化工社化工社 化学情報印刷レポート · 研究参考用
Triethylamine → 1-[4-(2-Chloro-4-nitrophenyl)piperazin-1-yl]-2-methylpropan-1-one
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | Isobutyryl chloride | HCID 62325 | — |
| 反応物 | 1-(2-Chloro-4-nitrophenyl)piperazine | HCID 2771331 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 1-[4-(2-Chloro-4-nitrophenyl)piperazin-1-yl]-2-methylpropan-1-one | HCID 2886337 | 100% |
反応手順
According to Scheme 4 Step 1: Isobutyryl chloride (1.24 mmol, 0.13 mL) and Et3N (2.48 mmol, 0.35 mL) were added to a solution of 1-(2-chloro-4-nitrophenyl)piperazine (0.83 mmol, 200 mg) in DCM (5 mL) at 0° C. The reaction mixture was stirred at room temperature for 2 hours. The organic phase was washed with a saturated solution of NaHCO3. The aqueous phase was extracted with AcOEt. The organic phase was washed with brine, was dried over Na2SO4, was filtered and was concentrated under reduced pressure to afford 1-(4-(2-chloro-4-nitrophenyl)piperazin-1-yl)-2-methylpropan-1-one (0.83 mmol, 261 mg, 100%). The product was used without further purification.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08524726B2 |
| 出典データセット | uspto-grants-2013_09 |
| ORD ID | ord-20b164a09da742bea74ca466d122cbe8 |
| 出典メモ | uspto-grants-2013_09 |