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HRID 1405309作成日:2026年10月27日

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

https://huagongshe.com/reaction/1405309

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物(S)-2-(4-Fluorophenyl)-3-(2-methylpyrrolidin-1-yl)quinoxaline-6-carbonitrileHCID 70654208—
反応物HCID 178514644HCID 178514644—
触媒Zinc bromide (ZnBr2); Zinc DibromideHCID 24375—
溶媒Dimethyl SulfoxideHCID 679—
生成物(S)-2-(4-fluorophenyl)-3-(2-methylpyrrolidin-1-yl)-6-(2H-tetrazol-5-yl)quinoxalineHCID 6017147363%

反応条件

温度125 °C

反応手順

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%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08916561B2
出典データセットuspto-grants-2014_12
ORD IDord-c9bee96bffa14a1fb7fe9c4edfb7a55f
出典メモuspto-grants-2014_12