2-(Chloromethyl)-3-methylpyridine hydrochloride → 3-[2-Methyl-1-(3-methyl-pyridin-2-ylmethyl)-1H-imidazol-4-ylethynyl]-benzonitrile
Reaction equation
[CH3:1][C:2]1[NH:3][CH:4]=[C:5]([C:7]#[C:8][C:9]2[CH:10]=[C:11]([CH:14]=[CH:15][CH:16]=2)[C:12]#[N:13])[N:6]=1.Cl.Cl[CH2:19][C:20]1[C:25]([CH3:26])=[CH:24][CH:23]=[CH:22][N:21]=1>>[CH3:1][C:2]1[N:3]([CH2:19][C:20]2[C:25]([CH3:26])=[CH:24][CH:23]=[CH:22][N:21]=2)[CH:4]=[C:5]([C:7]#[C:8][C:9]2[CH:10]=[C:11]([CH:14]=[CH:15][CH:16]=2)[C:12]#[N:13])[N:6]=1Participants
3
Procedure
The title compound, MS: m/e=313.2 (M+H+), was prepared in accordance with the general method of example 1 from 3-(2-methyl-1H-imidazol-4-ylethynyl)-benzonitrile and 2-chloromethyl-3-methyl-pyridine hydrochloride.
Sources & evidence
- ORD record
- ord-37da713474d94d63aa65a6b65c5abca0
- Source dataset
- uspto-grants-2011_06
- Patent number
- US07964620B2
Reaction notes
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