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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 736202Erstellt: 25. Oktober 2026

Diisopropylethylamine → (2-Chloro-5-methanesulfonyl-phenyl)-[4-(4-trifluoromethyl-phenyl)-piperazin-1-yl]-methanone

https://huagongshe.com/reaction/736202

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylethylamineHCID 81531—
Edukt1-(4-(Trifluoromethyl)phenyl)piperazineHCID 121718—
Edukt2-Chloro-5-(methylsulphonyl)benzoic acidHCID 2329132—
EduktO-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
LösungsmittelDimethylformamideHCID 6228—
Produkt(2-Chloro-5-methanesulfonyl-phenyl)-[4-(4-trifluoromethyl-phenyl)-piperazin-1-yl]-methanoneHCID 5979368988,4%

Reaktionsschritte

To a solution of 2-Chloro-5-methanesulfonyl-benzoic acid (102 mg, 0.43 mmol) in dimethylformamide (20 ml) were successively added TBTU (153 mg, 0.48 mmol), N-ethyldiisopropylamine (0.28 ml, 2.17 mmol) and 1-(4-trifluoromethylphenyl)piperazine (ABCR F07741NB, [30459-17-7], 100 mg, 0.43 mmol). The reaction was then stirred at room temperature for two hours, then concentrated in vacuo and purified by column chromatography (SiO2, 50 g, heptane/ethylacetate=0 to 100%), to give the title compound as a colorless gum (170 mg, 0.38 mmol). MS (m/e): 464.3 (M+NH4+, 100%)

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07595314B2
Quelldatensatzuspto-grants-2009_09
ORD IDord-168f61ed1d9e4caeb75a8b26b0fcc5d1
Quellennotizuspto-grants-2009_09