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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 519952Generated: October 29, 2026

Sodium borohydride → HCID 136063907, compound

https://huagongshe.com/reaction/519952

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 numberUS09115136B2
Source datasetuspto-grants-2015_08
ORD IDord-80b3b83063604e269094e70013239823
Source noteuspto-grants-2015_08