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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1068168Generated: November 2, 2026

Hydrochloric Acid → N2-(1-benzylpiperidin-4-yl)pyridine-2,3-diamine

https://huagongshe.com/reaction/1068168

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantStannous ChlorideHCID 24479—
ReactantN-(1-benzylpiperidin-4-yl)-3-nitropyridin-2-amineHCID 2823254—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductN2-(1-benzylpiperidin-4-yl)pyridine-2,3-diamineHCID 21192982—

Reaction Steps

To a solution of (1-Benzyl-piperidin-4-yl)-(3-nitro-pyridin-2-yl)-amine (from Step A) in 10 mL of THF was added 2.4 g of SnCl2 and 1 mL of concentrated HCl at room temperature, stirred at room temperature for 2 hours. The reaction was diluted with 40 mL of EtOAc and washed with 30 mL of saturated NaHCO3 aqueous solution. After separating layers, the aqueous phase was extracted with 2×15 mL EtOAc. The combined organic phases were washed with 15 mL of brine, dried over MgSO4 and concentrated under reduced pressure to give 603 mg of yellow soid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06248755B1
Source datasetuspto-grants-2001_06
ORD IDord-290f71f084b8469f867d3d61c5d8c8f1
Source noteuspto-grants-2001_06