Phenyl isocyanate → (5RS, 6SR)-6-phenyl-5-phenylcarbamoyloxy-2-(2-thienyl)-5,6-dihydro-4H-1,3-oxazine
Reaktionsgleichung
[C:1]1([CH:7]2[O:12][C:11]([C:13]3[S:14][CH:15]=[CH:16][CH:17]=3)=[N:10][CH2:9][CH:8]2[OH:18])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[C:19]1([N:25]=[C:26]=[O:27])[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1>>[C:1]1([CH:7]2[O:12][C:11]([C:13]3[S:14][CH:15]=[CH:16][CH:17]=3)=[N:10][CH2:9][CH:8]2[O:18][C:26](=[O:27])[NH:25][C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=2)[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1Komponenten
3
Versuchsvorschrift
Working in a manner similar to that described in Example 12, but starting with (5RS, 6SR)-6-phenyl-2-(2-thienyl)-5,6-dihydro-4H-1,3-oxazin-5-ol (1.55 g) and phenyl isocyanate (0.8 g), and after recrystallization in isopropanol, (5RS, 6SR)-6-phenyl-5-phenylcarbamoyloxy-2-(2-thienyl)-5,6-dihydro-4H-1,3-oxazine (1.75 g), m.p. 98° C., is obtained.
Aufarbeitung
- customafter recrystallization in isopropanol
Quellen und Nachweise
- ORD-Eintrag
- ord-2ed86a68dbc64c41b093204cb75cf510
- Quelldatensatz
- uspto-grants-1991_02
- Patentnummer
- US04994569
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