5-Bromo-2-(methylthio)pyrimidine-4-carbaldehyde → (S)-N-((5-bromo-2-(methylthio)pyrimidin-4-yl)methylene)-2-methylpropane-2-sulfinamide
Reaktionsgleichung
[Br:1][C:2]1C=C[C:5]([NH:16][C:17](=O)C)=[N:6][C:7]=1[CH:8]=[N:9][S@:10]([C:12]([CH3:15])([CH3:14])[CH3:13])=[O:11].BrC1C(C=O)=N[C:24]([S:27]C)=NC=1>>[Br:1][C:2]1[C:7]([CH:8]=[N:9][S@:10]([C:12]([CH3:13])([CH3:14])[CH3:15])=[O:11])=[N:6][C:5]([S:27][CH3:24])=[N:16][CH:17]=1Komponenten
3
Versuchsvorschrift
The title compound (11C) was prepared according to the method presented for the synthesis of compound 1D of Example 1 utilizing 11B. MS (m/z) 337.7 [M+H]+.
Quellen und Nachweise
- ORD-Eintrag
- ord-a1e710f277da4f048505b59ae3a399c1
- Quelldatensatz
- uspto-grants-2015_06
- Patentnummer
- US09050344B2
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