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Triethylamine → 4-amino-N-(oxan-4-yl)benzamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | 2H-pyran-4-amine | HCID 17791271 | — |
| 反応物 | 4-Amino-benzoic acid benzotriazol-1-yl ester | HCID 53844583 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | 4-amino-N-(oxan-4-yl)benzamide | HCID 43609562 | 54.3% |
反応手順
To a mixture of 1.1441 g (4.5 mmole) of 4-amino-benzoic acid benzotriazol-1-yl ester and 8 mL of dry dimethylformamide was added 0.6575 g (6.5 mmole) of 4-amino-pyran followed by 0.4554 g (0.45 mmole) of triethylamine. The mixture stirred at room temperature for 90 minutes. Volatiles were removed under reduced pressure and the residue taken up in ethyl acetate, and the organic layer washed once with 100 mL of 0.5 M sodium carbonate, twice with 75 mL water, and then 75 mL brine, dried over anhydrous sodium sulfate and concentrated under reduced pressure to give 0.5378 g 4-amino-N-(tetrahydro-pyran-4-yl)-benzamide, which was used without further purification.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08003785B2 |
| 出典データセット | uspto-grants-2011_08 |
| ORD ID | ord-f59a4f26f1b94892b120d6cb87f857fc |
| 出典メモ | uspto-grants-2011_08 |