HuagongsheHuagongshe Chemistry Print Report · For research reference only
Lithium borohydride → 6-Bromo-8-(2,6-dimethyl-4-fluorobenzylamino)-3-hydroxymethyl-2-methylimidazo[1,2-a]pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Lithium borohydride | HCID 4148881 | — |
| Reactant | 6-Bromo-3-carboethoxy-8-(2,6-dimethyl-4-fluorobenzylamino)-2-methylimidazo[1,2-a]pyridine | HCID 21717325 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 6-Bromo-8-(2,6-dimethyl-4-fluorobenzylamino)-3-hydroxymethyl-2-methylimidazo[1,2-a]pyridine | HCID 21717357 | 44.3% |
Reaction Steps
LiBH4 (70 mg) was added in portions and during 4 h to a refluxed solution of 6-bromo-3-carboethoxy-8-(2,6-dimethyl-4-fluorobenzylamino)-2-methylimidazo[1,2-a]pyridine (100 mg, 0.23 mmol) in THF. The reaction mixture was quenched by addition of diluted HCl and methylene chloride was added. The organic layer was separated, dried and evaporated in vacuo. The residue was purified by column chromatography on silica gel, using methylene chloride:ethyl acetate (100:10) as eluent to give 40 mg (44%) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06265415B1 |
| Source dataset | uspto-grants-2001_07 |
| ORD ID | ord-5f7e84c156db4b3cba044e5f36916c33 |
| Source note | uspto-grants-2001_07 |