戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 8157作成日:2026年10月24日

Pyridine → 5-Benzyloxycarbonylamino-2-(4-methylimidazol-1-yl)fluorobenzene

https://huagongshe.com/ja/reaction/8157

反応式

関与物質

役割名称HCID仕込み量
反応物PyridineHCID 1049—
反応物Benzyl chloroformateHCID 10387—
反応物Sodium BicarbonateHCID 516892—
反応物3-Fluoro-4-(4-methyl-1H-imidazol-1-yl)anilineHCID 21876638—
溶媒DichloromethaneHCID 6344—
生成物5-Benzyloxycarbonylamino-2-(4-methylimidazol-1-yl)fluorobenzeneHCID 2187667292.9%

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US07087629B2
出典データセットuspto-grants-2006_08
ORD IDord-f57646be41af44fcb4ffc0a07957ff78
出典メモuspto-grants-2006_08