Trimethylsilyl iodide → 2,4-Diamino-5-(2,3,5-trichlorophenyl)-6-hydroxymethylpyrimidine
Reaction equation
[NH2:1][C:2]1[N:7]=[C:6]([NH2:8])[C:5]([C:9]2[CH:14]=[C:13]([Cl:15])[CH:12]=[C:11]([Cl:16])[C:10]=2[Cl:17])=[C:4]([CH2:18][O:19]C)[N:3]=1.C[Si](I)(C)C>S1(CCCC1)(=O)=O>[NH2:1][C:2]1[N:7]=[C:6]([NH2:8])[C:5]([C:9]2[CH:14]=[C:13]([Cl:15])[CH:12]=[C:11]([Cl:16])[C:10]=2[Cl:17])=[C:4]([CH2:18][OH:19])[N:3]=1Participants
4
Procedure
This compound was made from the compound of Example 2 by reaction with trimethylsilyl iodide in sulpholane at 80° C. mp. 101°-105° C.
Sources & evidence
- ORD record
- ord-be5085cbe9f54f88b3cc5a6a5f8fa5a9
- Source dataset
- uspto-grants-1992_08
- Patent number
- US05136080
Reaction notes
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