HuagongsheHuagongshe Chemistry Print Report · For research reference only
Lithium borohydride → HCID 25269402, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Lithium borohydride | HCID 4148881 | — |
| Reactant | HCID 24808505 | HCID 24808505 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 25269402 | HCID 25269402 | — |
Reaction Steps
To a solution of ethyl 5-[(adamantan-1-ylmethyl)carbamoyl]imidazo[1,2-a]pyridine-2-carboxylate (7.0 g, 18.35 mmol) in THF (100 mL) at RT, is added portion-wise LiBH4 (799 mg, 36.7 mmol). The resulting mixture is stirred at RT for 16 h. The reaction is quenched by the slow addition of water, followed by the addition of EtOAc. The organic layer is separated, and the aqueous layer is back extracted with EtOAc. The combined organic layers are washed with water and brine, dried over sodium sulfate, and concentrated. The yellow solid is purified by re-crystallization from DCM to give the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08431593B2 |
| Source dataset | uspto-grants-2013_04 |
| ORD ID | ord-478337a85d3f41a092e3523792924270 |
| Source note | uspto-grants-2013_04 |