2-Fluoro-5-methylpyridine → HCID 66879278, compound
Reaction equation
[CH3:1][C:2]1[NH:3][CH:4]=[C:5]([C:7]#[C:8][C:9]2[CH:14]=[CH:13][CH:12]=[C:11]([C:15]([F:18])([F:17])[F:16])[CH:10]=2)[N:6]=1.F[C:20]1[CH:25]=[CH:24][C:23]([CH3:26])=[CH:22][N:21]=1>>[CH3:26][C:23]1[CH:24]=[CH:25][C:20]([N:3]2[CH:4]=[C:5]([C:7]#[C:8][C:9]3[CH:14]=[CH:13][CH:12]=[C:11]([C:15]([F:18])([F:16])[F:17])[CH:10]=3)[N:6]=[C:2]2[CH3:1])=[N:21][CH:22]=1Participants
3
Procedure
The title compound, MS: m/e=342.1 (M+), was prepared in accordance with the general method of example 1 from 2-methyl-4-(3-trifluoromethyl-phenylethynyl)-1H-imidazole and 2-fluoro-5-methylpyridine.
Sources & evidence
- ORD record
- ord-981e90da98e2471e8d40ff2fa14bbc46
- Source dataset
- uspto-grants-2007_07
- Patent number
- US07241760B2
Reaction notes
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