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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 452773Generated: October 29, 2026

Methanol → 2-[5-[2-[[4-(Methylthio)phenyl]amino]-4-pyridyl]-1,3,4-oxadiazol-2-yl]propan-2-ol

https://huagongshe.com/reaction/452773

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantTetrahydrofuranHCID 8028—
ReactantSodium HydroxideHCID 14798—
Reactant1-Methyl-1-[5-[2-[[4-(methylthio)phenyl]amino]-4-pyridyl]-1,3,4-oxadiazol-2-yl]ethyl acetateHCID 68664373—
SolventEthyl AcetateHCID 8857—
Product2-[5-[2-[[4-(Methylthio)phenyl]amino]-4-pyridyl]-1,3,4-oxadiazol-2-yl]propan-2-olHCID 6866453736%

Reaction Steps

A mixture of 1-methyl-1-[5-[2-[[4-(methylthio)phenyl]amino]-4-pyridyl]-1,3,4-oxadiazol-2-yl]ethyl acetate (192 mg, 4.99 mmol), 1 M aqueous sodium hydroxide solution (5 mL), tetrahydrofuran (5 mL) and methanol (5 mL) was stirred at room temperature for 1.5 hr. The reaction mixture was diluted with ethyl acetate, washed with water and saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified by basic silica gel column chromatography (hexane/ethyl acetate=10/1-0/1) and recrystallized from hexane/ethyl acetate to give the title compound (61.2 mg, yield 36%) as yellow crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492378B2
Source datasetuspto-grants-2013_07
ORD IDord-1466ec0cb3e944c8bc17c97d957ebcd2
Source noteuspto-grants-2013_07