反応式
N1[C:10]2[C:5](=NC=CN=2)[C:4](=O)NC1=O.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:4]=[CH:5][CH:10]=[CH:17][CH:16]=1参加物
4
実験手順
In a similar manner to the procedures described in Reference Example 3, reactions were carried out using pteridin-2,4-dione, instead of pyrimidine-2,4-dione, and using 2-(trimethylsilyl)ethoxymethyl chloride, instead of benzyloxymethyl chloride, to give the title compound (yield 53%) as a yellow powder.
出典と根拠
- ORDレコード
- ord-85db933605be4fb6a518977183ca41e0
- 出典データセット
- uspto-grants-2004_01
- 特許番号
- US06673804B1
関連ノート
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