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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1920955Erstellt: 26. Oktober 2026

Trifluoroacetic acid → 4-Chloro-2-isobutylimidazo[1,2-a]quinoxaline

https://huagongshe.com/reaction/1920955

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTrifluoroacetic acidHCID 6422—
Edukt2-(3-Chloroquinoxalin-2-ylamino)-4-methylpentanalHCID 57425908—
LösungsmittelTrifluoroacetic anhydrideHCID 9845—
Produkt4-Chloro-2-isobutylimidazo[1,2-a]quinoxalineHCID 5742590965,4%

Reaktionsschritte

To a solution of the 2-(3-chloroquinoxalin-2-ylamino)-4-methylpentanal (1.03 g, 3.71 mmol) in 8 mL of trifluoroacetic anhydride was added 0.2 mL trifluoroacetic acid at room temperature. The reaction mixture was stirred at that temperature overnight. The solvents were removed under reduced pressure. And then 20 mL of saturated aqueous sodium bicarbonate was added. The resulting mixture was extracted with ethyl acetate (50 mL×3). The combined organic layers were washed with water (20 mL), brine (20 mL), dried over MgSO4, filtered and concentrated. The crude product was purified by flash column chromatography eluted with ethyl acetate and hexanes to give the titled compound (630 mg, 65%). MS: MH+=260:262=3:1. 1H NMR (300 MHz, CDCl3): δ 8.05 (m, 1H), 7.93 (s, 1H), 7.86 (m, 1H), 7.67 (m, 1H), 7.59 (m, 1H), 2.87 (d, 2H), 2.17 (m, 1H), 1.02 (d, 6H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08173657B2
Quelldatensatzuspto-grants-2012_05
ORD IDord-6988a7e154e7418daa6046f35da0748e
Quellennotizuspto-grants-2012_05