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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 386406Generated: October 26, 2026

Triethylamine → 5-Chloro-3-(triethyl-silanylethynyl)-pyrazin-2-ylamine

https://huagongshe.com/reaction/386406

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant(Triethylsilyl)acetyleneHCID 637947—
Reactant3-Bromo-5-chloropyrazin-2-amineHCID 10488609—
CatalystCopper iodideHCID 83717—
CatalystHCID 178418476HCID 178418476—
SolventTetrahydrofuranHCID 8028—
Product5-Chloro-3-(triethyl-silanylethynyl)-pyrazin-2-ylamineHCID 59463522—

Reaction Steps

A 250 ml round bottom flask was charged with 3-bromo-5-chloro-pyrazin-2-ylamine (2) (1 g, 4.8 mmol), THF (10 ml), copper iodide (9 mg, 0.05 mM) and PdCl2(PPh3)2 (34 mg, 0.05 mmol) under nitrogen. To the reaction mixture, triethylamine (2 ml, 14.4 mmol) and triethylsilylacetylene (1 ml, 5.76 mmol) were added. The reaction mixture was stirred at room temperature for 3 h, then concentrated in vacuo and the residue was purified by flash chromatography, using as eluent pentane/EtOAc 10% to 30%, to give the title compound as an off white solid (1.2 g, 100%). 1H NMR (CDCl3): 0.7-0.8 (6H, qd), 1.0-1.1 (9H, t), 5.0-5.1 (2H, brs), 7.95 (1H, s). MS (ES+): 268.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08372835B2
Source datasetuspto-grants-2013_02
ORD IDord-2047b6b997224694964515edb1f25e62
Source noteuspto-grants-2013_02