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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1158996Generated: October 27, 2026

1H-Indazole → 2-(2,4-Difluorophenyl)-1-(2H-indazol-1-yl)-3-(1H-1,2,4-triazol-1-yl)propan-2-ol

https://huagongshe.com/reaction/1158996

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1H-IndazoleHCID 9221—
ReactantSodium hydrideHCID 24758—
Reactant1-(2-(2,4-Difluorophenyl)-2,3-epoxypropyl)-1H-1,2,4-triazoleHCID 10130921—
SolventDimethylformamideHCID 6228—
Product2-(2,4-Difluorophenyl)-1-(2H-indazol-1-yl)-3-(1H-1,2,4-triazol-1-yl)propan-2-olHCID 6864424444%

Reaction Steps

To a suspension of Indazole (0.27 g, 2.32 mmol) in N, N-dimethylformamide (10 ml) was slowly added sodium hydride (0.093 g, 2.32 mmol) at 0° C., followed by stirring for 30 min and then for an additional 30 min at room temperature. Then, 1-((2-(2,4-difluorophenyl)oxiran-2-yl)methyl)-1H-1,2,4-triazole (0.50 g, 2.11 mmol) was added, followed by stirring for 2 hrs at 60° C. The reaction was quenched with the addition of water (1 ml) at 0° C. Following dilution with ethyl acetate (20 ml), the reaction mixture was washed with saturated ammonium chloride solution (20 ml) and then with brine (20 ml). The organic layer was dried over anhydrous magnesium sulfate and concentrated by evaporation in a vacuum condition. The product was purified by chromatography on silica gel to give the title compound (Yield 44%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07812045B2
Source datasetuspto-grants-2010_10
ORD IDord-9e257a9ff2b34a68b5bf515e68524f44
Source noteuspto-grants-2010_10