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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 401805Generated: October 30, 2026

Hydrochloric Acid → 2-(Piperidin-3-ylmethyl)pyrimidine

https://huagongshe.com/reaction/401805

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactanttert-Butyl 3-(pyrimidin-2-ylmethyl)piperidine-1-carboxylateHCID 57732184—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
Product2-(Piperidin-3-ylmethyl)pyrimidineHCID 5773194586%

Reaction Steps

To a solution of tert-butyl 3-(pyrimidin-2-ylmethyl)piperidine-1-carboxylate (Preparation 70, 27.3 g, 98.4 mmol, 1 eq) in diethyl ether (160 mL) and DCM (50 mL) was added dropwise a 2M solution of hydrogen chloride in diethyl ether (246 mL, 492 mmol, 5 eq) while maintaining the internal temperature below 30° C. The reaction mixture was stirred at room temperature for 20 h. The solvent was decanted and fresh diethyl ether (300 mL) added. The solid was collected by filtration and washed with diethyl ether (3×100 mL) then dissolved in water (150 mL). The aqueous layer was washed with DCM (2×150 mL), basified with sodium hydroxide pellets to pH 13-14 and extracted with DCM (5×200 mL). The organic layer was separated, dried over sodium sulphate, filtered and concentrated under reduced pressure to afford title compound (15 g, 84.6 mmol, 86%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08741934B2
Source datasetuspto-grants-2014_06
ORD IDord-9703b677e0304db595f74e73e24f7a05
Source noteuspto-grants-2014_06