Reaktionsgleichung
[Cl:1][C:2]1[N:7]=[C:6]([CH3:8])[N:5]=[C:4]([NH2:9])[CH:3]=1.[I:10]Cl.S([O-])([O-])=O.[Na+].[Na+]>CO>[Cl:1][C:2]1[N:7]=[C:6]([CH3:8])[N:5]=[C:4]([NH2:9])[C:3]=1[I:10]Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 2.5 °C
Versuchsvorschrift
Combine 6-chloro-2-methylpyrimidin-4-amine (708 g, 4.93 mol) and MeOH (7.08 L) in a 20 L round bottom flask equipped with a mechanical stirrer. Cool to 0-5° C. Add iodine monochloride (4.806 kg, 29.6 mol) dissolved in MeOH (6 L) using an addition funnel over a period of 1 h. Warm the reaction mixture to RT and stir at RT for 16 h. Cool the reaction mixture to 0-5° C. and add sodium sulfite (46 L, 20% aqueous solution). Filter the resulting solid and wash with water (2 L) followed by hexane (3 L). Dry the solid under vacuum to afford the title compound as a white solid (1061 g, 80%). LC-ES/MS m/z 269.9 (M+1).
Aufarbeitung
- customof 1 h
- temperatureWarm the reaction mixture to RT
- temperatureCool the reaction mixture to 0-5° C.
- filtrationFilter the resulting solid
- washwash with water (2 L)
- customDry the solid under vacuum
Quellen und Nachweise
- ORD-Eintrag
- ord-f70f3c19650644a99b8c0b25040f25f2
- Quelldatensatz
- uspto-grants-2015_05
- Patentnummer
- US09035051B1
Verknüpfte Notizen
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