Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | HCID 86645974 | HCID 86645974 | — |
| Product | HCID 25265727 | HCID 25265727 | 67% |
Reaction Steps
To a solution of N-{4-[(1R)-1-(1H-pyrazol-5-yl)ethyl]phenyl}-4-(trifluoromethyl)-1,3-thiazol-2-amine (0.421 g, 1.24 mmol) in EtOAc (5 mL) m-CPBA (256 mg, 1.5 mmol) was added and the resulting mixture was stirred at room temperature overnight. The crude was diluted with EtOAc (10 ml), washed with water (2×10 ml) and dried over anhydrous Na2SO4. After solvent evaporation, the crude was purified by flash chromatography to give the pure 5-[(1R)-1-(4-{[4-(trifluoromethyl)-1,3-thiazol-2-yl]amino}phenyl)ethyl]-1H-pyrazol-1-ol (7) (0.295 g, 0.65 mmol) as a white solid (67%). [α]D=−28 (c=0.82; CH3OH); 1H-NMR (CD3OD): δ 9.40 (bs, 1H, NH); 7.55 (d, 1H, J=2.5 Hz); 7.40 (d, 2H, J=7 Hz); 7.35 (d, 2H, J=7 Hz); 7.15 (s, 1H), 6.25 (d, 1H, J=2.4 Hz); 3.80 (q, 1H, J=7 Hz); 1.60 (d, 3H, J=7 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08133911B2 |
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| Source dataset | uspto-grants-2012_03 |
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| ORD ID | ord-ace79fab50864477a32c3f681dd54336 |
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| Source note | uspto-grants-2012_03 |
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