3-Bromopyridine → HCID 66764988, compound
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][CH:10]=2)[CH:5]=[CH:6][CH:7]=1.Br[C:20]1[CH:21]=[N:22][CH:23]=[CH:24][CH:25]=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:20]3[CH:21]=[N:22][CH:23]=[CH:24][CH:25]=3)[CH:10]=2)[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-1H-indole and 3-bromopyridine.
Workup
- customPrepared
Sources & evidence
- ORD record
- ord-76a55ab4138a4e078fe2175c6a90115c
- Source dataset
- uspto-grants-2015_04
- Patent number
- US09000025B2
Reaction notes
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