HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → 4-(2,6-Dimethyl-4-fluorobenzylamino)-2,2-dimethylbenzimidazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 178432169 | HCID 178432169 | — |
| Catalyst | Tetrabutylammonium Bromide | HCID 74236 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | 4-(2,6-Dimethyl-4-fluorobenzylamino)-2,2-dimethylbenzimidazole | HCID 86758570 | 76.9% |
Reaction Steps
4-(2,6-Dimethyl-4-fluorobenzylamino)-2-methylbenzimidazole (0.1 g, 0.35 mmol) was dissolved in 1,2-dimethoxyethane (3 ml). Solid sodium hydroxide (25 mg, 0.63 mmol) and tetrabutylammonium bromide (5 mg, 0.016 mmol) were added. The mixture was stirred 15 minutes at ambient temperature. Methyl iodide (60 mg 0.42 mmol) was added and the reaction mixture was stirred at ambient temperature for 2.5 h. The solvent was evaporated under reduced pressure. The residue was purified by column chromatography on silica gel, using methylene chloride: ethyl acetate (50: 50) as eluent. 80 mg (76%) of the title compound was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06465505B1 |
| Source dataset | uspto-grants-2002_10 |
| ORD ID | ord-31147a9adb5e4e65967c3cea1f444ef4 |
| Source note | uspto-grants-2002_10 |