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HRID 22688作成日:2026年10月25日

Pyridine → 2-[2-(4-Fluorophenyl)acetyl]-4-(4-nitro-phenoxycarbonyloxy)-pyrazolidine-1-carboxylic acid benzyl ester

https://huagongshe.com/reaction/22688

反応式

関与物質

役割名称HCID仕込み量
反応物PyridineHCID 1049—
反応物4-Nitrophenyl chloroformateHCID 82129—
反応物2-[2-(4-Fluorophenyl)acetyl]-4-hydroxypyrazolidine-1-carboxylic acid benzyl esterHCID 20724744—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
生成物2-[2-(4-Fluorophenyl)acetyl]-4-(4-nitro-phenoxycarbonyloxy)-pyrazolidine-1-carboxylic acid benzyl esterHCID 2072474386%

反応条件

温度0 °C

反応手順

2-[2-(4-Fluorophenyl)acetyl]-4-hydroxy-pyrazolidine-1-carboxylic acid benzyl ester, 38, (366 mg, 1.02 mmol) is dissolved in dichloromethane (10 mL). The solution is cooled to 0° C. and p-nitrophenyl chloroformate (411 mg, 2.04 mmol) is added in one portion. The solution is stirred at 0° C., and pyridine (198 μL, 2.45 mmol) added. Stirring is continued at 0° C. for 1 hour followed by stirring at room temperature for 12 hours. The reaction is diluted with water (40 mL) and extracted with dichloromethane (40 mL). The organic layer is washed with 0.5 N NaOH (2×40 mL). The combined aqueous layers are back-extracted extracted with dichloromethane (30 mL). The combined organic layers are washed with brine (30 mL), dried, filtered, and concentrated in vacuo. The crude material is purified over silica (3:1 to 2:1 to 1:1 hexane/ethyl acetate) to afford 462 mg (86% yield) of the desired product as a white foam.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06849627B2
出典データセットuspto-grants-2005_02
ORD IDord-230ad8afcb884784baa19701dbf60b48
出典メモuspto-grants-2005_02