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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 452682Generated: October 30, 2026

Sodium Hydroxide → 5-[5-[[3-(trifluoromethyl)benzyl]thio]-1,3,4-oxadiazol-2-yl]-1H-indazole

https://huagongshe.com/reaction/452682

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant3-(Trifluoromethyl)benzyl chlorideHCID 69716—
ReactantHCID 178527939HCID 178527939—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product5-[5-[[3-(trifluoromethyl)benzyl]thio]-1,3,4-oxadiazol-2-yl]-1H-indazoleHCID 6866384974.1%

Reaction Steps

To a solution of 5-(1H-indazol-5-yl)-1,3,4-oxadiazole-2-thiol (218 mg, 1.00 mmol) and 1 M aqueous sodium hydroxide solution (1.00 mL, 1.00 mmol) in N,N-dimethylformamide (5 mL) was added 3-(trifluoromethyl)benzyl chloride (0.155 mL, 1.00 mmol) at room temperature, and the resulting mixture was stirred overnight. The reaction mixture was diluted with ethyl acetate, washed with water and saturated brine, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was purified by basic silica gel column chromatography (tetrahydrofuran) and recrystallized from methanol to give the title compound (279 mg, yield 74%) as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492378B2
Source datasetuspto-grants-2013_07
ORD IDord-570f80a1681649abb48b6ead548c350f
Source noteuspto-grants-2013_07