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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1625980Generated: October 30, 2026

Stannous chloride dihydrate → 5-Bromo-2-methoxypyridin-3-amine

https://huagongshe.com/reaction/1625980

Reaction equation

Participants

RoleNameHCIDCharge
ReactantStannous chloride dihydrateHCID 61436—
Reactant5-Bromo-2-methoxy-3-nitropyridineHCID 15645664—
SolventEthyl AcetateHCID 8857—
Product5-Bromo-2-methoxypyridin-3-amineHCID 4475486958.7%

Reaction Steps

To a solution of 5-bromo-2-(methyloxy)-3-nitropyridine (45 g, 193 mmol) in ethyl acetate (1 L) was added tin (II) chloride dihydrate (174 g, 772 mmol). The reaction mixture was heated at reflux for 4 h. LC/MS indicated some starting material remained, so added 20 mol % tin (II) chloride dihydrate and continued to heat at reflux. After 2 h, the reaction was allowed to cool to ambient temperature and concentrated in vacuo. The residue was treated with 2 N sodium hydroxide and the mixture stirred for 1 h. The mixture was then with methylene chloride (1 L), filtered through Celite, and washed with methylene chloride (500 mL). The layers were separated and the organics dried over magnesium sulfate and concentrated to give 5-bromo-2-(methyloxy)-3-pyridinamine (23 g, 113 mmol, 58.7% yield). The product was used crude in subsequent reactions. MS(ES)+ m/e 201.9, 203.9 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08785433B2
Source datasetuspto-grants-2014_07
ORD IDord-d065a902aea846a2a2df895301a3d68e
Source noteuspto-grants-2014_07