4-chloro-2-(difluoromethyl)-1H-indole-5-carbonitrile → 4-Chloro-2-(difluoromethyl)-1-{2-[(6-fluoro-3-pyridinyl)oxy]ethyl}-1H-indole-5-carbonitrile
Reaction equation
[Cl:1][C:2]1[C:10]([C:11]#[N:12])=[CH:9][CH:8]=[C:7]2[C:3]=1[CH:4]=[C:5]([CH:13]([F:15])[F:14])[NH:6]2.Br[CH2:17][CH2:18][O:19][C:20]1[CH:21]=[CH:22][C:23]([F:26])=[N:24][CH:25]=1>>[Cl:1][C:2]1[C:10]([C:11]#[N:12])=[CH:9][CH:8]=[C:7]2[C:3]=1[CH:4]=[C:5]([CH:13]([F:14])[F:15])[N:6]2[CH2:17][CH2:18][O:19][C:20]1[CH:25]=[N:24][C:23]([F:26])=[CH:22][CH:21]=1Participants
3
Procedure
Synthesized as described in Example 39 from 4-chloro-2-(difluoromethyl)-1H-indole-5-carbonitrile and 5-[(2-bromoethyl)oxy]-2-fluoropyridine: MS (ESI) m/z 366 (M+1).
Workup
- customSynthesized
Sources & evidence
- ORD record
- ord-cdf8458feb754cee9047a0d6c2994022
- Source dataset
- uspto-grants-2014_03
- Patent number
- US08673948B2
Reaction notes
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