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HRID 1896111作成日:2026年10月27日

Potassium Carbonate → 2-(4-Benzyl-1-(5-methoxy-2-nitrophenyl)piperazin-2-yl)acetic acid

https://huagongshe.com/reaction/1896111

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物18-Crown-6HCID 28557—
反応物3-Fluoro-4-nitroanisoleHCID 565654—
反応物2-Piperazineacetic acid, 4-(phenylmethyl)-, methyl esterHCID 15665466—
溶媒WaterHCID 962—
溶媒AcetonitrileHCID 6342—
生成物2-(4-Benzyl-1-(5-methoxy-2-nitrophenyl)piperazin-2-yl)acetic acidHCID 66769807—

反応条件

温度90 °C

反応手順

To a solution of Example 12C (0.907 g, 3.65 mmol) in acetonitrile (11.69 mL) was added 2-fluoro-4-methoxy-1-nitrobenzene (0.50 g, 2.92 mmol) and potassium carbonate (2.019 g, 14.61 mmol) in water (2.92 mL) followed by 18-crown-6 (0.039 g, 0.146 mmol), and the mixture was heated with an oil bath at 90° C. (reflux) for 24 hours. The solvent was evaporated and water was added followed by dichloromethane. The water phase was washed three times with dichloromethane to remove starting material and then acidified with 1 N HCl until pH=1. The acid product was extracted three times with dichloromethane, dried quickly with sodium sulfate and concentrated to give the title compound. MS (ESI) m/z 386.1 (M+H)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08518933B2
出典データセットuspto-grants-2013_08
ORD IDord-9880190aec6b457b8577ae8afd55e028
出典メモuspto-grants-2013_08