Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 573982Generated: November 1, 2026

5-Chloro-2-methoxy-3-nitropyridine → 5-Chloro-2-methoxypyridin-3-amine

https://huagongshe.com/reaction/573982

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Chloro-2-methoxy-3-nitropyridineHCID 26370218—
CatalystPlatinumHCID 23939—
CatalystZinc bromideHCID 10421208—
SolventEthyl AcetateHCID 8857—
Product5-Chloro-2-methoxypyridin-3-amineHCID 45122181100%

Reaction Steps

Zinc bromide (0.27 g, 1.2 mmol) and 10% platinum on carbon (0.58 g, 2.97 mmol) were added to a solution of 5-chloro-2-methoxy-3-nitropyridine (Preparation 6a, 1.13 g, 5.99 mmol) in ethyl acetate (20 mL) and the resulting mixture was hydrogenated in a Parr apparatus at 10 psi for 2 hours. The mixture was then filtered through diatomaceous earth (Celite®) and the filter cake was washed with ethyl acetate. The combined filtrate and washings were concentrated to give the title compound (0.95 g, 100%) as an oil which was used in the next synthetic step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09034311B2
Source datasetuspto-grants-2015_05
ORD IDord-9a2fd9244b1a4588b7db39fc72aff918
Source noteuspto-grants-2015_05