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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2471Erstellt: 23. Oktober 2026

N-{2-[4-(4-fluorobenzoyl)piperidino]ethyl}-4-hydroxymethyl-N-(2-methoxyphenyl)benzene sulfonamide → N-{2-[4-(4-Fluorobenzoyl)piperidino]ethyl}-4-formyl-N-(2-methoxyphenyl)benzenesulfonamide

https://huagongshe.com/de/reaction/2471

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN-{2-[4-(4-fluorobenzoyl)piperidino]ethyl}-4-hydroxymethyl-N-(2-methoxyphenyl)benzene sulfonamideHCID 19689938—
KatalysatorHCID 178418406HCID 178418406—
LösungsmittelDichloromethaneHCID 6344—
ProduktN-{2-[4-(4-Fluorobenzoyl)piperidino]ethyl}-4-formyl-N-(2-methoxyphenyl)benzenesulfonamideHCID 1968983281,7%

Reaktionsschritte

Activated manganese dioxide (870 mg, 10.0 mmol) was suspended in methylene chloride (10 ml), and N-{2-[4-(4-fluorobenzoyl)piperidino]ethyl}-4-hydroxymethyl-N-(2-methoxyphenyl)benzene sulfonamide (259 mg, 0.492 mmol) dissolved in methylene chloride (3 ml) was added to the suspension. After 30 minutes of stirring at room temperature, the reaction mixture was filtered through silica gel (1 g) which was further subjected to elution with ethyl acetate. Thereafter, the filtrate and eluate were combined, and the solvent was removed by evaporation to obtain 211 mg (81.7%) of the title compound in a colorless amorphous form.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05728835
Quelldatensatzuspto-grants-1998_03
ORD IDord-6642989d69874a4bb62b90deed971d65
Quellennotizuspto-grants-1998_03