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Ethyl Acetate → 2-(Bromomethyl)-3-(2-chlorophenyl)-5-nitroquinoxaline
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Ethyl Acetate | HCID 8857 | — |
| 反応物 | 3-Nitro-1,2-phenylenediamine | HCID 4359525 | — |
| 反応物 | 3-Bromo-1-(2-chlorophenyl)propane-1,2-dione | HCID 57556170 | — |
| 生成物 | 2-(Bromomethyl)-3-(2-chlorophenyl)-5-nitroquinoxaline | HCID 57707807 | — |
反応手順
To a solution of 3-bromo-1-(2-chlorophenyl)propane-1,2-dione (Prepared in Example 81, 4.2971 g, 16.4325 mmol) in ethyl acetate (109.55 mL, 16.433 mmol) was added 3-nitro-1,2-phenylenediamine (2.5165 g, 16.433 mmol) at room temperature and the resulting red mixture was stirred at room temperature. After 26 h of stirring at room temperature, the mixture was concentrated under reduced pressure to give 2-(bromomethyl)-3-(2-chlorophenyl)-5-nitroquinoxaline including its regioisomer as a red syrup: LC-MS (ESI) m/z 378.0 and 379.9 [M+H]+. The crude product as a red syrup was carried on crude without purification for the next step.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08193199B2 |
| 出典データセット | uspto-grants-2012_06 |
| ORD ID | ord-dd846b3575064eebb1e7b34bb85f63af |
| 出典メモ | uspto-grants-2012_06 |