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 | 100.9% |
Reaction Steps
To a solution of 10 g (39 mmol) of the product of Step C in DMF (70 mL) at rt was added NaH (1.3 g of an 80% oil dispersion, 43 mmol). After 20 minutes benzyl bromide (5.15 mL, 43 mmol) was added and the reaction was stirred for 16 hours. The mixture was poured onto 500 g of ice and the solid residue was filtered, washed with water and air dried to give 13 g of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05374638 |
| Source dataset | uspto-grants-1994_12 |
| ORD ID | ord-50c613d085e14b20872999e3ef77e0c8 |
| Source note | uspto-grants-1994_12 |