HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromhydrol → HCID 178454507, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromhydrol | HCID 166749 | — |
| Reactant | HCID 178489123 | HCID 178489123 | — |
| Solvent | Ethanethiol | HCID 6343 | — |
| Product | HCID 178454507 | HCID 178454507 | 39.3% |
Reaction Steps
To a solution of 118 mg (0.29 mmol) of N-[5-(4-Methoxy-phenyl)-4H-[1,2,4]triazol-3-yl]-2-methyl-2-(tetrahydro-pyran-4-sulfonyl)-propionamide in ethanethiol (5 mL) are added 750 mg (2.9 mmol) of aluminium tribromide. The reaction is stirred at room temperature for 20 h. The reaction is quenched by addition of 12M aqueous HCl solution (2 mL) and diluted with water (10 mL). The aqueous layer is extracted with ethyl acetate (3×20 mL). The combined organic extracts are dried over Na2SO4, filtered and the filtrate is concentrated under reduced pressure. The residual solid is washed with DCM to afford 45 mg of N-[5-(4-hydroxy-phenyl)-4H-[1,2,4]triazol-3-yl]-2-methyl-2-(tetrahydro-pyran-4-sulfonyl)-propionamide. Yield: 38%, ES-MS: m/z 395 [M+H].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08048899B2 |
| Source dataset | uspto-grants-2011_11 |
| ORD ID | ord-88f1c31e943b4215bce216d4a6e7e26d |
| Source note | uspto-grants-2011_11 |