Uracil → Benzyl chloromethyl ether
Reaction equation
F[C:2](F)(F)[C:3]1[C:4](=[O:10])NC(=O)N[CH:8]=1.N1[CH:18]=[CH:17][C:16](=O)NC1=O.C[Si](C)(C)CCO[CH2:26][Cl:27]>>[CH2:4]([O:10][CH2:26][Cl:27])[C:3]1[CH:2]=[CH:18][CH:17]=[CH:16][CH:8]=1Participants
4
Procedure
In a similar manner to the procedures described in Reference Example 3, reactions were carried out using 5-trifluoromethylpyrimidine-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 76%) as a white powder.
Sources & evidence
- ORD record
- ord-2ff02496eb1e41ebaf56a098b7c7495a
- Source dataset
- uspto-grants-2004_01
- Patent number
- US06673804B1
Reaction notes
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