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HRID 1179581作成日:2026年10月27日

Cesium carbonate → 1,1-Dimethylethyl 4-(6-fluoro-2-methyl-5-quinolinyl)-1-piperazinecarboxylate

https://huagongshe.com/reaction/1179581

反応式

関与物質

役割名称HCID仕込み量
反応物Cesium carbonateHCID 10796—
反応物tert-Butyl piperazine-1-carboxylateHCID 143452—
反応物5-Bromo-6-fluoro-2-methylquinolineHCID 13035313—
反応物Bis(diphenylphosphino)-1,1'-binaphthylHCID 18630801—
溶媒TolueneHCID 1140—
生成物1,1-Dimethylethyl 4-(6-fluoro-2-methyl-5-quinolinyl)-1-piperazinecarboxylateHCID 5744431365.8%

反応条件

温度120 °C

反応手順

A mixture of 5-bromo6-fluoro-2-methylquinoline (Chem. Pharm. Bull:, 1989, 37(8), 2103-8, 0.285 g), 1,1-dimethylethyl 1-piperazinecarboxylate (0.265 g, 1.2 equiv.), Pd(OA)2 (15 mol %, 0.04 g), bis(diphenylphosphino)-1,1′-binaphthyl (BINAP, 30 mol %, 0.221 g), cesium carbonate (1.5 equiv. 0.580 g) and toluene (3.5 mL) were stirred at 120° C. for 20 h in a sealed tube. The mixture was cooled to room temperature and partitioned between ethyl acetate and brine. The organic layer was dried over sodium sulfate, filtered and concentrated. This crude product was purified by flash chromatography [SiO2; DCM-MeOH (99:1)→(90:10)] to afford the title compound as colourless solid (0.270 g, 65% yield).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07279481B2
出典データセットuspto-grants-2007_10
ORD IDord-ea31da006d2347299f936ddf7a1cee26
出典メモuspto-grants-2007_10