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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1260309Generated: November 1, 2026

2-Methoxyethylamine → Ethyl 5-bromo-2-((2-methoxyethyl)amino)pyrimidine-4-carboxylate

https://huagongshe.com/reaction/1260309

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-MethoxyethylamineHCID 8018—
ReactantEthyl 5-bromo-2-(methylsulfonyl)pyrimidine-4-carboxylateHCID 67299941—
SolventDichloromethaneHCID 6344—
ProductEthyl 5-bromo-2-((2-methoxyethyl)amino)pyrimidine-4-carboxylateHCID 5836804389%

Reaction Steps

2-Methoxyethylamine (0.278 ml, 3.2 mmol) was added at room temperature to a solution of 5-bromo-2-methanesulfonyl-pyrimidine-4-carboxylic acid ethyl ester (0.2 g, 0.65 mmol) in dichloromethane (5 ml). Stirring was continued at 45° C. for 2 hours. The solvent was evaporated and the crude product was purified by silica gel chromatography using an ethyl acetate/heptane eluent to yield the title compound as colorless oil (0.175 g, 89%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08470820B2
Source datasetuspto-grants-2013_06
ORD IDord-1abf7d8d65ab444e9d0f8e28ffc62ae5
Source noteuspto-grants-2013_06