HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 21108270, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 21108120 | HCID 21108120 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 21108270 | HCID 21108270 | — |
Reaction Steps
Sodium borohydride (81 mg, 2.14 mmol) was added to a suspension of 4-[4-(4-chlorophenyl)-1-piperidinyl]-1-(3-isopropyl-2,3,4,5-tetrahydro-1H-3-benzazepin-7-yl)-4-oxo-1-butanone (0.50 g, 1.07 mmol) obtained in Example 30 in methanol (20 mL), and the mixture was stirred at room temperature for 30 minutes. The reaction solution was concentrated under reduced pressure, and the residues were partitioned into ethyl acetate and water. The ethyl acetate layer was washed with a saturated saline solution and dried over magnesium sulfate. The solvent was distilled away under reduced pressure, whereby the title compound was obtained as amorphous powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07229986B2 |
| Source dataset | uspto-grants-2007_06 |
| ORD ID | ord-a1a1082c10524d44875c94e2673b568e |
| Source note | uspto-grants-2007_06 |