Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2048177Generated: November 2, 2026

Sodium borohydride → HCID 67009846, compound

https://huagongshe.com/reaction/2048177

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 numberUS08592431B2
Source datasetuspto-grants-2013_11
ORD IDord-10fc05c2be944bb18587b6a8f2d4bfe8
Source noteuspto-grants-2013_11