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HRID 243103作成日:2026年10月24日

Ammonium Chloride → (5-Fluoro-2-nitrophenyl)-(5-fluoropyridin-3-yl)amine

https://huagongshe.com/ja/reaction/243103

反応式

関与物質

役割名称HCID仕込み量
反応物Ammonium ChlorideHCID 25517—
反応物2,4-DifluoronitrobenzeneHCID 67967—
反応物5-Fluoro-3-pyridinamineHCID 574450—
反応物Potassium tert-butoxideHCID 23665647—
溶媒TetrahydrofuranHCID 8028—
生成物(5-Fluoro-2-nitrophenyl)-(5-fluoropyridin-3-yl)amineHCID 6815775258%

反応条件

温度0 °C

反応手順

Alternative procedure: Potassium tert-butoxide (28.1 g, 0.25 mol) was added, in 2 portions, to a stirred solution of 3-amino-5-fluoropyridine (14.0 g, 0.125 mol) in anhydrous THF (400 mL) under a nitrogen atmosphere at 0° C. After 45 min stirring at 0° C., the resulting dark purple solution was transferred by cannula to a stirred solution of 2,4-difluoro-1-nitrobenzene (13.8 mL, 0.125 mol) in anhydrous THF (100 mL), at 0° C., over a period of 20 min. The resulting mixture was stirred for a further 45 min then poured onto a RT solution of NH4Cl (1:1 saturated solution:H2O, 1 L). The resulting yellow precipitate was filtered, washed with water and dried under vacuum at 50° C. to afford the title compound as an orange solid (18.2 g). The filtrate was partially evaporated, to remove some of the reaction solvent, the resulting precipitate was filtered then triturated with EtOAc to give a further 3.5 g of the title compound (overall 21.7 g, 69%) LCMS (Method C): RT 3.18 min [M+H]+ 252.13

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08653089B2
出典データセットuspto-grants-2014_02
ORD IDord-48475f8f719d4c65873c9c3e29bf3c28
出典メモuspto-grants-2014_02