Ethanol → 1-(4-oxo-3,4,6,7,8,9-hexahydro-benzo[g]quinazolin-2-yl)-1H-pyrazole-4-carboxylic acid
Reaktionsgleichung
C([O:3][C:4]([C:6]1[CH:7]=[N:8][N:9]([C:11]2[N:20](COCCOC)[C:19](=[O:27])[C:18]3[C:13](=[CH:14][C:15]4[CH2:31][CH2:30][CH2:29][CH2:28][C:16]=4[CH:17]=3)[N:12]=2)[CH:10]=1)=[O:5])C.C(O)C>CCOCC>[O:27]=[C:19]1[C:18]2[C:13](=[CH:14][C:15]3[CH2:31][CH2:30][CH2:29][CH2:28][C:16]=3[CH:17]=2)[N:12]=[C:11]([N:9]2[CH:10]=[C:6]([C:4]([OH:5])=[O:3])[CH:7]=[N:8]2)[NH:20]1Komponenten
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
Preparation of 1-(4-oxo-3,4,6,7,8,9-hexahydro-benzo[g]quinazolin-2-yl)-1H-pyrazole-4-carboxylic acid ethyl ester. HCl (4M in dioxane, 2.1 mL, 8.3 mmol) was added to a solution of 1-[3-(2-methoxy-ethoxymethyl)-4-oxo-3,4,6,7,8,9-hexahydro-benzo[g]quinazolin-2-yl]-1H-pyrazole-4-carboxylic acid ethyl ester (0.254 g, 0.596 mmol) and ethanol (2.0 mL). The reaction mixture was stirred at room temperature for 4 h, at which point ether (2 mL) was added and the precipitate was collected. The precipitate was triturated three times with ethanol, once with ethanol/THF (1:1), and once with DMSO. The filter cake was rinsed with ethanol and dried to yield the titled compound (89.4 mg, 44% yield). MS (ESI/Cl): mass calcd. for C18H18N4O3, 338.1; m/z found, 339.1 [M+H]+. 1H NMR (600 MHz, DMSO-d6): 12.66 (s, 1H), 8.98 (s, 1H), 8.30 (s, 1H), 7.84 (s, 1H), 7.40 (s, 1H), 4.30 (q, J=7.1 Hz, 2H), 2.95-2.83 (m, 4H), 1.82-1.74 (m, 4H), 1.32 (t, J=7.1 Hz, 3H).
Aufarbeitung
- additionwas added
- customthe precipitate was collected
- customThe precipitate was triturated three times with ethanol
- washThe filter cake was rinsed with ethanol
- customdried
Quellen und Nachweise
- ORD-Eintrag
- ord-69bcafbbd2344a63b4b765e6007ebfa1
- Quelldatensatz
- uspto-grants-2015_01
- Patentnummer
- US08937078B2
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