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HRID 1920251作成日:2026年10月26日

Ammonia → 5-amino-2-butyl-1-(2-methylpropyl)-1H-imidazole-4-carbonitrile

https://huagongshe.com/reaction/1920251

反応式

関与物質

役割名称HCID仕込み量
反応物AmmoniaHCID 222—
反応物IsobutylamineHCID 6558—
反応物Trimethyl orthovalerateHCID 83755—
反応物Aminomalononitrile p-toluenesulphonateHCID 563049—
溶媒AcetonitrileHCID 6342—
生成物5-amino-2-butyl-1-(2-methylpropyl)-1H-imidazole-4-carbonitrileHCID 5850013962.1%

反応手順

Dry ammonia was bubbled through a stirred solution of aminomalononitrile p-toluenesulfonate (25.0 g, 98.7 mmol) in anhydrous acetonitrile (1 L). The reaction warmed slightly, and precipitate formed. The precipitate was removed by filtration, and the filtrate was concentrated to a volume of about 500 mL. Trimethyl orthovalerate (17.0 mL, 98.7 mmol) was added, and the resulting solution was heated at reflux for 30 minutes and then allowed to cool to room temperature. Isobutylamine (9.8 mL, 99 mmol) was added, and the reaction was complete in minutes as evidenced by thin layer chromatography (TLC). The volatiles were removed under reduced pressure, and the residue was dissolved in ethyl acetate (400 mL). The resulting solution was washed sequentially with aqueous sodium hydroxide (75 mL of 2 M), water, and brine; dried over magnesium sulfate, and concentrated under reduced pressure to provide a dark solid. The crude product was purified by column chromatography on silica gel (eluting with 50/50 ethyl acetate/hexane) to provide 13.50 g (62%) of 5-amino-2-butyl-1-(2-methylpropyl)-1H-imidazole-4-carbonitrile as a brown solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08168802B2
出典データセットuspto-grants-2012_05
ORD IDord-eebb4b29fbff490aa010ed2a23676b60
出典メモuspto-grants-2012_05