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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 215967Generated: October 29, 2026

Sodium borohydride → HCID 59176789, compound

https://huagongshe.com/reaction/215967

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant3-[1-Naphthalen-1-yl-methylidene]-imidazo[1,2-a]pyridin-2-oneHCID 68699547—
SolventEthanolHCID 702—
SolventMethanolHCID 887—
ProductHCID 59176789HCID 59176789—

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a suspension of 137 mg (3.7 mmol) of sodium borohydride in 15 mL of ethanol is added a solution of 500 mg (1.8 mmol) of 3-[1-naphthalen-1-yl-methylidene]-imidazo[1,2-a]pyridin-2-one in 50 mL of methanol, dropwise at −78° C. After stirring for 10 min at −78° C., the reaction mixture is quenched with saturated aqueous ammonium chloride solution at −78° C. The product is extracted with dichloromethane. The organic layer is dried over magnesium sulfate, filtered and concentrated in vacuo to give the desired compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08193214B2
Source datasetuspto-grants-2012_06
ORD IDord-22fb3b9ad2bc48f99a18ffab9dce5bc0
Source noteuspto-grants-2012_06