関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Chlorobenzene | HCID 7964 | — |
| 反応物 | N-bromobutanimide | HCID 67184 | — |
| 反応物 | N,N-dimethyl-N'-[2-(4-methylphenyl)phenyl]sulfonylmethanimidamide | HCID 9972170 | — |
| 触媒 | Benzoyl Peroxide | HCID 7187 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | N'-[2-[4-(bromomethyl)phenyl]phenyl]sulfonyl-N,N-dimethylmethanimidamide | HCID 10317688 | 41% |
反応手順
4′-Methylbiphenyl-2-sulfonic acid 1-dimethylaminometh-(E)-ylideneamide (540.0 mg, 1786 μmol), NBS (318 mg, 1.8 mmol), and benzoyl peroxide (4.3 mg, 17.8 μmol) were dissolved in chlorobenzene (7.0 mL, 69 mmol) and the resulting solution was heated at 100° C. for 90 minutes. The mixture was cooled to room temperature and water was added. The mixture was extracted with DCM, washed with saturated NaHCO3 and saturated aqueous NaCl, extracted again with DCM, dried over MgSO4, filtered, and concentrated. The crude product was purified by flash chromatography (40 g, 0-100% EtOAc in hexanes), then taken up in EtOAc (4.5 mL) and DCM (1.5 mL). Additional DCM (3.0 mL) was added and the mixture was heated at 60° C. The mixture was cooled in the freezer overnight, then concentrated. The material was taken up in DCM (2 mL), EtOAc (6 mL) was added, and the resulting solution placed in the freezer. A precipitate formed and was filtered to yield the title compound (279 mg) as a white solid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08664227B2 |
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| 出典データセット | uspto-grants-2014_03 |
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| ORD ID | ord-c05f0c0217764d12a28a8c9a9031236d |
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| 出典メモ | uspto-grants-2014_03 |
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