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HRID 49720作成日:2026年10月25日

Ammonium formate → (RS) Methyl 3-{5-[2-(4-amino-3-hydroxy-phenyl)-acetylamino]-pyridin-2-yl}-butanoate

https://huagongshe.com/reaction/49720

反応式

関与物質

役割名称HCID仕込み量
反応物Ammonium formateHCID 2723923—
反応物(RS) methyl 3-{5-[2-(3-hydroxy-4-nitrophenyl)-acetylamino]-pyridin-2-yl}-butanoateHCID 17946659—
触媒PalladiumHCID 23938—
溶媒EthanolHCID 702—
生成物(RS) Methyl 3-{5-[2-(4-amino-3-hydroxy-phenyl)-acetylamino]-pyridin-2-yl}-butanoateHCID 1794663874.5%

反応条件

温度60 °C

反応手順

A solution of (RS) methyl 3-{5-[2-(3-hydroxy-4-nitrophenyl)-acetylamino]-pyridin-2-yl}-butanoate (2.0 g, Reference Example 25) in ethanol (80 mL), at 60° C., was treated with ammonium formate (4.0 g) and 10% palladium on charcoal (0.5 g). After stirring at 60° C. for 1 hour the reaction mixture was cooled and then filtered. The filtrate was evaporated and the residue was dissolved in ethyl acetate. This solution was washed twice with water, then dried over magnesium sulphate and then evaporated to give the title compound (1.37 g) as an oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06706738B2
出典データセットuspto-grants-2004_03
ORD IDord-c5851f05f1e04dd48d0249cc66ba9d27
出典メモuspto-grants-2004_03