HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1058634Generated: October 31, 2026
4-Fluorobenzenesulfonyl chloride → HCID 18668807, compound
https://huagongshe.com/reaction/1058634
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Fluorobenzenesulfonyl chloride | HCID 9588 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 18668816 | HCID 18668816 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 18668807 | HCID 18668807 | 63.5% |
Reaction Steps
To a suspension of 0.50 g of 4-chloro-1-[2-(4-piperidyl)ethyl]-1H-imidazo-[4,5-c]quinoline trifluoroacetate and 0.32 g of potassium carbonate in 2 ml of N,N-dimethylformamide, a solution of 0.23 g of p-fluorobenzenesulfonyl chloride in 3 ml of N,N-dimethylformamide was added dropwise at room temperature, and the mixture was stirred for 5 hours. The reaction mixture was adjusted to pH 10 with 10% aqueous sodium hydroxide solution, and extracted with ethyl acetate. The extract was washed successively with water and saturated brine, and dried, and then the solvent was evaporated to give 0.35 g of a colorless solid. Recrystallization from a mixture of methanol, ethanol and water gave colorless crystals having the melting point of from 175 to 178.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06518265B1 |
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| Source dataset | uspto-grants-2003_02 |
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| ORD ID | ord-5085c093352d423d8b26984b661d060d |
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| Source note | uspto-grants-2003_02 |
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