HuagongsheHuagongshe Chemistry Print Report · For research reference only
Lithium borohydride → HCID 25269405, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Lithium borohydride | HCID 4148881 | — |
| Reactant | HCID 25269403 | HCID 25269403 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 25269405 | HCID 25269405 | — |
Reaction Steps
To a solution of {5-[(adamantan-1-ylmethyl)-carbamoyl]-imidazo[1,2-a]pyridin-2-yl}-acetic acid ethyl ester (65 mg, 0.16 mmol) in THF (5 mL) at RT, is added portion-wise LiBH4 (10 mg, 0.46 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. Purification of the residue by PTLC (10% MeOH in DCM) the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08431593B2 |
| Source dataset | uspto-grants-2013_04 |
| ORD ID | ord-5d889f316b174595a6f67b804dbe6012 |
| Source note | uspto-grants-2013_04 |