Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1171127Generated: November 3, 2026

Pyridine → N-(5-bromo-3-((trimethylsilyl)ethynyl)pyrazin-2-yl)acetamide

https://huagongshe.com/reaction/1171127

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantAcetyl chlorideHCID 6367—
Reactant5-Bromo-3-((trimethylsilyl)ethynyl)pyrazin-2-amineHCID 53393189—
SolventTetrahydrofuranHCID 8028—
ProductN-(5-bromo-3-((trimethylsilyl)ethynyl)pyrazin-2-yl)acetamideHCID 5983602919%

Reaction Steps

To a solution of 5-Bromo-3-trimethylsilanylethynyl-pyrazin-2-ylamine (2.30 g, 8 mmol) in anhydrous THF (35 ml) and pyridine (1.62 ml, 20.0 mmol) was added acetyl chloride (682 μl, 9.6 mmol). The mixture was stirred at room temperature overnight, and then stirred at 60° C. for 5 hours. Solvents were removed in vacuum and the resulting brown residue was purified by silica gel chromatogrpahy with a gradient of ethyl acetate/hexane to afford the title compound (474 mg, 1.52 mmol) as light yellow as off white solid. MS: m/z 311.9/313.9 [MH+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07829558B2
Source datasetuspto-grants-2010_11
ORD IDord-43219bded6614ae99bb42959d8062597
Source noteuspto-grants-2010_11