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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1766028Generated: October 31, 2026

Sodium borohydride → HCID 21108270, compound

https://huagongshe.com/reaction/1766028

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 21108120HCID 21108120—
SolventMethanolHCID 887—
ProductHCID 21108270HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07229986B2
Source datasetuspto-grants-2007_06
ORD IDord-a1a1082c10524d44875c94e2673b568e
Source noteuspto-grants-2007_06