318 E 336 A

319 A 337 A

320 C 338 A

321 E 339 E

322 E 340 A

323 A 341 A

324 A 342 A

325 A 343 D

326 A 344 D

327 A 345 B

328 D 346 A

329 A 347 A

VWMD mutations were introduced into the genome of the HEK293T ATF4-Fluc stable cell lines by using Gene Art CRISPR nuclease vector with OFP Reporter kit (ThermoFisher; see Table 3 below). Guide RNAs were designed using the CRISPR Design Tool (http://crispr.mit.edu) and ligated into the CRISPR OFP Nuclease Vector. To obtain homology directed repair (HDR) incorporating VWMD point mutations in the genome, 150 bp ssDNA ultramer oligos were synthesized by Integrated DNA Technologies containing specific mutations of interest. In addition to the VWMD mutations, the ssDNA HDR templates contained a silent mutation to the PAM site of the CRISPR gRNA sequence (to avoid further Cas9 cutting) and 75 bp of homology on each side of the mutation.

HEK293T ATF4-Fluc cells were transfected with 500 ng of the CRISPR OFP Nuclease Vector and 1 uL of 10 μΜ ssDNA HDR template using lipofectamine 3000 (ThermoFisher) or SF Cell Line 4D-nucleofector X Kit (Lonza) according to the manufacturer's instructions. After 2-3 days of recovery, single cells were sorted for positive OFP expression on a FACS Aria II (BD Biosciences) into wells of a 96 well plate and allowed to recover for 1-2 weeks.

The resulting clones were surveyed for CRISPR editing and HDR by harvesting the genomic DNA with the PureLink Genomic DNA kit (ThermoFisher), amplifying a ~500bp locus near the editing site, and sequencing the amplicon. Clones that displayed an ambiguous chromatogram signal near the expected CRISPR editing site were further examined by TA cloning (Invitrogen) and sequencing of the amplicon, yielding the sequence of each allele in the clone. Typical clones obtained were hemizygous for the VWMD point mutation, with one or two alleles harboring the desired mutation, and the remaining alleles knocked out (edited to produce a premature stop codon).

Table 3: Exemplary VWMD point mutations introduced into eIF2B

eIF2B Subunit Mutation eIF2Bl V183F eIF2B3 H341Q eIF2B3 I346T eIF2B4 R483W eIF2B5 R113H eIF2B5 R195H EQUIVALENTS AND SCOPE

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Furthermore, the invention encompasses all variations, combinations, and permutations in which one or more limitations, elements, clauses, and descriptive terms from one or more of the listed claims are introduced into another claim. For example, any claim that is dependent on another claim can be modified to include one or more limitations found in any other claim that is dependent on the same base claim. Where elements are presented as lists, e.g., in Markush group format, each subgroup of the elements is also disclosed, and any element(s) can be removed from the group. It should it be understood that, in general, where the invention, or aspects of the invention, is/are referred to as comprising particular elements and/or features, certain embodiments of the invention or aspects of the invention consist, or consist essentially of, such elements and/or features. For purposes of simplicity, those embodiments have not been specifically set forth in haec verba herein. It is also noted that the terms "comprising" and "containing" are intended to be open and permits the inclusion of additional elements or steps. Where ranges are given, endpoints are included. Furthermore, unless otherwise indicated or otherwise evident from the context and understanding of one of ordinary skill in the art, values that are expressed as ranges can assume any specific value or sub-range within the stated ranges in different embodiments of the invention, to the tenth of the unit of the lower limit of the range, unless the context clearly dictates otherwise.

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Because such embodiments are deemed to be known to one of ordinary skill in the art, they may be excluded even if the exclusion is not set forth explicitly herein. Any particular embodiment of the invention can be excluded from any claim, for any reason, whether or not related to the existence of prior art.

Those skilled in the art will recognize or be able to ascertain using no more than routine experimentation many equivalents to the specific embodiments described herein. The scope of the present embodiments described herein is not intended to be limited to the above Description, but rather is as set forth in the appended claims. Those of ordinary skill in the art will appreciate that various changes and modifications to this description may be made without departing from the spirit or scope of the present invention, as defined in the following claims.