HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → HCID 58459243, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Potassium hydroxy sulfite | HCID 23707502 | — |
| Reactant | HCID 58459162 | HCID 58459162 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 58459243 | HCID 58459243 | — |
Reaction Steps
To a mixture of N-(1-(6-fluoro-1-(2-(methylthio)phenyl)-1H-benzo[d]imidazol-2-yl)ethyl)acetamide (1.1697 g, 3.41 mmol) in THF (25.5 mL) and water (8.52 mL) was added oxone (5.23 g, 8.52 mmol) and the mixture was stirred at rt. After 48 h, to the mixture was added water (50 mL), extracted with DCM (50 mL×2). The combined organic layers were dried over Na2SO4, filtered, combined with the white solid, and concentrated under reduced pressure to give N-(1-(6-fluoro-1-(2-(methylsulfonyl)phenyl)-1H-benzo[d]imidazol-2-yl)ethyl)acetamide as an orange solid: LC-MS (ESI) m/z 376.0 [M+H]+. The orange solid was carried on crude without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08575183B2 |
| Source dataset | uspto-grants-2013_11 |
| ORD ID | ord-53a69967e3c04936bbb1bda3fd56540b |
| Source note | uspto-grants-2013_11 |