2,6-Difluoropyridine → 2-[4-[2-(3-Chlorophenyl)ethynyl]-2-methyl-1H-imidazol-1-yl]-6-fluoropyridine
Reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]([C:8]#[C:9][C:10]2[N:11]=[C:12]([CH3:15])[NH:13][CH:14]=2)[CH:5]=[CH:6][CH:7]=1.[F:16][C:17]1[CH:22]=[CH:21][CH:20]=[C:19](F)[N:18]=1>>[Cl:1][C:2]1[CH:3]=[C:4]([C:8]#[C:9][C:10]2[N:11]=[C:12]([CH3:15])[N:13]([C:19]3[CH:20]=[CH:21][CH:22]=[C:17]([F:16])[N:18]=3)[CH:14]=2)[CH:5]=[CH:6][CH:7]=1Participants
3
Procedure
The title compound, off-white cristalline solid, MS: m/e=312.1, 314.1 (M+H+) was prepared in accordance with the general method of example 1b from 4-(3-chloro-phenylethynyl)-2-methyl-1H-imidazole and 2,6-difluoropyridine.
Sources & evidence
- ORD record
- ord-3dc954d3c2ec41b79a846026d80a4578
- Source dataset
- uspto-grants-2012_12
- Patent number
- US08334287B2
Reaction notes
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