HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1992588Generated: November 1, 2026
4-Toluenesulfonyl chloride → HCID 68536238, compound
https://huagongshe.com/reaction/1992588
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-1,3(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 funnel and was washed twice with 5% aqueous ammonium chloride and once with aqueous sodium carbonate solution, dried over magnesium sulfate, filtered, and concentrated under reduced pressure. 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 |
|---|
| Patent number | US07648997B2 |
|---|
| Source dataset | uspto-grants-2010_01 |
|---|
| ORD ID | ord-dc2598efb33c4e3292f194f7e157550f |
|---|
| Source note | uspto-grants-2010_01 |
|---|