HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 21905518, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 21904933 | HCID 21904933 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 21905518 | HCID 21905518 | 82.2% |
Reaction Steps
To a suspension of (RS)-N-(4-cyano-benzyl)-2-(3,5-difluoro-2′-formyl-biphenyl-4-yl)-2-ethoxy-acetamide (500 mg) in EtOH (1.2 ml) at 0° C. was added sodium borohydride (91 mg). After 5 min the ice bath was removed. Ice water was added and the mixture was extracted with EtOAc. The organic phase was dried, filtered and concentrated. The product was purified by chromatography (SiO2, cyclohexane/EtOAc 1:2=>EtOAc) to give (RS)-N-(4-cyano-benzyl)-2-(3,5-difluoro-2′-hydroxymethyl-biphenyl-4-yl)-2-ethoxy-acetamide (413 mg). Colorless solid. MS 437.0 ([M+H]+)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07129238B2 |
| Source dataset | uspto-grants-2006_10 |
| ORD ID | ord-2595bfdc9e1e489e889959023a3fbda5 |
| Source note | uspto-grants-2006_10 |