HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1710598Erstellt: 25. Oktober 2026
3-(Difluoromethoxy)benzenesulfonyl chloride → 4-[5-(3-Difluoromethoxy-benzenesulfonylamino)-2-methoxy-phenyl]-piperazine-1-carboxylic Acid tert-butyl Ester
https://huagongshe.com/reaction/1710598
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 3-(Difluoromethoxy)benzenesulfonyl chloride | HCID 2778226 | — |
| Edukt | Tert-butyl 4-(5-amino-2-methoxyphenyl)piperazine-1-carboxylate | HCID 10686178 | — |
| Lösungsmittel | Pyridine | HCID 1049 | — |
| Produkt | 4-[5-(3-Difluoromethoxy-benzenesulfonylamino)-2-methoxy-phenyl]-piperazine-1-carboxylic Acid tert-butyl Ester | HCID 57699506 | 75,5% |
Reaktionsschritte
0.745 g of 4-(5-Amino-2-methoxy-phenyl)-piperazine-1-carboxylic acid tert-butyl ester (2.423 mmol) were dissolved in 35 ml of pyridine. 0.588 g of 3-(difluoromethoxy)-benzene-sulfonylchloride were added dropwise and the reaction mixture was stirred for 72 h at room temperature. The solvent was evaporated, the residue was dissolved in 40 ml dichloromethane and the organic phase was washed twice with 30 ml aqueous saturated ammonium chloride. The organic phase was dried over magnesium sulfate, filtered, and the solvent was evaporated under reduced pressure. The crude product was purified three times via silica gel chromatography using dichloromethane-methanol, and dichloromethane-ethyl acetate as eluent. 0.94 g of the title compound were isolated.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07790727B2 |
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| Quelldatensatz | uspto-grants-2010_09 |
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| ORD ID | ord-0e696af7ba8c420c99894e94d037ad6f |
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| Quellennotiz | uspto-grants-2010_09 |
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