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HRID 340217作成日:2026年10月26日

Potassium Carbonate → 2-(Trifluoromethyl)benzo[f][1,7]naphthyridin-5-amine

https://huagongshe.com/reaction/340217

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物3-Chloro-5-(trifluoromethyl)pyridine-2-carbonitrileHCID 1473374—
反応物(2-BOC-aminophenyl)boronic acidHCID 2773226—
溶媒MethanolHCID 887—
溶媒WaterHCID 962—
溶媒TolueneHCID 1140—
溶媒DichloromethaneHCID 6344—
生成物2-(Trifluoromethyl)benzo[f][1,7]naphthyridin-5-amineHCID 58213640—

反応条件

温度100 °C

反応手順

A solution of 2-(tert-butoxycarbonylamino)phenylboronic acid (1.0 eq.) and 3-chloro-5-(trifluoromethyl)picolinonitrile (from step 2) (1.0 eq.) in toluene (0.44 M) was mixed with tetrakis(triphenyl-phosphine)palladium (5 mol %) and 2N aqueous potassium carbonate solution (2.0 eq.). The reaction was heated to 100° C. and stirred overnight. After cooling to ambient temperature, the reaction content was diluted with 2% methanol in dichloromethane and water. The two phases were separated, and the aqueous layer was extracted twice with 2% methanol in dichloromethane. The combined organic layers were washed with brine, dried over anhydrous MgSO4, and concentrated en vacuo. The crude product was purified by flash chromatography on a COMBIFLASH® system (ISCO) using 0-50% ethyl acetate in hexane to give 2-(trifluoromethyl)benzo[f][1,7]naphthyridin-5-amine. 1H NMR (acetone d-6): δ 9.44 (s, 1H), 9.20 (s, 1H), 8.65-8.63 (d, 1H), 7.70-7.61 (m, 2H), 7.44-7.36 (m, 1H), 6.84 (br, 2H). LRMS [M+H]=264.2

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08895577B2
出典データセットuspto-grants-2014_11
ORD IDord-cd26f8d24a984724bd2e9ee245eff791
出典メモuspto-grants-2014_11