HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sulfuric Acid → 5-Bromo-1-(4-fluorophenyl)-3-methyl-1,3-dihydro-benzimidazol-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| Reactant | 5-Bromo-1-(4-fluorophenyl)-1,3-dihydrobenzimidazol-2-one | HCID 59437201 | — |
| Solvent | Diglyme | HCID 8150 | — |
| Product | 5-Bromo-1-(4-fluorophenyl)-3-methyl-1,3-dihydro-benzimidazol-2-one | HCID 59437286 | 95.8% |
Reaction Steps
To a stirred room temperature suspension of 5-bromo-1-(4-fluorophenyl)-1,3-dihydro-benzimidazol-2-one (160 mg, 0.52 mmol) in anhydrous bis(2-methoxyethyl)ether (5 mL) was added lithium bis(trimethylsilyl)amide (0.55 mL of 1.06 M solution in THF, 0.58 mmol). After 30 minutes, methyl iodide (125 μL, 2 mmol) was added. After 2 hours, the mixture was poured into 1 N sulfuric acid containing ice. The resulting precipitate was filtered, washed with water, and dried to afford 160 mg of 5-bromo-1-(4-fluorophenyl)-3-methyl-1,3-dihydro-benzimidazol-2-one as an off-white solid. MS m/z 321/323 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08658637B2 |
| Source dataset | uspto-grants-2014_02 |
| ORD ID | ord-104da1b2cfac47e9a104beb41d3c2052 |
| Source note | uspto-grants-2014_02 |