돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 454921생성일: 2026년 10월 25일

Isopropanol → 1-(1-(3-((1-(Quinolin-2-YL)azetidin-3-YL)oxy)pyrazin-2-YL)piperidin-4-YL)ethanone

https://huagongshe.com/reaction/454921

반응식

참여 물질

역할이름HCID투입량
반응물IsopropanolHCID 3776—
반응물Potassium CarbonateHCID 11430—
반응물1-(Piperidin-4-yl)ethan-1-oneHCID 2723764—
반응물2-(3-(3-Chloropyrazin-2-yloxy)azetidin-1-yl)quinolineHCID 58547697—
용매WaterHCID 962—
생성물1-(1-(3-((1-(Quinolin-2-YL)azetidin-3-YL)oxy)pyrazin-2-YL)piperidin-4-YL)ethanoneHCID 5854784618%

반응 조건

온도160 °C

반응 단계

To a mixture of 2-(3-((3-chloropyrazin-2-yl)oxy)azetidin-1-yl)quinoline (see PREPARATION P2.6; 312 mg, 1.0 mmol) and 1-(piperidin-4-yl)ethanone (127 mg, 1.0 mmol) and K2CO3 (276 mg, 2.0 mmol) was added i-PrOH (3 mL) and water (1.0 ml). The solution was heated to 160° C. under microwave for 5 hours. Then the mixture was concentrated and extracted with EtOAc (2×30 mL). The combined organic extracts were washed with water (10 mL) and brine (10 mL), dried over Na2SO4, and filtered. The filtrate was evaporated in vacuo and the residue was purified by flash column chromatography on silica gel (20% to 60% EtOAc in petroleum ether) to give the title product (72 mg, 0.18 mmol, 18% yield) as white solid. ESI-MS (M+1): 404 calc. for C23H25N5O2 403.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08497265B2
출처 데이터셋uspto-grants-2013_07
ORD IDord-174739225df4471ea145f2c522cd939e
출처 메모uspto-grants-2013_07