HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 340182Erstellt: 25. Oktober 2026
Potassium Carbonate → Pyrazino[2,3-c]quinolin-5-amine
https://huagongshe.com/reaction/340182
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | 3-Chloropyrazine-2-carbonitrile | HCID 292465 | — |
| Edukt | (2-BOC-aminophenyl)boronic acid | HCID 2773226 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | Pyrazino[2,3-c]quinolin-5-amine | HCID 58213747 | — |
Reaktionsschritte
A solution of 2-(tert-butoxycarbonylamino)phenylboronic acid (1.0 eq.) and 3-chloropyrazine-2-carbonitrile (1.0 eq.) in toluene (0.44 M) was mixed with tetrakis(triphenyl-phosphine)palladium (5 mol %) and 2N aqueous potassium carbonate solution (2.0 eq.). The reaction was heated to 100° C. and stirred overnight. After cooling to ambient temperature, the reaction content was diluted with 2% methanol in dichloromethane and water. The two phases were separated, and the aqueous layer was extracted twice with 2% methanol in dichloromethane. The combined organic layers were washed with brine, dried over anhydrous MgSO4, and concentrated en vacuo. The crude product was purified by flash chromatography on a COMBIFLASH® system (ISCO) using 0-50% ethyl acetate in hexane to give a solid. 1H NMR (acetone d-6): δ 9.14 (s, 1H), 8.95 (s, 1H), 8.77 (d, 1H), 7.63-7.66 (m, 2H), 7.38 (t, 1H), 6.77 (br, 2H). LRMS [M+H]=197.1
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08895577B2 |
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| Quelldatensatz | uspto-grants-2014_11 |
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| ORD ID | ord-328bbb2683bf4e94b5d867507ecae260 |
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| Quellennotiz | uspto-grants-2014_11 |
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