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Triethylamine → N-benzyloxycarbonyl-L-tryptophan ethyl ester
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | benzyloxycarbonyl-L-tryptophan | HCID 101176 | — |
| 反応物 | Ethyl 2-ethoxycarbonyloxyimino-2-cyanoacetate | HCID 54447666 | — |
| 溶媒 | Ethyl Acetate | HCID 8857 | — |
| 生成物 | N-benzyloxycarbonyl-L-tryptophan ethyl ester | HCID 14036692 | — |
反応手順
To a solution of N-benzyloxycarbonyl-L-tryptophan (1.69 g) and triethylamine (0.70 ml) in ethyl acetate (15 ml), ethyl 2-ethoxycarbonyloxyimino-2-cyanoacetate (1.08 g) is added, and the resulting mixture is stirred at room temperature for 1 hour and allowed to stand over night. The reaction mixture is treated as in Example A whereby crystals are obtained. The crystals are triturated with petroleum ether, and the obtained powder is collected by filtration, dried and recrystallized from an ethyl acetate-petroleum ether mixture to give N-benzyloxycarbonyl-L-tryptophan ethyl ester (1.4 g). M.P. 80 - 83°C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US03976635 |
| 出典データセット | uspto-grants-1976_08 |
| ORD ID | ord-7f32931a2a48463098a161ffad852b05 |
| 出典メモ | uspto-grants-1976_08 |