関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Triphenylphosphine | HCID 11776 | — |
| 反応物 | Diethyl azodicarboxylate | HCID 5462977 | — |
| 反応物 | 2-{benzenesulfonyl-[2-(3-bromo-phenyl)-2-hydroxy-ethyl]-amino}-N-phenyl-acetamide | HCID 67001090 | — |
| 溶媒 | Ethyl Acetate | HCID 8857 | — |
| 生成物 | 4-Benzenesulfonyl-6-(3-bromo-phenyl)-1-phenyl-piperazin-2-one | HCID 67000436 | 89.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08063088B2 |
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| 出典データセット | uspto-grants-2011_11 |
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| ORD ID | ord-3b4eb96377374f32acfd1dd662c942df |
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| 出典メモ | uspto-grants-2011_11 |
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