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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1171066Generated: November 2, 2026

1H-1,2,4-Triazole → HCID 68770387, compound

https://huagongshe.com/reaction/1171066

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1H-1,2,4-TriazoleHCID 9257—
Reactant2,6-DifluorobenzonitrileHCID 74695—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
SolventDichloromethane methanolHCID 21226129—
ProductHCID 68770387HCID 68770387—

Reaction Conditions

Temperature50 °C

Reaction Steps

A mixture of 2,6-difluoro-benzonitrile (10.34 g, 74.4 mmol), 1H-[1,2,4]triazole (5.34 g, 77.4 mmol), and CsCO3 (25.19 g, 77.4 mmol) in DMSO (30 mL) was stirred at ˜50° C. for 24 h. The yellowish easily stirred slurry was then diluted with water (200 mL), stirred at rt for 15 min, and filtered. The filter cake was washed with water (1×100 mL) and the filter cake was then partitioned with water (100 mL) and DCM (200 mL). The aqueous layer was extracted with DCM (1×300 mL), and the organic layers were combined, washed with 4 M NaCl (1×100 mL), dried (Na2SO4), and concentrated under vacuum at 90° C. to provide the crude title compound as an off-white solid (8.96 g). A portion of this crude material (3.33 g) was dissolved in DCM/MeOH, silica gel (8.5 g) was added, and the mixture was concentrated to a free-flowing powder. The silica-adsorbed crude title compound was applied to a silica flash column (40 mm×6″) and eluted with EtOAc to afford the title compound as a white solid [1.60 g, 31% (calculated from chromatographic purification of a portion of the crude material)].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07829584B2
Source datasetuspto-grants-2010_11
ORD IDord-cd974fcc38144de596fffb5c65638a4e
Source noteuspto-grants-2010_11