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Trifluoroacetic acid → 4-acetyl-N-(3-methoxybenzyl)benzamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Trifluoroacetic acid | HCID 6422 | — |
| 反応物 | 4-Methylmorpholine | HCID 7972 | — |
| 反応物 | 4-Acetylbenzoic Acid | HCID 11470 | — |
| 反応物 | 3-Methoxybenzylamine | HCID 21156 | — |
| 反応物 | PyBOP | HCID 2724699 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 溶媒 | N-methyl-2-pyrrolidone | HCID 13387 | — |
| 生成物 | 4-acetyl-N-(3-methoxybenzyl)benzamide | HCID 59840895 | 97% |
反応手順
The Sasrin resin was prepared as described in Step 2 of Example 3. The resin (500 mg) was heated with a solution of 3-methoxybenzylamine (600 μl) in NMP (6 ml) at 70° C. for 4 hours. The resin was then washed with DMF and dichloromethane and then shaken with a solution of PyBop® (1.04 g, 2 mmol), 4-acetylbenzoic acid (0.33 g, 2 mmol), 4-methylmorpholine (4 mmol) in NMP (6 ml) at room temperature overnight. A small aliquot of the resin was treated with 20% TFA In dichloromethane to give the intermediate, (4-acetylphenyl)-N-[(3-methoxyphenyl)methyl]carboxamide (HPLC: 23.94 min (97%); MS; MH+=284 (as required)). The resin was then heated at 95° C. for 7 hours in DMFDMA (5 ml).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06417185B1 |
| 出典データセット | uspto-grants-2002_07 |
| ORD ID | ord-ca26b6a313984c20aa69ab7cc7498e6d |
| 出典メモ | uspto-grants-2002_07 |