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HRID 560118作成日:2026年10月25日

Triphenylphosphine → 4-Benzenesulfonyl-6-(3-bromo-phenyl)-1-phenyl-piperazin-2-one

https://huagongshe.com/reaction/560118

反応式

関与物質

役割名称HCID仕込み量
反応物TriphenylphosphineHCID 11776—
反応物Diethyl azodicarboxylateHCID 5462977—
反応物2-{benzenesulfonyl-[2-(3-bromo-phenyl)-2-hydroxy-ethyl]-amino}-N-phenyl-acetamideHCID 67001090—
溶媒Ethyl AcetateHCID 8857—
生成物4-Benzenesulfonyl-6-(3-bromo-phenyl)-1-phenyl-piperazin-2-oneHCID 6700043689.4%

反応手順

At 0° C. to a solution of 2-{benzenesulfonyl-[2-(3-bromo-phenyl)-2-hydroxy-ethyl]-amino}-N-phenyl-acetamide (1.15 g) and triphenylphosphine (678 mg) in ethylacetate (10 mL) was added a solution of diethylazodicarboxylate (0.4 mL) in ethylacetate (5 mL) dropwise. After 15 min. the cooling bath was removed and the mixture was stirred at RT for 3 h. Additional amounts of triphenylphosphine (31 mg) and diethylazodicarboxylate (0.18 mL) were added, and stirring was continued for 1 h. The mixture was diluted with water and ethyl acetate, the phases were separated, and the inorganic one was extracted with ethyl acetate (×2). The organic layers were combined, washed with brine, dried (Na2SO4) and concentrated in vacuo. The crude product was purified by flash chromatography (SiO2, n-heptane/ethyl acetate 7:3) to give 4-benzenesulfonyl-6-(3-bromo-phenyl)-1-phenyl-piperazin-2-one (0.99 g, 89%) as a white foam, MS: 471.4 (M+H, 1Br)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08063088B2
出典データセットuspto-grants-2011_11
ORD IDord-3b4eb96377374f32acfd1dd662c942df
出典メモuspto-grants-2011_11