1-(4-((2H-1,2,3-triazol-4-yl)methoxy)-3-fluorophenyl)-1H-tetrazole → 5-Ethyl-2-((trans)-3-fluoro-4-(4-((2-fluoro-4-(1H-tetrazol-1-yl)phenoxy)methyl)-2H-1,2,3-triazol-2-yl)piperidin-1-yl)pyrimidine
Reaction equation
[N:1]1[NH:2][N:3]=[C:4]([CH2:6][O:7][C:8]2[CH:13]=[CH:12][C:11]([N:14]3[CH:18]=[N:17][N:16]=[N:15]3)=[CH:10][C:9]=2[F:19])[CH:5]=1.[CH2:20]([C:22]1[CH:23]=[N:24][C:25]([N:28]2[CH2:33][CH2:32][C@H:31](O)[C@H:30]([F:35])[CH2:29]2)=[N:26][CH:27]=1)[CH3:21]>>[CH2:20]([C:22]1[CH:23]=[N:24][C:25]([N:28]2[CH2:33][CH2:32][C@@H:31]([N:2]3[N:3]=[C:4]([CH2:6][O:7][C:8]4[CH:13]=[CH:12][C:11]([N:14]5[CH:18]=[N:17][N:16]=[N:15]5)=[CH:10][C:9]=4[F:19])[CH:5]=[N:1]3)[C@H:30]([F:35])[CH2:29]2)=[N:26][CH:27]=1)[CH3:21]Participants
3
Reactant 2
Product 1
Procedure
The title compound was synthesized using 1-(4-((2H-1,2,3-triazol-4-yl)methoxy)-3-fluorophenyl)-1H-tetrazole (Intermediate 16) and cis-1-(5-ethylpyrimidin-2-yl)-3-fluoropiperidin-4-ol (Intermediate 17) in a manner similar to that described in Example 29.
Sources & evidence
- ORD record
- ord-770b48060d384af98762675d864d7990
- Source dataset
- uspto-grants-2014_09
- Patent number
- US08846675B2
Reaction notes
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