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Dichloromethane → 2-nitro-N-(2-pyridin-3-ylethyl)benzenesulfonamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Dichloromethane | HCID 6344 | — |
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | 2-Nitrobenzenesulfonyl chloride | HCID 15540 | — |
| 反応物 | 2-(Pyridin-3-yl)ethan-1-amine | HCID 854051 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | 2-nitro-N-(2-pyridin-3-ylethyl)benzenesulfonamide | HCID 46556534 | 32.9% |
反応手順
2-Nitrobenzene sulfonyl chloride (11.64 g) was added to a dichloromethane solution (100 ml) of 3-(2-aminoethyl)pyridine (6.11 g) and triethylamine (9 ml) at 0° C. The mixture was stirred at room temperature for 2 hours. Water was added to the reaction mixture, followed by extraction with dichloromethane. The organic layer was dried with anhydrous sodium sulfate, and condensed under reduced pressure. The residue was crystallized from ethyl acetate to give the title compound (5.06 g) as a yellow powder.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08822453B2 |
| 出典データセット | uspto-grants-2014_09 |
| ORD ID | ord-c3ccd1da4a8f4ca2bfbf69713a3fb167 |
| 出典メモ | uspto-grants-2014_09 |