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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2048691Generated: November 2, 2026

Sodium borohydride → HCID 136063907, compound

https://huagongshe.com/reaction/2048691

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 136063899HCID 136063899—
SolventMethanolHCID 887—
ProductHCID 136063907HCID 13606390772.3%

Reaction Steps

To a solution (10 mL) of 4-[4-(1-hydroxyethyl)phenyl]-6-{[2′-(5-oxo-4,5-dihydro-1,2,4-oxadiazol-3-yl)biphenyl-4-yl]methyl}-7-propyl[1,2,4]triazolo[1,5-a]pyrimidin-5(4H)-one (0.05 g) in methanol was added sodium borohydride (0.039 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 (0.036 g, 72%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08592431B2
Source datasetuspto-grants-2013_11
ORD IDord-460de908d19b480a881f51c70ebb14ba
Source noteuspto-grants-2013_11