5-Bromoindole → 5-(Thiophen-3-yl)-1H-indole
Reaction equation
Br[C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[NH:7][CH:6]=[CH:5]2.[S:11]1[CH:15]=[CH:14][C:13](B(O)O)=[CH:12]1>>[S:11]1[CH:15]=[CH:14][C:13]([C:2]2[CH:3]=[C:4]3[C:8](=[CH:9][CH:10]=2)[NH:7][CH:6]=[CH:5]3)=[CH:12]1Participants
3
Procedure
The title compound was prepared as in (D29) from 5-bromoindole and thiophene-3-boronic acid to give (D40) (1.1 g, 100%).
Workup
- customto give (D40) (1.1 g, 100%)
Sources & evidence
- ORD record
- ord-ba417346bf6e4daf94f286c3bb3ecfbd
- Source dataset
- uspto-grants-1998_11
- Patent number
- US05834494
Reaction notes
Loading…