HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → Imidazo[1,5-a]pyridin-8-ylmethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | ethyl 3H-imidazo[4,5-b]pyridine-2-carboxylate | HCID 13353748 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Imidazo[1,5-a]pyridin-8-ylmethanol | HCID 10351843 | — |
Reaction Steps
To a cold solution of lithium aluminum hydride (1.0 g, 26.3 mmol, 2.0 eq) in THF (40 mL) was added the crude ethyl imidazopyridine carboxylate (2.5 g, 13.2 mmol, 1.0 eq) and the reaction mixture was stirred at rt for 2 h. Reaction was cooled and water (1.7 mL), 15% NaOH (1.7 mL) and water (5.1 mL) were slowly added. Solution was next diluted with excess EtOAc and stirred at rt for 30 min. The solution was filtered and the solid was washed with ethyl acetate. Organic layers were combined, dried and solvent was removed to give crude imidazo[1,5-a]pyridine-8-methanol, which was purified by column chromatography (EtOAc/Hexane). MS: exact mass calculated for C8H8N2O, 148.06; m/z found, 149 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09018210B2 |
| Source dataset | uspto-grants-2015_04 |
| ORD ID | ord-62aeadd3de064a23bf3ed4c459f1bd6c |
| Source note | uspto-grants-2015_04 |