HCID 19787897, Verbindung → HCID 19787914, Verbindung
Reaktionsgleichung
C(OC([NH:11][C:12]1[C:17](=[O:18])[N:16]([CH2:19][C:20]([NH:22][CH:23]([CH:37]([CH3:39])[CH3:38])[CH:24]([O:29][Si:30]([C:33]([CH3:36])([CH3:35])[CH3:34])([CH3:32])[CH3:31])[C:25]([F:28])([F:27])[F:26])=[O:21])[C:15]([C:40]2[CH:45]=[CH:44][CH:43]=[CH:42][CH:41]=2)=[N:14][CH:13]=1)=O)C1C=CC=CC=1>O1CCCC1.C(O)C.[Pd]>[NH2:11][C:12]1[C:17](=[O:18])[N:16]([CH2:19][C:20]([NH:22][CH:23]([CH:37]([CH3:39])[CH3:38])[CH:24]([O:29][Si:30]([C:33]([CH3:36])([CH3:34])[CH3:35])([CH3:31])[CH3:32])[C:25]([F:28])([F:27])[F:26])=[O:21])[C:15]([C:40]2[CH:41]=[CH:42][CH:43]=[CH:44][CH:45]=2)=[N:14][CH:13]=1Komponenten
5
Edukt 1
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 3
Versuchsvorschrift
To a solution of 2-(5-benzyloxycarbonylamino-6-oxo-2-phenyl-1,6-dihydro-1-pyrimidinyl)-N-(2-tert-butyldimethylsilyloxy-3,3,3-trifluoro-1-isopropylpropyl)acetamide (12.4 g) in tetrahydrofuran (100 mL) and ethanol (60 mL) was added 10% (w/w) palladium on carbon (1 g) and the suspension was placed under a hydrogen atmosphere (3.4 bar) and shaken for 12 h. The solution was filtered through diatomaceous earth to give an oil which crystallized from ether to provide 2-(5-amino-6-oxo-2-phenyl-1,6-dihydro-1-pyrimidinyl)-N-(2-tert-butyldimethylsilyloxy-3,3,3-trifluoro-1-isopropylpropyl)acetamide as a white solid (8.7 g); MS: m/z=513(M+1).
Aufarbeitung
- filtrationThe solution was filtered through diatomaceous earth
- customto give an oil which
- customcrystallized from ether
Quellen und Nachweise
- ORD-Eintrag
- ord-d901f490fe994a828b1de93222f1ace3
- Quelldatensatz
- uspto-grants-1993_10
- Patentnummer
- US05254558
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