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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1253615Generated: November 3, 2026

Triethylamine → 5-bromo-N-ethyl-N-methylpyrimidine-2-carboxamide

https://huagongshe.com/reaction/1253615

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantN-MethylethylamineHCID 12219—
Reactant5-Bromopyrimidine-2-carbonyl chlorideHCID 59674657—
SolventDichloromethaneHCID 6344—
Product5-bromo-N-ethyl-N-methylpyrimidine-2-carboxamideHCID 59483315—

Reaction Steps

5-Bromo-pyrimidine-2-carbonyl chloride (1600 mg, 7.225 mmol) was dissolved in dichloromethane (25 ml) and triethylamine (4.03 ml, 28.9 mmol) was added followed by ethyl-methyl-amine (0.68 mL, 7.92 mmol). The reaction was stirred at room temperature under nitrogen for 16 ours, after which time, LCMS indicated completion. The mixture was diluted with dichloromethane (50 ml) and washed with water (50 ml) followed by 10% citric acid (50 ml) and brine (50 ml). The organic layer was separated and dried over MgSO4, the residue was filtered and the solvent was removed in vacuo to afford the title compound 5-bromo-N-ethyl-N-methylpyrimidine-2-carboxamide (SM-3): (1.4 g, 79.4%) as a brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08455496B2
Source datasetuspto-grants-2013_06
ORD IDord-c1f6237c9306414eb23cb53b323f4dc5
Source noteuspto-grants-2013_06