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HRID 730220作成日:2026年10月25日
6-Methoxy-m-toluenesulfonyl chloride → Benzo[b]thiophene-2sulfonic acid [2-(2-methoxy-5-methylbenzenesulfonylamino)phenyl]-amide
https://huagongshe.com/reaction/730220
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | 6-Methoxy-m-toluenesulfonyl chloride | HCID 145149 | — |
| 反応物 | Benzo[b]thiophene-2-sulfonic acid (2-aminophenyl)amide | HCID 86240018 | — |
| 溶媒 | Pyridine | HCID 1049 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | Benzo[b]thiophene-2sulfonic acid [2-(2-methoxy-5-methylbenzenesulfonylamino)phenyl]-amide | HCID 11518776 | 79.8% |
反応手順
To a solution of benzo[b]thiophene-2-sulfonic acid (2-aminophenyl)-amide (1 mmol, prepared as in Example 1) in DCM (2 mL) and pyridine (2 mL), 2-methoxy-5-methylbenzenesulfonyl chloride (1.1 mmol) was added at RT and the reaction mixture was then allowed to stir at RT overnight. The reaction mixture was then diluted with DCM (10 mL). The organic phase was washed with 10% aqueous HCl (10 mL), water (10 mL) and brine (10 mL). The organic phase was dried over anhydrous sodium sulfate and concentrated under vacuum. The residue obtained was purified by flash column chromatography eluting with DCM/EtOAc to obtain 390 mg of benzo[b]thiophene-2-sulfonic acid [2-(2-methoxy-5-methylbenzenesulfonylamino)phenyl]-amide. LC: Tr 1.25 min; MS: 489.1 (M+1)+.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07582673B2 |
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| 出典データセット | uspto-grants-2009_09 |
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| ORD ID | ord-a1631ad6ce614e76885649047060fa4d |
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| 出典メモ | uspto-grants-2009_09 |
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