関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 4-Chlorobenzenesulfonyl chloride | HCID 7398 | — |
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | tert-Butyl (2R)-2-methylpiperazine-1-carboxylate | HCID 10262201 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | (3R)-1-[(4-chlorophenyl)sulfonyl]-3-methylpiperazine | HCID 11630465 | 78.7% |
反応手順
To a solution of 1,1-dimethylethyl (2R)-2-methyl-1-piperazinecarboxylate (1.5 g, 07.5 mmol) in dry DCM (40 mL) was added triethylamine (2.59 mL, 18.8 mmol) and 4-chlorobenzenesulfonyl chloride (3.15 g, 10.5 mmol) and the reaction stirred at room temperature for 48 h. To the reaction was added resin supported-triamine (5 g) and the mixture stirred for 4 h. The reaction mixture was filtered and the filtrate washed with 0.5 M HCl (aq., 100 mL) followed by water (100 mL) before it was dried (MgSO4), filtered and the solvent removed in vacuo. The crude product was dissolved in DCM (40 mL) and TFA (10 mL) was added. The solution was stirred for 20 min. The solvent was evaporated and the residue tajen up in DCM (40 mL) and washed with 50% aqueous sodium bicarbonate (100 mL) followed by water (100 mL). The organic phase was dried (MgSO4), filtered and the solvent removed in vacuo to give the title compound (1.62 g).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08530478B2 |
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| 出典データセット | uspto-grants-2013_09 |
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| ORD ID | ord-d72421402bcd411a95caa05e81703400 |
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| 出典メモ | uspto-grants-2013_09 |
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