化工社化工社 化学情報印刷レポート · 研究参考用
Kinetin → 6-Furfurylamino-9-(2-bromoethyl)purine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Kinetin | HCID 3830 | — |
| 反応物 | 1,2-Dibromoethane | HCID 7839 | — |
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | 6-Furfurylamino-9-(2-bromoethyl)purine | HCID 53237266 | 60% |
反応手順
Kinetin (2 g, 9.3 mmol) and K2CO3 (2.4 g, 23 mmol) were mixed in 100 ml dimethylformamide (DMF). 1,2-Dibromoethane (5.2 g, 27.6 mmol) was added to the reaction mixture and then it was mixed at room temperature for 12 h, humidity was regulated by CaCl2 tube. Solvent was evaporated to dryness in vacuo to yellow solid and then 100 g ice was added. The mixture was shaken at least 1 h to until a white precipitate was formed. The solid was filtered off, washed with water and dried at 50° C. The product was recrystallised from methanol. Yield: 60%. 1H NMR (DMSO-d6): 3.95 (2H, t, J=5.91), 4.58 (2H, t, J=5.91), 4.69 (2H, s (br)), 6.23 (1H, d, J=2.94), 6.36 (1H, t, J=2.94), 7.54 (1H, d, J=2.94), 8.15 (2H, m), 8.24 (1H, s)
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US09220269B2 |
| 出典データセット | uspto-grants-2015_12 |
| ORD ID | ord-5a4bbcee3813456087da637d4a7c2544 |
| 出典メモ | uspto-grants-2015_12 |