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Sodium Hydroxide → 1-[2-Acetylthiomethyl-5-(trifluoroacetylamino)pentanoyl]-L-proline
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Sodium Hydroxide | HCID 14798 | — |
| 反応物 | 4-Nitrophenyl trifluoroacetate | HCID 69569 | — |
| 反応物 | L-Proline | HCID 145742 | — |
| 反応物 | 2-[(Acetylsulfanyl)methyl]-5-aminopentanoic acid | HCID 13424659 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | Pyridine | HCID 1049 | — |
| 生成物 | 1-[2-Acetylthiomethyl-5-(trifluoroacetylamino)pentanoyl]-L-proline | HCID 54098205 | — |
反応手順
A mixture of 2-acetylthiomethyl-5-aminopentanoic acid (2.05 g.) and p-nitrophenyltrifluoroacetate (5.6 g.) in pyridine (10 ml.) is stirred at room temperature for four hours, and then added dropwise to a vigorously stirred solution of L-proline (1.55 g.) in water (10 ml.) while keeping the pH at 9 with careful addition of 2N sodium hydroxide. When the consumption of sodium hydroxide stops, the reaction mixture is acidified with hydrochloric acid and extracted with ethyl acetate. The solvent is removed in vacuo and the residue is chromatographed on a silica gel column to yield 1-[2-acetylthiomethyl-5-(trifluoroacetylamino)pentanoyl]-L-proline.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04146611 |
| 出典データセット | uspto-grants-1979_03 |
| ORD ID | ord-320052e21a354b5f866e314ca8896daa |
| 出典メモ | uspto-grants-1979_03 |