Reaktionsgleichung
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[N:17]=[C:16](O)[C:15]3[CH2:14][CH2:13][CH2:12][CH2:11][C:10]=3[N:9]=2)=[CH:4][CH:3]=1.P(Cl)(Cl)([Cl:21])=O>>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[N:17]=[C:16]([Cl:21])[C:15]3[CH2:14][CH2:13][CH2:12][CH2:11][C:10]=3[N:9]=2)=[CH:4][CH:3]=1Komponenten
3
Versuchsvorschrift
8.0 g of 2-(4-chlorophenyl)-4-hydroxy-5,6,7,8-tetrahydroquinazoline were heated to 100° C. in 10 ml of phosphorus oxychloride. After 3 hours, the cooled solution was carefully poured onto ice water. The crystalline product was filtered off with suction, washed well with water and dried in vacuo at room temperature. Yield: 6.2 g; m.p.: 121° C.
Aufarbeitung
- additionthe cooled solution was carefully poured onto ice water
- filtrationThe crystalline product was filtered off with suction
- washwashed well with water
- customdried in vacuo at room temperature
Quellen und Nachweise
- ORD-Eintrag
- ord-17378f48516545b6a8122404210c0143
- Quelldatensatz
- uspto-grants-2006_05
- Patentnummer
- US07045526B2
Verknüpfte Notizen
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