Indole → 3-Bromo-1h-indole
Reaction equation
[NH:1]1[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[CH:3]=[CH:2]1.[Br:10]N1C(=O)CCC1=O>>[Br:10][C:3]1[C:4]2[C:9](=[CH:8][CH:7]=[CH:6][CH:5]=2)[NH:1][CH:2]=1Participants
3
Reactant 2
Product 1
Procedure
In step 3 indole compound k undergoes bromination by treatment with N-bromosuccinimide or other bromime source (not shown) to yield 3-bromo indole compound l. Bromoindole l is then subject to oxidation in step 4 to provide dihydroindolone compound m. Compound m is a compound of formula I in accordance with the invention.
Sources & evidence
- ORD record
- ord-1537cf4be3484571bd51d70d51c62c2d
- Source dataset
- uspto-grants-2009_09
- Patent number
- US07582760B2
Reaction notes
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