HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 178511148, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 178511147 | HCID 178511147 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178511148 | HCID 178511148 | 73.7% |
Reaction Steps
To a suspension of 3-(2-(2-Phenylethyl)benzimidazol-4-yl)3-oxopropionitrile (400 mg) obtained in Inventive Example 25 in ethanol (4.8 mL), while cooling in an ice bath, was added sodium borohydride (26 mg), and the mixture was stirred at the same temperature for 1 hour. The reaction solution was poured into ice water (20 mL) and extracted with ethyl acetate. The organic layer was washed with water and brine and dried over anhydrous sodium sulfate, and then the solvent was evaporated under a reduced pressure. The resulting residue was crystallized from ether and collected by filtration to obtain the title compound as crystal (297 mg)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06387938B1 |
| Source dataset | uspto-grants-2002_05 |
| ORD ID | ord-f981225ebde54970b419a032cc8ef632 |
| Source note | uspto-grants-2002_05 |