化工社化工社 化学情報印刷レポート · 研究参考用
Dimethylamine → Topotecan
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Dimethylamine | HCID 674 | — |
| 反応物 | Ethanol | HCID 702 | — |
| 反応物 | Formaldehyde | HCID 712 | — |
| 反応物 | Hydroxycamptothecin | HCID 97226 | — |
| 溶媒 | Acetic acid 10-acetoxymethyl-anthracen-9-ylmethyl ester | HCID 613145 | — |
| 生成物 | Topotecan | HCID 60700 | — |
反応手順
A mixture of 10-hydroxycamptothecin (728 mg 2.0 mmol), prepared as described in Example 2, in glacial acetic (50 mL), ethanol (20 mL), 37% aqueous formaldehyde (3 mL) and 40% aqueous dimethylamine (3 mL) was stirred at room temperature for 20 h. The solvents were removed under reduced pressure; the residue was heated at 50° under high vacuum for 2 h and triturated with isopropanol (10 mL) to precipitate the title compound (561 mg, 64%) as a yellow solid. FAB mass spectrum: m/e 422 (MH+). 1H NMR (CDCl3 /CD3OD) δ1.0 (t, 3), 1.9 (m, 2), 2.5 (s, 6), 4.3 (s, 2), 5.2 (s, 2), 5.4 (q, 2), 7.6 (s, 1), 7.7 (q, 2), 8.5 (s, 1).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05004758 |
| 出典データセット | uspto-grants-1991_04 |
| ORD ID | ord-a452c7c3aea64705b2836406f397f1a8 |
| 出典メモ | uspto-grants-1991_04 |