Reaktionsgleichung
[CH3:1][O:2][CH2:3][C:4](Cl)=[O:5].[NH2:7][C:8]1[N:13]=[C:12]([NH2:14])[N:11]=[C:10]([NH:15][CH:16]2[CH2:18][CH2:17]2)[N:9]=1>N1C=CC=CC=1>[CH3:1][O:2][CH2:3][C:4]([NH:14][C:12]1[N:13]=[C:8]([NH:7][C:4](=[O:5])[CH2:3][O:2][CH3:1])[N:9]=[C:10]([NH:15][CH:16]2[CH2:18][CH2:17]2)[N:11]=1)=[O:5]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 55 °C
Versuchsvorschrift
7.2 g of methoxyacetyl chloride are slowly added dropwise to a suspension of 5.0 g of 2,4-diamino-6-cyclopropylamino-1,3,5-triazine in 50 ml of pyridine. The reaction mixture is subsequently stirred for 1 hour at 55° C. and then for 16 hours at room temperature. After filtration of the reaction mixture, washing of the filter residue with water and finally drying, the product is obtained as white crystalline powder having a melting point of 175°-180° C.
Aufarbeitung
- waitfor 16 hours at room temperature
- filtrationAfter filtration of the reaction mixture
- washwashing of the filter residue with water
- customfinally drying
- customthe product is obtained as white crystalline powder
Quellen und Nachweise
- ORD-Eintrag
- ord-575bb544b3f7463cbafef8e1b91c713a
- Quelldatensatz
- uspto-grants-1989_04
- Patentnummer
- US04824845
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