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Allyl bromide → N-allyl-N-(2-trifluoromethylphenyl)-2-pyridinesulfonamide 1-oxide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Allyl bromide | HCID 7841 | — |
| 反応物 | Sodium hydride | HCID 24758 | — |
| 反応物 | N-(2-trifluoromethylphenyl)-2-pyridinesulfonamide 1-oxide | HCID 20152991 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | N-allyl-N-(2-trifluoromethylphenyl)-2-pyridinesulfonamide 1-oxide | HCID 14097714 | — |
反応手順
To N-(2-trifluoromethylphenyl)-2-pyridinesulfonamide 1-oxide (compound 129, Table A) (1.0 g, 3.0 mmol) in 10 ml of DMF is added NaH (0.30 g, 6.2 mmol) under N2, and the mixture is stirred at RT for 30 minutes. Allyl bromide (0.82 g, 0.59 ml, 6.8 mmol) is added dropwise, and the mixture is stirred at RT for 48 hours. It is then worked up and purified to give the title compound (compound 37, Table A). (DMF is dimethylformamide; RT is room temperature.)
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04722749 |
| 出典データセット | uspto-grants-1988_02 |
| ORD ID | ord-032d77276ec347c0b8611cfd56e26b51 |
| 出典メモ | uspto-grants-1988_02 |