HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1710604Generated: October 26, 2026
4-(Difluoromethoxy)benzenesulfonyl chloride → 4-Difluoromethoxy-N-[4-methoxy-3-(4-methyl-piperazin-1-yl)-phenyl]-benzenesulfonamide
https://huagongshe.com/reaction/1710604
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-(Difluoromethoxy)benzenesulfonyl chloride | HCID 2778223 | — |
| Reactant | 4-Methoxy-3-(4-methylpiperazin-1-yl)aniline | HCID 10331101 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 4-Difluoromethoxy-N-[4-methoxy-3-(4-methyl-piperazin-1-yl)-phenyl]-benzenesulfonamide | HCID 42602834 | 81.8% |
Reaction Steps
0.18 mL of 4-difluoromethoxybenzene sulfonyl chloride (1.13 mmol) were added to a solution of 0.25 g of (1.13 mmol) 4-methoxy-3-(4-methyl-piperazin-1-yl)-phenylamine in 10 mL of pyridine. The reaction mixture was stirred for 16 h at room temperature. The solvent was evaporated at reduced pressure. After addition of toluene and dichloromethane the mixture was again evaporated twice. The thus obtained residue was partitioned between dichloromethane and 5% aqueous ammoniumchloride. The organic phase was washed with saturated aqueous sodium chloride solution, dried over sodium sulfate, filtered, and the solvent was evaporated under reduced pressure. The obtained crude product was further purified via HPLC to yield 0.395 g of the desired title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07790727B2 |
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| Source dataset | uspto-grants-2010_09 |
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| ORD ID | ord-7741a19bab1b4660b445be4d6848dd4f |
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| Source note | uspto-grants-2010_09 |
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