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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1405309생성일: 2026년 10월 26일

Water → (S)-2-(4-fluorophenyl)-3-(2-methylpyrrolidin-1-yl)-6-(2H-tetrazol-5-yl)quinoxaline

https://huagongshe.com/reaction/1405309

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물(S)-2-(4-Fluorophenyl)-3-(2-methylpyrrolidin-1-yl)quinoxaline-6-carbonitrileHCID 70654208—
반응물HCID 178514644HCID 178514644—
촉매Zinc bromide (ZnBr2); Zinc DibromideHCID 24375—
용매Dimethyl SulfoxideHCID 679—
생성물(S)-2-(4-fluorophenyl)-3-(2-methylpyrrolidin-1-yl)-6-(2H-tetrazol-5-yl)quinoxalineHCID 6017147363%

반응 조건

온도125 °C

반응 단계

To a solution of (S)-2-(4-fluorophenyl)-3-(2-methylpyrrolidin-1-yl)quinoxaline-6-carbonitrile (100 mg, 0.30 mmol) in DMSO (10 mL) was added dibromozinc (33.8 mg, 0.15 mmol), water (10 mL), azidosodium (48.8 mg, 0.75 mmol) and water (5 mL). The resulting solution was stirred for 1 days at 125° C. and then quenched by the addition of water (100 mL), extracted with dichloromethane (3×30 mL). The organic layers were combined and dried over anhydrous sodium sulfate and concentrated in vacuo to give a residue, which was purified via silica gel column chromatography (2% dichloromethane in methanol) to afford (S)-2-(4-fluorophenyl)-3-(2-methylpyrrolidin-1-yl)-6-(2H-tetrazol-5-yl)quinoxaline as a yellow solid (70.9 mg, 63%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08916561B2
출처 데이터셋uspto-grants-2014_12
ORD IDord-c9bee96bffa14a1fb7fe9c4edfb7a55f
출처 메모uspto-grants-2014_12