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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1914279Generated: November 3, 2026

Stannous Chloride → 6-Chloro-5-methylpyridin-3-amine

https://huagongshe.com/reaction/1914279

Reaction equation

Participants

RoleNameHCIDCharge
ReactantStannous ChlorideHCID 24479—
Reactant2-Chloro-3-methyl-5-nitropyridineHCID 89648—
SolventMethanolHCID 887—
SolventEthyl AcetateHCID 8857—
Product6-Chloro-5-methylpyridin-3-amineHCID 12295607102.8%

Reaction Steps

2-Chloro-3-methyl-5-nitro-pyridine (2 g, 11.6 mmol) and SnCl2.(H2O)2 (7.86 g, 34.8 mmol) are refluxed in MeOH overnight. After cooled down, the mixture is diluted with ethyl acetate, washed with water, brine, dried over MgSO4, concentrated and purified by column chromatography to afford 6-chloro-5-methyl-pyridin-3-ylamine (1.7 g). To the solution of 6-chloro-5-methyl-pyridin-3-ylamine (1.7 g, 11.6 mmol) in 1N HCl is added the solution of NaNO2 (960 mg, 13.92 mmol) in water (10 ml) slowly at 0° C. After the addition, the solution is stirred for 20 min and then heated to 90° C. for 30 min. The solution is cooled down, quenched with K2CO3, extracted with ether, dried over MgSO4, and purified by column chromatography to afford the titled compound (560 mg) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08609892B2
Source datasetuspto-grants-2013_12
ORD IDord-e615999026c2449893b279bc3c705985
Source noteuspto-grants-2013_12