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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1616224Generated: November 3, 2026

Sodium borohydride → HCID 86691836, compound

https://huagongshe.com/reaction/1616224

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 86691837HCID 86691837—
SolventMethanolHCID 887—
ProductHCID 86691836HCID 86691836—

Reaction Steps

To a microwave vial was added 5-(5-acetyl-2-methylphenyl)-1-(2,2-dimethylpropyl)-3-methyl-1,3-dihydro-2H-imidazo[4,5-b]pyridin-2-one (15-7) (15 mg, 0.043 mmol) and sodium borohydride (2.5 mg, 0.064 mmol) under nitrogen. The mixture was dissolve in methanol (0.4 ml), and allowed to stir at room temperature for 1 hour. The reaction was diluted with methanol, and passed through a syringe filter. The solution was purified using reverse phase chromatography (10-100%, 0.1% TFA in H2O/Acetonitrile) and the desired fractions were collected and concentrated to produce 1-(2,2-dimethylpropyl)-5-{5-[(1S)-1-hydroxyethyl]-2-methylphenyl}-3-methyl-1,3-dihydro-2H-imidazo[4,5-b]pyridin-2-one (25-1). HRMS (M+H)+: observed=354.2178, calculated=354.2176.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08765784B2
Source datasetuspto-grants-2014_07
ORD IDord-9db0416204f643b5afa3dac831dccd87
Source noteuspto-grants-2014_07