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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2356880Generated: October 31, 2026

Sodium borohydride → HCID 10271065, compound

https://huagongshe.com/reaction/2356880

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 9969824HCID 9969824—
SolventMethanolHCID 887—
SolventEthyl AcetateHCID 8857—
ProductHCID 10271065HCID 1027106554.4%

Reaction Steps

3-(2-Cyanophenyl)-5-(2-pyridyl)-1-(3-formylphenyl)-1,2-dihydropyridin-2-one (585 mg) was dissolved in 20 ml of methanol, 260 mg of sodium borohydride were added with ice cooling and the mixture was stirred at room temperature for one night. The reaction solution was diluted with ethyl acetate, washed with a saturated saline solution and dried over anhydrous magnesium sulfate. The drying agent was filtered off and the filtrate was concentrated in vacuo and purified by an NH silica gel column chromatography (ethyl acetate). The resulting crude crystals were recrystallized from ethyl acetate-diethyl ether to give 320 mg of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07759367B2
Source datasetuspto-grants-2010_07
ORD IDord-9044903a8860467e8263376aca21759a
Source noteuspto-grants-2010_07