戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1920955作成日:2026年10月25日

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

https://huagongshe.com/reaction/1920955

反応式

関与物質

役割名称HCID仕込み量
反応物Trifluoroacetic acidHCID 6422—
反応物2-(3-Chloroquinoxalin-2-ylamino)-4-methylpentanalHCID 57425908—
溶媒Trifluoroacetic anhydrideHCID 9845—
生成物4-Chloro-2-isobutylimidazo[1,2-a]quinoxalineHCID 5742590965.4%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08173657B2
出典データセットuspto-grants-2012_05
ORD IDord-6988a7e154e7418daa6046f35da0748e
出典メモuspto-grants-2012_05