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HRID 130423作成日:2026年10月27日
p-Bromobenzenesulfonyl chloride → 4-Bromo-N-[2-chloro-5-(cis-3,5-dimethyl-1-piperazinyl)phenyl]benzenesulfonamide
https://huagongshe.com/reaction/130423
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | p-Bromobenzenesulfonyl chloride | HCID 7396 | — |
| 反応物 | 5-(cis-3,5-Dimethyl-1-piperazinyl)-2-chloroaniline | HCID 59007078 | — |
| 溶媒 | Pyridine methylene chloride | HCID 21875418 | — |
| 生成物 | 4-Bromo-N-[2-chloro-5-(cis-3,5-dimethyl-1-piperazinyl)phenyl]benzenesulfonamide | HCID 59007090 | — |
反応手順
A solution of 5-(cis-3,5-dimethyl-1-piperazinyl)-2-chloroaniline (D34) (108 mg, 0.45 mmol) in pyridine:dichloromethane (1:1, 4 ml) was treated with 4-bromobenzenesulfonyl chloride (138 mg, 0.54 mmol). The solution was stirred at room temperature for 2 hours, quenched with methanol and concentrated in vacuo. The residue was applied to a SCX cartridge (Varian bond-elute, 5 g) and washed with methanol and 2M ammonia in methanol. The combined basic fractions were concentrated in vacuo and the resulting residue was purified by column chromatography (FlashMaster) (dichloromethane to 5% methanol:dichloromethane) to afford some pure product. The impure fractions were purified further by MDAP, and combined with the above pure product to afford the title product (D35). MS (ES+) m/e 458/460/462 [M+H]+.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07381728B2 |
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| 出典データセット | uspto-grants-2008_06 |
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| ORD ID | ord-f07f4d9910774fc9810990896b77eba6 |
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| 出典メモ | uspto-grants-2008_06 |
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