化工社化工社 化学情報印刷レポート · 研究参考用
Diisopropylcarbodiimide → N-alpha-Benzyloxycarbonyl-L-lysine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Diisopropylcarbodiimide | HCID 12734 | — |
| 反応物 | Camptothecin | HCID 24360 | — |
| 反応物 | Dicarbobenzoxy-l-lysine | HCID 18595285 | — |
| 触媒 | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | N-alpha-Benzyloxycarbonyl-L-lysine | HCID 75172 | — |
反応手順
N,N-Bis CBZ-Lysine (311 mg, 0.75 mmol) was dissolved in 56 mL of anhydrous methylene chloride at room temperature. To this solution were added DIPC (0.12 mL, 0.75 mmol), DMAP (0.61 mg, 0.5 mmol) and camptothecin (0.087 g, 0.25 mmol) at 0° C. The reaction mixture was allowed to warm to room temperature and left for 16 h. The solution was washed with 0.1 N HCl, dried and evaporated under reduced pressure to yield a light yellow solid, which was recrystallized from methanol to give camptothecin-20-ester of N,N-Bis CBZ-Lys 13. Purification of 13 was satisfactory based on TLC and HPLC analysis.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07270808B2 |
| 出典データセット | uspto-grants-2007_09 |
| ORD ID | ord-b4763f1fae70488594e09ba58e389690 |
| 出典メモ | uspto-grants-2007_09 |