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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 44794Generated: October 29, 2026

Phthalimide potassium salt → HCID 57515472, compound

https://huagongshe.com/reaction/44794

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhthalimide potassium saltHCID 24194345—
ReactantHCID 57515471HCID 57515471—
SolventDimethylformamideHCID 6228—
ProductHCID 57515472HCID 57515472—

Reaction Steps

Potassium phthalimide (2.59 g, 14.0 mmol) was added to a solution of 1-{[4-amino-2-(chloromethyl)-1H-imidazo[4,5-c]quinolin-1-yl]methyl}cyclohexanol (5.07 g, 13.3 mmol) in DMF (50 mL), and the reaction mixture was stirred at room temperature overnight. An analysis by HPLC indicated the presence of starting material, and additional potassium phthalimide (1 g) was added. The reaction was stirred for an additional five hours, and then concentrated under reduced pressure. The residue was triturated with methanol, and the resulting white solid was isolated by filtration. The filtrate was concentrated under reduced pressure, and the residue was triturated with methanol to afford additional white solid, which was isolated by filtration. The two solids were combined to provide 2-({4-amino-1-[(1-hydroxycyclohexyl)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 numberUS08541438B2
Source datasetuspto-grants-2013_09
ORD IDord-0a402bb2b82a480a824f2f09313ec3e9
Source noteuspto-grants-2013_09