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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 645369Generated: October 30, 2026

Sodium borohydride → HCID 24771669, compound

https://huagongshe.com/reaction/645369

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 68615384HCID 68615384—
SolventMethanolHCID 887—
ProductHCID 24771669HCID 2477166977.3%

Reaction Steps

17.4 mg of sodium borohydride are added to a suspension, cooled to 0° C., of 157 mg of 6-benzoyl-N-phenylimidazo[1,2-a]pyridine-2-carboxamide in 10 ml of methanol. The reaction mixture is stirred for 16 hours, while allowing the temperature to rise to 20° C. 20 mg of sodium borohydride are added and the mixture is stirred at 20° C. for a further 1.5 hours. After evaporating to dryness, the residue is taken up in 50 ml of water and 200 ml of ethyl acetate. The organic phase is separated by settling, dried and concentrated to dryness under reduced pressure to give 122 mg of 6-[hydroxy(phenyl)methyl]-N-phenylimidazo[1,2-a]pyridine-2-carboxamide in the form of a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07704989B2
Source datasetuspto-grants-2010_04
ORD IDord-acb39054d57943dcb9a27cb55f99cce4
Source noteuspto-grants-2010_04