HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 883528Erstellt: 25. Oktober 2026
Sodium Bicarbonate → 8-(4-Methyl-piperazin-1-yl)-3phenylsulfonylquinoline
https://huagongshe.com/reaction/883528
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Sodium Bicarbonate | HCID 516892 | — |
| Edukt | Benzenesulfinic acid, sodium salt | HCID 2723840 | — |
| Edukt | 3-Bromo-8-(4-methyl-piperazin-1-yl)-quinoline | HCID 67313624 | — |
| Edukt | 3-Iodo-8-(4-methyl-piperazin-1-yl)-quinoline | HCID 67313746 | — |
| Katalysator | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 8-(4-Methyl-piperazin-1-yl)-3phenylsulfonylquinoline | HCID 9929162 | — |
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 (El) as an orange oil (0.152 g, 0.41 mmol, 7% over two steps);
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08236947B2 |
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| Quelldatensatz | uspto-grants-2012_08 |
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| ORD ID | ord-17846fc436b84853a0becb11ffbd535e |
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| Quellennotiz | uspto-grants-2012_08 |
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