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HRID 379396作成日:2026年10月26日

2-Bromoethanol → N-(3,5-Bis-trifluoromethyl-benzyl)-6-[4-(2-hydroxy-ethyl)-piperazin-1-yl]-N-methyl-4-o-tolyl-nicotinamide

https://huagongshe.com/reaction/379396

反応式

関与物質

役割名称HCID仕込み量
反応物2-BromoethanolHCID 10898—
反応物Potassium CarbonateHCID 11430—
反応物Sodium HydroxideHCID 14798—
反応物N-(3,5-bis-trifluoromethyl-benzyl)-N-methyl-6-piperazin-1-yl-4-o-tolyl-nicotinamideHCID 10280286—
溶媒AcetonitrileHCID 6342—
生成物N-(3,5-Bis-trifluoromethyl-benzyl)-6-[4-(2-hydroxy-ethyl)-piperazin-1-yl]-N-methyl-4-o-tolyl-nicotinamideHCID 993818878.7%

反応条件

温度45 °C

反応手順

A mixture of 100 mg (0.186 mmol) N-(3,5-bis-trifluoromethyl-benzyl)-N-methyl-6-piperazin-1-yl-4-o-tolyl-nicotinamide (Example 53), 0.030 ml (0.42 mmol)2-bromo-ethanol and 46 mg (0.33 mmol) potassium carbonate in 2 ml acetonitrile was stirred at 45° C. for 70 h. After cooling to room temperature 10 ml 1 N sodium hydroxide solution were added. Extraction with 3 15-ml portions of ethyl acetate, drying with sodium sulfate and concentration gave 138 mg of the crude product. Flash column chromatography afforded 85 mg (78.6%) of the title compound as a white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06297375B1
出典データセットuspto-grants-2001_10
ORD IDord-911c5194d69542a1ab0ef605ba97880a
出典メモuspto-grants-2001_10