HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1363632Generated: October 28, 2026
Phthalimide potassium salt → HCID 57515472, compound
https://huagongshe.com/reaction/1363632
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phthalimide potassium salt | HCID 24194345 | — |
| Reactant | HCID 57515471 | HCID 57515471 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 57515472 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07884207B2 |
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| Source dataset | uspto-grants-2011_02 |
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| ORD ID | ord-2761500eb14341bf8935cf44e4b1102e |
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| Source note | uspto-grants-2011_02 |
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