化工社化工社 化学情報印刷レポート · 研究参考用
Trifluoroacetic acid → L-Phenylalanyl-L-alanine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Trifluoroacetic acid | HCID 6422 | — |
| 反応物 | 1-(1(S)-t-butoxycarbonylethyl)-3(S)-azido-4(R)-phenylazetidin-2-one | HCID 13035214 | — |
| 触媒 | Palladium | HCID 23938 | — |
| 生成物 | Trifluoroacetic acid | HCID 6422 | — |
| 生成物 | L-Phenylalanyl-L-alanine | HCID 5488196 | 94% |
反応手順
After 1-(1(S)-t-butoxycarbonylethyl)-3(S)-azido-4(R)-phenylazetidin-2-one (300 mg., 0.95 mmol) was stirred in trifluoroacetic acid (2 ml.) at room temperature for 15 hours, the solvent was removed by distillation under reduced pressure. The thus obtained oil (360 mg.) was hydrogenated in 25 ml. of ethanol at 50° C. for 15 hours under ambient pressure using a 10% Pd-C (300 mg.) as a catalyst to give trifluoroacetic acid salt of L-phenylalanyl-L-alanine (311 mg., yield: 94%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04352752 |
| 出典データセット | uspto-grants-1982_10 |
| ORD ID | ord-8446506b615d4f04850806817179a906 |
| 出典メモ | uspto-grants-1982_10 |