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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1852856Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/1852856

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktHydroxyamine hydrochlorideHCID 443297—
EduktSodium BicarbonateHCID 516892—
Edukt2-(prop-1-en-2-yl)-3H-imidazo[4,5-c]pyridine-6-carbonitrileHCID 86724601—
LösungsmittelEthanolHCID 702—
Produkt2-(prop-1-en-2-yl)-3H-imidazo[4,5-c]pyridine-6-carboximidamideHCID 86724602—

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08962611B2
Quelldatensatzuspto-grants-2015_02
ORD IDord-8b82a2f0adf04cc9bf98b10275986a3c
Quellennotizuspto-grants-2015_02