戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1186760作成日:2026年10月25日

2-Fluoro-4-iodoaniline → HCID 57636896、化合物

https://huagongshe.com/reaction/1186760

反応式

関与物質

役割名称HCID仕込み量
反応物2-Fluoro-4-iodoanilineHCID 185694—
反応物Lithium HexamethyldisilazideHCID 2733832—
反応物Methyl 2-chloro-1,5-dimethyl-6-oxo-1,6-dihydropyridine-3-carboxylateHCID 58112585—
溶媒TetrahydrofuranHCID 8028—
生成物HCID 57636896HCID 5763689679.3%

反応条件

温度-78 °C

反応手順

An oven dried three-necked flask was charged with 2-fluoro-4-iodoaniline (2.08 g, 8.79 mmol) and dry THF (40 mL). The mixture was cooled at −78° C. and LiHMDS (17.79 mL, 1.0 M, THF) was added dropwise. The reaction was stirred an additional hour at this temperature and methyl 2-chloro-1,5-dimethyl-6-oxo-1,6-dihydropyridine-3-carboxylate (1.89 g, 8.79 mmol) previously dissolved in dry THF (30 mL) was added. The mixture was slowly warmed to room temperature and stirred an additional 2 hours and quenched with 2N aq. HCl. The resulting mixture was further diluted with EtOAc and the organic layer was washed with brine, dried (Na2SO4) and concentrated under reduced pressure. The brown residue was purified by flash chromatography (Biotage system) using a gradient of EtOAc (0-25%) in hexane to afford the title product (2.9 g, 79%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08673919B2
出典データセットuspto-grants-2014_03
ORD IDord-03ae1c5441b943d39f9ca6f6cc95b69d
出典メモuspto-grants-2014_03