化工社化工社 化学情報印刷レポート · 研究参考用
HRID 248832作成日:2026年10月27日
2-Furanmethanethiol → 8-chloro-N-[4-[(2-furanylmethyl)thio]-2-oxobutyl]dibenz[b,f][1,4]oxazepin-10(11H)-carboxamide
https://huagongshe.com/reaction/248832
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 2-Furanmethanethiol | HCID 7363 | — |
| 反応物 | Piperidine | HCID 8082 | — |
| 反応物 | Benzyltrimethylammonium hydroxide | HCID 66854 | — |
| 反応物 | 8-chloro-N-(2-oxo-3-butenyl)dibenz-[b,f][1,4]oxazepin-10(11H)-carboxamide | HCID 10831197 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 溶媒 | Ethyl Acetate | HCID 8857 | — |
| 生成物 | 8-chloro-N-[4-[(2-furanylmethyl)thio]-2-oxobutyl]dibenz[b,f][1,4]oxazepin-10(11H)-carboxamide | HCID 10742479 | — |
反応手順
A solution of 8-chloro-N-(2-oxo-3-butenyl)dibenz[b,f][1,4]oxazepin-10(11H)-carboxamide (0.75 gram), furfuryl mercaptan (0.23 mL), piperidine (0.069 mL), and N-benzyltrimethylammonium hydroxide (0.069 mL) in methylene chloride (12 mL) and methanol (3 mL) was stirred at room temperature for 6 hours. The reaction was diluted with methylene chloride (75 mL), washed with 75 mL each of 1N HCl (two times), water, saturated aqueous sodium bicarbonate, and brine, dried over MgSO4, and evaporated in vacuo. The crude product was purified by flash chromatography through silica gel 60 (350 mL) using 95:5 methylene chloride: ethyl acetate to yield a colorless oil. Analysis calculated for C23H21ClN2O4S×0.1 EtOAc: C, 60.34; H, 4.72; N, 6.01; Cl, 7.61; S, 6.88. Found: C, 59.94; H, 4.84; N, 5.87; Cl, 8.13; S, 6.65.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 特許番号 | US05212169 |
|---|
| 出典データセット | uspto-grants-1993_05 |
|---|
| ORD ID | ord-4f1d21f2d9974500b6b242551c69a2b2 |
|---|
| 出典メモ | uspto-grants-1993_05 |
|---|