Pyridinium hydrochloride → 4-Chloro-2-(5-fluoro-2-oxo-1,2-dihydropyridin-4-yl)benzonitrile
Reaction equation
[Cl:1][C:2]1[CH:9]=[CH:8][C:5]([C:6]#[N:7])=[C:4]([C:10]2[C:15]([F:16])=[CH:14][N:13]=[C:12]([O:17]C)[CH:11]=2)[CH:3]=1.Cl.[NH+]1C=CC=CC=1>>[Cl:1][C:2]1[CH:9]=[CH:8][C:5]([C:6]#[N:7])=[C:4]([C:10]2[C:15]([F:16])=[CH:14][NH:13][C:12](=[O:17])[CH:11]=2)[CH:3]=1Participants
3
Procedure
210 mg (0.77 mmol) of 4-chloro-2-(5-fluoro-2-methoxypyridin-4-yl)benzonitrile and pyridinium hydrochloride were reacted according to General Method 3A. Yield: 126 mg (66% of theory)
Sources & evidence
- ORD record
- ord-da6364b525004cfab0217d65648a0eb7
- Source dataset
- uspto-grants-2016_09
- Patent number
- US09434690B2
Reaction notes
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