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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 81251생성일: 2026년 10월 26일

Water → 2-(prop-1-en-2-yl)-3H-imidazo[4,5-c]pyridine-6-carboximidamide

https://huagongshe.com/reaction/81251

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Hydroxyamine hydrochlorideHCID 443297—
반응물Sodium BicarbonateHCID 516892—
반응물2-(prop-1-en-2-yl)-3H-imidazo[4,5-c]pyridine-6-carbonitrileHCID 86724601—
용매EthanolHCID 702—
생성물2-(prop-1-en-2-yl)-3H-imidazo[4,5-c]pyridine-6-carboximidamideHCID 86724602—

반응 조건

온도100 °C

반응 단계

Hydroxylamine hydrochloride (37.7 mg, 0.54 mmol), sodium bicarbonate (68.4 mg, 0.81 mmol), and water (0.54 mL) were combined in a vial and stirred for 15 minutes. This solution was added to a vial containing 4-(5-chloropyridin-3-yl)-3-[(1R or S)-1-(trans-4-methylcyclohexyl)ethyl]-2-(prop-1-en-2-yl)-3H-imidazo[4,5-c]pyridine-6-carbonitrile (114 mg, 0.27 mmol) dissolved in ethanol (1.3 mL). The mixture was sealed and heated at 100° C. for 1 hour. The reaction was cooled to room temperature, quenched with water, and extracted with ethyl acetate (2×). The combined organic layers were dried over sodium sulfate, filtered, and concentrated to afford 4-(5-chloropyridin-3-yl)-N-hydroxy-3-[(1R or S)-1-(trans-4-methylcyclohexyl)ethyl]-2-(prop-1-en-2-yl)-3H-imidazo[4,5-c]pyridine-6-carboximidamide. MS ESI calc'd. for C24H29ClN6O [M+H]+ 453. found 453.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08846657B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-586cbef5314540cb93ce5ff67db20aa2
출처 메모uspto-grants-2014_09