2-Chloro-4-fluoropyridine → 2-Chloro-4-(2-methyl-4-m-tolylethynyl-imidazol-1-yl)-pyridine
Reaction equation
[CH3:1][C:2]1[NH:3][CH:4]=[C:5]([C:7]#[C:8][C:9]2[CH:10]=[C:11]([CH3:15])[CH:12]=[CH:13][CH:14]=2)[N:6]=1.[Cl:16][C:17]1[CH:22]=[C:21](F)[CH:20]=[CH:19][N:18]=1>>[Cl:16][C:17]1[CH:22]=[C:21]([N:3]2[CH:4]=[C:5]([C:7]#[C:8][C:9]3[CH:10]=[C:11]([CH3:15])[CH:12]=[CH:13][CH:14]=3)[N:6]=[C:2]2[CH3:1])[CH:20]=[CH:19][N:18]=1Participants
3
Procedure
The title compound, light brown solid, MS: m/e=308.2, 310.1 (M+H+) was prepared in accordance with the general method of example 1b from 2-Methyl-4-m-tolylethynyl-1H-imidazole and 2-chloro-4-fluoropyridine
Sources & evidence
- ORD record
- ord-6162accd8436405ebccb93c94bf14c73
- Source dataset
- uspto-grants-2012_12
- Patent number
- US08334287B2
Reaction notes
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