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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 255342생성일: 2026년 10월 25일

2-Hydroxyquinoline-3-carbaldehyde → 7-Fluoro-1-[2-(4-{[(2-oxo-1,2-dihydroquinolin-3-yl)methyl]amino}piperidin-1-yl)ethyl]quinoxalin-2(1H)-one

https://huagongshe.com/reaction/255342

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참여 물질

역할이름HCID투입량
반응물2-Hydroxyquinoline-3-carbaldehydeHCID 589334—
반응물Sodium triacetoxyborohydrideHCID 5049666—
반응물1-(2-(4-aminopiperidin-1-yl)ethyl)-7-fluoroquinoxalin-2(1H)-oneHCID 59397907—
용매MethanolHCID 887—
생성물7-Fluoro-1-[2-(4-{[(2-oxo-1,2-dihydroquinolin-3-yl)methyl]amino}piperidin-1-yl)ethyl]quinoxalin-2(1H)-oneHCID 1598280235.4%

반응 조건

온도0 °C

반응 단계

A mixture of 1-[2-(4-aminopiperidin-1-yl)ethyl]-7-fluoroquinoxalin-2(1H)-one (Intermediate 140, 130 mg, 0.448 mmol), 2-oxo-1,2-dihydroquinoline-3-carbaldehyde (65 mg, 0.448 mmol) and 3 Å molecular sieves (100 mg) in methanol (6.0 mL) was heated at reflux for 2.5 hours under nitrogen atmosphere. It was cooled to 0° C. and sodium triacetoxy borohydride (189.5 mg, 0.996 mmol) was added and the mixture was allowed to warm to room temperature and stirred overnight. The mixture was filtered and purified through silica gel plug (eluting with 15% methanol in methylene chloride) to give title compound (71 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07875715B2
출처 데이터셋uspto-grants-2011_01
ORD IDord-9847802978ff4a55817ee19ba6ca6ede
출처 메모uspto-grants-2011_01