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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1009062Generated: October 30, 2026

2-(Piperidin-4-yl)pyridine → (2R,3R)-2-(2,4-difluorophenyl)-3-(4-pyridin-2-ylpiperidin-1-yl)-1-(1,2,4-triazol-1-yl)butan-2-ol

https://huagongshe.com/reaction/1009062

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Piperidin-4-yl)pyridineHCID 10374750—
Reactant1-((2-(2,4-Difluorophenyl)-3-methyl-2-oxiranyl)methyl)-1H-1,2,4-triazoleHCID 14706449—
ReactantLithium perchlorate trihydrateHCID 23708903—
SolventAcetonitrileHCID 6342—
Product(2R,3R)-2-(2,4-difluorophenyl)-3-(4-pyridin-2-ylpiperidin-1-yl)-1-(1,2,4-triazol-1-yl)butan-2-olHCID 4453860128.9%

Reaction Steps

(2R,3R)-2-(2,4-Difluorophenyl-3-methyl-2-(1H-1,2,4-triazol-1-ylmethyl)oxirane (0.76 g, 3.0 mmol) and 2-(4-piperidyl)pyridine (4.3 g, 26.5 mmol) were dissolved in acetonitrile (50 ml), and lithium perchlorate trihydrate (4.25 g, 26.5 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 0.37 g of the intended substance (yield 28.9%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07973056B2
Source datasetuspto-grants-2011_07
ORD IDord-d4250cb97f7d475aa01a91b29924fb11
Source noteuspto-grants-2011_07