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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2239593Generated: October 30, 2026

Hydrochloric Acid → 1-[5-(Trifluoromethyl)pyridin-2-yl]piperidin-4-amine dihydrochloride

https://huagongshe.com/reaction/2239593

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTert-butyl {1-[5-(trifluoromethyl)pyridin-2-yl]piperidin-4-yl}carbamateHCID 86625881—
Solvent1,4-DioxaneHCID 31275—
SolventDioxane tetrahydrofuranHCID 22018518—
Product1-[5-(Trifluoromethyl)pyridin-2-yl]piperidin-4-amine dihydrochlorideHCID 6724347289%

Reaction Steps

A mixture of tert-butyl {1-[5-(trifluoromethyl)pyridin-2-yl]piperidin-4-yl}carbamate (1.27 g, 3.68 mmol) in HCl in Dioxane/THF (4M, 1:1; 10 ml) was stirred at rt. After 6.5 h more HCl in Dioxane (4M, 2 ml) was added and the resulting mixture stirred for a further 18 h. The mixture was filtered and the residue was washed with EtOAc to give the title compound (1.04 g, 89%) as a solid. 1H NMR (500 MHz CD3OD): 8.35 (s, 1H), 8.20 (dd, 1H), 7.60 (d, 1H), 4.46 (d, 2H), 3.66-3.56 (m, 1H), 3.48 (td, 2H), 2.28 (d, 2H), 1.90-1.80 (m, 2H); 13C NMR (125 MHz CD3OD): 153.5, 139.2, 136.3, 126.1, 123.9, 121.8, 120.0, 116.2, 115.9, 115.6, 115.3, 113.9, 45.2, 29.1; Mass Spectrum: M+H+ 246.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07723333B2
Source datasetuspto-grants-2010_05
ORD IDord-e811fe7c6d2f4e88a11bd57ca52a83f4
Source noteuspto-grants-2010_05