7-Nitroquinazolin-4(3H)-one → 7-Amino-quinazolin-4-ol
Reaktionsgleichung
[N+:1]([C:4]1[CH:13]=[C:12]2[C:7]([C:8](=[O:14])[NH:9][CH:10]=[N:11]2)=[CH:6][CH:5]=1)([O-])=O>CO.[Pd]>[NH2:1][C:4]1[CH:13]=[C:12]2[C:7]([C:8](=[O:14])[NH:9][CH:10]=[N:11]2)=[CH:6][CH:5]=1Komponenten
4
Edukt 1
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 2
Versuchsvorschrift
Pd/C (100 mg) was added as a single portion to a degassed and flushed (3×Ar) suspension of 7-nitroquinazolin-4-one (1.15 g, 6.02 mmol) in methanol (150 mL). The resulting black mixture was degassed, flushed with hydrogen and allowed to stir for 4 hours. The mixture was filtered through celite, washed well with methanol, and the filtrate concentrated to give a tanned solid. This was purified by column chromatography (silica) using 10% methanol/ethyl acetate as the eluent. Combined fractions gave a beige solid (949 mg, 98% yield).
Aufarbeitung
- customa degassed
- customflushed
- customThe resulting black mixture was degassed
- customflushed with hydrogen
- filtrationThe mixture was filtered through celite
- washwashed well with methanol
- concentrationthe filtrate concentrated
- customto give a tanned solid
- customThis was purified by column chromatography (silica)
Quellen und Nachweise
- ORD-Eintrag
- ord-0d04f88957a74bfa9a556ca827f0dfd3
- Quelldatensatz
- uspto-grants-2011_05
- Patentnummer
- US07951955B2
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