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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1009069Generated: November 2, 2026

1-((2-(2,4-Difluorophenyl)-3-methyloxiran-2-yl)methyl)-1H-1,2,4-triazole, (2R-cis)- → (2R,3R)-2-(2,4-difluorophenyl)-3-(5',6'-dihydro-2,3'-bipyridin-1'(2'H)-yl)-1-(1,2,4-triazol-1-yl)butan-2-ol

https://huagongshe.com/reaction/1009069

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-((2-(2,4-Difluorophenyl)-3-methyloxiran-2-yl)methyl)-1H-1,2,4-triazole, (2R-cis)-HCID 10131191—
Reactant2-(1,2,5,6-Tetrahydropyridin-3-yl)pyridineHCID 18328010—
ReactantLithium perchlorate trihydrateHCID 23708903—
SolventAcetonitrileHCID 6342—
Product(2R,3R)-2-(2,4-difluorophenyl)-3-(5',6'-dihydro-2,3'-bipyridin-1'(2'H)-yl)-1-(1,2,4-triazol-1-yl)butan-2-olHCID 4453871561.9%

Reaction Steps

(2R,3S)-2-(2,4-Difluorophenyl)-3-methyl-2-(1H-1,2,4-triazol-1-ylmethyl)oxirane (0.83 g, 3.3 mmol) and 1′,2′,5′,6′-tetrahydro-2,3′-bipyridine (3.51 g, 21.9 mmol) were dissolved in acetonitrile (50 ml), and lithiumperchlorate trihydrate (1.50 g, 9.3 mmol) was added thereto and refluxed for 40 hours. The solvent was evaporated under a reduced pressure, and the thus obtained residue was dissolved in ethyl acetate and washed with water. The solvent was again evaporated under a reduced pressure, and the residue was purified using a silica gel column to obtain 0.87 g of the intended substance (yield 61.9%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07973056B2
Source datasetuspto-grants-2011_07
ORD IDord-686c51868abe4795a54c5eb1c1eaef21
Source noteuspto-grants-2011_07