HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1857622Erstellt: 26. Oktober 2026
Sodium Iodide → 7-chloro-3-(3,5-dimethylphenyl)-4-[2-(1-methylpiperidin-2-yl)-ethoxy]-6-nitro-1H-quinolin-2-one
https://huagongshe.com/reaction/1857622
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Sodium Iodide | HCID 5238 | — |
| Edukt | Sodium Bicarbonate | HCID 516892 | — |
| Edukt | 2-(2-Chloroethyl)-1-methylpiperidine--hydrogen chloride (1/1) | HCID 12432704 | — |
| Edukt | 7-chloro-3-(3,5-dimethylphenyl)-4-hydroxy-6-nitro-1H-quinolin-2-one | HCID 54711238 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | 7-chloro-3-(3,5-dimethylphenyl)-4-[2-(1-methylpiperidin-2-yl)-ethoxy]-6-nitro-1H-quinolin-2-one | HCID 9982147 | 49,1% |
Reaktionsschritte
A mixture of 7-chloro-3-(3,5-dimethylphenyl)-4-hydroxy-6-nitro-1H-quinolin-2-one (100 mg) and sodium bicarbonate (54 mg) was suspended in 2 mL dry N,N-dimethylformamide and heated to 80° C. on an oil bath. After 30 minutes, sodium iodide (48 mg) was added followed by 2-(2-chloroethyl)-1-methylpiperidine hydrochloride (64 mg) and the mixture stirred at 80° C. for 7 hours. At this time the reaction was cooled to room temperature and quenched by the addition of 25 mL ice/water. The mixture was filtered and the residue washed (1×) with ice water then dried at 40° C. Purification of the crude product by flash chromatography on silica gel (chloroform:10% ammonium hydroxide in methanol, 95:5) gave the title compound (67 mg).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06147088 |
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| Quelldatensatz | uspto-grants-2000_11 |
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| ORD ID | ord-cf5fe14dfd464d14a753b1d117efa825 |
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| Quellennotiz | uspto-grants-2000_11 |
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