Aniline → N-phenyl-2-methyl-2-(6-methyl-5-phenyl-2 3-dihydro-4-oxo-4H-1,3-oxazin-3-yl)-propanamide
Reaktionsgleichung
[CH3:1][C:2]([N:7]1[C:12](=[O:13])[C:11]([C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)=[C:10]([CH3:20])[O:9][CH2:8]1)([CH3:6])[C:3]([OH:5])=O.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.[NH2:40][C:41]1[CH:46]=[CH:45][CH:44]=[CH:43][CH:42]=1.C(N(CC)CC)C>C(Cl)(Cl)(Cl)Cl.C(Cl)Cl>[C:41]1([NH:40][C:3](=[O:5])[C:2]([CH3:1])([N:7]2[C:12](=[O:13])[C:11]([C:14]3[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=3)=[C:10]([CH3:20])[O:9][CH2:8]2)[CH3:6])[CH:46]=[CH:45][CH:44]=[CH:43][CH:42]=1Komponenten
6
Edukt 4
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
To a suspension of 2-methyl-2-(6-methyl-5-phenyl-2,3-dihydro-4-oxo-4H-1,3-oxazin-3-yl)-propionic acid (0.83 g) in 10.4 ml of CCl4 --CH2Cl2 (1:1) was added triphenylphosphin (1.04 g), then the mixture was refluxed for 40 min. The reaction mixture was ice-cooled and aniline (0.28 g) and triethylamine (0.3 g) were slowly added, then it was stirred at room temperature for 1 h. After evaporation of the solvent, the residue was dissolved in ethyl acetate. The insolubles were filtered off and the filtrate was evaporated. The residue was purified by chromatography on a silica gel column to get the captioned compound (0.58 g).
Aufarbeitung
- temperaturethe mixture was refluxed for 40 min
- temperaturecooled
- customAfter evaporation of the solvent
- dissolutionthe residue was dissolved in ethyl acetate
- filtrationThe insolubles were filtered off
- customthe filtrate was evaporated
- customThe residue was purified by chromatography on a silica gel column
Quellen und Nachweise
- ORD-Eintrag
- ord-b620cbd457d64dee8bd73ac6f4c4cc3d
- Quelldatensatz
- uspto-grants-1999_11
- Patentnummer
- US05977025
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