戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 510856作成日:2026年10月27日

Nitrogen → 1-[4-Chloro-6-(2,6-difluoropyridin-4-yl)-5-methylbiphenyl-2-yl]ethanone

https://huagongshe.com/reaction/510856

反応式

関与物質

役割名称HCID仕込み量
反応物NitrogenHCID 947—
反応物WaterHCID 962—
反応物2,6-Difluoropyridine-4-boronic acidHCID 2762747—
反応物1-(6-Bromo-4-chloro-5-methylbiphenyl-2-yl)ethanoneHCID 86666787—
触媒HCID 178418397HCID 178418397—
溶媒Sodium CarbonateHCID 10340—
溶媒1,4-DioxaneHCID 31275—
生成物1-[4-Chloro-6-(2,6-difluoropyridin-4-yl)-5-methylbiphenyl-2-yl]ethanoneHCID 8666678830%

反応条件

温度100 °C

反応手順

A biphasic solution of 1-(6-bromo-4-chloro-5-methylbiphenyl-2-yl)ethanone (0.20 g, 0.62 mmol) and (2,6-difluoropyridin-4-yl)boronic acid (0.12 g, 0.74 mmol) in 1,4-dioxane (2.0 mL) and 10% Na2CO3 in water (0.98 mL, 0.93 mmol)) was bubbled with N2 to degas. After tetrakis(triphenylphosphine)palladium(0) (29 mg, 0.025 mmol) was added the mixture was bubbled with N2 for 5 min. and heated at 100° C. overnight. The mixture was cooled to room temperature and diluted with ethyl acetate. The layers were separated and the aq. layer was extracted with more ethyl acetate. The combined extracts were washed with brine, dried over Na2SO4, filtered and concentrated. The residue was purified on silica gel column, eluting with 0-30% of ethyl acetate in hexane, to give the desired product (60 mg, 30%). LCMS calculated for C20H15ClF2NO (M+H)+: m/z=358.1. found: 358.0.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09096600B2
出典データセットuspto-grants-2015_08
ORD IDord-5c02a9856bba4c47b9bc7ab66ea54f41
出典メモuspto-grants-2015_08