HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 24771669, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 68615384 | HCID 68615384 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 24771669 | HCID 24771669 | 77.3% |
Reaction Steps
17.4 mg of sodium borohydride are added to a suspension, cooled to 0° C., of 157 mg of 6-benzoyl-N-phenylimidazo[1,2-a]pyridine-2-carboxamide in 10 ml of methanol. The reaction mixture is stirred for 16 hours, while allowing the temperature to rise to 20° C. 20 mg of sodium borohydride are added and the mixture is stirred at 20° C. for a further 1.5 hours. After evaporating to dryness, the residue is taken up in 50 ml of water and 200 ml of ethyl acetate. The organic phase is separated by settling, dried and concentrated to dryness under reduced pressure to give 122 mg of 6-[hydroxy(phenyl)methyl]-N-phenylimidazo[1,2-a]pyridine-2-carboxamide in the form of a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07704989B2 |
| Source dataset | uspto-grants-2010_04 |
| ORD ID | ord-acb39054d57943dcb9a27cb55f99cce4 |
| Source note | uspto-grants-2010_04 |