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HRID 541029作成日:2026年10月25日

Acetonitrile → Efinaconazole

https://huagongshe.com/reaction/541029

反応式

関与物質

役割名称HCID仕込み量
反応物AcetonitrileHCID 6342—
反応物1-((2-(2,4-Difluorophenyl)-3-methyloxiran-2-yl)methyl)-1H-1,2,4-triazole, (2R-cis)-HCID 10131191—
生成物EfinaconazoleHCID 489181—

反応条件

温度100 °C

反応手順

21.26 g (119.4 mmol) of the 4-methylenepiperidine hydrobromide (4-MP.HBr) obtained in Production 1 and 2.859 g (119.4 mmol) of lithium hydroxide were added to 80 mL of acetonitrile and stirred for a while. Thereafter, 20 g (79.6 mmol) of (2R,3S)-2-(2,4-difluorophenyl)-3-methyl-2-[(1H-1,2,4-triazol-1-yl)methyl]oxirane was added and the mixture was heated under reflux in an oil bath (external temperature: 100° C.) for 14 hours. After the reaction completed, ethanol and distilled water were added to the reaction mixture, whereupon a crystal was precipitated. Thereafter, the crystal was filtered off, washed with 40 mL of an ethanol/water mixture, dried with air at room temperature and further dried under reduced pressure at 40° C. for 12 hours to give a pale yellow crystal of KP-103 in an amount of 24.2 g (yield, 87.3%; purity on HPLC, 95.3%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08871942B2
出典データセットuspto-grants-2014_10
ORD IDord-1c949d4a2db146d892c62822d9539674
出典メモuspto-grants-2014_10