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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1698232Generated: October 30, 2026

N-Methylacetamide → HCID 59278270, compound

https://huagongshe.com/reaction/1698232

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-MethylacetamideHCID 6582—
ReactantSodium hydrideHCID 24758—
Reactant5-Bromo-2-chloropyrimidineHCID 606665—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59278270HCID 59278270—

Reaction Steps

To a solution of 5-bromo-2-chloroprimidine (2.00 g, 10.34 mmol) in THF was added 60% NaH (0.34 g, 14.00 mmol) in mineral oil. After 20 minutes, N-methylacetamide (0.80 g, 11.00 mmol) was added dropwise. After 2 hours, the reaction was diluted with water and extracted with ethyl acetate. The combined organic layers were washed with brine, dried over sodium sulfate and concentrated in vacuo. The residue was purified by silica gel chromatography eluting with 30% ethyl acetate in heptane. The major fractions were combined and the solvent was concentrated in vacuo to afford N-(5-bromo-pyrimidin-2-yl)-N-methyl-acetamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08163918B2
Source datasetuspto-grants-2012_04
ORD IDord-8f659d5a431a4bdf96b2c5ee5fa91878
Source noteuspto-grants-2012_04