Reaktionsgleichung
CN1[C:10]2[C:9](=O)NC(=O)N[C:5]=2N=C1.N1C=[CH:17][C:16](=O)NC1=O.C[Si](C)(C)[CH2:23][CH2:24][O:25][CH2:26][Cl:27]>>[CH2:24]([O:25][CH2:26][Cl:27])[C:23]1[CH:17]=[CH:16][CH:9]=[CH:10][CH:5]=1Komponenten
4
Versuchsvorschrift
In a similar manner to the procedures described in Reference Example 3, reactions were carried out using 7-methylxanthine, instead of pyrimidine-2,4-dione, and using 2-(trimethylsilyl)ethoxymethyl chloride, instead of benzyloxymethyl chloride, to give the title compound (yield 69%) as a pale yellow powder.
Quellen und Nachweise
- ORD-Eintrag
- ord-aabbc1fe7b634686ad862928f82d70f5
- Quelldatensatz
- uspto-grants-2004_01
- Patentnummer
- US06673804B1
Verknüpfte Notizen
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