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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1619712Generated: November 2, 2026

Ammonium formate → N-(2,4-Dimethoxybenzyl)pyrimidin-4-amine

https://huagongshe.com/reaction/1619712

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium formateHCID 2723923—
ReactantHCID 55190931HCID 55190931—
SolventEthanolHCID 702—
ProductN-(2,4-Dimethoxybenzyl)pyrimidin-4-amineHCID 6336299597%

Reaction Conditions

Temperature80 °C

Reaction Steps

6-Chloro-N-(2,4-dimethoxybenzyl)pyrimidin-4-amine (Preparation 112, 3.46 g, 12.39 mmol) was dissolved in ethanol (140 mL). The solution was degassed and then 10% palladium on carbon (0.98 g) was added followed by ammonium formate (4.55 g, 72.15 mmol) and the reaction was heated at 80° C. for 2 hours. The reaction was cooled to room temperature, filtered through pad of Celite™ and the filtrate was concentrated in vacuo. The residue was partitioned between dichloromethane (30 mL) and water (15 mL). The organic layer was separated, dried over anhydrous MgSO4, filtered and evaporated to give the title compound (2.94 g, 97%) as viscous oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08772293B2
Source datasetuspto-grants-2014_07
ORD IDord-f5c571e401594ebf840393c41adefd7e
Source noteuspto-grants-2014_07