関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | o-Chlorophenylacetic acid | HCID 17124 | — |
| 反応物 | Thionyl Chloride | HCID 24386 | — |
| 生成物 | Acetyl chloride, 2-(2-chlorophenyl)- | HCID 182669 | — |
反応手順
15 ml of thionyl chloride was added to 0.44 g of 2-chlorophenylacetic acid. The mixture was stirred at room temperature for 2 hours. The reaction mixture was subjected to distillation to remove the remaining thionyl chloride and then to azeotropy with toluene twice to completely remove the thionyl chloride. The residue was dissolved in 10 ml of dichloromethane. 0.36 ml of triethylamine was added, with ice-cooling, to a dichloromethane solution containing 0.40 g of 5-dimethylamino-1-(4-aminobenzoyl)-2,3,4,5-tetrahydro-1H-benzoazepine. Thereto was dropwise added the above obtained 2-(2-chlorophenyl)acetyl chloride solution. The resulting mixture was stirred at room temperature for 1 hour. The reaction mixture was water-washed twice, then dried over magnesium sulfate and concentrated. The residue was purified by silica gel column chromatography (elutant: chloroform/methanol=200/1) and then recrystallized from methanol-diethyl ether to obtain 0.29 g of 5-dimethylamino-1-{4-[2-(2-chlorophenyl)acetylamino]benzoyl}-2,3,4,5-tetrahydro-1H-benzoazepine.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05622947 |
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| 出典データセット | uspto-grants-1997_04 |
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| ORD ID | ord-d0c460ed1540444c85bf2a050d61eee3 |
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| 出典メモ | uspto-grants-1997_04 |
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