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HRID 1920251생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/1920251

반응식

참여 물질

역할이름HCID투입량
반응물AmmoniaHCID 222—
반응물IsobutylamineHCID 6558—
반응물Trimethyl orthovalerateHCID 83755—
반응물Aminomalononitrile p-toluenesulphonateHCID 563049—
용매AcetonitrileHCID 6342—
생성물5-amino-2-butyl-1-(2-methylpropyl)-1H-imidazole-4-carbonitrileHCID 5850013962.1%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08168802B2
출처 데이터셋uspto-grants-2012_05
ORD IDord-eebb4b29fbff490aa010ed2a23676b60
출처 메모uspto-grants-2012_05