Thiophenol → 5-Bromo-2-chloro-4-(phenylthio)pyrimidine
Reaction equation
[Br:1][C:2]1[C:3](Cl)=[N:4][C:5]([Cl:8])=[N:6][CH:7]=1.[C:10]1([SH:16])[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1>>[Br:1][C:2]1[C:3]([S:16][C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=2)=[N:4][C:5]([Cl:8])=[N:6][CH:7]=1Participants
3
Procedure
Using an analogous method to that described in Method 1, but starting from 5-bromo-2,4-dichloropyrimidine and thiophenol, the product was obtained. NMR: 7.6 (m, 5H), 8.8 (s, 1H).
Workup
- customthe product was obtained
Sources & evidence
- ORD record
- ord-99b646fbcedb4fa08746bae593920360
- Source dataset
- uspto-grants-2004_03
- Patent number
- US06710052B2
Reaction notes
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