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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Potassium Acetate | HCID 517044 | — |
| 반응물 | 4,7-Dimethoxy-1,10-phenanthroline | HCID 10462298 | — |
| 반응물 | 2,6-Dibromo-4-fluorobenzaldehyde | HCID 44474666 | — |
| 반응물 | 6,7,8,9-Tetrahydropyrazino[1,2-a]indol-1(2H)-one | HCID 86683755 | — |
| 생성물 | 2-Bromo-4-fluoro-6-(1-oxo-6,7,8,9-tetrahydropyrazino[1,2-a]indol-2(1H)-yl)benzaldehyde | HCID 86683756 | 49.3% |
반응 단계
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08729072B2 |
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| 출처 데이터셋 | uspto-grants-2014_05 |
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| ORD ID | ord-6c67023df6bd4e6a876cecd42924a331 |
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| 출처 메모 | uspto-grants-2014_05 |
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