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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1713002Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/1713002

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
Edukt(Triethylsilyl)acetyleneHCID 637947—
Edukt3-Bromo-5-chloropyrazin-2-amineHCID 10488609—
KatalysatorCopper iodideHCID 83717—
KatalysatorHCID 178418476HCID 178418476—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt5-Chloro-3-(triethyl-silanylethynyl)-pyrazin-2-ylamineHCID 59463522—

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07795259B2
Quelldatensatzuspto-grants-2010_09
ORD IDord-f28f29cf42754ab08b61aa342508e942
Quellennotizuspto-grants-2010_09