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HRID 1192839作成日:2026年10月25日

N-[(6-chloropyridin-3-yl)methyl]-2,2-difluoroethanamine → N-[(6-chloropyridin-3-yl)methyl]-N-(2,2-difluoroethyl)-4-hydroxy-2-oxo-2,5-dihydrofuran-3-carboxamide

https://huagongshe.com/reaction/1192839

反応式

関与物質

役割名称HCID仕込み量
反応物N-[(6-chloropyridin-3-yl)methyl]-2,2-difluoroethanamineHCID 44604123—
反応物Methyl 4-hydroxy-2-oxo-2,5-dihydrofuran-3-carboxylateHCID 54677706—
溶媒ButyronitrileHCID 8008—
生成物N-[(6-chloropyridin-3-yl)methyl]-N-(2,2-difluoroethyl)-4-hydroxy-2-oxo-2,5-dihydrofuran-3-carboxamideHCID 86661408—

反応条件

温度65 °C

反応手順

10 g of methyl 4-hydroxy-2-oxo-2,5-dihydrofuran-3-carboxylate are initially introduced in 111 g of butyronitrile and admixed with 5 g of N-[(6-chloropyridin-3-yl)methyl]-2,2-difluoroethanamine. The solution is heated at 65° C. for 3 h. The solution is then extracted with 300 ml of water and then washed with 300 ml of 5% strength hydrochloric acid solution. The organic phase is dried over magnesium sulphate and the solvent is removed in vacuo. For purification, recrystallization from isopropanol is carried out.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08680285B2
出典データセットuspto-grants-2014_03
ORD IDord-33b2f7e565e44cbd870ad14183a7eeae
出典メモuspto-grants-2014_03