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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1431341Generated: November 1, 2026

Stannous chloride dihydrate → 5-Bromo-2-(piperidin-1-yl)pyridin-3-amine

https://huagongshe.com/reaction/1431341

Reaction equation

Participants

RoleNameHCIDCharge
ReactantStannous chloride dihydrateHCID 61436—
Reactant5-Bromo-3-nitro-2-(piperidin-1-yl)pyridineHCID 46738792—
SolventEthyl AcetateHCID 8857—
Product5-Bromo-2-(piperidin-1-yl)pyridin-3-amineHCID 59631488—

Reaction Conditions

Temperature90 °C

Reaction Steps

To a stirred mixture of 5-bromo-3-nitro-2-(piperidin-1-yl)pyridine (5.88 g, 20.5 mmol) in EtOAc (50 mL) was added tin(II) chloride dihydrate (23.5 g, 104 mmol) in portions. Upon complete addition of the reducing agent, the mixture was carefully heated to 90° C. After 1 h, the reaction was cooled in an ice bath, then washed with 1M NaOH, water, and brine. After drying over anhydrous sodium sulfate and filtration, the organic solvent was removed under reduced pressure. The residue was purified with silica gel chromatography (0-15% EtOAc in hexanes) to provide a white solid as 5-bromo-2-(piperidin-1-yl)pyridin-3-amine. 1H NMR (400 MHz, DMSO-d6) δ ppm 7.57 (1H, d, J=2.2 Hz), 7.09 (1H, d, J=2.3 Hz), 5.04 (2H, s), 2.98 (4H, m), 1.73 (4H, m), 1.58 (2H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08940724B2
Source datasetuspto-grants-2015_01
ORD IDord-cb217b42873c4e26b36a07b85ef7d915
Source noteuspto-grants-2015_01