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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1678756Generated: November 1, 2026

1,4-Dioxane hydrochloride → 2-(5-Piperidin-4-yl-4h-1,2,4-triazol-3-yl)-pyridine dihydrochloride

https://huagongshe.com/reaction/1678756

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-Dioxane hydrochlorideHCID 20443148—
ReactantHCID 178420141HCID 178420141—
SolventMethanolHCID 887—
SolventDiethyl EtherHCID 3283—
SolventAcetonitrileHCID 6342—
Product2-(5-Piperidin-4-yl-4h-1,2,4-triazol-3-yl)-pyridine dihydrochlorideHCID 178478534—

Reaction Steps

This material (2.68 g, 8.14 mmol) was suspended in 4 N HCl/dioxane. The stoppered reaction mixture was stirred at room temperature for 16 hours and then diluted with diethyl ether. The solids were isolated by filtration and the hygroscopic solid was digested in acetonitrile. This solid was isolated by filtration and partially dissolved in hot methanol. Upon cooling and addition of some ethyl ether to the solution 2-(3-piperidin-4-yl-1H-1,2,4-triazol-5-yl)pyridine slowly precipitated as the dihydrochloride salt. 1H NMR (500 MHz, DMSO-d6): δ 9.10 (1H, br s), 8.92 (1H, br s), 8.73 (1H, d, J=4.9 Hz), 8.10-8.20 (2H, m), 7.64 (1H, t, J=5.7 Hz), 3.33 (2H, br d, J=12.7 Hz), 3.16 (1H, m), 3.05 (2H, br q, J=11.9 Hz, J=21.8 Hz), 2.18 (2H, br d, J=11.5 Hz), 1.99 (2H, br q, j=11.0 Hz, J=22.2 Hz): m/e (m+1): 230.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08008317B2
Source datasetuspto-grants-2011_08
ORD IDord-bdc58db9c08f483d80c1cc1e750b67a1
Source noteuspto-grants-2011_08