戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 8153作成日:2026年10月24日

Pyridine → 5-Benzyloxycarbonylamino-2-(2-methyl-imidazol-1-yl)fluorobenzene

https://huagongshe.com/ja/reaction/8153

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-(2-methyl-1H-imidazol-1-yl)anilineHCID 21876620—
溶媒DichloromethaneHCID 6344—
生成物5-Benzyloxycarbonylamino-2-(2-methyl-imidazol-1-yl)fluorobenzeneHCID 2187665193.5%

反応手順

5-Amino-2-(2-methylimidazol-1-yl)fluorobenzene (34.25 g, 0.179 M) was dissolved in dry dichloromethane (600 ml) under nitrogen, and cooled to −5°. Pyridine (17.7 g, 0.224 M) was added, followed by benzyl chloroformate (33.7 g, 0.197 M) over 20 minutes. The mixture was stirred and the temperature allowed to rise to ambient over 16 hours. Aqueous sodium bicarbonate (5%, 250 ml) was added, the organic layer separated, the aqueous layer re-extracted with dichloromethane (2×300 ml), and combined extracts dried (magnesium sulfate). After filtration and evaporation, the residue was recrystallised from toluene (400 ml) to give title product (54.5 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-d9bb5586c23743ebb695b08c565f0db1
出典メモuspto-grants-2006_08