HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1187410Generated: November 1, 2026
4-Toluenesulfonyl chloride → HCID 68536238, compound
https://huagongshe.com/reaction/1187410
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | HCID 68536377 | HCID 68536377 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 68536238 | HCID 68536238 | — |
Reaction Steps
To a solution of 2-{2-[2-(2-ethyl-1H-imidazo[4,5-c]quinolin-1-yl)ethoxy]ethoxy}-1H-isoindole-l,3(2H)-dione (11.0 g, 25.5 mmol) in chloroform (150 mL) was added mCPBA (11.4 g, 51.1 mmol). The solution was stirred at room temperature for 2 hours. Concentrated ammonium hydroxide (100 mL) was added, followed by p-toluenesulfonyl chloride (5.40 g, 28.1 mmol). The mixture was stirred overnight at room temperature. The mixture was transferred to a separatory fimnel and was washed twice with 5% aqueous ammonium chloride and once with aqueous sodium carbonate solution, dried over magnesium sulfate, filtered, and concentrated. The crude product was purified by flash chromatography (silica gel, gradient elution with 0-5% methanol in dichloromethane) to provide 6 g of 1-{2-[2-(aminooxy)ethoxy]ethyl}-2-ethyl-1H-imidazo[4,5-c]quinolin-4-amine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08673932B2 |
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| Source dataset | uspto-grants-2014_03 |
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| ORD ID | ord-0496fdfb89504598b2d1b8bfdca45dfa |
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| Source note | uspto-grants-2014_03 |
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