HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → (S)-N-{3-[4-(4-hydroxy-3,3-dimethyl-piperidin-1-yl)-3-fluorophenyl]-2-oxo-oxazolidin-5-ylmethyl}-acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 59754027 | HCID 59754027 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (S)-N-{3-[4-(4-hydroxy-3,3-dimethyl-piperidin-1-yl)-3-fluorophenyl]-2-oxo-oxazolidin-5-ylmethyl}-acetamide | HCID 11291908 | 78% |
Reaction Steps
The title compound was prepared by reacting (S)-N-{3-[4-(4-oxo-3,3-dimethyl-piperidin-1-yl)-3-fluoro-phenyl]-2-oxo-oxazolidin-5-ylmethyl}-acetamide (1.0 mmol), with sodiumborohydride (1.2 mmol)) methanol (10 ml) at a temperature 0-25° C. for 2 hours in 78% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07687627B2 |
| Source dataset | uspto-grants-2010_03 |
| ORD ID | ord-eadc9a9c6ebe41e39f94721e9315c400 |
| Source note | uspto-grants-2010_03 |