7-Methoxy-2-(1-methyl-4-phenyl-1H-imidazol-5-yl)[1,3]thiazolo[5,4-d]pyrimidine → 2-(2-Bromo-1-methyl-4-phenyl-1H-imidazol-5-yl)-7-methoxy[1,3]thiazolo[5,4-d]pyrimidine
Reaction equation
[Br:1][C:2]1[N:3]([CH3:24])[C:4]([C:13]2[S:14][C:15]3[N:16]=[CH:17][N:18]=[C:19](SC)[C:20]=3[N:21]=2)=[C:5]([C:7]2[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=2)[N:6]=1.[CH3:25][O:26]C1C2N=C(C3N(C)C=NC=3C3C=CC=CC=3)SC=2N=CN=1.CN1C(C2SC3N=CN=C(SC)C=3N=2)=C(C2C=CC=CC=2)N=C1>>[Br:1][C:2]1[N:3]([CH3:24])[C:4]([C:13]2[S:14][C:15]3[N:16]=[CH:17][N:18]=[C:19]([O:26][CH3:25])[C:20]=3[N:21]=2)=[C:5]([C:7]2[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=2)[N:6]=1Participants
4
Reactant 3
Product 1
Procedure
The title compound was prepared by a similar process to that described for Intermediate 37 but using 7-Methoxy-2-(1-methyl-4-phenyl-1H-imidazol-5-yl)[1,3]thiazolo[5,4-d]pyrimidine (Example 33) in place of 2-(1-methyl-4-phenyl-1H-imidazol-5-yl)-7-(methylthio)[1,3]thiazolo[5,4-d]pyrimidine (Intermediate 42). Light brown solid (0.47 g, 45%);
Sources & evidence
- ORD record
- ord-2eaac9c14bb94d5f84938ce52fd54b81
- Source dataset
- uspto-grants-2008_09
- Patent number
- US07427616B2
Reaction notes
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