HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 22736932, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 6-{[4-Hydroxy-4-(3-methoxyphenyl)-1-piperidinyl]acetyl}-3,4-dihydroquinolin-2(1h)-one | HCID 22736940 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 22736932 | HCID 22736932 | 69% |
Reaction Steps
To a stirred solution of sodium borohydride (1.15 g, 30.3 mmol) in ethanol (100 ml) was added suspension of 6-{[4-Hydroxy-4-(3-methoxyphenyl)-1-piperidinyl]acetyl}-3,4-dihydroquinolin-2(1H)-one (5.98 g, 15.2 mmol) in ethanol (40 ml) at 0° C. and the reaction mixture was stirred at room temperature overnight. The precipitate was filtered and added to methanol (20 ml). The precipitate was collected by filtration to afford the title compound (4.13 g, 69%) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06713490B2 |
| Source dataset | uspto-grants-2004_03 |
| ORD ID | ord-de7cfd67a4e444bfa6aef484216011e4 |
| Source note | uspto-grants-2004_03 |