N-Iodosuccinimide → 5-Iodo-2-methylsulfanyl-6-(3-trifluoromethyl-phenyl)-pyrimidin-4-ylamine
Reaction equation
[CH3:1][S:2][C:3]1[N:8]=[C:7]([NH2:9])[CH:6]=[C:5]([C:10]2[CH:15]=[CH:14][CH:13]=[C:12]([C:16]([F:19])([F:18])[F:17])[CH:11]=2)[N:4]=1.C1C(=O)N([I:27])C(=O)C1>>[I:27][C:6]1[C:7]([NH2:9])=[N:8][C:3]([S:2][CH3:1])=[N:4][C:5]=1[C:10]1[CH:15]=[CH:14][CH:13]=[C:12]([C:16]([F:19])([F:17])[F:18])[CH:11]=1Participants
3
Procedure
The title compound is synthesized according to general procedure GP2 starting from 2.0 g (7.0 mmol) 2-methylsulfanyl-6-(3-trifluoromethyl-phenyl)-pyrimidin-4-ylamine and 1.6 g (7.0 mmol) NIS. Yield after precipitation: 1.9 g (66%).
Workup
- customYield
- customafter precipitation
Sources & evidence
- ORD record
- ord-9f61f229d26842f7bf28adfc27d02f10
- Source dataset
- uspto-grants-2014_12
- Patent number
- US08916548B2
Reaction notes
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