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Pyridine → Ethyl N-(6,7-dichloro-2-methoxyquinoxalin-3-yl)carbamate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Pyridine | HCID 1049 | — |
| 反応物 | Ethyl chloroformate | HCID 10928 | — |
| 反応物 | 2-Amino-6,7-dichloro-3-methoxyquinoxaline | HCID 69243349 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | Ethyl N-(6,7-dichloro-2-methoxyquinoxalin-3-yl)carbamate | HCID 69243293 | 86% |
反応手順
2-Amino-6,7-dichloro-3-methoxyquinoxaline (1.16 g, 4.75 mmol) and ethyl chloroformate (1.03 g, 9.50 mmol) were dissolved in dichloromethane (50 ml) at room temperature and thereto pyridine (751 mg, 9.50 mmol) was added. The mixture was stirred at room temperature for 24 hours and concentrated under the reduced pressure to remove the solvent, and purified by SiO2 column chromatography. Extraction of the residue with a n-hexane:ethyl acetate (2:1) mixture and concentration gave 1.29 g of the titled compound (yield, 86%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08314100B2 |
| 出典データセット | uspto-grants-2012_11 |
| ORD ID | ord-882ee2faa6a347c5b2f867c1bbfcd2cb |
| 出典メモ | uspto-grants-2012_11 |