HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 18442933, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 18442934 | HCID 18442934 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 18442933 | HCID 18442933 | — |
Reaction Steps
A solution of sodium borohydride (7.7 mg) in ethanol (1 ml) was added to a solution of N-[1-(3-[3,4-difluorophenyl]-3-ketopropyl)-piperidin-4-yl]-N-ethyl-4-methanesulphonylphenylacetamide (0.25 g) in ethanol (3.2 ml) at 0° C. under argon and the reaction allowed to warm to room temperature over 20 hours. The reaction was quenched with brine, extracted three times with ether and the combined extracts dried. The filtrate was then concentrated to a clear oil, yield 0.21 g. MS (MH+) 495.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07192973B2 |
| Source dataset | uspto-grants-2007_03 |
| ORD ID | ord-0c18c74e721540958fa5b6afa2794113 |
| Source note | uspto-grants-2007_03 |