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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 431640Erstellt: 24. Oktober 2026

Pyridine → N-{2-[4-(1H-Benzimidazol-2-yl)-piperazin-1-yl]-ethyl}-2,4-dichloro-5,N-dimethyl-benzenesulfonamide

https://huagongshe.com/de/reaction/431640

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPyridineHCID 1049—
Edukt2,4-Dichloro-5-methylbenzene-1-sulphonyl chlorideHCID 119914—
Edukt{2-[4-(1h-Benzimidazol-2-yl)-piperazin-1-yl]-ethyl}-methyl-amine hydrochloride saltHCID 18761519—
LösungsmittelDichloromethaneHCID 6344—
ProduktN-{2-[4-(1H-Benzimidazol-2-yl)-piperazin-1-yl]-ethyl}-2,4-dichloro-5,N-dimethyl-benzenesulfonamideHCID 991311717%

Reaktionsschritte

A mixture of 2,4-dichloro-5-methylbenzenesulphonyl chloride (81 mg, 0.31 mmol), {2-[4-(1H-Benzimidazol-2-yl)-piperazin-1-yl]-ethyl}-methyl-amine hydrochloride salt (D23) (80 mg, 0.31 mmol) and pyridine (0.5 ml) in dry dichloromethane (5 ml) was stirred at room temperature for 17 h. The mixture was then diluted with dichloromethane (30 ml), washed with aqueous sodium bicarbonate (1×10 ml) and dried.(MgSO4). The solvent was evaporated and the residue was co-evaporated with toluene (5 ml). Column chromatography of the residue (eluting with methanol-dichloromethane gradient) gave the product as a yellowish solid (25 mg, 17%); MS: m/z (MH+)=482.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06660751B1
Quelldatensatzuspto-grants-2003_12
ORD IDord-c1a2f00cd6634f2db97f4d28c6888f51
Quellennotizuspto-grants-2003_12