m,alpha-Dichlorotoluene → 4-Amino-2-(3-chlorophenylmethylthio)-6-hydroxypyrimidine
Reaktionsgleichung
O.[NH2:2][C:3]1[CH:8]=[C:7]([OH:9])[N:6]=[C:5]([SH:10])[N:4]=1.[Cl:11][C:12]1[CH:13]=[C:14]([CH:17]=[CH:18][CH:19]=1)[CH2:15]Cl>>[NH2:2][C:3]1[N:4]=[C:5]([S:10][CH2:15][C:14]2[CH:17]=[CH:18][CH:19]=[C:12]([Cl:11])[CH:13]=2)[NH:6][C:7](=[O:9])[CH:8]=1Komponenten
3
Versuchsvorschrift
The subtitle compound was prepared according to the procedure of Example 1 step i) treating 4-amino-6-hydroxy-2-mercaptopyrimidine monohydrate (10.00 g) with 3-chlorobenzyl chloride (9.98 g) to afford the subtitle compound as a white solid. Yield: 15.00 g.
Aufarbeitung
- customThe subtitle compound was prepared
Quellen und Nachweise
- ORD-Eintrag
- ord-89c04bfe57524176ae897c385dc54249
- Quelldatensatz
- uspto-grants-2012_01
- Patentnummer
- US08106063B2
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