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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1428952Erstellt: 25. Oktober 2026

Triethylamine → N-Cyclopropyl-N-piperidin-4-yl-3-(trifluoromethyl)benzenesulfonamide

https://huagongshe.com/reaction/1428952

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktPotassium CarbonateHCID 11430—
Edukt3-(Trifluoromethyl)benzenesulfonyl chlorideHCID 2733250—
Edukt1-Benzyl-N-cyclopropylpiperidin-4-amineHCID 2735481—
EduktN-(1-benzylpiperidin-4-yl)-N-cyclopropyl-3-trifluoromethyl-benzenesulfonamideHCID 4114155—
LösungsmittelDichloromethaneHCID 6344—
ProduktN-Cyclopropyl-N-piperidin-4-yl-3-(trifluoromethyl)benzenesulfonamideHCID 2773944—
ProduktN-(1-benzylpiperidin-4-yl)-N-cyclopropyl-3-trifluoromethyl-benzenesulfonamideHCID 4114155—

Reaktionsschritte

N-(1-Benzylpiperidin-4-yl)-N-cyclopropyl-3-trifluoromethyl-benzenesulfonamide: N-Benzyl-4-cyclopropylaminopiperidine (5.0 g, 21.71 mmol) and triethylamine (3.6 mL, 26.05 mmol) were dissolved in dichloromethane (DCM, 100 mL). 3-Trifluoromethylbenzenesulfonyl chloride (3.47 mL, 21.71 mmol) was added and the resulting reaction mixture was stirred overnight. The mixture then was poured into potassium carbonate solution (200 mL), extracted with ether (2×200 mL), dried (MgSO4), and concentrated in vacuum to give a crude product as a yellow gum, which was purified by column chromatography on silica gel (hexane/EtOAc, 2:1). The title compound N-(1-benzylpiperidin-4-yl)-N-cyclopropyl-3-trifluoromethyl-benzenesulfonamide was obtained (9 g, 95% yield) as a pale yellow gum. Rf=0.42 (UV detection).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08937181B2
Quelldatensatzuspto-grants-2015_01
ORD IDord-1f6641ea8fe248938efe7100e90267a5
Quellennotizuspto-grants-2015_01