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HRID 2113412作成日:2026年10月27日

Aminopyralid → 4-Amino-3,6-dichloro-5-fluoropyridine-2-carboxylic acid

https://huagongshe.com/reaction/2113412

反応式

関与物質

役割名称HCID仕込み量
反応物AminopyralidHCID 213012—
反応物SelectfluorHCID 2724933—
溶媒WaterHCID 962—
生成物4-Amino-3,6-dichloro-5-fluoropyridine-2-carboxylic acidHCID 2169664666.5%

反応手順

A solution of 4-amino-3,6-dichloropyridine-2-carboxylic acid (1100 g, 5.31 mol), 1-chloromethyl-4-fluoro-1,4-diazoniabicyclo[2.2.2]octanebis(tetrafluoroborate) (2100 g, 5.93 mol) in water (6000 mL) was warmed to 65° C. for six hours. After cooling to ambient temperature, the reaction mixture was stirred an additional 18 hours. The solution was concentrated and the resulting solid washed with 6 N hydrochloric acid (5×1000 mL) and dried to give 4-amino-3,6-dichloro-5-fluoropyridine-2-carboxylic acid (757 g, 3.53 mol. 58% purity). This crude material was added to methanol (3000 mL) which had been saturated with anhydrous hydrogen chloride and the reaction mixture was warmed to 45° C. for 2 hours. The solution was added with vigorous stirring to ice water (4000 mL) and the resulting solid collected. The crude ester was dissolved in ethyl acetate (1000 mL) and washed with saturated sodium bicarbonate solution (2×1000 mL), dried, and concentrated. The resulting solid was recrystallized from ethyl acetate/hexanes to give methyl 4-amino-3,6-dichloro-5-fluoropyridine-2-carboxylate (402.5 g, 1.67 mol), mp 128-131° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07432227B2
出典データセットuspto-grants-2008_10
ORD IDord-f297286f481c497dbbb33e5e8efc3b3c
出典メモuspto-grants-2008_10