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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2411227Erstellt: 26. Oktober 2026

Hydrogen Bromide → HCID 83698021, Verbindung

https://huagongshe.com/reaction/2411227

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrogen BromideHCID 260—
EduktSodium HydroxideHCID 14798—
Edukt1-(4,6-Dimethylpyridin-3-yl)-4-(toluene-4-sulfonyl)piperazineHCID 71252181—
LösungsmittelAcetic AcidHCID 176—
ProduktHCID 83698021HCID 8369802162,3%

Reaktionsbedingungen

Temperatur100 °C

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-567da05e6a364c3f873dd3bbccd9f107
Quellennotizuspto-grants-2014_08