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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2411226Erstellt: 23. Oktober 2026

Diisopropylethylamine → HCID 71252181, Verbindung

https://huagongshe.com/de/reaction/2411226

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylethylamineHCID 81531—
EduktN,N-bis(2-chloroethyl)-p-toluenesulphonamideHCID 96039—
Edukt4,6-Dimethylpyridin-3-amineHCID 7060669—
LösungsmittelWaterHCID 962—
ProduktHCID 71252181HCID 7125218115,7%

Reaktionsschritte

To 5-amino-2,4-dimethylpyridine (883 mg) were added N,N-diisopropylethylamine (2.1 mL) and N,N-bis(2-chloroethyl)-p-toluenesulfonamide (2.08 g), and the mixture was stirred with heating under reflux. After completion of the reaction, water was added to the reaction mixture, the mixture was extracted with chloroform, and the solvent was evaporated. The obtained residue was purified by column chromatography (chloroform:methanol) to give 1-(4,6-dimethylpyridin-3-yl)-4-(toluene-4-sulfonyl)piperazine (380 mg). The obtained 1-(4,6-dimethylpyridin-3-yl)-4-(toluene-4-sulfonyl)piperazine (380 mg) was dissolved in acetic acid (2 mL), 40% hydrobromic acid (2 mL) was added, and the mixture was stirred at 100° C. After completion of the reaction, the reaction mixture was neutralized with aqueous sodium hydroxide solution, and the mixture was extracted with ethyl acetate. The solvent was evaporated from the organic layer to give the title compound (131 mg).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08816079B2
Quelldatensatzuspto-grants-2014_08
ORD IDord-eb0674f3edd244f3995b85e2b604a5a1
Quellennotizuspto-grants-2014_08