HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → 3-Benzyl-5-bromo-2-ethyl-7-methylimidazo[4,5-b]pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 5-Bromo-2-ethyl-7-methyl-1H-imidazo[4,5-b]pyridine | HCID 19385648 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-Benzyl-5-bromo-2-ethyl-7-methylimidazo[4,5-b]pyridine | HCID 19385661 | — |
Reaction Steps
To a solution of 5-bromo-2-ethyl-7-methylimidazo[4,5-b]pyridine (10 g, 39 mmol) in DMF (70 mL) at room temperature was added NaH (1.3 g of an 80% dispersion, 43 mmol). After 20 min benzyl bromide (5.15 mL, 43 mmol) was added and the reaction was stirred for 16 h. The mixture was poured onto 500 g of ice and the solid residue was filtered, washed with water and air dried to afford 3-benzyl-5-bromo-2-ethyl-7-methylimidazo[4,5-b]pyridine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05412097 |
| Source dataset | uspto-grants-1995_05 |
| ORD ID | ord-bc4654fcb7834a6b9ddb49d96b3fda2b |
| Source note | uspto-grants-1995_05 |