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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 519437Generated: November 1, 2026

Sodium borohydride → HCID 67009846, compound

https://huagongshe.com/reaction/519437

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 67009035HCID 67009035—
SolventMethanolHCID 887—
ProductHCID 67009846HCID 67009846100%

Reaction Steps

To a solution (15 mL) of 4′-({4-[2-(4-fluorophenyl)-2-oxoethyl]-5-oxo-7-propyl-4,5-dihydro[1,2,4]triazolo[1,5-a]pyrimidin-6-yl}methyl)biphenyl-2-carbonitrile (0.78 g) in methanol was added sodium borohydride (0.12 g), and the mixture was stirred at room temperature for 1 hr. After evaporation of the solvent under reduced pressure, the residue was extracted with water and ethyl acetate. The obtained ethyl acetate layer was washed with saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography to give the title compound as a colorless solid (0.78 g, 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09115136B2
Source datasetuspto-grants-2015_08
ORD IDord-50b6341794364702b61903eede8606c4
Source noteuspto-grants-2015_08