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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2426357Generated: November 2, 2026

Water → HCID 73152965, compound

https://huagongshe.com/reaction/2426357

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantO-Methylhydroxylamine hydrochlorideHCID 521874—
ReactantHCID 67052308HCID 67052308—
SolventPyridineHCID 1049—
ProductHCID 73152965HCID 7315296561.2%

Reaction Steps

Methoxylamine hydrochloride (0.26 g, 3.1 mmol) was added to a stirred solution of 4-[4-amino-1-(2-hydroxy-2-methylpropyl)-1H-imidazo[4,5-c]quinolin-2-yl]butan-2-one (0.600 g, 1.84 mmol) in pyridine (9 mL), and the reaction was stirred at room temperature for 45 minutes. Water (50 mL) was added. The aqueous layer was separated, extracted with dichloromethane (2×50 mL), adjusted to pH 10 with the addition of saturated aqueous sodium carbonate, and extracted with dichloromethane (2×25 mL). The combined organic fractions were washed sequentially with saturated aqueous sodium bicarbonate (50 mL) and brine (50 mL), dried over sodium sulfate, filtered, and concentrated under reduced pressure. The resulting white powder was stirred with diethyl ether for one hour, isolated by filtration, and washed with diethyl ether. The resulting solid (0.45 g) was recrystallized from acetonitrile (20 mL), and the crystals were isolated by filtration, washed with acetonitrile, and dried for 15 hours under vacuum at 60° C. to provide 0.40 g of 4-[4-amino-1-(2-hydroxy-2-methylpropyl)-1H-imidazo[4,5-c]quinolin-2-yl]butan-2-one O-methyloxime as white needles, mp 182-184° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07968563B2
Source datasetuspto-grants-2011_06
ORD IDord-67b6f92bfc32417a866f7e49ace19957
Source noteuspto-grants-2011_06