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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1026487생성일: 2026년 10월 26일

Potassium Acetate → 2-Bromo-4-fluoro-6-(1-oxo-6,7,8,9-tetrahydropyrazino[1,2-a]indol-2(1H)-yl)benzaldehyde

https://huagongshe.com/reaction/1026487

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참여 물질

역할이름HCID투입량
반응물Potassium AcetateHCID 517044—
반응물4,7-Dimethoxy-1,10-phenanthrolineHCID 10462298—
반응물2,6-Dibromo-4-fluorobenzaldehydeHCID 44474666—
반응물6,7,8,9-Tetrahydropyrazino[1,2-a]indol-1(2H)-oneHCID 86683755—
생성물2-Bromo-4-fluoro-6-(1-oxo-6,7,8,9-tetrahydropyrazino[1,2-a]indol-2(1H)-yl)benzaldehydeHCID 8668375649.3%

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온도100 °C

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A 100-mL single-neck round-bottomed flask equipped with a magnetic stirrer and a reflux condenser was charged with 121e (500 mg, 2.66 mmol), 2,6-dibromo-4-fluorobenzaldehyde (1.50 g, 5.32 mmol), and potassium acetate (521 mg, 5.32 mmol). After bubbling argon through the suspension for 30 minutes, 4,7-dimethoxy-1,10-phenanthroline (638.4 mg, 2.66 mmol) and cuprous iodide (506 mg, 2.66 mmol) were added. The system was subjected to three cycles of vacuum/argon flush and then heated at 100° C. for 16 h. It was then cooled to room temperature and filtered. The solid was washed with dichloromethane (2×100 ml). The combined filtrate was concentrated under reduced pressure and the residue was purified by silica-gel column chromatography eluting with petroleum ether/ethyl acetate (10:1 to 3:1) to afford 121f (510 mg, 49%) as a yellow solid. MS: [M+H]+ 389.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08729072B2
출처 데이터셋uspto-grants-2014_05
ORD IDord-6c67023df6bd4e6a876cecd42924a331
출처 메모uspto-grants-2014_05