Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Bromo-4-(trifluoromethyl)pyridine | HCID 2781543 | — |
| Reactant | HCID 21897507 | HCID 21897507 | — |
| Product | HCID 21897585 | HCID 21897585 | 32% |
Reaction Steps
A mixture of [1-(4-methanesulfonyl-phenyl)-1H-pyrazolo[3,4-d]pyrimidin-4-yl]-piperidin-4-yl-amine (100 mg, 0.24 mmol), 2-bromo-4-trifluoromethylpyridine (166 mg, 0.73 mmol), and potassium carbonate (102 mg, 0.73 mmol) in DMF (1.0 mL) was heated under microwave irradiation for 20 minutes at 165° C. The crude mixture was purified by HPLC to provide compound A128 as a white solid (41 mg, 32%). Exact mass calculated for C23H22F3N7O2S 517.15, found 518.2 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07625906B2 |
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| Source dataset | uspto-grants-2009_12 |
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| ORD ID | ord-b985d79eada04b1a997d3021b5118fe7 |
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| Source note | uspto-grants-2009_12 |
|---|