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Triethylamine → (S)-3-((tert-Butoxycarbonyl)amino)-5-fluoro-4-oxopentanoic acid
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | Acetic acid, 2-fluoro-, 1,1'-anhydride | HCID 67886 | — |
| 反応物 | N-(tert-butoxycarbonyl)-L-aspartic acid | HCID 99718 | — |
| 触媒 | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| 溶媒 | Benzene | HCID 241 | — |
| 生成物 | (S)-3-((tert-Butoxycarbonyl)amino)-5-fluoro-4-oxopentanoic acid | HCID 10131156 | — |
反応手順
A suspension of Boc-Asp-OH (8.11 mmol) and fluoroacetic anhydride (16.2 mmol) in benzene (30 ml) was treated with triethylamine (16.2 mmol) at room temperature. The catalyst 4-dimethylaminopyridine (0.41 mmol) was added to the solution and the reaction stirred for about 2 h at room temperature. About 100 ml benzene was added to the reaction mixture. The organic solution was washed with 1N HCl (2×50 ml), saturated NaHCO3 (2×50 ml), and saturated NaCl (2×50 ml), followed by drying over anhydrous MgSO4. The solvent was then removed by evaporation under reduced pressure. The resulting oil was applied to a 2.5×80 cm column of silica gel (60-200 mesh). The title compound was eluded with 2% methanol in chloroform.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05416013 |
| 出典データセット | uspto-grants-1995_05 |
| ORD ID | ord-1f37921e0a2e4e799336bdb217625c12 |
| 出典メモ | uspto-grants-1995_05 |