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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1718834Generated: October 31, 2026

Pyridine → 3-[2-[4-[[4-butyl-1-[(2Z)-3,3-dimethyl-2-propan-2-yloxyiminobutyl]-2-methyl-6-oxopyrimidin-5-yl]methyl]-3-fluorophenyl]phenyl]-4H-1,2,4-oxadiazol-5-one

https://huagongshe.com/reaction/1718834

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantO-(propan-2-yl)hydroxylamine hydrochlorideHCID 12696235—
Reactant6-butyl-3-(3,3-dimethyl-2-oxobutyl)-5-{[3-fluoro-2'-(5-oxo-4,5-dihydro-1,2,4-oxadiazol-3-yl)biphenyl-4-yl]methyl}-2-methylpyrimidin-4(3H)-oneHCID 136026990—
SolventEthyl AcetateHCID 8857—
Product3-[2-[4-[[4-butyl-1-[(2Z)-3,3-dimethyl-2-propan-2-yloxyiminobutyl]-2-methyl-6-oxopyrimidin-5-yl]methyl]-3-fluorophenyl]phenyl]-4H-1,2,4-oxadiazol-5-oneHCID 13614690122%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 6-butyl-3-(3,3-dimethyl-2-oxobutyl)-5-{[3-fluoro-2′-(5-oxo-4,5-dihydro-1,2,4-oxadiazol-3-yl)biphenyl-4-yl]methyl}-2-methylpyrimidin-4(3H)-one (0.15 g), 2-(aminooxy)propane hydrochloride (0.63 g) and pyridine (5 mL) was stirred at 100° C. for 16 hr. The mixture was allowed to cool to room temperature, and the reaction mixture was diluted with ethyl acetate, washed with 1 M hydrochloric acid and then with saturated brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography to give the title compound as a colorless amorphous solid (0.036 g, 22%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07803940B2
Source datasetuspto-grants-2010_09
ORD IDord-665263da40a744eaa9d4b0f72c8bc794
Source noteuspto-grants-2010_09