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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 271137Erstellt: 26. Oktober 2026

Sodium Bicarbonate → 8-(4-Methyl-piperazin-1-yl)-3phenylsulfonylquinoline

https://huagongshe.com/reaction/271137

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium BicarbonateHCID 516892—
EduktBenzenesulfinic acid, sodium saltHCID 2723840—
Edukt3-Bromo-8-(4-methyl-piperazin-1-yl)-quinolineHCID 67313624—
Edukt3-Iodo-8-(4-methyl-piperazin-1-yl)-quinolineHCID 67313746—
KatalysatorCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
LösungsmittelMethanolHCID 887—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelDichloromethaneHCID 6344—
Produkt8-(4-Methyl-piperazin-1-yl)-3phenylsulfonylquinolineHCID 99291627%

Reaktionsbedingungen

Temperatur120 °C

Reaktionsschritte

A 4:1 mixture of 3-iodo-8-(4-methyl-piperazin-1-yl)-quinoline (D2) and 3-bromo-8-(4-methyl-piperazin-1-yl)-quinoline (D1) (1.5 g), phenylsulfinic acid sodium salt, dihydrate (2.52 g, 12.6 mmol) and copper (I) iodide (2.4 g, 12.6 mmol) in N,N-dimethylformamide (25 ml) was stirred in an oil bath at 120° C. for 40 h under argon. To the reaction mixture, cooled to ambient temperature, was added 5% sodium hydrogen carbonate solution (100 ml) and dichloromethane (100 ml) with vigorous shaking. The insoluble material was filtered, washed with dichloromethane (3×20 ml) and discarded. The filtrate and washings were transferred to a separating funnel and the layers separated. The aqueous layer was extracted with dichloromethane (100 ml) and the combined organic extracts were washed with water (100 ml), dried (MgSO4) and concentrated in vacuo to an oil (0.9 g). The oil was purified by chromatography over silica gel eluting with a gradient of methanol/dichloromethane to afford an orange oil (0.28 g, Rf 0.11, methanol/dichloromethane 1:19). This material was further purified by passage through a strong cation exchange (SCX) column eluting firstly with methanol (fractions discarded) and then with methanol/aqueous ammonia-880 (10:1) to give the title compound (E1) as an orange oil (0.152 g, 0.41 mmol, 7% over two steps);

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07452888B2
Quelldatensatzuspto-grants-2008_11
ORD IDord-cc38edef63f141558aa66e6471a9b3f5
Quellennotizuspto-grants-2008_11