HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → HCID 25263632, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | HCID 86645986 | HCID 86645986 | — |
| Solvent | m-Chloroperbenzoic acid | HCID 70297 | — |
| Product | HCID 25263632 | HCID 25263632 | 67% |
Reaction Steps
To a solution of intermediate 15b (0.21 g, 0.62 mmol) in EtOAc (5 ml), m-CPBA was added (0.17 g, 0.97 mmol) and the resulting mixture was stirred at room temperature overnight. The reaction mixture was washed with water (2×10 ml) and anhydrous Na2SO4 and evaporated under vacuum to give a crude that, after purification by flash chromatography, afforded the pure 5-[(1R)-1-(4-{[4-(trifluoromethyl)-1,3-thiazol-2-yl]amino}phenyl)ethyl]-1H-1,2,4-triazol-1-ol (15) as a white solid (67%). [α]D=−35 (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 |
|---|---|
| Patent number | US08133911B2 |
| Source dataset | uspto-grants-2012_03 |
| ORD ID | ord-69f1b347659d478680965713adc2a1d4 |
| Source note | uspto-grants-2012_03 |