Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1027703Generated: November 2, 2026

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

https://huagongshe.com/reaction/1027703

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 numberUS08735396B2
Source datasetuspto-grants-2014_05
ORD IDord-0c14297aed774874a82f544e3ae66413
Source noteuspto-grants-2014_05