Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1009067Generated: October 30, 2026

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

https://huagongshe.com/reaction/1009067

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-((2-(2,4-Difluorophenyl)-3-methyloxiran-2-yl)methyl)-1H-1,2,4-triazole, (2R-cis)-HCID 10131191—
Reactant5-Chloro-1',2',3',6'-tetrahydro-2,4'-bipyridineHCID 21105524—
ReactantLithium perchlorate trihydrateHCID 23708903—
SolventAcetonitrileHCID 6342—
Product(2R,3R)-3-(5-chloro-3',6'-dihydro-2,4'-bipyridin-1'(2'H)-yl)-2(2,4-difluorophenyl)-1-(1,2,4-triazol-1-yl)butan-2-olHCID 4453860663.8%

Reaction Steps

(2R,3S)-2-(2,4-Difluorophenyl)-3-methyl-2-(1H-1,2,4-triazol-1-ylmethyl)oxirane (0.76 g, 3.0 mmol) and 5-chloro-1′,2′,3′,6′-tetrahydro-2,4′-bipyridine (1.31 g, 6.7 mmol) were dissolved in acetonitrile (20 ml), and lithium perchlorate 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 0.88 g of the intended substance (yield 63.8%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07973056B2
Source datasetuspto-grants-2011_07
ORD IDord-3e3e30816abe4e6d94f4ba69de98aea9
Source noteuspto-grants-2011_07