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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1469339Generated: October 31, 2026

Phthalimide potassium salt → HCID 57515602, compound

https://huagongshe.com/reaction/1469339

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhthalimide potassium saltHCID 24194345—
Reactant1-{[4-amino-2-(chloromethyl)-1H-imidazo[4,5-c]quinolin-1-yl]methyl}cyclobutanolHCID 57515522—
SolventDimethylformamideHCID 6228—
ProductHCID 57515602HCID 5751560295.5%

Reaction Steps

Under a nitrogen atmosphere, potassium phthalimide (1.21 g, 6.52 mmol) was added to a solution of 1-{[4-amino-2-(chloromethyl)-1H-imidazo[4,5-c]quinolin-1-yl]methyl}cyclobutanol (1.88 g, 5.93 mmol) in DMF (30 mL), and the reaction mixture was stirred at room temperature overnight and then concentrated under reduced pressure. The residue was partitioned between chloroform (200 mL) and water (25 mL)/saturated aqueous sodium bicarbonate (2×40 mL). The organic layer was washed with brine (2×40 mL), dried over sodium sulfate, filtered, and concentrated under reduced pressure to provide 2.42 g of 2-({4-amino-1-[(1-hydroxycyclobutyl)methyl]-1H-imidazo[4,5-c]quinolin-2-yl}methyl)-1H-isoindole-1,3(2H)-dione.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09006264B2
Source datasetuspto-grants-2015_04
ORD IDord-e9f73f989aba4922aec6eb41e3e5e331
Source noteuspto-grants-2015_04