2H-1,2,4-Oxadiazin-3(4H)-one, dihydro-5-thioxo- → HCID 178442899, Verbindung
Reaktionsgleichung
[O:1]1[CH2:6][C:5](=S)[NH:4][C:3](=[O:8])[NH:2]1.[CH2:9]([NH2:27])[CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16]/[CH:17]=[CH:18]\[CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH3:26]>>[CH2:9]([NH:27][C:5]1[CH2:6][O:1][NH:2][C:3](=[O:8])[N:4]=1)[CH2:10][CH2:11][CH:12]=[CH:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH3:26]Komponenten
3
Versuchsvorschrift
To 0.66 g (0.005 mole) of 6H-1,2,4-oxadiazin-3(2H)-one-5(4H)-thione dissolved in 10 ml of freshly distilled dry dioxane is added 1.33 g (0.0051 mole) of oleylamine. The reaction mixture is stirred for 17 hours at room temperature and the crystalline material filtered, washed with additional dry dioxane and chloroform, and dried to give 0.3 g (16 percent) of 5-(4-octadecenylamino)-6H-1,2,4-oxadiazin-3(2H)-one.
Aufarbeitung
- distillationof freshly distilled dry dioxane
- filtrationthe crystalline material filtered
- washwashed with additional dry dioxane and chloroform
- customdried
Quellen und Nachweise
- ORD-Eintrag
- ord-f780cc7bcec741a1980ac2d72229e5d4
- Quelldatensatz
- uspto-grants-1984_07
- Patentnummer
- US04459403
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