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HRID 333945作成日:2026年10月26日

Diethyl methylphosphonate → 2-Diethoxyphosphoryl-1-[4-(4-quinolyl)piperazin-1-yl]ethanone

https://huagongshe.com/reaction/333945

反応式

関与物質

役割名称HCID仕込み量
反応物Diethyl methylphosphonateHCID 12685—
反応物Sodium HydroxideHCID 14798—
反応物Ethyl 4-(4-quinolyl)piperazine-1-carboxylateHCID 66835834—
反応物ButyllithiumHCID 178418339—
溶媒Acetic AcidHCID 176—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
溶媒HexaneHCID 8058—
生成物2-Diethoxyphosphoryl-1-[4-(4-quinolyl)piperazin-1-yl]ethanoneHCID 86691595—

反応条件

温度-78 °C

反応手順

Diethylmethylphosphonate (302.8 mg, 2 mmol) was dissolved in anhydrous THF (2.5 ml), the mixture was cooled to −78° C. under argon, n-butyllithium (2.11 mmol, 846 μl of a 2.5 M solution in hexane) was added dropwise with stirring. After addition was complete, stirring was continued for 20 minutes, after which ethyl 4-(4-quinolyl)piperazine-1-carboxylate (284 mg, 1 mmol) dissolved in 0.5 μl THF was added dropwise. The mixture was allowed to reach room temperature overnight with continued stirring. Glacial acetic acid (0.25 ml) and water (2 ml) was added, after which the mixture was basified with 0.1 NaOH and extracted with diethylether (2×). The organic phases were combined, washed with 5% sodium bicarbonate and water. The aqueous phases were back-extracted with diethylether after basification with 0.1 N NaOH and the combined organic phases dried over magnesium sulfate and the solvent was removed under reduced pressure to yield 271 mg (0.693 mmol, 69%). MS (ESI): m/z=392.1 [M+1]+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08883791B2
出典データセットuspto-grants-2014_11
ORD IDord-35905a4a66f54338a085c9c0a7ee01a4
出典メモuspto-grants-2014_11