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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1850350생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1850350

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물1-(Piperidin-4-yl)ethan-1-oneHCID 2723764—
반응물2-(3-(3-Chloropyrazin-2-yl)azetidin-1-yl)quinolineHCID 58546741—
용매Dimethyl SulfoxideHCID 679—
용매WaterHCID 962—
생성물1-{1-[3-(1-Quinolin-2-yl-azetidin-3-yl)-pyrazin-2-yl]-piperidin-4-yl}-ethanoneHCID 5854722963%

반응 조건

온도100 °C

반응 단계

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%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08957073B2
출처 데이터셋uspto-grants-2015_02
ORD IDord-5682078ac7aa4504a7b635e4daa2aa78
출처 메모uspto-grants-2015_02