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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 368899Generated: October 26, 2026

1H-1,2,4-Triazole → (2S,3R)-2-(2,4-difluorophenyl)-1-(1H-1,2,4-triazol-1-yl)butane-2,3-diol

https://huagongshe.com/reaction/368899

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1H-1,2,4-TriazoleHCID 9257—
ReactantPotassium CarbonateHCID 11430—
Reactant(2S,3R)-1,2-Epoxy-2-(2,4-difluorophenyl)butan-3-olHCID 10867332—
SolventDimethylformamideHCID 6228—
Product(2S,3R)-2-(2,4-difluorophenyl)-1-(1H-1,2,4-triazol-1-yl)butane-2,3-diolHCID 981685138%

Reaction Conditions

Temperature80 °C

Reaction Steps

To an ice cooled suspension of anhydrous K2CO3 (0.691 g, 0.005 mole) in N,N-dimethylformamide (7 ml), 1H-1,2,4-triazole (0.345, 0.005 mole) was added in small portions under art atmosphere of nitrogen. The mixture was slowly brought to room temperature and a solution of compound 7c (2R, 3S)-3-(2,4-Difluorophenyl)-3,4-epoxy-2-butanol (0.5 g, 0.0025 mole) in N,N-dimethylformamide (1 ml) was added. The resulting mixture was heated at 80° C. for 2 hours. The solvent was removed under reduced pressure and 25 g of crushed ice was added to the residue. The so formed mixture was extracted with ethyl acetate (50 ml, 2×25 ml). The combined organic layers were washed with water (10 ml) brine (25 ml) and dried over MgSO4. The solvent was removed in vacuo and the residue was chromatographed on silica gel. Elution with methanol in chloroform (0% -3%) gave the title compound 9c as an amorphous solid (0.26 g, 38%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06133485
Source datasetuspto-grants-2000_10
ORD IDord-feb19ed6c85c434cbda9a14ba43464e7
Source noteuspto-grants-2000_10