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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 458954Generated: October 30, 2026

Sodium borohydride → HCID 18442933, compound

https://huagongshe.com/reaction/458954

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 18442934HCID 18442934—
SolventEthanolHCID 702—
ProductHCID 18442933HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07192973B2
Source datasetuspto-grants-2007_03
ORD IDord-0c18c74e721540958fa5b6afa2794113
Source noteuspto-grants-2007_03