HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1019822Erstellt: 25. Oktober 2026
Dimethylformamide → 2-(1-(3-Chloro-6-fluoroquinoxalin-2-yl)ethyl)isoindoline-1,3-dione
https://huagongshe.com/reaction/1019822
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Dimethylformamide | HCID 6228 | — |
| Edukt | Phthalimide potassium salt | HCID 24194345 | — |
| Edukt | 2-(1-Bromoethyl)-3-chloro-6-fluoroquinoxaline | HCID 86698520 | — |
| Edukt | 3-Chloro-2-(1-chloroethyl)-6-fluoroquinoxaline | HCID 86698522 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | 2-(1-(3-Chloro-6-fluoroquinoxalin-2-yl)ethyl)isoindoline-1,3-dione | HCID 86698521 | 76% |
Reaktionsschritte
To a mixture of 2-(1-bromoethyl)-3-chloro-6-fluoroquinoxaline (57.17 g, 197.5 mmol) containing 3-chloro-2-(1-chloroethyl)-6-fluoroquinoxaline (48.39 g, 197.5 mmol) in N,N-dimethylformamide (700.0 ml, 197.5 mmol) was added potassium phthalimide (91.43 g, 493.6 mmol) at rt and the mixture was stirred at rt for 1 h. After 1 h, to the mixture was added water (2 L). The mixture was extracted with DCM (500 mL×3). The combined organic layers were washed with brine (1 L×1), dried over MgSO4, filtered, and concentrated under reduced pressure to give a red liquid. The red liquid was filtered though a plug of silica (5.5 inch diameter×5 inch height), and eluented with 20% of EtOAc in hexane, then 30% of EtOAc in hexane, and then 100% of EtOAc as eluent to give two fractions. Second fraction, desired product 2-(1-(3-chloro-6-fluoroquinoxalin-2-yl)ethyl)isoindoline-1,3-dione (53.367 g, 75.97% yield) as a pink solid. 1H NMR (400 MHz, DMSO-d6) δ ppm 8.25 (dd, J=9.4, 5.9 Hz, 1H), 7.81-7.95 (m, 6H), 5.86 (q, J=6.8 Hz, 1H), 1.86 (d, J=7.0 Hz, 3H). Mass Spectrum (ESI) m/e=356.0 (M+1).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08716290B2 |
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| Quelldatensatz | uspto-grants-2014_05 |
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| ORD ID | ord-b97005f02d9b4d6489adc2d723555f97 |
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| Quellennotiz | uspto-grants-2014_05 |
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