Methyl iodide → HCID 58464069, compound
Reaction equation
[F:1][C:2]1[CH:3]=[C:4]([C:8]#[C:9][C:10]2[N:11]=[CH:12][C:13]([N:16]3[CH2:21][CH2:20][C:19]([CH3:23])([CH3:22])[NH:18][C:17]3=[O:24])=[N:14][CH:15]=2)[CH:5]=[CH:6][CH:7]=1.[CH3:25]I>>[F:1][C:2]1[CH:3]=[C:4]([C:8]#[C:9][C:10]2[N:11]=[CH:12][C:13]([N:16]3[CH2:21][CH2:20][C:19]([CH3:22])([CH3:23])[N:18]([CH3:25])[C:17]3=[O:24])=[N:14][CH:15]=2)[CH:5]=[CH:6][CH:7]=1Participants
3
Procedure
The title compound, a light yellow solid, MS: m/e=339.1 (M+H+), was prepared in accordance with the general method of Example 165, by alkylation of 1-(5-((3-fluorophenyl)ethynyl)pyrazin-2-yl)-4,4-dimethyltetrahydropyrimidin-2(1H)-one (Example 166) with methyl iodide.
Sources & evidence
- ORD record
- ord-3bd9b7b2baa149ae962b9bea3e39ffb2
- Source dataset
- uspto-grants-2013_08
- Patent number
- US08513273B2
Reaction notes
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