Acetonitrile → HCID 58215831, compound
Reaction equation
[F:1][C:2]1[CH:3]=[C:4]([C:8]2[NH:9][C:10]3[C:15]([CH:16]=2)=[CH:14][CH:13]=[CH:12][CH:11]=3)[CH:5]=[N:6][CH:7]=1.ClCCl.[C:20](#[N:22])C>>[F:1][C:2]1[CH:3]=[C:4]([C:8]2[NH:9][C:10]3[C:15]([C:16]=2[C:20]#[N:22])=[CH:14][CH:13]=[CH:12][CH:11]=3)[CH:5]=[N:6][CH:7]=1Participants
4
Procedure
2-(5-Fluoro-pyridin-3-yl)-1H-indole (Example 92) is processed according to the method described in Example 140, using a mixture of dichloromethane and acetonitrile instead of dichloromethane, to give 2-(5-fluoro-pyridin-3-yl)-1H-indole-3-carbonitrile. MS (ESI) m/z 238.0 (M+H)+.
Sources & evidence
- ORD record
- ord-2ef200702bbc47ccb2830bc718c32065
- Source dataset
- uspto-grants-2011_10
- Patent number
- US08030334B2
Reaction notes
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