5-Bromoindole → 5-Bromoindoline
Reaction equation
[Br:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[NH:7][CH:6]=[CH:5]2.C([BH3-])#N.[Na+]>>[Br:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[NH:7][CH2:6][CH2:5]2Participants
3
Procedure
5-Bromoindole (0.7 g, 3.6 mmol) was treated with sodium cyanoborohydride as in the method of Description 10 to yield the title compound (0.5 g, 71%).
Sources & evidence
- ORD record
- ord-949ff44e6d7c45ba94b489f276085474
- Source dataset
- uspto-grants-1998_11
- Patent number
- US05834494
Reaction notes
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