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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 883531Erstellt: 24. Oktober 2026

Diisopropylethylamine → 3-Phenylsulfonyl-8-piperazin-1-yl-quinoline hydrochloride

https://huagongshe.com/de/reaction/883531

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylethylamineHCID 81531—
Edukt1-Chloroethyl chloroformateHCID 521305—
Edukt8-(4-Methyl-piperazin-1-yl)-3phenylsulfonylquinolineHCID 9929162—
Lösungsmittel1,2-DichloroethaneHCID 11—
Produkt3-Phenylsulfonyl-8-piperazin-1-yl-quinoline hydrochlorideHCID 5697214152,5%

Reaktionsschritte

A stirred solution of 8-(4-methyl-piperazin-1-yl)-3-phenylsulfonylquinoline (E1) (0.148 g, 0.4 mmol), 1-chloroethyl chloroformate (0.093 ml, 0.85 mmol) and N,N-diisopropylethylamine (0.148 ml, 0.85 mmol) in 1,2-dichloroethane (9 ml) was heated at reflux for 1.25 h under argon. The reaction mixture was cooled to ambient temperature and concentrated in vacuo to an oil. The oil was purified by chromatography over silica gel eluting with a gradient of methanol/dichloromethane, pooling fractions which contained the major component (Rf 0.9, methanol/dichloromethane 1:19). The purified material was redissolved in methanol (15 ml) and the solution was refluxed for 1 h under argon. The reaction mixture was cooled to ambient temperature and concentrated in vacuo to a solid which was stirred with diethyl ether (5 ml) and filtered to afford the title compound (E2) (0.08 g, 0.21 mmol, 51%);

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08236947B2
Quelldatensatzuspto-grants-2012_08
ORD IDord-3b50d8856611446ba3e29aa96b6acfa8
Quellennotizuspto-grants-2012_08