Reaktionsgleichung
[Cl:1][C:2]1[N:7]=[C:6](Cl)[C:5]([N+:9]([O-:11])=[O:10])=[C:4](Cl)[N:3]=1.[CH3:13][C:14]1[NH:18][N:17]=[C:16]([NH2:19])[CH:15]=1.[CH3:20][O-:21].[Na+]>>[Cl:1][C:2]1[N:7]=[C:6]([NH:19][C:16]2[CH:15]=[C:14]([CH3:13])[NH:18][N:17]=2)[C:5]([N+:9]([O-:11])=[O:10])=[C:4]([O:21][CH3:20])[N:3]=1Komponenten
4
Versuchsvorschrift
The title compound was prepared using a procedure similar to the one described for the synthesis of Intermediate 18 using 2,4,6-trichloro-5-nitropyrimidine (Intermediate 37), 5-methyl-1H-pyrazol-3-amine and sodium methoxide as the starting materials. LCMS: 285 [M+1].
Quellen und Nachweise
- ORD-Eintrag
- ord-142abff36d424c32981f1d185e0f9f1c
- Quelldatensatz
- uspto-grants-2013_07
- Patentnummer
- US08486966B2
Verknüpfte Notizen
Wird geladen…