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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 70814생성일: 2026년 10월 25일

Phosphorus oxybromide → 4-bromo-2-cyano-N-[2-ethyl-6-methyl-4-(1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl)phenyl]quinoline-6-carboxamide

https://huagongshe.com/reaction/70814

반응식

참여 물질

역할이름HCID투입량
반응물Phosphorus oxybromideHCID 24613—
반응물Sodium BicarbonateHCID 516892—
반응물2-cyano-N-[2-ethyl-6-methyl-4-(1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl)phenyl]quinoline-6-carboxamide-1-oxideHCID 86672970—
용매AcetonitrileHCID 6342—
생성물4-bromo-2-cyano-N-[2-ethyl-6-methyl-4-(1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl)phenyl]quinoline-6-carboxamideHCID 8667297243%

반응 조건

온도100 °C

반응 단계

2-Cyano-N-[2-ethyl-6-methyl-4-(1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl)phenyl]-quinoline-6-carboxamide-1-oxide (96 mg) was dissolved in acetonitrile, added with phosphoryl bromide (250 mg), and stirred at 100° C. for 5 hours. After cooling to room temperature, the reaction solution was poured into ice water and neutralized with sodium hydrogen carbonate. After extracting the mixture twice with ethyl acetate, the organic phases were combined and washed with water, and dried over anhydrous magnesium sulfate. The drying agent was filtered off and the solvent was removed by distillation under the reduced pressure. The resulting residues were purified by column chromatography to obtain 4-bromo-2-cyano-N-[2-ethyl-6-methyl-4-(1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl)phenyl]quinoline-6-carboxamide (46 mg, 43%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08822691B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-7bddf54d950647c9b202ef8fb1175e47
출처 메모uspto-grants-2014_09