6-(1-Methyl-4-phenyl-1H-imidazol-5-yl)-4-(methylsulfonyl)thieno[2,3-d]pyrimidine → 6-(4-(3-iodophenyl)-1-methyl-1H-imidazol-5-yl)-4-(methylsulfonyl)thieno[2,3-d]pyrimidine
Reaction equation
[CH3:1][N:2]1[C:6]([C:7]2[S:19][C:10]3[N:11]=[CH:12][N:13]=[C:14]([S:15]([CH3:18])(=[O:17])=[O:16])[C:9]=3[CH:8]=2)=[C:5]([C:20]2[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=2)[N:4]=[CH:3]1.[I:26]C1C=C(C2N=CN(C)C=2C2SC3N=CN=C(SC)C=3C=2)C=CC=1>>[I:26][C:22]1[CH:21]=[C:20]([C:5]2[N:4]=[CH:3][N:2]([CH3:1])[C:6]=2[C:7]2[S:19][C:10]3[N:11]=[CH:12][N:13]=[C:14]([S:15]([CH3:18])(=[O:17])=[O:16])[C:9]=3[CH:8]=2)[CH:25]=[CH:24][CH:23]=1Participants
3
Reactant 2
Product 1
Procedure
The title compound was prepared by a similar process to that described for Intermediate 17 but using 6-[4-(3-iodophenyl)-1-methyl-1H-imidazol-5-yl]-4-(methylthio)thieno[2,3-d]pyrimidine (Intermediate 54) in place of 6-(1-methyl-4-phenyl-1H-imidazol-5-yl)-4-(methylthio)thieno[2,3-d]pyrimidine (example 7). Yellow solid (220 mg, 68%);
Sources & evidence
- ORD record
- ord-0df96b4f8a25448c91eb5b29ebd04b76
- Source dataset
- uspto-grants-2008_09
- Patent number
- US07427616B2
Reaction notes
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