Substituted heteroaryl compounds and methods of use
The present invention provides novel heteroaryl compounds, pharmaceutical acceptable salts and formulations thereof. They are useful in preventing, managing, treating or lessening the severity of a protein kinase-mediated disease. The invention also provides pharmaceutically acceptable compositions comprising such compounds and methods of using the compositions in the treatment of protein kinase-mediated disease.
1. A compound having Formula (II):
or a stereoisomer, a tautomer, an N-oxide, a solvate, a pharmaceutically acceptable salt or a prodrug thereof, wherein:
W is C 7 -C 12 spiro bicycloalkyl, C 7 -C 12 fused bicycloalkyl, 7-12 membered spiro heterobicyclyl or 7-12 membered fused heterobicycloalkyl, wherein W is substituted by 1, 2, 3, 4 or 5 R 14 groups;
W 1 is H, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 alkoxyl, C 1 -C 6 aminoalkyl, C 1 -C 6 hydroxyalkyl, C 3 -C 6 cycloalkyl or 4-7 membered heterocyclyl;
R 12 is H, F, Cl, Br, I, N 3 , CN, —NO 2 , C 1 -C 12 alkyl, C 1 -C 12 alkoxyl, C 2 -C 12 alkenyl, C 2 -C 12 alkynyl, C 3 -C 12 cycloalkyl, 3-12 membered heterocyclyl, C 6 -C 12 aryl, 5-12 membered heteroaryl, —NR 15a R 15b , —OR 15c , —C(═O)OR 15c , —C(═O)NR 15a R 15b or —S(═O) 2 NR 15a R 15b , wherein each of the C 1 -C 12 alkyl, C 1 -C 12 alkoxyl, C 2 -C 12 alkenyl, C 2 -C 12 alkynyl, C 3 -C 12 cycloalkyl, 3-12 membered heterocyclyl, C 6 -C 12 aryl and 5-12 membered heteroaryl is optionally independently substituted by 1, 2, 3, 4 or 5 R 17 groups;
each R 13 is independently H, F, Cl, CN, C 1 -C 12 alkyl, C 2 -C 12 alkenyl, C 1 -C 12 alkoxyl, —(C 0 -C 4 alkylene)-(C 3 -C 12 cycloalkyl), —(C 0 -C 4 alkylene)-(3-12 membered heterocyclyl), C 6 -C 12 aryl or 5-12 membered heteroaryl, wherein each of the C 1 -C 12 alkyl, C 2 -C 12 alkenyl, C 1 -C 12 alkoxyl, —(C 0 -C 4 alkylene)-(C 3 -C 12 cycloalkyl), —(C 0 -C 4 alkylene)-(3-12 membered heterocyclyl), C 6 -C 12 aryl and 5-12 membered heteroaryl is optionally independently substituted by 1, 2, 3, 4 or 5 R 17 groups;
each R 14 is independently F, Cl, Br, I, NO 2 , N 3 , CN, C 3 -C 12 alkyl, C 2 -C 12 alkenyl, C 2 -C 12 alkynyl, C 1 -C 12 hydroxyalkyl, C 3 -C 12 alkoxyl, C 1 -C 12 alkylamino, C 1 -C 12 aminoalkyl, C 3 -C 12 cycloalkyl, 4-7 membered heterocyclyl, C 6 -C 12 aryl, 6-cyanopyridazine-3-yl, —CH 2 CN, —CH 2 CH 2 CN, —C(═O)R 16d , —S(═O) 2 R 16e , —C(═O)NR 16a R 16b , —S(═O) 2 NR 16a R 16b , —C(═O)O—R 16c , —N(R 16a )C(═O)R 16f , —N(R 16a )S(═O) 2 R 16g or —OC(═O)R 16f , wherein each of the —CH 2 CN, —CH 2 CH 2 CN, C 3 -C 12 alkyl, C 2 -C 12 alkenyl, C 2 -C 12 alkynyl, C 1 -C 12 hydroxyalkyl, C 3 -C 12 alkoxyl, C 1 -C 12 alkylamino, C 1 -C 12 aminoalkyl, C 3 -C 12 cycloalkyl, 4-7 membered heterocyclyl, C 6 -C 12 aryl and 6-cyanopyridazine-3-yl is optionally independently substituted by 1, 2, 3, 4 or 5 R 17 groups;
each R 15a , R 15b , R 15e , R 16a and R 16b is independently H, C 1 -C 12 alkyl, C 2 -C 12 alkenyl, C 2 -C 12 alkynyl, C 3 -C 12 cycloalkyl, 3-12 membered heterocyclyl, C 6 -C 12 aryl, 5-12 membered heteroaryl, —(C 1 -C 4 alkylene)-(C 3 -C 12 cycloalkyl), —(C 1 -C 4 alkylene)-(3-12 membered heterocyclyl), —(C 1 -C 4 alkylene)-(C 6 -C 12 aryl), or —(C 1 -C 4 alkylene)-(5-12 membered heteroaryl), or R 15a and R 15b , taken together with the nitrogen atom to which they are attached form a 3-12 membered heterocyclyl group, wherein each of the C 1 -C 12 alkyl, C 2 -C 12 alkenyl, C 2 -C 12 alkynyl, C 3 -C 12 cycloalkyl, 3-12 membered heterocyclyl, C 6 -C 12 aryl, 5-12 membered heteroaryl, —(C 1 -C 4 alkylene)-(C 3 -C 12 cycloalkyl), —(C 1 -C 4 alkylene)-(3-12 membered heterocyclyl), —(C 1 -C 4 alkylene)-(C 6 -C 12 aryl), and —(C 1 -C 4 alkylene)-(5-12 membered heteroaryl) is optionally substituted by 1, 2 or 3 substitutents independently selected from F, Cl, Br, CN, N 3 , —NO 2 , —OH, —NH 2 , C 1 -C 4 alkyl, C 1 -C 4 haloalkyl, C 1 -C 4 alkoxy, C 1 -C 4 hydroxyalkyl, C 1 -C 4 aminoalkyl and C 1 -C 4 alkylamino;
each R 16d , R 16e and R 16g is independently C 2 -C 12 alkyl, C 3 -C 12 cycloalkyl, 3-12 membered heterocyclyl, C 6 -C 12 aryl, 5-12 membered heteroaryl, —(C 1 -C 4 alkylene)-(C 3 -C 12 cycloalkyl), —(C 1 -C 4 alkylene)-(3-12 membered heterocyclyl), —(C 1 -C 4 alkylene)-(C 6 -C 12 aryl) or —(C 1 -C 4 alkylene)-(5-12 membered heteroaryl), wherein each of the above substituents is optionally substituted by 1, 2, 3 or 4 substitutents independently selected from F, Cl, Br, CN, N 3 , —OH, —NH 2 , C 1 -C 4 alkyl, C 1 -C 4 haloalkyl, C 1 -C 4 alkoxy, C 1 -C 4 hydroxyalkyl, C 1 -C 4 aminoalkyl and C 1 -C 4 alkylamino;
each R 16c and R 16f is independently C 1 -C 3 alkyl, C 3 -C 12 cycloalkyl, 3-12 membered heterocyclyl, C 6 -C 12 aryl, 5-12 membered heteroaryl, —(C 1 -C 4 alkylene)-(C 3 -C 12 cycloalkyl), —(C 1 -C 4 alkylene)-(3-12 membered heterocyclyl), —(C 1 -C 4 alkylene)-(C 6 -C 12 aryl), or —(C 1 -C 4 alkylene)-(5-12 membered heteroaryl), wherein each of the above substituents is optionally substituted by 1, 2, 3 or 4 substitutents independently selected from F, Cl, Br, CN, N 3 , —OH, —NH 2 , C 1 -C 4 alkyl, C 1 -C 4 haloalkyl, C 1 -C 4 alkoxy, C 1 -C 4 hydroxyalkyl, C 1 -C 4 aminoalkyl and C 1 -C 4 alkylamino;
each R 17 is independently F, Cl, Br, I, CN, NO 2 , N 3 , —OH, —NH 2 , C 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C 1 -C 6 haloalkyl, C 3 -C 6 cycloalkyl, C 6 -C 12 aryl, 4-7 membered heterocyclyl, 5-12 membered heteroaryl, C 1 -C 6 aminoalkyl, C 1 -C 6 alkylamino, C 1 -C 6 alkoxyl, C 1 -C 6 hydroxyalkyl, —NH(C 0 -C 4 alkylene)-(C 3 -C 6 cycloalkyl), —NH(C 0 -C 4 alkylene)-(4-7 membered heterocyclyl), —N[(C 0 -C 4 alkylene)-(C 3 -C 6 cycloalkyl)]2, —N[(C 0 -C 4 alkylene)-(4-7 membered heterocyclyl)] 2 , —O(C 0 -C 4 alkylene)-(C 3 -C 6 cycloalkyl) or —O(C 0 -C 4 alkylene)-(4-7 membered heterocyclyl); and
n is 0, 1 or 2.
2. The compound of claim 1 , wherein W is 8-11 membered spiro heterobicyclyl or 8-10 membered fused heterobicycloalkyl, wherein W is substituted by 1, 2, 3 or 4 R 14 groups.
3. The compound of claim 1 , wherein W is:
or a stereoisomer thereof, wherein each Y, Y′, Y 2 and Y 3 is independently —CH 2 —, —NH— or —O—, with the proviso that Y 2 and Y 3 are not —O— simultaneously; and wherein W is substituted by 1, 2 or 3 R 14 groups.
4. The compound of claim 1 , wherein W is:
or a stereoisomer thereof, and wherein W is substituted by 1, 2 or 3 R 14 groups.
5. The compound of claim 1 , wherein W 1 is H, methyl, ethyl, n-propyl, isopropyl or cyclopropyl.
6. The compound of claim 1 , wherein R 12 is H, F, Cl, Br, I, N 3 , CN, —NO 2 , C 1 -C 4 alkyl, C 1 -C 4 alkoxyl, C 2 -C 4 alkenyl, C 2 -C 4 alkynyl, C 3 -C 6 cycloalkyl, 4-7 membered heterocyclyl, —NR 15a R 15b , —OR 15c , —C(═O)OR 15c , —C(═O)NR 15a R 15b or —S(═O) 2 NR 15a R 15b , wherein each of the C 1 -C 4 alkyl, C 1 -C 4 alkoxyl, C 2 -C 4 alkenyl, C 2 -C 4 alkynyl, C 3 -C 6 cycloalkyl and 4-7 membered heterocyclyl is optionally independently substituted by 1, 2 or 3 R 17 groups.
7. The compound of claim 1 , wherein each R 13 is independently H, F, Cl, CN, C 1 -C 4 alkyl, C 2 -C 4 alkenyl, C 1 -C 4 alkoxyl, —(C 0 -C 3 alkylene)-(C 3 -C 6 cycloalkyl) or —(C 0 -C 3 alkylene)-(4-7 membered heterocyclyl), wherein each of the C 1 -C 4 alkyl, C 2 -C 4 alkenyl, C 1 -C 4 alkoxyl, —(C 0 -C 3 alkylene)-(C 3 -C 6 cycloalkyl) and —(C 0 -C 3 alkylene)-(4-7 membered heterocyclyl) is optionally independently substituted by 1, 2 or 3 R 17 groups.
8. The compound of claim 1 , wherein each R 14 is independently F, Cl, Br, I, —NO 2 , N 3 , CN, C 3 -C 6 alkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C 1 -C 6 hydroxyalkyl, C 3 -C 6 alkoxyl, C 1 -C 6 alkylamino, C 1 -C 6 aminoalkyl, C 3 -C 6 cycloalkyl, 4-7 membered heterocyclyl, phenyl, 6-cyanopyridazine-3-yl, —CH 2 CN, —CH 2 CH 2 CN, —C(═O)R 16d , —S(═O) 2 R 16e , —C(═O)NR 16a R 16b , —S(═O) 2 NR 16a R 16b , —C(═O)O—R 16c , —N(R 16a )C(═O)R 16f , —N(R 16a )S(═O) 2 R 16g or —OC(═O)R 16f , wherein each of the —CH 2 CN, —CH 2 CH 2 CN, C 3 -C 6 alkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C 1 -C 6 hydroxyalkyl, C 3 -C 6 alkoxyl, C 1 -C 6 alkylamino, C 1 -C 6 aminoalkyl, C 3 -C 6 cycloalkyl, 4-7 membered heterocyclyl, phenyl and 6-cyanopyridazine-3-yl is optionally independently substituted by 1, 2 or 3 R 17 groups.
9. The compound of claim 1 , wherein each R 14 is independently F, Cl, Br, —NO 2 , CN,
10. The compound of claim 1 , wherein each R 15a , R 15b , R 15c , R 16a and R 16b is independently H, C 1 -C 4 alkyl, C 2 -C 4 alkenyl, C 2 -C 4 alkynyl, C 3 -C 6 cycloalkyl, 4-7 membered heterocyclyl, phenyl, 5-6 membered heteroaryl, —(C 1 -C 3 alkylene)-(C 3 -C 6 cycloalkyl), —(C 1 -C 3 alkylene)-(4-7 membered heterocyclyl), —(C 1 -C 3 alkylene)-phenyl or —(C 1 -C 3 alkylene)-(5-6 membered heteroaryl), or R 15a and R 15b , taken together with the nitrogen atom to which they are attached form a 4-7 membered heterocyclyl group, wherein each of the C 1 -C 4 alkyl, C 2 -C 4 alkenyl, C 2 -C 4 alkynyl, C 3 -C 6 cycloalkyl, 4-7 membered heterocyclyl, phenyl, 5-6 membered heteroaryl, —(C 1 -C 3 alkylene)-(C 3 -C 6 cycloalkyl), —(C 1 -C 3 alkylene)-(4-7 membered heterocyclyl), —(C 1 -C 3 alkylene)-phenyl and —(C 1 -C 3 alkylene)-(5-6 membered heteroaryl) is optionally substituted by 1, 2 or 3 substitutents independently selected from F, Cl, Br, CN, N 3 , —NO 2 , —OH, —NH 2 , C 1 -C 3 alkyl, C 1 -C 3 haloalkyl, C 1 -C 3 alkoxy, C 1 -C 3 hydroxyalkyl, C 1 -C 3 aminoalkyl and C 1 -C 3 alkylamino.
11. The compound of claim 1 , wherein each R 16d , R 16e and R 16g is independently C 2 -C 6 alkyl, C 3 -C 6 cycloalkyl, 4-7 membered heterocyclyl, phenyl, 5-6 membered heteroaryl, —(C 1 -C 3 alkylene)-(C 3 -C 6 cycloalkyl), —(C 1 -C 3 alkylene)-(4-7 membered heterocyclyl), —(C 1 -C 3 alkylene)-phenyl, or —(C 1 -C 3 alkylene)-(5-6 membered heteroaryl), wherein each of the above substituents is optionally substituted by 1, 2, 3 or 4 substitutents independently selected from F, Cl, Br, CN, N 3 , —OH, —NH 2 , C 1 -C 3 alkyl, C 1 -C 3 haloalkyl, C 1 -C 3 alkoxy, C 1 -C 3 hydroxyalkyl, C 1 -C 3 aminoalkyl and C 1 -C 3 alkylamino.
12. The compound of claim 1 , wherein each R 16c and R 16f is independently C 1 -C 3 alkyl, C 3 -C 6 cycloalkyl, 4-7 membered heterocyclyl, phenyl, 5-6 membered heteroaryl, —(C 1 -C 3 alkylene)-(C 3 -C 6 cycloalkyl), —(C 1 -C 3 alkylene)-(4-7 membered heterocyclyl), —(C 1 -C 3 alkylene)-phenyl, or —(C 1 -C 3 alkylene)-(5-6 membered heteroaryl), wherein each of the above substituents is optionally substituted by 1, 2, 3 or 4 substitutents independently selected from F, Cl, Br, CN, N 3 , —OH, —NH 2 , C 1 -C 3 alkyl, C 1 -C 3 haloalkyl, C 1 -C 3 alkoxy, C 1 -C 3 hydroxyalkyl, C 1 -C 3 aminoalkyl and C 1 -C 3 alkylamino.
13. The compound of claim 1 having one of the following structures:
a stereoisomer, a tautomer, an N-oxide, a solvate, or a pharmaceutically acceptable salt thereof.
14. A pharmaceutical composition comprising the compound of claim 1 , and a pharmaceutically acceptable excipient, carrier, adjuvant, vehicle or a combination thereof.
15. The pharmaceutical composition of claim 14 further comprising a therapeutic agent selected from the group consisting of chemotherapeutic agents, anti-proliferative agents, phosphodiesterase 4 (PDE4) inhibitors, β 2 -adrenoreceptor agonists, corticosteroids, non-steroidal GR agonists, anticholinergic agents, antihistamines, anti-inflammatory agents, immunosuppressants, immunomodulators, agents for treating atherosclerosis, agents for treating pulmonary fibrosis and combinations thereof.
16. A method of managing, treating or lessening the severity of a protein kinase-mediated disease in a patient by administering to the patient the compound of claim 1 ,
wherein the protein kinase is selected from JAK1, JAK2, Aurora A, Aurora B and FLT3, and
wherein the disease is a cancer selected from head and neck cancer, prostate cancer, breast cancer, ovarian cancer, melanoma, lung cancer, brain tumor, pancreatic cancer and renal carcinoma; or wherein the disease is selected from polycythemia vera, essential thrombocytosis, myelofibrosis, chronic myelogenous leukemia (CML), acute myeloid leukemia (AML), acute lymphocytic leukemia (ALL), chronic obstruction pulmonary disease (COPD), asthma, systemic lupus erythematosis, cutaneous lupus erythematosis, lupus nephritis, dermatomyositis, Sjogren's syndrome, psoriasis, type I diabetes mellitus, allergic airway disease, sinusitis, eczema, hives, food allergies, allergies to insect venom, inflammatory bowel syndrome, Chron's disease, rheumatoid arthritis, juvenile arthritis and psoriatic arthritis, or a graft-versus-host disease selected from organ transplant rejection, tissue transplant rejection and cell transplant rejection.
17. A method of managing, treating or lessening the severity of a protein kinase-mediated disease in a patient by administering to the patient the pharmaceutical composition of claim 14 ,
wherein the protein kinase is selected from JAK1, JAK2, Aurora A, Aurora B and FLT3, and
wherein the disease is a cancer selected from head and neck cancer, prostate cancer, breast cancer, ovarian cancer, melanoma, lung cancer, brain tumor, pancreatic cancer and renal carcinoma; or wherein the disease is selected from polycythemia vera, essential thrombocytosis, myelofibrosis, chronic myelogenous leukemia (CML), acute myeloid leukemia (AML), acute lymphocytic leukemia (ALL), chronic obstruction pulmonary disease (COPD), asthma, systemic lupus erythematosis, cutaneous lupus erythematosis, lupus nephritis, dermatomyositis, Sjogren's syndrome, psoriasis, type I diabetes mellitus, allergic airway disease, sinusitis, eczema, hives, food allergies, allergies to insect venom, inflammatory bowel syndrome, Chron's disease, rheumatoid arthritis, juvenile arthritis and psoriatic arthritis, or a graft-versus-host disease selected from organ transplant rejection, tissue transplant rejection and cell transplant rejection.
18. A method of inhibiting the activity of a protein kinase with the compound of claim 1 , wherein the protein kinase is JAK kinase, FLT3 kinase, Aurora kinase or a combination thereof.
19. A method of inhibiting the activity of a protein kinase with the pharmaceutical composition of claim 14 , wherein the protein kinase is JAK kinase, FLT3 kinase, Aurora kinase or a combination thereof.