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Pyridine → 5-Benzyloxycarbonylamino-2-(4-methylimidazol-1-yl)fluorobenzene
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Pyridine | HCID 1049 | — |
| 反応物 | Benzyl chloroformate | HCID 10387 | — |
| 反応物 | Sodium Bicarbonate | HCID 516892 | — |
| 反応物 | 3-Fluoro-4-(4-methyl-1H-imidazol-1-yl)aniline | HCID 21876638 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 5-Benzyloxycarbonylamino-2-(4-methylimidazol-1-yl)fluorobenzene | HCID 21876672 | 92.9% |
反応手順
5-Amino-2-(4-methylimidazol-1-yl)fluorobenzene (50.6 g, 0.265 M) was dissolved in dry dichloromethane (800 ml) under nitrogen, and cooled to −5°. Pyridine (26.1 g, 0.33 M) was added, followed by benzyl chloroformate (49.9 g, 0.292 M) over 30 minutes. The mixture was stirred and the temperature allowed to rise to ambient over 16 hours. Aqueous sodium bicarbonate (5%, 350 ml) was added, the organic layer separated, and the aqueous layer re-extracted with dichloromethane (2×200 ml), and combined organics dried (magnesium sulfate). After filtration and evaporation, the residue was recrystallised from toluene (300 ml) to give title product (80 g).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07087629B2 |
| 出典データセット | uspto-grants-2006_08 |
| ORD ID | ord-f57646be41af44fcb4ffc0a07957ff78 |
| 出典メモ | uspto-grants-2006_08 |