化工社化工社 化学情報印刷レポート · 研究参考用
Potassium Carbonate → N-[1(S)-Ethoxycarbonyl-3-phenylpropyl]-L-alanine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | (2S)-2-(ethylamino)-4-phenylbutanoic acid | HCID 18647272 | — |
| 反応物 | benzyl (R)-alpha-toluenesulfonyloxypropionate | HCID 86745135 | — |
| 溶媒 | Acetonitrile | HCID 6342 | — |
| 生成物 | N-[1(S)-Ethoxycarbonyl-3-phenylpropyl]-L-alanine | HCID 5702571 | — |
反応手順
Ethyl (S)-homophenylalanine (I') and benzyl (R)-α-toluenesulfonyloxypropionate (II') in the presence or absence of potassium carbonate were added to acetonitrile (15 ml, bp 82° C.), and refluxed for a predetermined time, while stirring. After completing the reaction, the mixture was concentrated under reduced pressure and water (10 ml) was added to the oily residue. Then the mixture was extracted with toluene (10 ml). The organic layer was concentrated under reduced pressure to remove toluene. The oily residue was subjected to silica gel column chromatography to give the compound N-[(lS)-1-ethoxycarbonyl-3-phenylpropyl]-L-alanine. The reaction conditions are shown in Table 3.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05055588 |
| 出典データセット | uspto-grants-1991_10 |
| ORD ID | ord-a514b0037b054f80bd8b3b0a39c51b65 |
| 出典メモ | uspto-grants-1991_10 |