戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1963881作成日:2026年10月27日

Sodium Carbonate → 5'-Chloro-2'-fluoro-6-(3-fluorobenzylamino)-2,4'-bipyridine-5-carbonitrile

https://huagongshe.com/reaction/1963881

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium CarbonateHCID 10340—
反応物(5-Chloro-2-fluoropyridin-4-yl)boronic acidHCID 44754822—
反応物HCID 86650611HCID 86650611—
触媒HCID 178418807HCID 178418807—
溶媒1,2-DimethoxyethaneHCID 8071—
生成物5'-Chloro-2'-fluoro-6-(3-fluorobenzylamino)-2,4'-bipyridine-5-carbonitrileHCID 6693715333%

反応条件

温度120 °C

反応手順

6-chloro-2-(3-fluorobenzylamino)nicotinonitrile (0.602 g, 2.30 mmol), 5-chloro-2-fluoropyridin-4-ylboronic acid (1.21 g, 6.91 mmol), and sodium carbonate (2.99 mL, 5.99 mmol, 2M in H2O) were dissolved in DME (10.5 mL). The resulting solution was then degassed by sparging with argon for 5 min. It was then treated with PdCl2(dppf) CH2Cl2 adduct (0.376 g, 0.460 mmol). The resulting reaction mixture was heated in the microwave at 120° C. for 10 min. It was then filtered through a pad of Celite. The filtrate was concentrated in vacuo. The resulting residue was subjected to silica gel column chromatography. Elution using 5 EtOAc/95 hexanes to 50 EtOAc/50 hexanes yielded 0.2689 g (33%) of 5′-chloro-2′-fluoro-6-(3-fluorobenzylamino)-2,4′-bipyridine-5-carbonitrile. LCMS (m/z): 357.2 (MH+), retention time=1.02 min.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08415381B2
出典データセットuspto-grants-2013_04
ORD IDord-cc9f1fe7b1e342d399118193725b94cb
出典メモuspto-grants-2013_04