3-Bromopyridine → 3-(3-Bromo-phenylsulfanyl)-6-chloro-2-methyl-1-pyridin-3-yl-1H-indole
Reaction equation
[Br:1][C:2]1[CH:3]=[C:4]([S:8][C:9]2[C:17]3[C:12](=[CH:13][C:14]([Cl:18])=[CH:15][CH:16]=3)[NH:11][C:10]=2[CH3:19])[CH:5]=[CH:6][CH:7]=1.Br[C:21]1[CH:22]=[N:23][CH:24]=[CH:25][CH:26]=1>>[Br:1][C:2]1[CH:3]=[C:4]([S:8][C:9]2[C:17]3[C:12](=[CH:13][C:14]([Cl:18])=[CH:15][CH:16]=3)[N:11]([C:21]3[CH:22]=[N:23][CH:24]=[CH:25][CH:26]=3)[C:10]=2[CH3:19])[CH:5]=[CH:6][CH:7]=1Participants
3
Procedure
Prepared according to the procedure described in Example 27, Step 1, using the following starting materials: 3-(3-bromo-phenylsulfanyl)-6-chloro-2-methyl-1H-indole and 3-bromopyridine.
Workup
- customPrepared
Sources & evidence
- ORD record
- ord-6b20cceb68694c6bbeebced0c066545e
- Source dataset