Triazole n-linked carbamoyl cyclohexyl acids as LPA antagonists

1. A compound of Formula (IIa):

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

X 1 , X 2 , X 3 , and X 4 are each independently CR 6 or N; provided that no more than two of X 1 , X 2 , X 3 , or X 4 are N;

R 1 is (—CH 2 ) a R 9 ;

a is an integer of 0 or 1;

R 2 is each independently halo, cyano, hydroxyl, amino, C 1-6 alkyl, C 3-6 cycloalkyl, C 4-6 heterocyclyl, alkylamino, haloalkyl, hydroxyalkyl, aminoalkyl, alkoxy, alkoxyalkyl, haloalkoxyalkyl, or haloalkoxy;

R 3 is independently hydrogen or C 1-4 alkyl;

R 4 is C 1-10 alkyl, C 3-8 cycloalkyl, 6 to 10-membered aryl, —(C 1-6 alkylene)-(C 3-8 cycloalkyl), or —(C 1-6 alkylene)-(6 to 10-membered aryl); wherein each of the alkyl, alkenyl, cycloalkyl, aryl, heterocyclyl, and heteroaryl, by itself or as part of other moiety, is independently substituted with 0 to 3 R 8 ; or alternatively, R 3 and R 4 , taken together with the N and O to which they are attached, form a 4- to 6-membered heterocyclic ring moiety which is substituted with 0 to 3 R 8 ;

R 5 is hydrogen, C 1-6 alkyl, alkylamino, haloalkyl, hydroxyalkyl, aminoalkyl, alkoxyalkyl, haloalkoxyalkyl, alkoxy, or haloalkoxy;

R 6 is hydrogen, halo, cyano, hydroxyl, amino, C 1-6 alkyl, alkylamino, haloalkyl, hydroxyalkyl, aminoalkyl, alkoxyalkyl, haloalkoxyalkyl, alkoxy, or haloalkoxy;

R 7a is independently hydrogen, halo, oxo, cyano, hydroxyl, amino, C 1-6 alkyl, C 3-6 cycloalkyl, C 4-6 heterocyclyl, alkylamino, haloalkyl, hydroxyalkyl, aminoalkyl, alkoxyalkyl, haloalkoxyalkyl, alkoxy, or haloalkoxy;

R 8 is each independently deuterium, halo, hydroxyl, amino, cyano, C 1-6 alkyl, C 1-6 deuterated alkyl, C 2-6 alkenyl, C 2-6 alkynyl, alkylamino, haloalkyl, hydroxyalkyl, aminoalkyl, alkoxyalkyl, haloalkoxyalkyl, alkoxy, haloalkoxy, —CHO, phenyl, or 5 to 6 membered heteroaryl; or alternatively, two R 8 , taken together with the atoms to which they are attached, form a 3 to 6-membered carbocyclic ring or a 3 to 6-membered heterocyclic ring each of which is independently substituted with 0 to 3 R 12 ;

R 9 is selected from —CN, —C(O)OR 10 , —C(O)NR 11a R 11b ,

R e is C 1-6 alkyl, C 3-6 cycloalkyl, haloalkyl, hydroxyalkyl, aminoalkyl, alkoxyalkyl, or haloalkoxyalkyl;

R 10 is hydrogen or C 1-10 alkyl;

R 11a and R 11b are each independently hydrogen, C 1-6 alkyl, C 3-6 cycloalkyl, C 4-6 heterocyclyl, alkylamino, haloalkyl, hydroxyalkyl, aminoalkyl, alkoxyalkyl, haloalkoxyalkyl, alkoxy, or haloalkoxy;

R 12 is halo, cyano, hydroxyl, amino, C 1-6 alkyl, alkylamino, haloalkyl, hydroxyalkyl, aminoalkyl, alkoxyalkyl, haloalkoxyalkyl, alkoxy, haloalkoxy, phenyl, or 5 to 6 membered heteroaryl;

f is an integer of 0, 1, or 2; and

n is 0 or 1.

2. The compound according to claim 1 , wherein R 1 is CO 2 H.

3. The compound according to claim 1 , wherein

R 4 is C 1-10 alkyl, C 1-10 haloalkyl, C 3-6 cycloalkyl, —(C 1-4 alkylene)-(C 3-6 cycloalkyl), —(C 1-4 alkylene)-(C 1-6 alkoxy), or —(C 1-4 alkylene)-phenyl; wherein each of the alkyl, alkylene, cycloalkyl, and phenyl, by itself or as part of another group, is independently substituted with 0 to 3 R 8 ; and

R 8 is each independently halo, hydroxyl, amino, cyano, C 1-6 alkyl, alkylamino, haloalkyl, hydroxyalkyl, aminoalkyl, alkoxyalkyl, haloalkoxyalkyl, alkoxy, or haloalkoxy; or alternatively, two R 8 , taken together with the atom(s) to which they are attached, form a 3 to 6-membered carbocyclic ring.

4. The compound according to claim 1 , wherein X 1 is CR 6 , where R 6 is hydrogen, C 1-4 alkyl, C 1-4 haloalkyl, or C 1-4 alkoxyalkyl.

5. The compound according to claim 1 , wherein X 3 is N.

6. The compound according to claim 1 , wherein

the

moiety is selected from

R 6a is each independently halo, cyano, hydroxyl, amino, C 1-6 alkyl, alkylamino, haloalkyl, hydroxyalkyl, aminoalkyl, alkoxyalkyl, haloalkoxyalkyl, alkoxy, or haloalkoxy; and

d is an integer of 0, 1, or 2.

7. The compound according to claim 6 , wherein

the

moiety is selected from

and

R 6 is each independently hydrogen, halo, cyano, hydroxyl, amino, C 1-6 alkyl, alkylamino, haloalkyl, hydroxyalkyl, aminoalkyl, alkoxyalkyl, haloalkoxyalkyl, alkoxy, or haloalkoxy.

8. The compound according to claim 1 , wherein f is 0 or 1.

9. A compound of Formula (IIIb):

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

X 1 , X 2 , X 3 , and X 4 are each independently CR 6 or N; provided that no more than two of X 1 , X 2 , X 3 , or X 4 are N;

R 1 is (—CH 2 ) a R 9 ;

a is an integer of 0 or 1;

R 2a is hydrogen, chloro, fluoro, or C 1-4 alkyl;

R 3 is hydrogen or C 1-6 alkyl;

R 4 is C 1-10 alkyl, C 3-8 cycloalkyl, 6 to 10-membered aryl, —(C 1-6 alkylene)-(C 3-8 cycloalkyl), or —(C 1-6 alkylene)-(6 to 10-membered aryl); wherein each of the alkyl, alkenyl, cycloalkyl, aryl, heterocyclyl, and heteroaryl, by itself or as part of other moiety, is independently substituted with 0 to 3 R 8 ; or alternatively, R 3 and R 4 , taken together with the N and O to which they are attached, form a 4- to 6-membered heterocyclic ring moiety which is substituted with 0 to 3 R 8 ;

R 6 is hydrogen, halo, cyano, hydroxyl, amino, C 1-6 alkyl, alkylamino, haloalkyl, hydroxyalkyl, aminoalkyl, alkoxyalkyl, haloalkoxyalkyl, alkoxy, or haloalkoxy;

R 8 is each independently deuterium, halo, hydroxyl, amino, cyano, C 1-6 alkyl, C 1-6 deuterated alkyl, C 2-6 alkenyl, C 2-6 alkynyl, alkylamino, haloalkyl, hydroxyalkyl, aminoalkyl, alkoxyalkyl, haloalkoxyalkyl, alkoxy, haloalkoxy, —CHO, phenyl, or 5 to 6 membered heteroaryl; or alternatively, two R 8 , taken together with the atoms to which they are attached, form a 3 to 6-membered carbocyclic ring or a 3 to 6-membered heterocyclic ring each of which is independently substituted with 0 to 3 R 12 ;

R 9 is selected from —CN, —C(O)OR 10 , —C(O)NR 11a R 11b ,

R e is C 1-6 alkyl, C 3-6 cycloalkyl, haloalkyl, hydroxyalkyl, aminoalkyl, alkoxyalkyl, or haloalkoxyalkyl;

R 10 is hydrogen or C 1-10 alkyl;

R 11a and R 11b are each independently hydrogen, C 1-6 alkyl, C 3-6 cycloalkyl, C 4-6 heterocyclyl, alkylamino, haloalkyl, hydroxyalkyl, aminoalkyl, alkoxyalkyl, haloalkoxyalkyl, alkoxy, or haloalkoxy; and

R 12 is halo, cyano, hydroxyl, amino, C 1-6 alkyl, alkylamino, haloalkyl, hydroxyalkyl, aminoalkyl, alkoxyalkyl, haloalkoxyalkyl, alkoxy, haloalkoxy, phenyl, or 5 to 6 membered heteroaryl.

10. The compound according to claim 9 , wherein the

moiety is selected from

11. The compound according to claim 9 , wherein R 1 is CO 2 H.

12. The compound according to claim 9 , wherein

the

moiety is selected from

R 6 is each independently hydrogen, CH 3 , CH 2 CH 3 , CH 2 OCH 3 , CHF 2 , or CF 3 .

13. The compound according to claim 9 , wherein

R 4 is C 3-10 alkyl, C 3-10 haloalkyl, C 3-6 cycloalkyl, phenyl, —(C 1-4 alkylene)-(C 1-3 alkoxy), —(C 1-4 alkylene)-(C 3-6 cycloalkyl), or benzyl; wherein the alkyl, alkylene, cycloalkyl, and benzyl are each independently substituted with 0 to 3 R 8 ; and

R 8 is each independently halo, C 1-6 alkyl, alkylamino, haloalkyl, hydroxyalkyl, aminoalkyl, alkoxyalkyl, haloalkoxyalkyl, alkoxy, or haloalkoxy; or alternatively, two R 8 , taken together with the atoms to which they are attached, form a 3 to 6-membered carbocyclic ring.

14. The compound according to claim 9 , wherein

R 4 is C 3-10 alkyl, C 3-10 haloalkyl, cyclobutyl, cyclopentyl, —(CH 2 ) 1-2 —(C 1-3 alkoxy), —(CHR 8a ) 1-2 -cyclopropyl, —(CHR 8a ) 1-2 -cyclobutyl, or —(CHR 8a ) 1-2 -phenyl; wherein the cyclopropyl, cyclobutyl, cyclopentyl, and phenyl are each independently substituted with 0 to 3 R 8 ; or alternatively, two R 8 , taken together with the atom to which they are attached, form cyclopropyl;

R 8a is each independently hydrogen or methyl; and

R 8 is each independently halo or C 1-4 alkyl.

15. The compound according to claim 9 , wherein

X 1 is CR 6 , where R 6 is hydrogen, C 1-4 alkyl, C 1-4 haloalkyl, or C 1-4 alkoxyalkyl;

X 2 and X 4 are N;

X 3 is N;

R 1 is CO 2 H;

R 2a is hydrogen, chloro, fluoro, or C 1-4 alkyl;

R 3 is hydrogen or C 1-6 alkyl;

R 4 is C 1-10 alkyl, —(C 1-6 alkylene) 0-1 -phenyl, or —(C 1-6 alkylene) 0-1 -(C 3-8 cycloalkyl); and

R 6 is hydrogen, C 1-6 alkyl, alkylamino, haloalkyl, hydroxyalkyl, aminoalkyl, alkoxyalkyl, haloalkoxyalkyl, alkoxy, or haloalkoxy.

16. A pharmaceutical composition comprising one or more compounds according to claim 1 , or a stereoisomer, tautomer, or pharmaceutically acceptable salt or solvate thereof; and a pharmaceutically acceptable carrier or diluent.

17. A method of treating a disease, disorder, or condition associated with dysregulation of lysophosphatidic acid receptor 1 (LPA1) in a patient having the disease, disorder, or condition, comprising administering a therapeutically effective amount of a compound according to claim 1 , or a stereoisomer, a tautomer, or a pharmaceutically acceptable salt or solvate thereof, to the patient.

18. The method according to claim 17 , wherein the disease, disorder, or condition is pathological fibrosis, transplant rejection, cancer, osteoporosis, or inflammatory disorders.

19. The method according to claim 18 , wherein the pathological fibrosis is pulmonary, liver, renal, cardiac, dernal, ocular, or pancreatic fibrosis.

20. The method according to claim 17 , wherein the disease, disorder, or condition is idiopathic pulmonary fibrosis (IPF), non-alcoholic steatohepatitis (NASH), non-alcoholic fatty liver disease (NAFLD), chronic kidney disease, diabetic kidney disease, and systemic sclerosis.

21. The method according to claim 19 , wherein the cancer is of the bladder, blood, bone, brain, breast, central nervous system, cervix, colon, endometrium, esophagus, gall bladder, genitalia, genitourinary tract, head, kidney, larynx, liver, lung, muscle tissue, neck, oral or nasal mucosa, ovary, pancreas, prostate, skin, spleen, small intestine, large intestine, stomach, testicle, or thyroid.

22. A method of treating fibrosis in a mammal having fibrosis, comprising administering a therapeutically effective amount of a compound according to claim 1 , or a stereoisomer, a tautomer, or a pharmaceutically acceptable salt or solvate thereof, to the mammal.

23. The method according to claim 22 , wherein the fibrosis is idiopathic pulmonary fibrosis (IPF), nonalcoholic steatohepatitis (NASH), chronic kidney disease, diabetic kidney disease, and systemic sclerosis.

24. A method of treating a disease, disorder, or condition selected from: lung fibrosis (idiopathic pulmonary fibrosis), asthma, chronic obstructive pulmonary disease (COPD), renal fibrosis, acute kidney injury, chronic kidney disease, liver fibrosis (non-alcoholic steatohepatitis), skin fibrosis, fibrosis of the gut, breast cancer, pancreatic cancer, ovarian cancer, prostate cancer, glioblastoma, bone cancer, colon cancer, bowel cancer, head and neck cancer, melanoma, multiple myeloma, chronic lymphocytic leukemia, cancer pain, tumor metastasis, transplant organ rejection, scleroderma, ocular fibrosis, age related macular degeneration (AMD), diabetic retinopathy, collagen vascular disease, atherosclerosis, Raynaud's phenomenon, or neuropathic pain in a mammal having the disease, disorder, or condition, comprising administering a therapeutically effective amount of a compound according to claim 1 , or a stereoisomer, a tautomer, or a pharmaceutically acceptable salt or solvate thereof, to the mammal.