Potassium Carbonate → Pyrazino[2,3-c]quinolin-5-amine
Reaktionsgleichung
C(OC([NH:8][C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=1B(O)O)=O)(C)(C)C.Cl[C:19]1[C:20]([C:25]#[N:26])=[N:21][CH:22]=[CH:23][N:24]=1.C(=O)([O-])[O-].[K+].[K+]>C1(C)C=CC=CC=1.CO.ClCCl.O>[N:24]1[C:19]2[C:14]3[CH:13]=[CH:12][CH:11]=[CH:10][C:9]=3[N:8]=[C:25]([NH2:26])[C:20]=2[N:21]=[CH:22][CH:23]=1Komponenten
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 4
Reaktionsbedingungen
- Temperatur
- 100 °C
Versuchsvorschrift
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
Aufarbeitung
- temperatureAfter cooling to ambient temperature
- customThe two phases were separated
- extractionthe aqueous layer was extracted twice with 2% methanol in dichloromethane
- washThe combined organic layers were washed with brine
- dry with materialdried over anhydrous MgSO4
- concentrationconcentrated en vacuo
- customThe crude product was purified by flash chromatography on a COMBIFLASH® system (ISCO)
- customto give a solid
Quellen und Nachweise
- ORD-Eintrag
- ord-328bbb2683bf4e94b5d867507ecae260
- Quelldatensatz
- uspto-grants-2014_11
- Patentnummer
- US08895577B2
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