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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 33506Generated: October 26, 2026

Water → 2-[4-(4-[1,2,3]Triazol-1-yl-butyl)-phenoxymethyl]-6-(4-trifluoromethyl-phenyl)-pyridine

https://huagongshe.com/reaction/33506

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
Reactant4-(4-[1,2,3]Triazol-1-yl-butyl)phenolHCID 12109494—
Reactant2-Chloromethyl-6-(4-trifluoromethyl-phenyl)-pyridineHCID 69106617—
SolventDimethylformamideHCID 6228—
Product2-[4-(4-[1,2,3]Triazol-1-yl-butyl)-phenoxymethyl]-6-(4-trifluoromethyl-phenyl)-pyridineHCID 1606558160.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

16 mg (0.39 mmol) of 60% sodium hydride were added at 0° C. to a solution of 80 mg (0.37 mmol) 4-(4-[1,2,3]triazol-1-yl-butyl)-phenol in 4.0 ml N,N-dimethylformamide and stirred for 30 min. at 0° C. 100 mg (0.37 mmol) 2-chloromethyl-6-(4-trifluoromethyl-phenyl)-pyridine (WO 2004/007439) were given to the reaction mixture and stirring continued at r.t for 2 days. After addition of 8 ml water the mixture was stirred for 1 h, the formed precipitate isolated by filtration, washed with water, methanol/water 1:1, and a small amount of ether. The residue was dried at 40° C. to give 101 mg (60%) of the title compound as white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07429605B2
Source datasetuspto-grants-2008_09
ORD IDord-cbad8edbeb3c4836b5af369697c463a0
Source noteuspto-grants-2008_09