Pyrazolopyrimidine Derivatives Useful as Inhibitors of Bruton's Tyrosine Kinase
US-2019119281-A1 · Apr 25, 2019 · US
US12220401B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-12220401-B2 |
| Application number | US-202318362249-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jul 31, 2023 |
| Priority date | Dec 16, 2015 |
| Publication date | Feb 11, 2025 |
| Grant date | Feb 11, 2025 |
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This invention relates to novel compounds. The compounds of the invention are tyrosine kinase inhibitors. Specifically, the compounds of the invention are useful as inhibitors of Bruton's tyrosine kinase (BTK). The invention also contemplates the use of the compounds for treating conditions treatable by the inhibition of Bruton's tyrosine kinase, for example cancer, lymphoma, leukemia and immunological diseases.
Opening claim text (preview).
The invention claimed is: 1. A compound of the formula: wherein * indicates a chiral center, or a pharmaceutically acceptable salt thereof. 2. A pharmaceutical composition, wherein the pharmaceutical composition comprises a compound of the formula: wherein * indicates a chiral center, or a pharmaceutically acceptable salt thereof, and pharmaceutically acceptable excipients. 3. A method of treating a condition which is modulated by BTK in a patient in need thereof comprising administering to the patient a compound of the formula: wherein * indicates a chiral center, or a pharmaceutically acceptable salt thereof. 4. The method according to claim 3 wherein the condition modulated by BTK is cancer, lymphoma, leukemia, autoimmune diseases, inflammatory disorders, heteroimmune conditions, or fibrosis. 5. The method according to claim 4 wherein the condition modulated by BTK is selected from B-cell malignancy, B-cell lymphoma, diffuse large B cell lymphoma, chronic lymphocytic leukemia, non-Hodgkin lymphoma, ABC-DLBCL, mantle cell lymphoma, follicular lymphoma, hairy cell leukemia, B-cell non-Hodgkin lymphoma, Waldenstrom's macroglobulinemia, multiple myeloma, bone cancer, bone metastasis, arthritis, multiple sclerosis, osteoporosis, irritable bowel syndrome, inflammatory bowel disease, Crohn's disease, Sjögren's syndrome, and lupus. 6. The method according to claim 5 wherein the condition modulated by BTK is selected from arthritis, multiple sclerosis, osteoporosis, irritable bowel syndrome, inflammatory bowel disease, Crohn's disease, and lupus.
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