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HRID 1850350作成日:2026年10月27日

Triethylamine → 1-{1-[3-(1-Quinolin-2-yl-azetidin-3-yl)-pyrazin-2-yl]-piperidin-4-yl}-ethanone

https://huagongshe.com/reaction/1850350

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物1-(Piperidin-4-yl)ethan-1-oneHCID 2723764—
反応物2-(3-(3-Chloropyrazin-2-yl)azetidin-1-yl)quinolineHCID 58546741—
溶媒Dimethyl SulfoxideHCID 679—
溶媒WaterHCID 962—
生成物1-{1-[3-(1-Quinolin-2-yl-azetidin-3-yl)-pyrazin-2-yl]-piperidin-4-yl}-ethanoneHCID 5854722963%

反応条件

温度100 °C

反応手順

To a solution of 2-[3-(3-chloro-pyrazin-2-yl)-azetidin-1-yl]-quinoline (80 mg, 0.27 mmol) and 1-piperidin-4-yl-ethanone (WUXI APPTEC) (34.3 mg, 0.27 mmol) in DMSO (5 mL) was added Et3N (54.5 mg, 0.54 mmol). The reaction mixture was stirred at 100° C. overnight. The reaction mixture was diluted with water, extracted with EtOAc (20 mL×3). The combined organic extracts were washed with water (30 mL) and brine (30 mL), dried over Na2SO4 and filtered. The filtrate was evaporated in vacuo and the residue was purified by flash column chromatography on silica gel to give 1-{1-[3-(1-quinolin-2-yl-azetidin-3-yl)-pyrazin-2-yl]-piperidin-4-yl}-ethanone (65.8 mg, 0.17 mmol, yield 62.9%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08957073B2
出典データセットuspto-grants-2015_02
ORD IDord-5682078ac7aa4504a7b635e4daa2aa78
出典メモuspto-grants-2015_02