Phosphorus pentachloride → HCID 12901645, Verbindung
Reaktionsgleichung
[NH2:1][C:2]1[N:7]=[C:6]([O:8][CH3:9])[C:5]([C:10]([OH:12])=O)=[CH:4][N:3]=1.P(Cl)(Cl)(Cl)(Cl)[Cl:14]>C(OCC)C>[ClH:14].[NH2:1][C:2]1[N:7]=[C:6]([O:8][CH3:9])[C:5]([C:10]([Cl:14])=[O:12])=[CH:4][N:3]=1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
To 16.9 g of 2-amino 4-methoxy 5-pyrimidinyl carboxylic acid prepared in stage 2, in suspension in 300 ml of anhydrous ethyl ether, were added at 0° C., 20.8 g of phosphorous pentachloride while stirring. After returning to room temperature for 3 hours, the precipitate was separated by filtration, rinsed several times with 50 ml of absolute ethyl ether. The hydrochloride of the 2-amino 4-methoxy 5-chlorocarbonyl pyrimidine thus obtained was used in the raw state in the following stage.
Aufarbeitung
- customthe precipitate was separated by filtration
- washrinsed several times with 50 ml of absolute ethyl ether
Quellen und Nachweise
- ORD-Eintrag
- ord-e5e9dcf3a4c2432699fbb661ca6a4b19
- Quelldatensatz
- uspto-grants-1981_02
- Patentnummer
- US04250178
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