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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1643470Erstellt: 26. Oktober 2026

Triethylamine → 1-(1-Methylpiperidin-4-yl)-4-((1-(3-(trifluoromethyl)phenylsulfonyl)piperidin-2-yl)methylsulfonyl)piperazine

https://huagongshe.com/reaction/1643470

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
Edukt1-(1-Methyl-4-piperidinyl)piperazineHCID 566324—
Edukt(1-(3-(Trifluoromethyl)phenylsulfonyl)piperidin-2-yl)methanesulfonyl chlorideHCID 59367748—
LösungsmittelDichloromethaneHCID 6344—
Produkt1-(1-Methylpiperidin-4-yl)-4-((1-(3-(trifluoromethyl)phenylsulfonyl)piperidin-2-yl)methylsulfonyl)piperazineHCID 4620497630%

Reaktionsschritte

1-(1-Methyl-4-piperidinyl)piperazine (1.126 mmol) was dissolved in methylene chloride (7 ml), the solution was cooled in an ice bath and triethylamine (2.8 mmol) and (1-(3-(trifluoromethyl)phenylsulfonyl)piperidin-2-yl)methanesulfonic acid chloride (dissolved in methylene chloride (3 ml)) were added. The mixture was stirred for 16 h, during which it was allowed to warm slowly to room temperature. The reaction mixture was diluted with methylene chloride and washed with water and the organic phase was dried over sodium sulfate and concentrated in vacuo. The crude product was purified by column chromatography (silica gel) with methylene chloride/methanol (19:1). Yield: 30%. MS, Rt=2.4 min, m/z=553.0 [MH]+

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08119805B2
Quelldatensatzuspto-grants-2012_02
ORD IDord-64b94bdc6da8478e9d722c226b99b3b0
Quellennotizuspto-grants-2012_02