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Dimethylformamide → N-[2-(3,4-dimethoxyphenyl)ethyl]-2-(N-benzyloxycarbonyl-p-toluidino)-acetamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Dimethylformamide | HCID 6228 | — |
| 反応物 | Benzyl chloroformate | HCID 10387 | — |
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | N-[2-(3,4-dimethoxyphenyl)ethyl]-2-(p-toluidino)acetamide | HCID 10042154 | — |
| 溶媒 | Chloroform | HCID 6212 | — |
| 生成物 | N-[2-(3,4-dimethoxyphenyl)ethyl]-2-(N-benzyloxycarbonyl-p-toluidino)-acetamide | HCID 20460509 | 84.8% |
反応手順
A mixture of N-[2-(3,4-dimethoxyphenyl)ethyl]-2-(p-toluidino)acetamide (3.6 g) and anhydrous potassium carbonate (2.5 g) was added to anhydrous dimethylformamide (25 ml). The mixture was vigorously stirred under ice cooling and to the solution was dropwise added over 20 minutes an anhydrous chloroform solution (5 ml) containing benzyl chloroformate (2.04 g). The reaction mixture was poured into ice-water and extracted with chloroform. The extract was washed with water, dried and the solvent was distilled off. The residue was crystallized by treating with ether to give N-[2-(3,4-dimethoxyphenyl)ethyl]-2-(N-benzyloxycarbonyl-p-toluidino)-acetamide (4.3 g), mp 81° to 85° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04447436 |
| 出典データセット | uspto-grants-1984_05 |
| ORD ID | ord-1160d815c9d64b1188751560b0021423 |
| 出典メモ | uspto-grants-1984_05 |