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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 43386Erstellt: 25. Oktober 2026

Diisopropylethylamine → (2S)-4-{[2-bromo-4-(trifluoromethyl)phenyl]sulfonyl}-2-methyl-1-[(6-methyl-3-pyridinyl)carbonyl]piperazine

https://huagongshe.com/reaction/43386

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylethylamineHCID 81531—
Edukt2-Bromo-4-(trifluoromethyl)benzenesulfonyl chlorideHCID 2778611—
Edukt(2S)-2-Methyl-1-[(6-methyl-3-pyridinyl)carbonyl]piperazineHCID 59161378—
LösungsmittelDichloromethaneHCID 6344—
Produkt(2S)-4-{[2-bromo-4-(trifluoromethyl)phenyl]sulfonyl}-2-methyl-1-[(6-methyl-3-pyridinyl)carbonyl]piperazineHCID 5916138846,8%

Reaktionsschritte

To a solution of (2S)-2-methyl-1-[(6-methyl-3-pyridinyl)carbonyl]piperazine (may be prepared as described in Description 13) (200 mg, 0.912 mmol) in DCM (10 mL) was added 2-bromo-4-(trifluoromethyl)benzenesulfonyl chloride (295 mg, 0.912 mmol) followed by DIPEA (0.159 mL, 0.912 mmol). The reaction mixture was left stirring at room temperature for 15 h. The solvent was removed by evaporation and the crude residue was dissolved in DCM (30 ml), washed with saturated sodium bicarbonate (40 ml), dried (hydrophobic frit) and evaporated under vacuum. The crude product was purified by silica chromatography using a gradient EtOAc/iso-hexane from 20/80 to 100/0. The desired fractions were combined and concentrated under vacuum to give the title compound (216 mg).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08536183B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-268b1917a9fa4ff28bdd9e1cfbb036f2
Quellennotizuspto-grants-2013_09