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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1185385Generated: October 26, 2026

Ethyl 2,6-dichloro-5-nitropyrimidine-4-carboxylate → Ethyl 5-amino-2-chloropyrimidine-4-carboxylate

https://huagongshe.com/reaction/1185385

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 2,6-dichloro-5-nitropyrimidine-4-carboxylateHCID 2761044—
ReactantMagnesium monoxideHCID 6850729—
CatalystPalladiumHCID 23938—
Solvent1,4-DioxaneHCID 31275—
ProductEthyl 5-amino-2-chloropyrimidine-4-carboxylateHCID 1225891055%

Reaction Steps

In a Parr hydrogenator, ethyl 2,6-dichloro-5-nitropyrimidine-4-carboxylate (2.16 g, 8.12 mmol), 10% Pd/C (2.0 g, 0.94 mmol), magnesium monoxide (1.60 g, 39.7 mmol) and 1,4-dioxane (100 mL) were charged. The hydrogenation was allowed to go at room temperature under 50-60 psi for 2 days while monitored by LCMS. The reaction mixture was filtered through Celite and washed with methanol. The filtrate was concentrated and purified via flash chromatography eluting with 50 to 100% ethyl acetate in heptane to give ethyl 5-amino-2-chloropyrimidine-4-carboxylate (0.90 g, 55%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08669361B2
Source datasetuspto-grants-2014_03
ORD IDord-c63cd1facfe646fd9e80e0a7e2cad924
Source noteuspto-grants-2014_03